(471623, 'HP:0034974', 'Bathrocephaly', 'XPO:0142059', 'abnormal nasal region morphology', 0.45652173913043476, 4.5318002188002176, 1.4383550734357495, 'UPHENO:0087907', 'abnormal head morphology'),
(471624, 'HP:0034974', 'Bathrocephaly', 'XPO:0102538', 'abnormal lateral nasal prominence morphology', 0.4375, 4.5318002188002176, 1.4080705222839853, 'UPHENO:0087907', 'abnormal head morphology'),
(471625, 'HP:0034974', 'Bathrocephaly', 'XPO:0129688', 'increased size of the olfactory region', 0.5081967213114754, 7.024697770424301, 1.8894254087244782, 'HP:0000929', 'Abnormal skull morphology'),
(471626, 'HP:0034974', 'Bathrocephaly', 'XPO:0131600', 'decreased size of the intercanthal region', 0.40384615384615385, 4.5318002188002176, 1.3528303989641963, 'UPHENO:0087907', 'abnormal head morphology'),
(471627, 'HP:0034974', 'Bathrocephaly', 'XPO:0102401', 'abnormal neurocranium morphology', 0.5740740740740741, 7.024697770424301, 2.008157580521644, 'HP:0000929', 'Abnormal skull morphology'),
(471628, 'HP:0034974', 'Bathrocephaly', 'XPO:0130138', 'increased size of the braincase and otic capsule skeleton', 0.4126984126984127, 4.638757693672553, 1.3836213127410304, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(471629, 'HP:0034974', 'Bathrocephaly', 'XPO:0115526', 'abnormally incomplete structure of head', 0.45652173913043476, 4.5318002188002176, 1.4383550734357495, 'UPHENO:0087907', 'abnormal head morphology'),
(471630, 'HP:0034974', 'Bathrocephaly', 'XPO:0101764', 'abnormal cranium morphology', 0.5098039215686274, 4.638757693672553, 1.5378091115092631, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(471631, 'HP:0034974', 'Bathrocephaly', 'XPO:0139715', 'abnormally necrotic head', 0.42, 4.5318002188002176, 1.3796217205799897, 'UPHENO:0087907', 'abnormal head morphology'),
(471632, 'HP:0034974', 'Bathrocephaly', 'XPO:0130062', 'increased size of the head region', 0.40384615384615385, 4.5318002188002176, 1.3528303989641963, 'UPHENO:0087907', 'abnormal head morphology'),
(471633, 'HP:0034974', 'Bathrocephaly', 'XPO:0128846', 'decreased size of the choana', 0.47692307692307695, 7.024697770424301, 1.8303662133915815, 'HP:0000929', 'Abnormal skull morphology'),
(471634, 'HP:0034974', 'Bathrocephaly', 'XPO:0100420', 'abnormal choana', 0.4528301886792453, 4.5318002188002176, 1.4325278175784049, 'UPHENO:0087907', 'abnormal head morphology'),
(471635, 'HP:0034974', 'Bathrocephaly', 'XPO:0129771', 'increased size of the dermatocranium', 0.4262295081967213, 4.638757693672553, 1.4061206955371255, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(471636, 'HP:0034974', 'Bathrocephaly', 'XPO:0129718', 'increased size of the ethmoid region', 0.4406779661016949, 4.638757693672553, 1.4297546312868548, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(471637, 'HP:0034974', 'Bathrocephaly', 'XPO:0103332', 'decreased size of the chondrocranium', 0.4262295081967213, 4.638757693672553, 1.4061206955371255, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(471638, 'HP:0034974', 'Bathrocephaly', 'XPO:0140672', 'abnormally necrotic olfactory region', 0.5254237288135594, 7.024697770424301, 1.9211826816637279, 'HP:0000929', 'Abnormal skull morphology'),
(471639, 'HP:0034974', 'Bathrocephaly', 'XPO:0129406', 'decreased size of the suspensorium', 0.43333333333333335, 4.638757693672553, 1.4177899470389728, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(471640, 'HP:0034974', 'Bathrocephaly', 'XPO:0107372', 'abnormal flexural organ morphology', 0.425531914893617, 4.638757693672553, 1.404969552736279, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(471641, 'HP:0034974', 'Bathrocephaly', 'XPO:0131638', 'increased size of the intercanthal region', 0.40384615384615385, 4.5318002188002176, 1.3528303989641963, 'UPHENO:0087907', 'abnormal head morphology'),
(471642, 'HP:0034974', 'Bathrocephaly', 'XPO:0102795', 'abnormal branchial basket morphology', 0.4126984126984127, 4.638757693672553, 1.3836213127410304, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(471643, 'HP:0034974', 'Bathrocephaly', 'XPO:0103152', 'abnormal otic region morphology', 0.5740740740740741, 7.024697770424301, 2.008157580521644, 'HP:0000929', 'Abnormal skull morphology'),
(471644, 'HP:0034974', 'Bathrocephaly', 'XPO:0102567', 'abnormal skeleton morphology', 0.425531914893617, 4.638757693672553, 1.404969552736279, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(471645, 'HP:0034974', 'Bathrocephaly', 'XPO:0139775', 'abnormally necrotic braincase and otic capsule skeleton', 0.4262295081967213, 4.638757693672553, 1.4061206955371255, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(471646, 'HP:0034974', 'Bathrocephaly', 'XPO:0128947', 'decreased size of the otic region', 0.5081967213114754, 7.024697770424301, 1.8894254087244782, 'HP:0000929', 'Abnormal skull morphology'),
(471647, 'HP:0034974', 'Bathrocephaly', 'XPO:0129514', 'increased size of the cranium', 0.4482758620689655, 4.638757693672553, 1.4420274283314136, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(471648, 'HP:0034974', 'Bathrocephaly', 'XPO:0140510', 'abnormally necrotic postcranial axial skeleton', 0.40350877192982454, 6.272837960958401, 1.5909573036826314, 'UPHENO:0022529', 'abnormal postcranial axial skeleton morphology'),
(471649, 'HP:0034974', 'Bathrocephaly', 'XPO:0139745', 'abnormally necrotic chondrocranium', 0.4406779661016949, 4.638757693672553, 1.4297546312868548, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(471650, 'HP:0034974', 'Bathrocephaly', 'XPO:0139832', 'abnormally necrotic splanchnocranium', 0.4406779661016949, 4.638757693672553, 1.4297546312868548, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(471651, 'HP:0034974', 'Bathrocephaly', 'XPO:0102828', 'abnormal occipital region morphology', 0.5849056603773585, 7.024697770424301, 2.027013933933702, 'HP:0000929', 'Abnormal skull morphology'),
(471652, 'HP:0034974', 'Bathrocephaly', 'XPO:0128238', 'decreased size of the ethmoid region', 0.4406779661016949, 4.638757693672553, 1.4297546312868548, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(471653, 'HP:0034974', 'Bathrocephaly', 'XPO:0102272', 'abnormal notochordal sheath morphology', 0.425531914893617, 4.638757693672553, 1.404969552736279, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(471654, 'HP:0034974', 'Bathrocephaly', 'XPO:0130449', 'increased size of the fenestra subocularis', 0.45614035087719296, 4.638757693672553, 1.4546217934659431, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(471655, 'HP:0034974', 'Bathrocephaly', 'XPO:0140223', 'abnormally necrotic head region', 0.42, 4.5318002188002176, 1.3796217205799897, 'UPHENO:0087907', 'abnormal head morphology'),
(471656, 'HP:0034974', 'Bathrocephaly', 'XPO:0101659', 'abnormal lower jaw morphology', 0.45588235294117646, 7.024697770424301, 1.78953506483714, 'HP:0000929', 'Abnormal skull morphology'),
(471657, 'HP:0034974', 'Bathrocephaly', 'XPO:0141185', 'abnormally necrotic occipital region', 0.5344827586206896, 7.024697770424301, 1.9376738226061134, 'HP:0000929', 'Abnormal skull morphology'),
(471658, 'HP:0034974', 'Bathrocephaly', 'XPO:0102010', 'abnormal perichondrium morphology', 0.4166666666666667, 4.638757693672553, 1.3902574242552699, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(471659, 'HP:0034974', 'Bathrocephaly', 'XPO:0129513', 'increased size of the splanchnocranium', 0.4262295081967213, 4.638757693672553, 1.4061206955371255, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(471660, 'HP:0034974', 'Bathrocephaly', 'XPO:0102572', 'abnormal hatching gland primordium morphology', 0.42, 4.5318002188002176, 1.3796217205799897, 'UPHENO:0087907', 'abnormal head morphology'),
(471661, 'HP:0034974', 'Bathrocephaly', 'XPO:0101957', 'abnormal axial skeleton morphology', 0.42, 6.211345574613551, 1.61516721776344, 'UPHENO:0087089', 'abnormal axial skeleton plus cranial skeleton morphology'),
(471662, 'HP:0034974', 'Bathrocephaly', 'XPO:0102564', 'abnormal olfactory region morphology', 0.5740740740740741, 7.024697770424301, 2.008157580521644, 'HP:0000929', 'Abnormal skull morphology'),
(471663, 'HP:0034974', 'Bathrocephaly', 'XPO:0141829', 'increased width of head', 0.5081967213114754, 7.024697770424301, 1.8894254087244782, 'HP:0000929', 'Abnormal skull morphology'),
(471664, 'HP:0034974', 'Bathrocephaly', 'XPO:0115586', 'abnormally decreased volume of chondrocranium', 0.4126984126984127, 4.638757693672553, 1.3836213127410304, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(471665, 'HP:0034974', 'Bathrocephaly', 'XPO:0140132', 'abnormally necrotic ethmoid region', 0.45614035087719296, 4.638757693672553, 1.4546217934659431, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(471666, 'HP:0034974', 'Bathrocephaly', 'XPO:0102351', 'abnormal sphenoid region morphology', 0.5740740740740741, 7.024697770424301, 2.008157580521644, 'HP:0000929', 'Abnormal skull morphology'),
(471667, 'HP:0034974', 'Bathrocephaly', 'XPO:0102259', 'abnormal pharyngeal region morphology', 0.4772727272727273, 4.5318002188002176, 1.4706816956370683, 'UPHENO:0087907', 'abnormal head morphology'),
(471668, 'HP:0034974', 'Bathrocephaly', 'XPO:0141061', 'abnormally necrotic suspensorium', 0.4482758620689655, 4.638757693672553, 1.4420274283314136, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(471669, 'HP:0034974', 'Bathrocephaly', 'XPO:0141339', 'decreased pigmentation in the head', 0.4375, 4.5318002188002176, 1.4080705222839853, 'UPHENO:0087907', 'abnormal head morphology'),
(471670, 'HP:0034974', 'Bathrocephaly', 'XPO:0101634', 'abnormal head morphology', 0.4666666666666667, 4.5318002188002176, 1.4542489821577214, 'UPHENO:0087907', 'abnormal head morphology'),
(471671, 'HP:0034974', 'Bathrocephaly', 'XPO:0128582', 'decreased size of the head region', 0.40384615384615385, 4.5318002188002176, 1.3528303989641963, 'UPHENO:0087907', 'abnormal head morphology'),
(471672, 'HP:0034974', 'Bathrocephaly', 'XPO:0102921', 'abnormal orbital region morphology', 0.5081967213114754, 7.024697770424301, 1.8894254087244782, 'HP:0000929', 'Abnormal skull morphology'),
(471673, 'HP:0034974', 'Bathrocephaly', 'XPO:0141839', 'edematous pharyngeal region', 0.45652173913043476, 4.5318002188002176, 1.4383550734357495, 'UPHENO:0087907', 'abnormal head morphology'),
(471674, 'HP:0034974', 'Bathrocephaly', 'XPO:0102665', 'abnormal suspensorium morphology', 0.49056603773584906, 4.638757693672553, 1.508514826510376, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(471675, 'HP:0034974', 'Bathrocephaly', 'XPO:0130425', 'increased size of the otic region', 0.5081967213114754, 7.024697770424301, 1.8894254087244782, 'HP:0000929', 'Abnormal skull morphology'),
(471676, 'HP:0034974', 'Bathrocephaly', 'XPO:0128033', 'decreased size of the splanchnocranium', 0.4262295081967213, 4.638757693672553, 1.4061206955371255, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(471677, 'HP:0034974', 'Bathrocephaly', 'XPO:0141723', 'abnormal posterior notochord morphology', 0.425531914893617, 4.638757693672553, 1.404969552736279, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(471678, 'HP:0034974', 'Bathrocephaly', 'XPO:0141719', 'abnormal anterior notochord morphology', 0.425531914893617, 4.638757693672553, 1.404969552736279, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(471679, 'HP:0034974', 'Bathrocephaly', 'XPO:0129291', 'decreased size of the orbital region', 0.44285714285714284, 7.024697770424301, 1.7637850163909, 'HP:0000929', 'Abnormal skull morphology'),
(471680, 'HP:0034974', 'Bathrocephaly', 'XPO:0103721', 'increased size of the chondrocranium', 0.4262295081967213, 4.638757693672553, 1.4061206955371255, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(471681, 'HP:0034974', 'Bathrocephaly', 'XPO:0103707', 'increased pigmentation in the head', 0.4375, 4.5318002188002176, 1.4080705222839853, 'UPHENO:0087907', 'abnormal head morphology'),
(471682, 'HP:0034974', 'Bathrocephaly', 'XPO:0103358', 'decreased size of the pharyngeal region', 0.42857142857142855, 4.5318002188002176, 1.3936283915633758, 'UPHENO:0087907', 'abnormal head morphology'),
(471683, 'HP:0034974', 'Bathrocephaly', 'XPO:0141201', 'abnormally necrotic sphenoid region', 0.5254237288135594, 7.024697770424301, 1.9211826816637279, 'HP:0000929', 'Abnormal skull morphology'),
(471684, 'HP:0034974', 'Bathrocephaly', 'XPO:0130324', 'increased size of the choana', 0.47692307692307695, 7.024697770424301, 1.8303662133915815, 'HP:0000929', 'Abnormal skull morphology'),
(471685, 'HP:0034974', 'Bathrocephaly', 'XPO:0102082', 'abnormal circumpharyngeal ridge morphology', 0.42857142857142855, 4.5318002188002176, 1.3936283915633758, 'UPHENO:0087907', 'abnormal head morphology'),
(471686, 'HP:0034974', 'Bathrocephaly', 'XPO:0128208', 'decreased size of the olfactory region', 0.5081967213114754, 7.024697770424301, 1.8894254087244782, 'HP:0000929', 'Abnormal skull morphology'),
(471687, 'HP:0034974', 'Bathrocephaly', 'XPO:0102776', 'abnormal fenestra subocularis morphology', 0.5, 4.638757693672553, 1.5229507040072823, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(471688, 'HP:0034974', 'Bathrocephaly', 'XPO:0128905', 'decreased size of the occipital region', 0.5166666666666667, 7.024697770424301, 1.9051055564944135, 'HP:0000929', 'Abnormal skull morphology'),
(471689, 'HP:0034974', 'Bathrocephaly', 'XPO:0130383', 'increased size of the occipital region', 0.5166666666666667, 7.024697770424301, 1.9051055564944135, 'HP:0000929', 'Abnormal skull morphology'),
(471690, 'HP:0034974', 'Bathrocephaly', 'XPO:0128668', 'decreased size of the fenestra basicranialis', 0.45614035087719296, 4.638757693672553, 1.4546217934659431, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(471691, 'HP:0034974', 'Bathrocephaly', 'XPO:0101860', 'abnormal skeletal subdivision morphology', 0.4166666666666667, 4.638757693672553, 1.3902574242552699, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(471692, 'HP:0034974', 'Bathrocephaly', 'XPO:0128880', 'decreased size of the lower jaw', 0.41333333333333333, 7.024697770424301, 1.7039782114536297, 'HP:0000929', 'Abnormal skull morphology'),
(471693, 'HP:0034974', 'Bathrocephaly', 'XPO:0130880', 'increased size of the suspensorium', 0.43333333333333335, 4.638757693672553, 1.4177899470389728, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(471694, 'HP:0034974', 'Bathrocephaly', 'XPO:0102217', 'abnormal elastica externa morphology', 0.4444444444444444, 4.638757693672553, 1.4358516936218344, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(471695, 'HP:0034974', 'Bathrocephaly', 'XPO:0128291', 'decreased size of the dermatocranium', 0.4262295081967213, 4.638757693672553, 1.4061206955371255, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(471696, 'HP:0034974', 'Bathrocephaly', 'XPO:0139784', 'abnormally necrotic cranium', 0.4642857142857143, 4.638757693672553, 1.4675520192501232, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(471697, 'HP:0034974', 'Bathrocephaly', 'XPO:0102092', 'abnormal ethmoid region morphology', 0.5, 4.638757693672553, 1.5229507040072823, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(471698, 'HP:0034974', 'Bathrocephaly', 'XPO:0139880', 'abnormally necrotic dermatocranium', 0.4406779661016949, 4.638757693672553, 1.4297546312868548, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(471699, 'HP:0034974', 'Bathrocephaly', 'XPO:0128034', 'decreased size of the cranium', 0.4482758620689655, 4.638757693672553, 1.4420274283314136, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(471700, 'HP:0034974', 'Bathrocephaly', 'XPO:0102054', 'abnormal notochord morphology', 0.425531914893617, 4.638757693672553, 1.404969552736279, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(471701, 'HP:0034974', 'Bathrocephaly', 'XPO:0129225', 'decreased size of the upper jaw', 0.4025974025974026, 7.024697770424301, 1.6817030286006471, 'HP:0000929', 'Abnormal skull morphology'),
(471702, 'HP:0034974', 'Bathrocephaly', 'XPO:0103739', 'increased size of the pharyngeal region', 0.42857142857142855, 4.5318002188002176, 1.3936283915633758, 'UPHENO:0087907', 'abnormal head morphology'),
(471703, 'HP:0034974', 'Bathrocephaly', 'XPO:0128659', 'decreased size of the braincase and otic capsule skeleton', 0.4126984126984127, 4.638757693672553, 1.3836213127410304, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(471704, 'HP:0005407', 'Decreased proportion of CD4-positive helper T cells', 'XPO:0131221', 'abnormally decreased number of thymocyte', 0.5517241379310345, 11.379159829460056, 2.5056251011051724, 'UPHENO:0085346', 'abnormally decreased number of T cell'),
(471705, 'HP:0010603', 'Odontogenic keratocysts of the jaw', 'XPO:0100647', 'abnormal mouth', 0.42592592592592593, 7.0866363731414825, 1.7373491758799184, 'HP:0000153', 'Abnormality of the mouth'),
(471706, 'HP:0010603', 'Odontogenic keratocysts of the jaw', 'XPO:0126046', 'absent tooth', 0.43023255813953487, 9.181382707377857, 1.9874933382160715, 'UPHENO:0002826', 'abnormal dentition'),
(471707, 'HP:0010603', 'Odontogenic keratocysts of the jaw', 'XPO:0130701', 'increased size of the upper jaw', 0.4074074074074074, 7.312692920701687, 1.7260490329042149, 'UPHENO:0076800', 'abnormal mouth morphology'),
(471708, 'HP:0010603', 'Odontogenic keratocysts of the jaw', 'XPO:0129152', 'decreased size of the oral cavity', 0.49230769230769234, 7.884497199543557, 1.970177307075115, 'UPHENO:0076786', 'abnormal oral cavity morphology'),
(471709, 'HP:0010603', 'Odontogenic keratocysts of the jaw', 'XPO:0140789', 'abnormally necrotic roof of mouth', 0.4411764705882353, 7.312692920701687, 1.7961592505261732, 'UPHENO:0076800', 'abnormal mouth morphology'),
(471710, 'HP:0010603', 'Odontogenic keratocysts of the jaw', 'XPO:0140639', 'abnormally necrotic upper jaw', 0.4177215189873418, 7.312692920701687, 1.7477611949930372, 'UPHENO:0076800', 'abnormal mouth morphology'),
(471711, 'HP:0010603', 'Odontogenic keratocysts of the jaw', 'XPO:0102861', 'abnormal cementum morphology', 0.4457831325301205, 9.181382707377857, 2.0230930636658266, 'UPHENO:0002826', 'abnormal dentition'),
(471712, 'HP:0010603', 'Odontogenic keratocysts of the jaw', 'XPO:0101506', 'abnormal upper jaw', 0.48148148148148145, 7.0866363731414825, 1.8471827683422974, 'HP:0000153', 'Abnormality of the mouth'),
(471713, 'HP:0010603', 'Odontogenic keratocysts of the jaw', 'XPO:0101464', 'abnormal oral cavity', 0.41818181818181815, 7.0866363731414825, 1.721482641014341, 'HP:0000153', 'Abnormality of the mouth'),
(471714, 'HP:0010603', 'Odontogenic keratocysts of the jaw', 'XPO:0131573', 'decreased size of the roof of mouth', 0.42857142857142855, 7.312692920701687, 1.7703138850862843, 'UPHENO:0076800', 'abnormal mouth morphology'),
(471715, 'HP:0010603', 'Odontogenic keratocysts of the jaw', 'XPO:0139736', 'abnormally necrotic tooth', 0.45121951219512196, 9.181382707377857, 2.0353916150214837, 'UPHENO:0002826', 'abnormal dentition'),
(471716, 'HP:0010603', 'Odontogenic keratocysts of the jaw', 'XPO:0130628', 'increased size of the oral cavity', 0.49230769230769234, 7.884497199543557, 1.970177307075115, 'UPHENO:0076786', 'abnormal oral cavity morphology'),
(471717, 'HP:0010603', 'Odontogenic keratocysts of the jaw', 'XPO:0100184', 'abnormal tooth', 0.4406779661016949, 7.0866363731414825, 1.7671798163792727, 'HP:0000153', 'Abnormality of the mouth'),
(471718, 'HP:0010603', 'Odontogenic keratocysts of the jaw', 'XPO:0127103', 'abnormally localised upper jaw', 0.4126984126984127, 7.0866363731414825, 1.7101589348848036, 'HP:0000153', 'Abnormality of the mouth'),
(471719, 'HP:0010603', 'Odontogenic keratocysts of the jaw', 'XPO:0130466', 'increased size of the tooth', 0.43023255813953487, 9.181382707377857, 1.9874933382160715, 'UPHENO:0002826', 'abnormal dentition'),
(471720, 'HP:0010603', 'Odontogenic keratocysts of the jaw', 'XPO:0130358', 'increased size of the lower jaw', 0.4177215189873418, 7.312692920701687, 1.7477611949930372, 'UPHENO:0076800', 'abnormal mouth morphology'),
(471721, 'HP:0010603', 'Odontogenic keratocysts of the jaw', 'XPO:0129225', 'decreased size of the upper jaw', 0.4074074074074074, 7.312692920701687, 1.7260490329042149, 'UPHENO:0076800', 'abnormal mouth morphology'),
(471722, 'HP:0010603', 'Odontogenic keratocysts of the jaw', 'XPO:0115558', 'abnormally incomplete structure of mouth', 0.4918032786885246, 7.312692920701687, 1.8964193508935339, 'UPHENO:0076800', 'abnormal mouth morphology'),
(471723, 'HP:0010603', 'Odontogenic keratocysts of the jaw', 'XPO:0101816', 'abnormal tooth morphology', 0.5, 9.181382707377857, 2.1425898706212836, 'UPHENO:0002826', 'abnormal dentition'),
(471724, 'HP:0010603', 'Odontogenic keratocysts of the jaw', 'XPO:0131651', 'abnormal roof of mouth', 0.4107142857142857, 7.0866363731414825, 1.7060430229369012, 'HP:0000153', 'Abnormality of the mouth'),
(471725, 'HP:0010603', 'Odontogenic keratocysts of the jaw', 'XPO:0101659', 'abnormal lower jaw morphology', 0.4583333333333333, 7.312692920701687, 1.830751463740579, 'UPHENO:0076800', 'abnormal mouth morphology'),
(471726, 'HP:0010603', 'Odontogenic keratocysts of the jaw', 'XPO:0102890', 'abnormal dentine morphology', 0.43529411764705883, 9.181382707377857, 1.999150290595484, 'UPHENO:0002826', 'abnormal dentition'),
(471727, 'HP:0010603', 'Odontogenic keratocysts of the jaw', 'XPO:0103199', 'abnormal tongue morphology', 0.5333333333333333, 7.884497199543557, 2.0506255565290066, 'UPHENO:0076786', 'abnormal oral cavity morphology'),
(471728, 'HP:0010603', 'Odontogenic keratocysts of the jaw', 'XPO:0103828', 'decreased width of the mouth', 0.43243243243243246, 7.884497199543557, 1.8464864750399128, 'UPHENO:0076786', 'abnormal oral cavity morphology'),
(471729, 'HP:0010603', 'Odontogenic keratocysts of the jaw', 'XPO:0140626', 'abnormally necrotic tongue', 0.49230769230769234, 7.884497199543557, 1.970177307075115, 'UPHENO:0076786', 'abnormal oral cavity morphology'),
(471730, 'HP:0010603', 'Odontogenic keratocysts of the jaw', 'XPO:0131611', 'increased size of the roof of mouth', 0.42857142857142855, 7.312692920701687, 1.7703138850862843, 'UPHENO:0076800', 'abnormal mouth morphology'),
(471731, 'HP:0010603', 'Odontogenic keratocysts of the jaw', 'XPO:0103735', 'increased size of the mouth', 0.463768115942029, 7.884497199543557, 1.9122181913637677, 'UPHENO:0076786', 'abnormal oral cavity morphology'),
(471732, 'HP:0010603', 'Odontogenic keratocysts of the jaw', 'XPO:0127750', 'abnormally localised tongue', 0.5161290322580645, 7.884497199543557, 2.017279829235854, 'UPHENO:0076786', 'abnormal oral cavity morphology'),
(471733, 'HP:0010603', 'Odontogenic keratocysts of the jaw', 'XPO:0128880', 'decreased size of the lower jaw', 0.4177215189873418, 7.312692920701687, 1.7477611949930372, 'UPHENO:0076800', 'abnormal mouth morphology'),
(471734, 'HP:0010603', 'Odontogenic keratocysts of the jaw', 'XPO:0101567', 'abnormal tongue', 0.6274509803921569, 7.884497199543557, 2.22421570396237, 'UPHENO:0076786', 'abnormal oral cavity morphology'),
(471735, 'HP:0010603', 'Odontogenic keratocysts of the jaw', 'XPO:0126089', 'absent tongue', 0.5, 7.884497199543557, 1.9855096574360394, 'UPHENO:0076786', 'abnormal oral cavity morphology'),
(471736, 'HP:0010603', 'Odontogenic keratocysts of the jaw', 'XPO:0115393', 'abnormally decreased volume of oral cavity', 0.47761194029850745, 7.884497199543557, 1.9405488929043109, 'UPHENO:0076786', 'abnormal oral cavity morphology'),
(471737, 'HP:0010603', 'Odontogenic keratocysts of the jaw', 'XPO:0103352', 'decreased size of the mouth', 0.463768115942029, 7.884497199543557, 1.9122181913637677, 'UPHENO:0076786', 'abnormal oral cavity morphology'),
(471738, 'HP:0010603', 'Odontogenic keratocysts of the jaw', 'XPO:0102960', 'abnormal oral epithelium morphology', 0.43478260869565216, 7.312692920701687, 1.7830961007901136, 'UPHENO:0076800', 'abnormal mouth morphology'),
(471739, 'HP:0010603', 'Odontogenic keratocysts of the jaw', 'XPO:0141830', 'increased width of mouth', 0.43243243243243246, 7.884497199543557, 1.8464864750399128, 'UPHENO:0076786', 'abnormal oral cavity morphology'),
(471740, 'HP:0010603', 'Odontogenic keratocysts of the jaw', 'XPO:0141006', 'abnormally necrotic cementum', 0.4065934065934066, 9.181382707377857, 1.9321205118290519, 'UPHENO:0002826', 'abnormal dentition'),
(471741, 'HP:0010603', 'Odontogenic keratocysts of the jaw', 'XPO:0103138', 'abnormal upper jaw morphology', 0.44594594594594594, 7.312692920701687, 1.8058421198805104, 'UPHENO:0076800', 'abnormal mouth morphology'),
(471742, 'HP:0010603', 'Odontogenic keratocysts of the jaw', 'XPO:0128989', 'decreased size of the tooth', 0.43023255813953487, 9.181382707377857, 1.9874933382160715, 'UPHENO:0002826', 'abnormal dentition'),
(471743, 'HP:0010603', 'Odontogenic keratocysts of the jaw', 'XPO:0141311', 'abnormal roof of mouth morphology', 0.47619047619047616, 7.312692920701687, 1.8660746834314161, 'UPHENO:0076800', 'abnormal mouth morphology'),
(471744, 'HP:0010603', 'Odontogenic keratocysts of the jaw', 'XPO:0128105', 'decreased size of the tongue', 0.4383561643835616, 7.884497199543557, 1.859090624602482, 'UPHENO:0076786', 'abnormal oral cavity morphology'),
(471745, 'HP:0010603', 'Odontogenic keratocysts of the jaw', 'XPO:0103096', 'abnormal oral cavity morphology', 0.5333333333333333, 7.884497199543557, 2.0506255565290066, 'UPHENO:0076786', 'abnormal oral cavity morphology'),
(471746, 'HP:0010603', 'Odontogenic keratocysts of the jaw', 'XPO:0102279', 'abnormal mouth morphology', 0.5, 7.312692920701687, 1.9121575406725366, 'UPHENO:0076800', 'abnormal mouth morphology'),
(471747, 'HP:0010603', 'Odontogenic keratocysts of the jaw', 'XPO:0140897', 'abnormally necrotic lower jaw', 0.42857142857142855, 7.312692920701687, 1.7703138850862843, 'UPHENO:0076800', 'abnormal mouth morphology'),
(471748, 'HP:0010603', 'Odontogenic keratocysts of the jaw', 'XPO:0129585', 'increased size of the tongue', 0.42857142857142855, 7.884497199543557, 1.8382247491467985, 'UPHENO:0076786', 'abnormal oral cavity morphology'),
(471749, 'HP:0010603', 'Odontogenic keratocysts of the jaw', 'XPO:0127611', 'abnormally localised lower jaw', 0.4126984126984127, 7.0866363731414825, 1.7101589348848036, 'HP:0000153', 'Abnormality of the mouth'),
(471750, 'HP:0010603', 'Odontogenic keratocysts of the jaw', 'XPO:0100027', 'abnormal lower jaw', 0.48148148148148145, 7.0866363731414825, 1.8471827683422974, 'HP:0000153', 'Abnormality of the mouth'),
(471751, 'HP:0032451', 'Oral melanotic macule', 'XPO:0101506', 'abnormal upper jaw', 0.40350877192982454, 7.0866363731414825, 1.6910115138695967, 'HP:0000153', 'Abnormality of the mouth'),
(471752, 'HP:0032451', 'Oral melanotic macule', 'XPO:0102445', 'abnormal branchial arch 3 morphology', 0.4426229508196721, 5.725717590856133, 1.5919591752381232, 'UPHENO:0076803', 'abnormal digestive system morphology'),
(471753, 'HP:0032451', 'Oral melanotic macule', 'XPO:0102890', 'abnormal dentine morphology', 0.40229885057471265, 7.884497199543557, 1.7809896576723612, 'UPHENO:0076786', 'abnormal oral cavity morphology'),
(471754, 'HP:0032451', 'Oral melanotic macule', 'XPO:0115526', 'abnormally incomplete structure of head', 0.40384615384615385, 4.5318002188002176, 1.3528303989641963, 'UPHENO:0087907', 'abnormal head morphology'),
(471755, 'HP:0032451', 'Oral melanotic macule', 'XPO:0103199', 'abnormal tongue morphology', 0.6140350877192983, 7.884497199543557, 2.2003085987070747, 'UPHENO:0076786', 'abnormal oral cavity morphology'),
(471756, 'HP:0032451', 'Oral melanotic macule', 'XPO:0139863', 'abnormally necrotic pharyngeal arch', 0.43548387096774194, 5.725717590856133, 1.5790686053918375, 'UPHENO:0076803', 'abnormal digestive system morphology'),
(471757, 'HP:0032451', 'Oral melanotic macule', 'XPO:0102259', 'abnormal pharyngeal region morphology', 0.42, 4.5318002188002176, 1.3796217205799897, 'UPHENO:0087907', 'abnormal head morphology'),
(471758, 'HP:0032451', 'Oral melanotic macule', 'XPO:0103096', 'abnormal oral cavity morphology', 0.6140350877192983, 7.884497199543557, 2.2003085987070747, 'UPHENO:0076786', 'abnormal oral cavity morphology'),
(471759, 'HP:0032451', 'Oral melanotic macule', 'XPO:0102420', 'abnormal branchial arch 4 morphology', 0.43548387096774194, 5.725717590856133, 1.5790686053918375, 'UPHENO:0076803', 'abnormal digestive system morphology'),
(471760, 'HP:0032451', 'Oral melanotic macule', 'XPO:0139987', 'abnormally necrotic branchial arch', 0.4153846153846154, 5.725717590856133, 1.5421981063659433, 'UPHENO:0076803', 'abnormal digestive system morphology'),
(471761, 'HP:0032451', 'Oral melanotic macule', 'XPO:0100647', 'abnormal mouth', 0.42592592592592593, 7.0866363731414825, 1.7373491758799184, 'HP:0000153', 'Abnormality of the mouth'),
(471762, 'HP:0032451', 'Oral melanotic macule', 'XPO:0102279', 'abnormal mouth morphology', 0.5789473684210527, 7.312692920701687, 2.0575870145662134, 'UPHENO:0076800', 'abnormal mouth morphology'),
(471763, 'HP:0032451', 'Oral melanotic macule', 'XPO:0102204', 'abnormal branchial arch morphology', 0.4576271186440678, 5.725717590856133, 1.6187166655326515, 'UPHENO:0076803', 'abnormal digestive system morphology'),
(471764, 'HP:0032451', 'Oral melanotic macule', 'XPO:0129152', 'decreased size of the oral cavity', 0.5645161290322581, 7.884497199543557, 2.1097217443189065, 'UPHENO:0076786', 'abnormal oral cavity morphology'),
(471765, 'HP:0032451', 'Oral melanotic macule', 'XPO:0102525', 'abnormal hyoid arch morphology', 0.45, 5.725717590856133, 1.6051706812315194, 'UPHENO:0076803', 'abnormal digestive system morphology'),
(471766, 'HP:0032451', 'Oral melanotic macule', 'XPO:0128880', 'decreased size of the lower jaw', 0.4177215189873418, 7.312692920701687, 1.7477611949930372, 'UPHENO:0076800', 'abnormal mouth morphology'),
(471767, 'HP:0032451', 'Oral melanotic macule', 'XPO:0102960', 'abnormal oral epithelium morphology', 0.5230769230769231, 11.317232080316854, 2.4330604049878386, 'UPHENO:0087132', 'abnormal mouth mucosa morphology'),
(471768, 'HP:0032451', 'Oral melanotic macule', 'XPO:0141830', 'increased width of mouth', 0.49295774647887325, 7.884497199543557, 1.971477611236298, 'UPHENO:0076786', 'abnormal oral cavity morphology'),
(471769, 'HP:0032451', 'Oral melanotic macule', 'XPO:0139736', 'abnormally necrotic tooth', 0.4166666666666667, 7.884497199543557, 1.812514045870123, 'UPHENO:0076786', 'abnormal oral cavity morphology'),
(471770, 'HP:0032451', 'Oral melanotic macule', 'XPO:0127750', 'abnormally localised tongue', 0.5409836065573771, 7.884497199543557, 2.06528054532565, 'UPHENO:0076786', 'abnormal oral cavity morphology'),
(471771, 'HP:0032451', 'Oral melanotic macule', 'XPO:0130358', 'increased size of the lower jaw', 0.4177215189873418, 7.312692920701687, 1.7477611949930372, 'UPHENO:0076800', 'abnormal mouth morphology'),
(471772, 'HP:0032451', 'Oral melanotic macule', 'XPO:0101634', 'abnormal head morphology', 0.4117647058823529, 4.5318002188002176, 1.3660290568695288, 'UPHENO:0087907', 'abnormal head morphology'),
(471773, 'HP:0032451', 'Oral melanotic macule', 'XPO:0140639', 'abnormally necrotic upper jaw', 0.4177215189873418, 7.312692920701687, 1.7477611949930372, 'UPHENO:0076800', 'abnormal mouth morphology'),
(471774, 'HP:0032451', 'Oral melanotic macule', 'XPO:0140430', 'abnormally necrotic hyoid arch', 0.4090909090909091, 5.725717590856133, 1.5304701939081158, 'UPHENO:0076803', 'abnormal digestive system morphology'),
(471775, 'HP:0032451', 'Oral melanotic macule', 'XPO:0129585', 'increased size of the tongue', 0.4666666666666667, 7.884497199543557, 1.9181845652735452, 'UPHENO:0076786', 'abnormal oral cavity morphology'),
(471776, 'HP:0032451', 'Oral melanotic macule', 'XPO:0103138', 'abnormal upper jaw morphology', 0.44594594594594594, 7.312692920701687, 1.8058421198805104, 'UPHENO:0076800', 'abnormal mouth morphology'),
(471777, 'HP:0032451', 'Oral melanotic macule', 'XPO:0131611', 'increased size of the roof of mouth', 0.4925373134328358, 7.312692920701687, 1.8978340615348135, 'UPHENO:0076800', 'abnormal mouth morphology'),
(471778, 'HP:0032451', 'Oral melanotic macule', 'XPO:0130628', 'increased size of the oral cavity', 0.5645161290322581, 7.884497199543557, 2.1097217443189065, 'UPHENO:0076786', 'abnormal oral cavity morphology'),
(471779, 'HP:0032451', 'Oral melanotic macule', 'XPO:0129225', 'decreased size of the upper jaw', 0.4074074074074074, 7.312692920701687, 1.7260490329042149, 'UPHENO:0076800', 'abnormal mouth morphology'),
(471780, 'HP:0032451', 'Oral melanotic macule', 'XPO:0142059', 'abnormal nasal region morphology', 0.40384615384615385, 4.5318002188002176, 1.3528303989641963, 'UPHENO:0087907', 'abnormal head morphology'),
(471781, 'HP:0032451', 'Oral melanotic macule', 'XPO:0128105', 'decreased size of the tongue', 0.5, 7.884497199543557, 1.9855096574360394, 'UPHENO:0076786', 'abnormal oral cavity morphology'),
(471782, 'HP:0032451', 'Oral melanotic macule', 'XPO:0131573', 'decreased size of the roof of mouth', 0.4925373134328358, 7.312692920701687, 1.8978340615348135, 'UPHENO:0076800', 'abnormal mouth morphology'),
(471783, 'HP:0032451', 'Oral melanotic macule', 'XPO:0130132', 'increased size of the oral epithelium', 0.4594594594594595, 11.317232080316854, 2.2803090435727427, 'UPHENO:0087132', 'abnormal mouth mucosa morphology'),
(471784, 'HP:0032451', 'Oral melanotic macule', 'XPO:0140789', 'abnormally necrotic roof of mouth', 0.5076923076923077, 7.312692920701687, 1.9268103031581083, 'UPHENO:0076800', 'abnormal mouth morphology'),
(471785, 'HP:0032451', 'Oral melanotic macule', 'XPO:0102203', 'abnormal branchial arch 1 morphology', 0.43548387096774194, 5.725717590856133, 1.5790686053918375, 'UPHENO:0076803', 'abnormal digestive system morphology'),
(471786, 'HP:0032451', 'Oral melanotic macule', 'XPO:0115558', 'abnormally incomplete structure of mouth', 0.5689655172413793, 7.312692920701687, 2.039772073064637, 'UPHENO:0076800', 'abnormal mouth morphology'),
(471787, 'HP:0032451', 'Oral melanotic macule', 'XPO:0103352', 'decreased size of the mouth', 0.5303030303030303, 7.884497199543557, 2.044791617092975, 'UPHENO:0076786', 'abnormal oral cavity morphology'),
(471788, 'HP:0032451', 'Oral melanotic macule', 'XPO:0142061', 'abnormal digestive tract morphology', 0.40384615384615385, 5.725717590856133, 1.520627839767678, 'UPHENO:0076803', 'abnormal digestive system morphology'),
(471789, 'HP:0032451', 'Oral melanotic macule', 'XPO:0101567', 'abnormal tongue', 0.6274509803921569, 7.884497199543557, 2.22421570396237, 'UPHENO:0076786', 'abnormal oral cavity morphology'),
(471790, 'HP:0032451', 'Oral melanotic macule', 'XPO:0102125', 'abnormal liver and biliary system morphology', 0.40384615384615385, 5.725717590856133, 1.520627839767678, 'UPHENO:0076803', 'abnormal digestive system morphology'),
(471791, 'HP:0032451', 'Oral melanotic macule', 'XPO:0141311', 'abnormal roof of mouth morphology', 0.55, 7.312692920701687, 2.0054877477526327, 'UPHENO:0076800', 'abnormal mouth morphology'),
(471792, 'HP:0032451', 'Oral melanotic macule', 'XPO:0131651', 'abnormal roof of mouth', 0.4107142857142857, 7.0866363731414825, 1.7060430229369012, 'HP:0000153', 'Abnormality of the mouth'),
(471793, 'HP:0032451', 'Oral melanotic macule', 'XPO:0102223', 'abnormal pharyngeal arch morphology', 0.47368421052631576, 5.725717590856133, 1.6468703703453182, 'UPHENO:0076803', 'abnormal digestive system morphology'),
(471794, 'HP:0032451', 'Oral melanotic macule', 'XPO:0103828', 'decreased width of the mouth', 0.49295774647887325, 7.884497199543557, 1.971477611236298, 'UPHENO:0076786', 'abnormal oral cavity morphology'),
(471795, 'HP:0032451', 'Oral melanotic macule', 'XPO:0141833', 'edematous alimentary system', 0.40384615384615385, 5.725717590856133, 1.520627839767678, 'UPHENO:0076803', 'abnormal digestive system morphology'),
(471796, 'HP:0032451', 'Oral melanotic macule', 'XPO:0101816', 'abnormal tooth morphology', 0.4605263157894737, 7.884497199543557, 1.9055231426456665, 'UPHENO:0076786', 'abnormal oral cavity morphology'),
(471797, 'HP:0032451', 'Oral melanotic macule', 'XPO:0126089', 'absent tongue', 0.5238095238095238, 7.884497199543557, 2.032233924421703, 'UPHENO:0076786', 'abnormal oral cavity morphology'),
(471798, 'HP:0032451', 'Oral melanotic macule', 'XPO:0102861', 'abnormal cementum morphology', 0.4117647058823529, 7.884497199543557, 1.8018206543383524, 'UPHENO:0076786', 'abnormal oral cavity morphology'),
(471799, 'HP:0032451', 'Oral melanotic macule', 'XPO:0141009', 'abnormally necrotic oral epithelium', 0.4722222222222222, 11.317232080316854, 2.311763067957408, 'UPHENO:0087132', 'abnormal mouth mucosa morphology'),
(471800, 'HP:0032451', 'Oral melanotic macule', 'XPO:0101659', 'abnormal lower jaw morphology', 0.4583333333333333, 7.312692920701687, 1.830751463740579, 'UPHENO:0076800', 'abnormal mouth morphology'),
(471801, 'HP:0032451', 'Oral melanotic macule', 'XPO:0102522', 'abnormal pharyngeal cavity morphology', 0.42, 5.725717590856133, 1.5507422055775666, 'UPHENO:0076803', 'abnormal digestive system morphology'),
(471802, 'HP:0032451', 'Oral melanotic macule', 'XPO:0101464', 'abnormal oral cavity', 0.41818181818181815, 7.0866363731414825, 1.721482641014341, 'HP:0000153', 'Abnormality of the mouth'),
(471803, 'HP:0032451', 'Oral melanotic macule', 'XPO:0140897', 'abnormally necrotic lower jaw', 0.42857142857142855, 7.312692920701687, 1.7703138850862843, 'UPHENO:0076800', 'abnormal mouth morphology'),
(471804, 'HP:0032451', 'Oral melanotic macule', 'XPO:0115393', 'abnormally decreased volume of oral cavity', 0.546875, 7.884497199543557, 2.076495703342625, 'UPHENO:0076786', 'abnormal oral cavity morphology'),
(471805, 'HP:0032451', 'Oral melanotic macule', 'XPO:0102261', 'abnormal branchial arch 2 morphology', 0.43548387096774194, 5.725717590856133, 1.5790686053918375, 'UPHENO:0076803', 'abnormal digestive system morphology'),
(471806, 'HP:0032451', 'Oral melanotic macule', 'XPO:0103735', 'increased size of the mouth', 0.5303030303030303, 7.884497199543557, 2.044791617092975, 'UPHENO:0076786', 'abnormal oral cavity morphology'),
(471807, 'HP:0032451', 'Oral melanotic macule', 'XPO:0103357', 'decreased size of the pharyngeal arch', 0.4153846153846154, 5.725717590856133, 1.5421981063659433, 'UPHENO:0076803', 'abnormal digestive system morphology'),
(471808, 'HP:0032451', 'Oral melanotic macule', 'XPO:0140626', 'abnormally necrotic tongue', 0.5645161290322581, 7.884497199543557, 2.1097217443189065, 'UPHENO:0076786', 'abnormal oral cavity morphology'),
(471809, 'HP:0032451', 'Oral melanotic macule', 'XPO:0103738', 'increased size of the pharyngeal arch', 0.4153846153846154, 5.725717590856133, 1.5421981063659433, 'UPHENO:0076803', 'abnormal digestive system morphology'),
(471810, 'HP:0032451', 'Oral melanotic macule', 'XPO:0100027', 'abnormal lower jaw', 0.40350877192982454, 7.0866363731414825, 1.6910115138695967, 'HP:0000153', 'Abnormality of the mouth'),
(471811, 'HP:0032451', 'Oral melanotic macule', 'XPO:0128653', 'decreased size of the oral epithelium', 0.4594594594594595, 11.317232080316854, 2.2803090435727427, 'UPHENO:0087132', 'abnormal mouth mucosa morphology'),
(471812, 'HP:0032451', 'Oral melanotic macule', 'XPO:0101784', 'abnormal alimentary system morphology', 0.42, 5.725717590856133, 1.5507422055775666, 'UPHENO:0076803', 'abnormal digestive system morphology'),
(471813, 'HP:0032451', 'Oral melanotic macule', 'XPO:0130701', 'increased size of the upper jaw', 0.4074074074074074, 7.312692920701687, 1.7260490329042149, 'UPHENO:0076800', 'abnormal mouth morphology'),
(471814, 'HP:0032451', 'Oral melanotic macule', 'XPO:0107375', 'abnormal larval alimentary system morphology', 0.40384615384615385, 5.725717590856133, 1.520627839767678, 'UPHENO:0076803', 'abnormal digestive system morphology'),
(471815, 'HP:0032451', 'Oral melanotic macule', 'XPO:0115392', 'abnormally incomplete structure of alimentary system', 0.4117647058823529, 5.725717590856133, 1.5354635846428564, 'UPHENO:0076803', 'abnormal digestive system morphology'),
(471816, 'HP:0032451', 'Oral melanotic macule', 'XPO:0102735', 'abnormal pharyngeal mesenchyme morphology', 0.4426229508196721, 5.725717590856133, 1.5919591752381232, 'UPHENO:0076803', 'abnormal digestive system morphology'),
(471817, 'HP:0032451', 'Oral melanotic macule', 'XPO:0141839', 'edematous pharyngeal region', 0.40384615384615385, 4.5318002188002176, 1.3528303989641963, 'UPHENO:0087907', 'abnormal head morphology'),
(471818, 'HP:0031143', 'Decreased hepatic echogenicity', 'XPO:0115392', 'abnormally incomplete structure of alimentary system', 0.42857142857142855, 5.725717590856133, 1.5664861849086864, 'UPHENO:0076803', 'abnormal digestive system morphology'),
(471819, 'HP:0031143', 'Decreased hepatic echogenicity', 'XPO:0128672', 'decreased size of the liver', 0.4430379746835443, 10.01729298920255, 2.1066658960898295, 'UPHENO:0019492', 'abnormal liver morphology'),
(471820, 'HP:0031143', 'Decreased hepatic echogenicity', 'XPO:0142061', 'abnormal digestive tract morphology', 0.42, 5.725717590856133, 1.5507422055775666, 'UPHENO:0076803', 'abnormal digestive system morphology'),
(471821, 'HP:0031143', 'Decreased hepatic echogenicity', 'XPO:0101674', 'abnormal hepatic vein morphology', 0.4430379746835443, 10.01729298920255, 2.1066658960898295, 'UPHENO:0019492', 'abnormal liver morphology'),
(471822, 'HP:0031143', 'Decreased hepatic echogenicity', 'XPO:0127068', 'abnormally localised hepatic vein', 0.4861111111111111, 10.01729298920255, 2.20669830862916, 'UPHENO:0019492', 'abnormal liver morphology'),
(471823, 'HP:0031143', 'Decreased hepatic echogenicity', 'XPO:0103168', 'abnormal liver parenchyme morphology', 0.5384615384615384, 10.01729298920255, 2.322482937329355, 'UPHENO:0019492', 'abnormal liver morphology'),
(471824, 'HP:0031143', 'Decreased hepatic echogenicity', 'XPO:0101788', 'abnormal foregut morphology', 0.40384615384615385, 5.725717590856133, 1.520627839767678, 'UPHENO:0076803', 'abnormal digestive system morphology'),
(471825, 'HP:0031143', 'Decreased hepatic echogenicity', 'XPO:0140114', 'abnormally necrotic liver and biliary system', 0.4074074074074074, 8.69832224767236, 1.8824879589836343, 'UPHENO:0087100', 'abnormal hepatobiliary system morphology'),
(471826, 'HP:0031143', 'Decreased hepatic echogenicity', 'XPO:0140388', 'abnormally necrotic biliary tree', 0.421875, 8.69832224767236, 1.9156212303680435, 'UPHENO:0087100', 'abnormal hepatobiliary system morphology'),
(471827, 'HP:0031143', 'Decreased hepatic echogenicity', 'XPO:0141005', 'abnormally necrotic bile duct', 0.4090909090909091, 8.69832224767236, 1.8863733871813304, 'UPHENO:0087100', 'abnormal hepatobiliary system morphology'),
(471828, 'HP:0031143', 'Decreased hepatic echogenicity', 'XPO:0101820', 'abnormal delta cell morphology', 0.43103448275862066, 7.428233084304616, 1.7893643020088765, 'UPHENO:0076812', 'abnormal endocrine system morphology'),
(471829, 'HP:0031143', 'Decreased hepatic echogenicity', 'XPO:0130724', 'increased size of the liver parenchyme', 0.4861111111111111, 10.01729298920255, 2.20669830862916, 'UPHENO:0019492', 'abnormal liver morphology'),
(471830, 'HP:0031143', 'Decreased hepatic echogenicity', 'XPO:0141125', 'abnormally necrotic liver parenchyme', 0.5, 10.01729298920255, 2.2380005573281867, 'UPHENO:0019492', 'abnormal liver morphology'),
(471831, 'HP:0031143', 'Decreased hepatic echogenicity', 'XPO:0129248', 'decreased size of the liver parenchyme', 0.4861111111111111, 10.01729298920255, 2.20669830862916, 'UPHENO:0019492', 'abnormal liver morphology'),
(471832, 'HP:0031143', 'Decreased hepatic echogenicity', 'XPO:0130756', 'increased size of the hepatocyte', 0.4024390243902439, 9.184143847054914, 1.9225134302959865, 'UPHENO:0086622', 'abnormal liver morphology'),
(471833, 'HP:0031143', 'Decreased hepatic echogenicity', 'XPO:0130806', 'increased size of the biliary tree', 0.4090909090909091, 8.69832224767236, 1.8863733871813304, 'UPHENO:0087100', 'abnormal hepatobiliary system morphology'),
(471834, 'HP:0031143', 'Decreased hepatic echogenicity', 'XPO:0141833', 'edematous alimentary system', 0.42, 5.725717590856133, 1.5507422055775666, 'UPHENO:0076803', 'abnormal digestive system morphology'),
(471835, 'HP:0031143', 'Decreased hepatic echogenicity', 'XPO:0102426', 'abnormal liver morphology', 0.5384615384615384, 10.01729298920255, 2.322482937329355, 'UPHENO:0019492', 'abnormal liver morphology'),
(471836, 'HP:0031143', 'Decreased hepatic echogenicity', 'XPO:0102367', 'abnormal hindgut morphology', 0.40384615384615385, 5.725717590856133, 1.520627839767678, 'UPHENO:0076803', 'abnormal digestive system morphology'),
(471837, 'HP:0031143', 'Decreased hepatic echogenicity', 'XPO:0130151', 'increased size of the liver', 0.4117647058823529, 10.01729298920255, 2.0309524124007297, 'UPHENO:0019492', 'abnormal liver morphology'),
(471838, 'HP:0031143', 'Decreased hepatic echogenicity', 'XPO:0140645', 'abnormally necrotic hepatic vein', 0.4069767441860465, 10.01729298920255, 2.019110023327942, 'UPHENO:0019492', 'abnormal liver morphology'),
(471839, 'HP:0031143', 'Decreased hepatic echogenicity', 'XPO:0140793', 'abnormally necrotic hepatic portal vein', 0.4069767441860465, 10.01729298920255, 2.019110023327942, 'UPHENO:0019492', 'abnormal liver morphology'),
(471840, 'HP:0031143', 'Decreased hepatic echogenicity', 'XPO:0107375', 'abnormal larval alimentary system morphology', 0.42, 5.725717590856133, 1.5507422055775666, 'UPHENO:0076803', 'abnormal digestive system morphology'),
(471841, 'HP:0031143', 'Decreased hepatic echogenicity', 'XPO:0102211', 'abnormal biliary tree morphology', 0.4576271186440678, 8.69832224767236, 1.9951411346668921, 'UPHENO:0087100', 'abnormal hepatobiliary system morphology'),
(471842, 'HP:0031143', 'Decreased hepatic echogenicity', 'XPO:0140908', 'abnormally necrotic hepatocyte', 0.44594594594594594, 9.184143847054914, 2.0237667147125786, 'UPHENO:0086622', 'abnormal liver morphology'),
(471843, 'HP:0031143', 'Decreased hepatic echogenicity', 'XPO:0129280', 'decreased size of the hepatocyte', 0.4024390243902439, 9.184143847054914, 1.9225134302959865, 'UPHENO:0086622', 'abnormal liver morphology'),
(471844, 'HP:0031143', 'Decreased hepatic echogenicity', 'XPO:0102118', 'abnormal oral evagination morphology', 0.4117647058823529, 5.725717590856133, 1.5354635846428564, 'UPHENO:0076803', 'abnormal digestive system morphology'),
(471845, 'HP:0031143', 'Decreased hepatic echogenicity', 'XPO:0129330', 'decreased size of the biliary tree', 0.4090909090909091, 8.69832224767236, 1.8863733871813304, 'UPHENO:0087100', 'abnormal hepatobiliary system morphology'),
(471846, 'HP:0031143', 'Decreased hepatic echogenicity', 'XPO:0102655', 'abnormal ultimobranchial body morphology', 0.40384615384615385, 7.767034997756375, 1.7710695103898046, 'UPHENO:0087376', 'abnormal endocrine gland morphology'),
(471847, 'HP:0031143', 'Decreased hepatic echogenicity', 'XPO:0139877', 'abnormally necrotic liver', 0.4605263157894737, 10.01729298920255, 2.147842413796034, 'UPHENO:0019492', 'abnormal liver morphology'),
(471848, 'HP:0031143', 'Decreased hepatic echogenicity', 'XPO:0103088', 'abnormal capillary system of liver morphology', 0.4074074074074074, 9.184143847054914, 1.9343443938413178, 'UPHENO:0086622', 'abnormal liver morphology'),
(471849, 'HP:0031143', 'Decreased hepatic echogenicity', 'XPO:0101787', 'abnormal hepatic portal vein morphology', 0.4430379746835443, 10.01729298920255, 2.1066658960898295, 'UPHENO:0019492', 'abnormal liver morphology'),
(471850, 'HP:0031143', 'Decreased hepatic echogenicity', 'XPO:0100042', 'abnormal hepatic vein', 0.5645161290322581, 10.01729298920255, 2.378008297219882, 'UPHENO:0019492', 'abnormal liver morphology'),
(471851, 'HP:0031143', 'Decreased hepatic echogenicity', 'XPO:0102522', 'abnormal pharyngeal cavity morphology', 0.4375, 5.725717590856133, 1.582719635943005, 'UPHENO:0076803', 'abnormal digestive system morphology'),
(471852, 'HP:0031143', 'Decreased hepatic echogenicity', 'XPO:0102801', 'abnormal hepato-pancreatic duct morphology', 0.4074074074074074, 8.69832224767236, 1.8824879589836343, 'UPHENO:0087100', 'abnormal hepatobiliary system morphology'),
(471853, 'HP:0031143', 'Decreased hepatic echogenicity', 'XPO:0101784', 'abnormal alimentary system morphology', 0.4375, 5.725717590856133, 1.582719635943005, 'UPHENO:0076803', 'abnormal digestive system morphology'),
(471854, 'HP:0031143', 'Decreased hepatic echogenicity', 'XPO:0126004', 'absent hepatic portal vein', 0.4069767441860465, 10.01729298920255, 2.019110023327942, 'UPHENO:0019492', 'abnormal liver morphology'),
(471855, 'HP:0031143', 'Decreased hepatic echogenicity', 'XPO:0102155', 'abnormal midgut morphology', 0.40384615384615385, 5.725717590856133, 1.520627839767678, 'UPHENO:0076803', 'abnormal digestive system morphology'),
(471856, 'HP:0031143', 'Decreased hepatic echogenicity', 'XPO:0102825', 'abnormal bile duct morphology', 0.45, 8.69832224767236, 1.9784450994284786, 'UPHENO:0087100', 'abnormal hepatobiliary system morphology'),
(471857, 'HP:0031143', 'Decreased hepatic echogenicity', 'XPO:0125433', 'absent hepatic vein', 0.4666666666666667, 10.01729298920255, 2.162113948961646, 'UPHENO:0019492', 'abnormal liver morphology'),
(471858, 'HP:0031143', 'Decreased hepatic echogenicity', 'XPO:0102763', 'abnormal hepatocyte morphology', 0.4782608695652174, 9.184143847054914, 2.0958093001283595, 'UPHENO:0086622', 'abnormal liver morphology'),
(471859, 'HP:0031143', 'Decreased hepatic echogenicity', 'XPO:0103009', 'abnormal manicotto glandulare morphology', 0.4117647058823529, 5.725717590856133, 1.5354635846428564, 'UPHENO:0076803', 'abnormal digestive system morphology'),
(471860, 'HP:0031143', 'Decreased hepatic echogenicity', 'XPO:0102125', 'abnormal liver and biliary system morphology', 0.4489795918367347, 8.69832224767236, 1.9762006913328223, 'UPHENO:0087100', 'abnormal hepatobiliary system morphology'),
(471861, 'HP:0031143', 'Decreased hepatic echogenicity', 'XPO:0141647', 'neoplastic liver', 0.5147058823529411, 10.01729298920255, 2.2706738265976094, 'UPHENO:0019492', 'abnormal liver morphology'),
(471862, 'HP:0034952', 'Gangliocytoma', 'XPO:0101663', 'abnormal central nervous system morphology', 0.42857142857142855, 5.483278994082134, 1.5329633758669794, 'HP:0002011', 'Morphological central nervous system abnormality'),
(471863, 'HP:0034952', 'Gangliocytoma', 'XPO:0142031', 'abnormally necrotic cerebrospinal fluid', 0.4090909090909091, 5.483278994082134, 1.4977181271815287, 'HP:0002011', 'Morphological central nervous system abnormality'),
(471864, 'HP:0034952', 'Gangliocytoma', 'XPO:0101790', 'abnormal neuromere morphology', 0.4090909090909091, 5.483278994082134, 1.4977181271815287, 'HP:0002011', 'Morphological central nervous system abnormality'),
(471865, 'HP:0034952', 'Gangliocytoma', 'XPO:0101796', 'abnormal neural nucleus morphology', 0.4186046511627907, 5.483278994082134, 1.515033362849152, 'HP:0002011', 'Morphological central nervous system abnormality'),
(471866, 'HP:0034952', 'Gangliocytoma', 'XPO:0142058', 'abnormal cerebrospinal fluid morphology', 0.43902439024390244, 5.483278994082134, 1.5515454285692403, 'HP:0002011', 'Morphological central nervous system abnormality'),
(471867, 'HP:0001135', 'Chorioretinal dystrophy', 'XPO:0103186', 'abnormal peripheral retina morphology', 0.48314606741573035, 8.040873045973026, 1.9710190741722953, 'HP:0000479', 'Abnormal retinal morphology'),
(471868, 'HP:0001135', 'Chorioretinal dystrophy', 'XPO:0102882', 'abnormal retinal cone cell morphology', 0.4095238095238095, 8.040873045973026, 1.8146429295275122, 'HP:0000479', 'Abnormal retinal morphology'),
(471869, 'HP:0001135', 'Chorioretinal dystrophy', 'XPO:0129309', 'decreased size of the hyaloid artery', 0.40350877192982454, 10.24626555896271, 2.0333366746714376, 'UPHENO:0087915', 'abnormal vasculature of eye morphology'),
(471870, 'HP:0001135', 'Chorioretinal dystrophy', 'XPO:0128643', 'decreased size of the retinal layer', 0.4725274725274725, 8.040873045973026, 1.9492391893577128, 'HP:0000479', 'Abnormal retinal morphology'),
(471871, 'HP:0001135', 'Chorioretinal dystrophy', 'XPO:0103226', 'abnormal retinal outer plexiform layer morphology', 0.43, 8.040873045973026, 1.859455675666511, 'HP:0000479', 'Abnormal retinal morphology'),
(471872, 'HP:0001135', 'Chorioretinal dystrophy', 'XPO:0102815', 'abnormal retinal ganglion cell morphology', 0.4056603773584906, 8.040873045973026, 1.8060630094548564, 'HP:0000479', 'Abnormal retinal morphology'),
(471873, 'HP:0001135', 'Chorioretinal dystrophy', 'XPO:0128300', 'decreased size of the retina', 0.46236559139784944, 8.040873045973026, 1.9281657141584967, 'HP:0000479', 'Abnormal retinal morphology'),
(471874, 'HP:0001135', 'Chorioretinal dystrophy', 'XPO:0102017', 'abnormal retinal neural layer morphology', 0.43434343434343436, 8.040873045973026, 1.8688232698432123, 'HP:0000479', 'Abnormal retinal morphology'),
(471875, 'HP:0001135', 'Chorioretinal dystrophy', 'XPO:0102239', 'abnormal retinal pigmented epithelium morphology', 0.43, 8.040873045973026, 1.859455675666511, 'HP:0000479', 'Abnormal retinal morphology'),
(471876, 'HP:0001135', 'Chorioretinal dystrophy', 'XPO:0141333', 'increased pigmentation in the retinal pigmented epithelium', 0.4174757281553398, 8.040873045973026, 1.8321761186829812, 'HP:0000479', 'Abnormal retinal morphology'),
(471877, 'HP:0001135', 'Chorioretinal dystrophy', 'XPO:0130785', 'increased size of the hyaloid artery', 0.40350877192982454, 10.24626555896271, 2.0333366746714376, 'UPHENO:0087915', 'abnormal vasculature of eye morphology'),
(471878, 'HP:0001135', 'Chorioretinal dystrophy', 'XPO:0103155', 'abnormal bipolar neuron morphology', 0.40186915887850466, 8.040873045973026, 1.797603651429875, 'HP:0000479', 'Abnormal retinal morphology'),
(471879, 'HP:0001135', 'Chorioretinal dystrophy', 'XPO:0140240', 'abnormally necrotic eye photoreceptor cell', 0.40186915887850466, 8.040873045973026, 1.797603651429875, 'HP:0000479', 'Abnormal retinal morphology'),
(471880, 'HP:0001135', 'Chorioretinal dystrophy', 'XPO:0140006', 'abnormally necrotic retinal neural layer', 0.40186915887850466, 8.040873045973026, 1.797603651429875, 'HP:0000479', 'Abnormal retinal morphology'),
(471881, 'HP:0001135', 'Chorioretinal dystrophy', 'XPO:0102117', 'abnormal retina morphology', 0.5, 8.040873045973026, 2.0051026215599324, 'HP:0000479', 'Abnormal retinal morphology'),
(471882, 'HP:0001135', 'Chorioretinal dystrophy', 'XPO:0101961', 'abnormal retinal blood vessel morphology', 0.5869565217391305, 10.24626555896271, 2.452368731105541, 'UPHENO:0087915', 'abnormal vasculature of eye morphology'),
(471883, 'HP:0001135', 'Chorioretinal dystrophy', 'XPO:0141253', 'abnormally necrotic hyaloid vein', 0.4158415841584158, 10.24626555896271, 2.064176179919454, 'UPHENO:0087915', 'abnormal vasculature of eye morphology'),
(471884, 'HP:0001135', 'Chorioretinal dystrophy', 'XPO:0141033', 'abnormally necrotic photoreceptor layer', 0.4056603773584906, 8.040873045973026, 1.8060630094548564, 'HP:0000479', 'Abnormal retinal morphology'),
(471885, 'HP:0001135', 'Chorioretinal dystrophy', 'XPO:0103086', 'abnormal amacrine cell morphology', 0.40186915887850466, 8.040873045973026, 1.797603651429875, 'HP:0000479', 'Abnormal retinal morphology'),
(471886, 'HP:0001135', 'Chorioretinal dystrophy', 'XPO:0103022', 'abnormal ciliary body morphology', 0.41304347826086957, 9.773257991046536, 2.0091740777151936, 'HP:0000553', 'Abnormal uvea morphology'),
(471887, 'HP:0001135', 'Chorioretinal dystrophy', 'XPO:0125589', 'absent hyaloid blood vessel', 0.4157303370786517, 9.463856994035337, 1.9835353433187084, 'UPHENO:0005090', 'abnormal vasculature of eye'),
(471888, 'HP:0001135', 'Chorioretinal dystrophy', 'XPO:0102939', 'abnormal retinal ganglion cell layer morphology', 0.43, 8.040873045973026, 1.859455675666511, 'HP:0000479', 'Abnormal retinal morphology'),
(471889, 'HP:0001135', 'Chorioretinal dystrophy', 'XPO:0128787', 'decreased size of the peripheral retina', 0.44329896907216493, 8.040873045973026, 1.8879911895239345, 'HP:0000479', 'Abnormal retinal morphology'),
(471890, 'HP:0001135', 'Chorioretinal dystrophy', 'XPO:0127563', 'abnormally localised retinal blood vessel', 0.550561797752809, 9.463856994035337, 2.282638412081859, 'HP:0008047', 'Abnormality of the vasculature of the eye'),
(471891, 'HP:0001135', 'Chorioretinal dystrophy', 'XPO:0140317', 'abnormally necrotic retinal progenitor cell', 0.41346153846153844, 8.040873045973026, 1.8233463028623837, 'HP:0000479', 'Abnormal retinal morphology'),
(471892, 'HP:0001135', 'Chorioretinal dystrophy', 'XPO:0140945', 'abnormally necrotic retinal ganglion cell layer', 0.40186915887850466, 8.040873045973026, 1.797603651429875, 'HP:0000479', 'Abnormal retinal morphology'),
(471893, 'HP:0001135', 'Chorioretinal dystrophy', 'XPO:0102963', 'abnormal retinal outer nuclear layer morphology', 0.43, 8.040873045973026, 1.859455675666511, 'HP:0000479', 'Abnormal retinal morphology'),
(471894, 'HP:0001135', 'Chorioretinal dystrophy', 'XPO:0129045', 'decreased size of the hyaloid vein', 0.4077669902912621, 10.24626555896271, 2.0440373941548233, 'UPHENO:0087915', 'abnormal vasculature of eye morphology'),
(471895, 'HP:0001135', 'Chorioretinal dystrophy', 'XPO:0140346', 'abnormally necrotic retinal blood vessel', 0.5454545454545454, 10.24626555896271, 2.3640795509184054, 'UPHENO:0087915', 'abnormal vasculature of eye morphology'),
(471896, 'HP:0001135', 'Chorioretinal dystrophy', 'XPO:0102947', 'abnormal hyaloid vascular plexus morphology', 0.45652173913043476, 10.24626555896271, 2.162785928512097, 'UPHENO:0087915', 'abnormal vasculature of eye morphology'),
(471897, 'HP:0001135', 'Chorioretinal dystrophy', 'XPO:0140531', 'abnormally necrotic retinal progenitor cell region', 0.46236559139784944, 8.040873045973026, 1.9281657141584967, 'HP:0000479', 'Abnormal retinal morphology'),
(471898, 'HP:0001135', 'Chorioretinal dystrophy', 'XPO:0101817', 'abnormal eye morphology', 0.40229885057471265, 6.887869297006056, 1.6646266551675757, 'UPHENO:0021474', 'abnormal camera-type eye morphology'),
(471899, 'HP:0001135', 'Chorioretinal dystrophy', 'XPO:0102196', 'abnormal central retina morphology', 0.5, 8.040873045973026, 2.0051026215599324, 'HP:0000479', 'Abnormal retinal morphology'),
(471900, 'HP:0001135', 'Chorioretinal dystrophy', 'XPO:0101359', 'abnormal hyaloid artery', 0.4606741573033708, 9.463856994035337, 2.088002477385226, 'UPHENO:0005090', 'abnormal vasculature of eye'),
(471901, 'HP:0001135', 'Chorioretinal dystrophy', 'XPO:0127783', 'abnormally localised hyaloid vascular plexus', 0.4065934065934066, 9.463856994035337, 1.9616171529423536, 'HP:0008047', 'Abnormality of the vasculature of the eye'),
(471902, 'HP:0001135', 'Chorioretinal dystrophy', 'XPO:0130506', 'increased size of the Muller cell', 0.40186915887850466, 8.040873045973026, 1.797603651429875, 'HP:0000479', 'Abnormal retinal morphology'),
(471903, 'HP:0001135', 'Chorioretinal dystrophy', 'XPO:0102162', 'abnormal ciliary marginal zone morphology', 0.4574468085106383, 8.040873045973026, 1.9178820903589395, 'HP:0000479', 'Abnormal retinal morphology'),
(471904, 'HP:0001135', 'Chorioretinal dystrophy', 'XPO:0140161', 'abnormally necrotic hyaloid vascular plexus', 0.4158415841584158, 10.24626555896271, 2.064176179919454, 'UPHENO:0087915', 'abnormal vasculature of eye morphology'),
(471905, 'HP:0001135', 'Chorioretinal dystrophy', 'XPO:0130829', 'increased size of the hyaloid vascular plexus', 0.4077669902912621, 10.24626555896271, 2.0440373941548233, 'UPHENO:0087915', 'abnormal vasculature of eye morphology'),
(471906, 'HP:0001135', 'Chorioretinal dystrophy', 'XPO:0140439', 'abnormally necrotic retinal stem cell', 0.41346153846153844, 8.040873045973026, 1.8233463028623837, 'HP:0000479', 'Abnormal retinal morphology'),
(471907, 'HP:0001135', 'Chorioretinal dystrophy', 'XPO:0102784', 'abnormal retinal progenitor cell region morphology', 0.4777777777777778, 8.040873045973026, 1.960038381077836, 'HP:0000479', 'Abnormal retinal morphology'),
(471908, 'HP:0001135', 'Chorioretinal dystrophy', 'XPO:0130522', 'increased size of the hyaloid vein', 0.4077669902912621, 10.24626555896271, 2.0440373941548233, 'UPHENO:0087915', 'abnormal vasculature of eye morphology'),
(471909, 'HP:0001135', 'Chorioretinal dystrophy', 'XPO:0102818', 'abnormal optic chiasm morphology', 0.41414141414141414, 7.796308075334707, 1.7968789751681224, 'UPHENO:0021656', 'abnormal ocular fundus morphology'),
(471910, 'HP:0001135', 'Chorioretinal dystrophy', 'XPO:0100329', 'abnormal retinal blood vessel', 0.620253164556962, 9.463856994035337, 2.4228056565612017, 'UPHENO:0005090', 'abnormal vasculature of eye'),
(471911, 'HP:0001135', 'Chorioretinal dystrophy', 'XPO:0125909', 'absent retinal blood vessel', 0.5212765957446809, 9.463856994035337, 2.2211004381759123, 'UPHENO:0005090', 'abnormal vasculature of eye'),
(471912, 'HP:0001135', 'Chorioretinal dystrophy', 'XPO:0102003', 'abnormal hyaloid blood vessel morphology', 0.49411764705882355, 10.24626555896271, 2.2500801383805236, 'UPHENO:0087915', 'abnormal vasculature of eye morphology'),
(471913, 'HP:0001135', 'Chorioretinal dystrophy', 'XPO:0129355', 'decreased size of the hyaloid vascular plexus', 0.4077669902912621, 10.24626555896271, 2.0440373941548233, 'UPHENO:0087915', 'abnormal vasculature of eye morphology'),
(471914, 'HP:0001135', 'Chorioretinal dystrophy', 'XPO:0127566', 'abnormally localised hyaloid artery', 0.40594059405940597, 9.463856994035337, 1.9600417674763895, 'UPHENO:0005090', 'abnormal vasculature of eye'),
(471915, 'HP:0001135', 'Chorioretinal dystrophy', 'XPO:0139912', 'abnormally necrotic optic fiber layer', 0.40186915887850466, 8.040873045973026, 1.797603651429875, 'HP:0000479', 'Abnormal retinal morphology'),
(471916, 'HP:0001135', 'Chorioretinal dystrophy', 'XPO:0140520', 'abnormally necrotic retinal outer nuclear layer', 0.40186915887850466, 8.040873045973026, 1.797603651429875, 'HP:0000479', 'Abnormal retinal morphology'),
(471917, 'HP:0001135', 'Chorioretinal dystrophy', 'XPO:0140732', 'abnormally necrotic hyaloid artery', 0.4107142857142857, 10.24626555896271, 2.051411133899847, 'UPHENO:0087915', 'abnormal vasculature of eye morphology'),
(471918, 'HP:0001135', 'Chorioretinal dystrophy', 'XPO:0127230', 'abnormally localised hyaloid blood vessel', 0.43023255813953487, 9.463856994035337, 2.017835326385816, 'UPHENO:0005090', 'abnormal vasculature of eye'),
(471919, 'HP:0001135', 'Chorioretinal dystrophy', 'XPO:0140487', 'abnormally necrotic retinal layer', 0.4777777777777778, 8.040873045973026, 1.960038381077836, 'HP:0000479', 'Abnormal retinal morphology'),
(471920, 'HP:0001135', 'Chorioretinal dystrophy', 'XPO:0139722', 'abnormally necrotic hyaloid blood vessel', 0.46153846153846156, 10.24626555896271, 2.1746368990243345, 'UPHENO:0087915', 'abnormal vasculature of eye morphology'),
(471921, 'HP:0001135', 'Chorioretinal dystrophy', 'XPO:0140391', 'abnormally necrotic central retina', 0.48314606741573035, 8.040873045973026, 1.9710190741722953, 'HP:0000479', 'Abnormal retinal morphology'),
(471922, 'HP:0001135', 'Chorioretinal dystrophy', 'XPO:0130353', 'increased size of the photoreceptor layer', 0.40186915887850466, 8.040873045973026, 1.797603651429875, 'HP:0000479', 'Abnormal retinal morphology'),
(471923, 'HP:0001135', 'Chorioretinal dystrophy', 'XPO:0100779', 'abnormal optic choroid vascular plexus', 0.47435897435897434, 9.463856994035337, 2.1187886862947445, 'UPHENO:0005090', 'abnormal vasculature of eye'),
(471924, 'HP:0001135', 'Chorioretinal dystrophy', 'XPO:0128875', 'decreased size of the photoreceptor layer', 0.40186915887850466, 8.040873045973026, 1.797603651429875, 'HP:0000479', 'Abnormal retinal morphology'),
(471925, 'HP:0001135', 'Chorioretinal dystrophy', 'XPO:0129955', 'increased size of the retinal stem cell region', 0.45263157894736844, 8.040873045973026, 1.9077612698957138, 'HP:0000479', 'Abnormal retinal morphology'),
(471926, 'HP:0001135', 'Chorioretinal dystrophy', 'XPO:0130013', 'increased size of the optic choroid vascular plexus', 0.53, 11.854497839006713, 2.5065681428346522, 'HP:0000610', 'Abnormal choroid morphology'),
(471927, 'HP:0001135', 'Chorioretinal dystrophy', 'XPO:0128533', 'decreased size of the optic choroid vascular plexus', 0.53, 11.854497839006713, 2.5065681428346522, 'HP:0000610', 'Abnormal choroid morphology'),
(471928, 'HP:0001135', 'Chorioretinal dystrophy', 'XPO:0140489', 'abnormally necrotic ciliary marginal zone', 0.4215686274509804, 8.040873045973026, 1.8411354685352277, 'HP:0000479', 'Abnormal retinal morphology'),
(471929, 'HP:0001135', 'Chorioretinal dystrophy', 'XPO:0102266', 'abnormal horizontal cell morphology', 0.41346153846153844, 8.040873045973026, 1.8233463028623837, 'HP:0000479', 'Abnormal retinal morphology'),
(471930, 'HP:0001135', 'Chorioretinal dystrophy', 'XPO:0140754', 'abnormally necrotic optic choroid vascular plexus', 0.5408163265306123, 11.854497839006713, 2.5320161875779332, 'HP:0000610', 'Abnormal choroid morphology'),
(471931, 'HP:0001135', 'Chorioretinal dystrophy', 'XPO:0102505', 'abnormal retinal stem cell region morphology', 0.4777777777777778, 8.040873045973026, 1.960038381077836, 'HP:0000479', 'Abnormal retinal morphology'),
(471932, 'HP:0001135', 'Chorioretinal dystrophy', 'XPO:0130413', 'increased size of the central retina', 0.4725274725274725, 8.040873045973026, 1.9492391893577128, 'HP:0000479', 'Abnormal retinal morphology'),
(471933, 'HP:0001135', 'Chorioretinal dystrophy', 'XPO:0103926', 'decreased pigmentation in the retinal pigmented epithelium', 0.4174757281553398, 8.040873045973026, 1.8321761186829812, 'HP:0000479', 'Abnormal retinal morphology'),
(471934, 'HP:0001135', 'Chorioretinal dystrophy', 'XPO:0102851', 'abnormal retinal rod cell morphology', 0.4095238095238095, 8.040873045973026, 1.8146429295275122, 'HP:0000479', 'Abnormal retinal morphology'),
(471935, 'HP:0001135', 'Chorioretinal dystrophy', 'XPO:0103210', 'abnormal pupil morphology', 0.40425531914893614, 9.773257991046536, 1.9876849670648034, 'HP:0000553', 'Abnormal uvea morphology'),
(471936, 'HP:0001135', 'Chorioretinal dystrophy', 'XPO:0100371', 'abnormal hyaloid blood vessel', 0.4805194805194805, 9.463856994035337, 2.1325026720931706, 'HP:0008047', 'Abnormality of the vasculature of the eye'),
(471937, 'HP:0001135', 'Chorioretinal dystrophy', 'XPO:0128669', 'decreased size of the ciliary marginal zone', 0.41346153846153844, 8.040873045973026, 1.8233463028623837, 'HP:0000479', 'Abnormal retinal morphology'),
(471938, 'HP:0001135', 'Chorioretinal dystrophy', 'XPO:0102991', 'abnormal hyaloid artery morphology', 0.4423076923076923, 10.24626555896271, 2.128849941671931, 'UPHENO:0087915', 'abnormal vasculature of eye morphology'),
(471939, 'HP:0001135', 'Chorioretinal dystrophy', 'XPO:0103184', 'abnormal inner limiting membrane morphology', 0.43, 8.040873045973026, 1.859455675666511, 'HP:0000479', 'Abnormal retinal morphology'),
(471940, 'HP:0001135', 'Chorioretinal dystrophy', 'XPO:0102996', 'abnormal optic fiber layer morphology', 0.43, 8.040873045973026, 1.859455675666511, 'HP:0000479', 'Abnormal retinal morphology'),
(471941, 'HP:0001135', 'Chorioretinal dystrophy', 'XPO:0141014', 'abnormally necrotic retinal outer plexiform layer', 0.40186915887850466, 8.040873045973026, 1.797603651429875, 'HP:0000479', 'Abnormal retinal morphology'),
(471942, 'HP:0001135', 'Chorioretinal dystrophy', 'XPO:0140553', 'abnormally necrotic retinal stem cell region', 0.46236559139784944, 8.040873045973026, 1.9281657141584967, 'HP:0000479', 'Abnormal retinal morphology'),
(471943, 'HP:0001135', 'Chorioretinal dystrophy', 'XPO:0130122', 'increased size of the retinal layer', 0.4725274725274725, 8.040873045973026, 1.9492391893577128, 'HP:0000479', 'Abnormal retinal morphology'),
(471944, 'HP:0001135', 'Chorioretinal dystrophy', 'XPO:0141182', 'abnormally necrotic inner limiting membrane', 0.40186915887850466, 8.040873045973026, 1.797603651429875, 'HP:0000479', 'Abnormal retinal morphology'),
(471945, 'HP:0001135', 'Chorioretinal dystrophy', 'XPO:0102441', 'abnormal retinal inner plexiform layer morphology', 0.43, 8.040873045973026, 1.859455675666511, 'HP:0000479', 'Abnormal retinal morphology'),
(471946, 'HP:0001135', 'Chorioretinal dystrophy', 'XPO:0102663', 'abnormal retinal progenitor cell morphology', 0.43434343434343436, 8.040873045973026, 1.8688232698432123, 'HP:0000479', 'Abnormal retinal morphology'),
(471947, 'HP:0001135', 'Chorioretinal dystrophy', 'XPO:0102450', 'abnormal retinal stem cell morphology', 0.43434343434343436, 8.040873045973026, 1.8688232698432123, 'HP:0000479', 'Abnormal retinal morphology'),
(471948, 'HP:0001135', 'Chorioretinal dystrophy', 'XPO:0140948', 'abnormally necrotic retinal inner nuclear layer', 0.40186915887850466, 8.040873045973026, 1.797603651429875, 'HP:0000479', 'Abnormal retinal morphology'),
(471949, 'HP:0001135', 'Chorioretinal dystrophy', 'XPO:0102756', 'abnormal Muller cell morphology', 0.4574468085106383, 8.040873045973026, 1.9178820903589395, 'HP:0000479', 'Abnormal retinal morphology'),
(471950, 'HP:0001135', 'Chorioretinal dystrophy', 'XPO:0127907', 'abnormally localised optic choroid vascular plexus', 0.4157303370786517, 9.463856994035337, 1.9835353433187084, 'UPHENO:0005090', 'abnormal vasculature of eye'),
(471951, 'HP:0001135', 'Chorioretinal dystrophy', 'XPO:0128935', 'decreased size of the central retina', 0.4725274725274725, 8.040873045973026, 1.9492391893577128, 'HP:0000479', 'Abnormal retinal morphology'),
(471952, 'HP:0001135', 'Chorioretinal dystrophy', 'XPO:0129029', 'decreased size of the Muller cell', 0.40186915887850466, 8.040873045973026, 1.797603651429875, 'HP:0000479', 'Abnormal retinal morphology'),
(471953, 'HP:0001135', 'Chorioretinal dystrophy', 'XPO:0102342', 'abnormal hyaloid vein morphology', 0.45161290322580644, 10.24626555896271, 2.1511266202401336, 'UPHENO:0087915', 'abnormal vasculature of eye morphology'),
(471954, 'HP:0001135', 'Chorioretinal dystrophy', 'XPO:0102805', 'abnormal retinal layer morphology', 0.5119047619047619, 8.040873045973026, 2.028832472656439, 'HP:0000479', 'Abnormal retinal morphology'),
(471955, 'HP:0001135', 'Chorioretinal dystrophy', 'XPO:0128475', 'decreased size of the retinal stem cell region', 0.45263157894736844, 8.040873045973026, 1.9077612698957138, 'HP:0000479', 'Abnormal retinal morphology'),
(471956, 'HP:0001135', 'Chorioretinal dystrophy', 'XPO:0101861', 'abnormal photoreceptor layer morphology', 0.43434343434343436, 8.040873045973026, 1.8688232698432123, 'HP:0000479', 'Abnormal retinal morphology'),
(471957, 'HP:0001135', 'Chorioretinal dystrophy', 'XPO:0129780', 'increased size of the retina', 0.46236559139784944, 8.040873045973026, 1.9281657141584967, 'HP:0000479', 'Abnormal retinal morphology'),
(471958, 'HP:0001135', 'Chorioretinal dystrophy', 'XPO:0140271', 'abnormally necrotic peripheral retina', 0.45263157894736844, 8.040873045973026, 1.9077612698957138, 'HP:0000479', 'Abnormal retinal morphology'),
(471959, 'HP:0001135', 'Chorioretinal dystrophy', 'XPO:0127645', 'abnormally localised hyaloid vein', 0.4111111111111111, 9.463856994035337, 1.9724849211627773, 'UPHENO:0005090', 'abnormal vasculature of eye'),
(471960, 'HP:0001135', 'Chorioretinal dystrophy', 'XPO:0102232', 'abnormal eye photoreceptor cell morphology', 0.4174757281553398, 8.040873045973026, 1.8321761186829812, 'HP:0000479', 'Abnormal retinal morphology'),
(471961, 'HP:0001135', 'Chorioretinal dystrophy', 'XPO:0128564', 'decreased size of the hyaloid blood vessel', 0.45161290322580644, 10.24626555896271, 2.1511266202401336, 'UPHENO:0087915', 'abnormal vasculature of eye morphology'),
(471962, 'HP:0001135', 'Chorioretinal dystrophy', 'XPO:0128330', 'decreased size of the retinal progenitor cell region', 0.45263157894736844, 8.040873045973026, 1.9077612698957138, 'HP:0000479', 'Abnormal retinal morphology'),
(471963, 'HP:0001135', 'Chorioretinal dystrophy', 'XPO:0102946', 'abnormal retinal inner nuclear layer morphology', 0.43, 8.040873045973026, 1.859455675666511, 'HP:0000479', 'Abnormal retinal morphology'),
(471964, 'HP:0001135', 'Chorioretinal dystrophy', 'XPO:0102411', 'abnormal optic choroid vascular plexus morphology', 0.5888888888888889, 11.854497839006713, 2.642154813925255, 'HP:0000610', 'Abnormal choroid morphology'),
(471965, 'HP:0001135', 'Chorioretinal dystrophy', 'XPO:0102862', 'abnormal iris morphology', 0.40425531914893614, 9.773257991046536, 1.9876849670648034, 'HP:0000553', 'Abnormal uvea morphology'),
(471966, 'HP:0001135', 'Chorioretinal dystrophy', 'XPO:0130044', 'increased size of the hyaloid blood vessel', 0.45161290322580644, 10.24626555896271, 2.1511266202401336, 'UPHENO:0087915', 'abnormal vasculature of eye morphology'),
(471967, 'HP:0001135', 'Chorioretinal dystrophy', 'XPO:0130148', 'increased size of the ciliary marginal zone', 0.41346153846153844, 8.040873045973026, 1.8233463028623837, 'HP:0000479', 'Abnormal retinal morphology'),
(471968, 'HP:0001135', 'Chorioretinal dystrophy', 'XPO:0101315', 'abnormal hyaloid vascular plexus', 0.46835443037974683, 9.463856994035337, 2.105335923703579, 'UPHENO:0005090', 'abnormal vasculature of eye'),
(471969, 'HP:0001135', 'Chorioretinal dystrophy', 'XPO:0100710', 'abnormal hyaloid vein', 0.46835443037974683, 9.463856994035337, 2.105335923703579, 'UPHENO:0005090', 'abnormal vasculature of eye'),
(471970, 'HP:0001135', 'Chorioretinal dystrophy', 'XPO:0130257', 'increased size of the retinal blood vessel', 0.5346534653465347, 10.24626555896271, 2.340555786124369, 'UPHENO:0087915', 'abnormal vasculature of eye morphology'),
(471971, 'HP:0001135', 'Chorioretinal dystrophy', 'XPO:0140192', 'abnormally necrotic retina', 0.4725274725274725, 8.040873045973026, 1.9492391893577128, 'HP:0000479', 'Abnormal retinal morphology'),
(471972, 'HP:0001135', 'Chorioretinal dystrophy', 'XPO:0128779', 'decreased size of the retinal blood vessel', 0.5346534653465347, 10.24626555896271, 2.340555786124369, 'UPHENO:0087915', 'abnormal vasculature of eye morphology'),
(471973, 'HP:0001135', 'Chorioretinal dystrophy', 'XPO:0141138', 'abnormally necrotic retinal inner plexiform layer', 0.40186915887850466, 8.040873045973026, 1.797603651429875, 'HP:0000479', 'Abnormal retinal morphology'),
(471974, 'HP:0001135', 'Chorioretinal dystrophy', 'XPO:0130265', 'increased size of the peripheral retina', 0.44329896907216493, 8.040873045973026, 1.8879911895239345, 'HP:0000479', 'Abnormal retinal morphology'),
(471975, 'HP:0001135', 'Chorioretinal dystrophy', 'XPO:0141156', 'abnormally necrotic outer limiting membrane', 0.40186915887850466, 8.040873045973026, 1.797603651429875, 'HP:0000479', 'Abnormal retinal morphology'),
(471976, 'HP:0001135', 'Chorioretinal dystrophy', 'XPO:0102581', 'abnormal outer limiting membrane morphology', 0.43, 8.040873045973026, 1.859455675666511, 'HP:0000479', 'Abnormal retinal morphology'),
(471977, 'HP:0001135', 'Chorioretinal dystrophy', 'XPO:0129810', 'increased size of the retinal progenitor cell region', 0.45263157894736844, 8.040873045973026, 1.9077612698957138, 'HP:0000479', 'Abnormal retinal morphology'),
(471978, 'HP:0001135', 'Chorioretinal dystrophy', 'XPO:0139887', 'abnormally necrotic Muller cell', 0.43434343434343436, 8.040873045973026, 1.8688232698432123, 'HP:0000479', 'Abnormal retinal morphology'),
(471979, 'HP:0031274', 'Hypovolemic shock', 'XPO:0100108', 'abnormal cell part', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(471980, 'HP:0031274', 'Hypovolemic shock', 'XPO:0101583', 'abnormal truncus arteriosus', 0.42424242424242425, 5.249153838287537, 1.4922847414540332, 'UPHENO:0080362', 'abnormal cardiovascular system'),
(471981, 'HP:0031274', 'Hypovolemic shock', 'XPO:0101206', 'abnormal ischiadic vein', 0.4117647058823529, 5.249153838287537, 1.4701755971154233, 'UPHENO:0080362', 'abnormal cardiovascular system'),
(471982, 'HP:0031274', 'Hypovolemic shock', 'XPO:0100285', 'abnormal progenitor cell', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(471983, 'HP:0031274', 'Hypovolemic shock', 'XPO:0101326', 'abnormal cementoblast', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(471984, 'HP:0031274', 'Hypovolemic shock', 'XPO:0100791', 'abnormal multiciliated cell precursor', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(471985, 'HP:0031274', 'Hypovolemic shock', 'XPO:0101333', 'abnormal barrier epithelial cell', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(471986, 'HP:0031274', 'Hypovolemic shock', 'XPO:0100172', 'abnormal stem cell', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(471987, 'HP:0031274', 'Hypovolemic shock', 'XPO:0100054', 'abnormal blood vessel', 0.4375, 5.249153838287537, 1.5154223187781013, 'UPHENO:0080362', 'abnormal cardiovascular system'),
(471988, 'HP:0031274', 'Hypovolemic shock', 'XPO:0101435', 'abnormal paracrine cell', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(471989, 'HP:0031274', 'Hypovolemic shock', 'XPO:0100691', 'abnormal keratin accumulating cell', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(471990, 'HP:0031274', 'Hypovolemic shock', 'XPO:0100980', 'abnormal dorsal longitudinal anastomosing vessel - left branch', 0.4117647058823529, 5.249153838287537, 1.4701755971154233, 'UPHENO:0080362', 'abnormal cardiovascular system'),
(471991, 'HP:0031274', 'Hypovolemic shock', 'XPO:0101585', 'abnormal dorsal longitudinal anastomosing vessel - right branch', 0.4117647058823529, 5.249153838287537, 1.4701755971154233, 'UPHENO:0080362', 'abnormal cardiovascular system'),
(471992, 'HP:0031274', 'Hypovolemic shock', 'XPO:0101237', 'abnormal mucus secreting cell', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(471993, 'HP:0031274', 'Hypovolemic shock', 'XPO:0100549', 'abnormal mitotic cell', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(471994, 'HP:0031274', 'Hypovolemic shock', 'XPO:0100080', 'abnormal aorta', 0.4117647058823529, 5.249153838287537, 1.4701755971154233, 'UPHENO:0080362', 'abnormal cardiovascular system'),
(471995, 'HP:0031274', 'Hypovolemic shock', 'XPO:0100026', 'abnormal germ cell', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(471996, 'HP:0031274', 'Hypovolemic shock', 'XPO:0101241', 'abnormal nucleate erythrocyte', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(471997, 'HP:0031274', 'Hypovolemic shock', 'XPO:0100477', 'abnormal pericyte', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(471998, 'HP:0031274', 'Hypovolemic shock', 'XPO:0100337', 'abnormal zygote', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(471999, 'HP:0031274', 'Hypovolemic shock', 'XPO:0100081', 'abnormal anatomical entity in vitro', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(472000, 'HP:0031274', 'Hypovolemic shock', 'XPO:0101431', 'abnormal ischiadic artery', 0.4117647058823529, 5.249153838287537, 1.4701755971154233, 'UPHENO:0080362', 'abnormal cardiovascular system'),
(472001, 'HP:0031274', 'Hypovolemic shock', 'XPO:0100076', 'abnormal artery', 0.42424242424242425, 5.249153838287537, 1.4922847414540332, 'UPHENO:0080362', 'abnormal cardiovascular system'),
(472002, 'HP:0031274', 'Hypovolemic shock', 'XPO:0100638', 'abnormal polar body', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(472003, 'HP:0031274', 'Hypovolemic shock', 'XPO:0101132', 'abnormal apoptotic cell', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(472004, 'HP:0031274', 'Hypovolemic shock', 'XPO:0101297', 'abnormal barrier cell', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(472005, 'HP:0031274', 'Hypovolemic shock', 'XPO:0100852', 'abnormal interdigital region', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(472006, 'HP:0031274', 'Hypovolemic shock', 'XPO:0101243', 'abnormal vertebral artery', 0.4117647058823529, 5.249153838287537, 1.4701755971154233, 'UPHENO:0080362', 'abnormal cardiovascular system'),
(472007, 'HP:0031274', 'Hypovolemic shock', 'XPO:0100987', 'abnormal larval aorta', 0.4117647058823529, 5.249153838287537, 1.4701755971154233, 'UPHENO:0080362', 'abnormal cardiovascular system'),
(472008, 'HP:0031274', 'Hypovolemic shock', 'XPO:0101373', 'abnormal oxygen accumulating cell', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(472009, 'HP:0031274', 'Hypovolemic shock', 'XPO:0101467', 'abnormal alkali secreting cell', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(472010, 'HP:0031274', 'Hypovolemic shock', 'XPO:0100981', 'abnormal dorsal longitudinal anastomosing vessel', 0.42424242424242425, 5.249153838287537, 1.4922847414540332, 'UPHENO:0080362', 'abnormal cardiovascular system'),
(472011, 'HP:0031274', 'Hypovolemic shock', 'XPO:0100792', 'abnormal capillary', 0.42424242424242425, 5.249153838287537, 1.4922847414540332, 'UPHENO:0080362', 'abnormal cardiovascular system'),
(472012, 'HP:0031274', 'Hypovolemic shock', 'XPO:0100481', 'abnormal anatomical line', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(472013, 'HP:0031274', 'Hypovolemic shock', 'XPO:0101004', 'abnormal acid secreting cell', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(472014, 'HP:0031274', 'Hypovolemic shock', 'XPO:0100754', 'abnormal electrically active cell', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(472015, 'HP:0031274', 'Hypovolemic shock', 'XPO:0101448', 'abnormal myelin accumulating cell', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(472016, 'HP:0031274', 'Hypovolemic shock', 'XPO:0100137', 'abnormal cardinal vein', 0.4117647058823529, 5.249153838287537, 1.4701755971154233, 'UPHENO:0080362', 'abnormal cardiovascular system'),
(472017, 'HP:0031274', 'Hypovolemic shock', 'XPO:0100043', 'abnormal vein', 0.42424242424242425, 5.249153838287537, 1.4922847414540332, 'UPHENO:0080362', 'abnormal cardiovascular system'),
(472018, 'HP:0031274', 'Hypovolemic shock', 'XPO:0100789', 'abnormal occipitovertebral artery', 0.4117647058823529, 5.249153838287537, 1.4701755971154233, 'UPHENO:0080362', 'abnormal cardiovascular system'),
(472019, 'HP:0031274', 'Hypovolemic shock', 'XPO:0100289', 'abnormal chondroblast', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(472020, 'HP:0031274', 'Hypovolemic shock', 'XPO:0100344', 'abnormal portion of organism substance', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(472021, 'HP:0031274', 'Hypovolemic shock', 'XPO:0100802', 'abnormal exocrine cell', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(472022, 'HP:0031274', 'Hypovolemic shock', 'XPO:0100522', 'abnormal subinterstitial vein', 0.4117647058823529, 5.249153838287537, 1.4701755971154233, 'UPHENO:0080362', 'abnormal cardiovascular system'),
(472023, 'HP:0031274', 'Hypovolemic shock', 'XPO:0100933', 'abnormal branchial vein', 0.4117647058823529, 5.249153838287537, 1.4701755971154233, 'UPHENO:0080362', 'abnormal cardiovascular system'),
(472024, 'HP:0031274', 'Hypovolemic shock', 'XPO:0100533', 'abnormal melanoblast', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(472025, 'HP:0031274', 'Hypovolemic shock', 'XPO:0100653', 'abnormal myoblast', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(472026, 'HP:0031274', 'Hypovolemic shock', 'XPO:0101557', 'abnormal Jacobsons vein', 0.4117647058823529, 5.249153838287537, 1.4701755971154233, 'UPHENO:0080362', 'abnormal cardiovascular system'),
(472027, 'HP:0031274', 'Hypovolemic shock', 'XPO:0100715', 'abnormal ciliated cell', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(472028, 'HP:0031274', 'Hypovolemic shock', 'XPO:0101535', 'abnormal absorptive cell', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(472029, 'HP:0031274', 'Hypovolemic shock', 'XPO:0100004', 'abnormal cell', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(472030, 'HP:0031274', 'Hypovolemic shock', 'XPO:0100006', 'abnormal anatomical structure', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(472031, 'HP:0031274', 'Hypovolemic shock', 'XPO:0100780', 'abnormal vascular plexus', 0.42424242424242425, 5.249153838287537, 1.4922847414540332, 'UPHENO:0080362', 'abnormal cardiovascular system'),
(472032, 'HP:0031274', 'Hypovolemic shock', 'XPO:0100704', 'abnormal Merkel cell', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(472033, 'HP:0010054', 'Abnormality of the first metatarsal bone', 'XPO:0102880', 'abnormal digit-joint region morphology', 0.4492753623188406, 6.173473740856008, 1.6654097548918498, 'UPHENO:0087006', 'abnormal autopod region morphology'),
(472034, 'HP:0010054', 'Abnormality of the first metatarsal bone', 'XPO:0141569', 'abnormal digit-joint region morphology in the regenerating hindlimb', 0.41333333333333333, 6.173473740856008, 1.5974049203485685, 'UPHENO:0087006', 'abnormal autopod region morphology'),
(472035, 'HP:0010054', 'Abnormality of the first metatarsal bone', 'XPO:0133357', 'fused hindlimb digits', 0.40860215053763443, 7.61213700143767, 1.76361434247245, 'UPHENO:0079871', 'abnormal anatomical entity morphology in the skeleton of pelvic complex'),
(472036, 'HP:0010054', 'Abnormality of the first metatarsal bone', 'XPO:0101810', 'abnormal digit morphology', 0.4492753623188406, 6.173473740856008, 1.6654097548918498, 'UPHENO:0087006', 'abnormal autopod region morphology'),
(472037, 'HP:0010054', 'Abnormality of the first metatarsal bone', 'XPO:0102051', 'abnormal hindlimb digit 2 morphology', 0.4418604651162791, 7.61213700143767, 1.833985385978876, 'UPHENO:0079871', 'abnormal anatomical entity morphology in the skeleton of pelvic complex'),
(472038, 'HP:0010054', 'Abnormality of the first metatarsal bone', 'XPO:0101872', 'abnormal hindlimb digit 1 morphology', 0.4418604651162791, 7.61213700143767, 1.833985385978876, 'UPHENO:0079871', 'abnormal anatomical entity morphology in the skeleton of pelvic complex'),
(472039, 'HP:0010054', 'Abnormality of the first metatarsal bone', 'XPO:0139961', 'abnormally necrotic hindlimb digit', 0.41304347826086957, 7.61213700143767, 1.7731732978116046, 'UPHENO:0079871', 'abnormal anatomical entity morphology in the skeleton of pelvic complex'),
(472040, 'HP:0010054', 'Abnormality of the first metatarsal bone', 'XPO:0102948', 'abnormal hindlimb digit 5 morphology', 0.4418604651162791, 7.61213700143767, 1.833985385978876, 'UPHENO:0079871', 'abnormal anatomical entity morphology in the skeleton of pelvic complex'),
(472041, 'HP:0010054', 'Abnormality of the first metatarsal bone', 'XPO:0141568', 'abnormal digit-joint region morphology in the regenerating forelimb', 0.41333333333333333, 6.173473740856008, 1.5974049203485685, 'UPHENO:0087006', 'abnormal autopod region morphology'),
(472042, 'HP:0010054', 'Abnormality of the first metatarsal bone', 'XPO:0103008', 'abnormal iliac process morphology', 0.42857142857142855, 7.61213700143767, 1.806196121462886, 'UPHENO:0079871', 'abnormal anatomical entity morphology in the skeleton of pelvic complex'),
(472043, 'HP:0010054', 'Abnormality of the first metatarsal bone', 'XPO:0103759', 'increased size of the hindlimb digit', 0.40425531914893614, 7.61213700143767, 1.7542083322460909, 'UPHENO:0079871', 'abnormal anatomical entity morphology in the skeleton of pelvic complex'),
(472044, 'HP:0010054', 'Abnormality of the first metatarsal bone', 'XPO:0101809', 'abnormal hindlimb digit morphology', 0.4523809523809524, 7.61213700143767, 1.855690110542345, 'UPHENO:0079871', 'abnormal anatomical entity morphology in the skeleton of pelvic complex'),
(472045, 'HP:0010054', 'Abnormality of the first metatarsal bone', 'XPO:0141567', 'abnormal joint region morphology in the femur', 0.4148936170212766, 7.61213700143767, 1.7771401334132233, 'UPHENO:0079871', 'abnormal anatomical entity morphology in the skeleton of pelvic complex'),
(472046, 'HP:0010054', 'Abnormality of the first metatarsal bone', 'XPO:0102180', 'abnormal hindlimb digit 3 morphology', 0.4418604651162791, 7.61213700143767, 1.833985385978876, 'UPHENO:0079871', 'abnormal anatomical entity morphology in the skeleton of pelvic complex'),
(472047, 'HP:0010054', 'Abnormality of the first metatarsal bone', 'XPO:0102876', 'abnormal hindlimb digit 4 morphology', 0.4418604651162791, 7.61213700143767, 1.833985385978876, 'UPHENO:0079871', 'abnormal anatomical entity morphology in the skeleton of pelvic complex'),
(472048, 'HP:0010054', 'Abnormality of the first metatarsal bone', 'XPO:0128497', 'decreased size of the digit-joint region', 0.41333333333333333, 6.173473740856008, 1.5974049203485685, 'UPHENO:0087006', 'abnormal autopod region morphology'),
(472049, 'HP:0010054', 'Abnormality of the first metatarsal bone', 'XPO:0141208', 'abnormally necrotic digit-joint region', 0.4246575342465753, 6.173473740856008, 1.619139319678172, 'UPHENO:0087006', 'abnormal autopod region morphology'),
(472050, 'HP:0010054', 'Abnormality of the first metatarsal bone', 'XPO:0101859', 'abnormal hindlimb skeleton morphology', 0.4027777777777778, 7.61213700143767, 1.7509996075325265, 'UPHENO:0079871', 'abnormal anatomical entity morphology in the skeleton of pelvic complex'),
(472051, 'HP:0010054', 'Abnormality of the first metatarsal bone', 'XPO:0129977', 'increased size of the digit-joint region', 0.41333333333333333, 6.173473740856008, 1.5974049203485685, 'UPHENO:0087006', 'abnormal autopod region morphology'),
(472052, 'HP:0010054', 'Abnormality of the first metatarsal bone', 'XPO:0130149', 'increased size of the claw primordium', 0.4222222222222222, 7.61213700143767, 1.7927669677364697, 'UPHENO:0079871', 'abnormal anatomical entity morphology in the skeleton of pelvic complex'),
(472053, 'HP:0010054', 'Abnormality of the first metatarsal bone', 'XPO:0103436', 'decreased size of the hindlimb digit', 0.40425531914893614, 7.61213700143767, 1.7542083322460909, 'UPHENO:0079871', 'abnormal anatomical entity morphology in the skeleton of pelvic complex'),
(472054, 'HP:0010054', 'Abnormality of the first metatarsal bone', 'XPO:0141547', 'abnormal hindlimb digit morphology in the regenerating hindlimb', 0.4222222222222222, 7.61213700143767, 1.7927669677364697, 'UPHENO:0079871', 'abnormal anatomical entity morphology in the skeleton of pelvic complex'),
(472055, 'HP:0010054', 'Abnormality of the first metatarsal bone', 'XPO:0139962', 'abnormally necrotic digit', 0.40789473684210525, 6.173473740856008, 1.5868608782524412, 'UPHENO:0087006', 'abnormal autopod region morphology'),
(472056, 'HP:0010054', 'Abnormality of the first metatarsal bone', 'XPO:0102566', 'abnormal claw primordium morphology', 0.4578313253012048, 7.61213700143767, 1.8668354967009138, 'UPHENO:0079871', 'abnormal anatomical entity morphology in the skeleton of pelvic complex'),
(472057, 'HP:0010054', 'Abnormality of the first metatarsal bone', 'XPO:0139979', 'abnormally necrotic claw primordium', 0.4318181818181818, 7.61213700143767, 1.8130248646148572, 'UPHENO:0079871', 'abnormal anatomical entity morphology in the skeleton of pelvic complex'),
(472058, 'HP:0010054', 'Abnormality of the first metatarsal bone', 'XPO:0140858', 'abnormally necrotic iliac process', 0.4090909090909091, 7.61213700143767, 1.764668820499383, 'UPHENO:0079871', 'abnormal anatomical entity morphology in the skeleton of pelvic complex'),
(472059, 'HP:0010054', 'Abnormality of the first metatarsal bone', 'XPO:0128670', 'decreased size of the claw primordium', 0.4222222222222222, 7.61213700143767, 1.7927669677364697, 'UPHENO:0079871', 'abnormal anatomical entity morphology in the skeleton of pelvic complex'),
(472060, 'HP:0010054', 'Abnormality of the first metatarsal bone', 'XPO:0100178', 'abnormal digit', 0.41935483870967744, 5.802924133159483, 1.5599629206829213, 'UPHENO:0076727', 'abnormal limb bone morphology'),
(472061, 'HP:0034594', 'Elevated circulating dihydrothymine concentration', 'XPO:0141917', 'abnormal tryptophan metabolic process', 0.45, 8.366559792680423, 1.9403483982795953, 'UPHENO:0049618', 'abnormal small molecule metabolic process'),
(472062, 'HP:0034594', 'Elevated circulating dihydrothymine concentration', 'XPO:0141918', 'abnormal tyrosine metabolic process', 0.45, 8.366559792680423, 1.9403483982795953, 'UPHENO:0049618', 'abnormal small molecule metabolic process'),
(472063, 'HP:0034594', 'Elevated circulating dihydrothymine concentration', 'XPO:0141869', 'abnormal alpha-amino acid metabolic process', 0.47368421052631576, 8.366559792680423, 1.9907554521379673, 'UPHENO:0049618', 'abnormal small molecule metabolic process'),
(472064, 'HP:0034594', 'Elevated circulating dihydrothymine concentration', 'XPO:0141919', 'abnormal uracil metabolic process', 0.45454545454545453, 14.30515924801628, 2.549969629767122, 'UPHENO:0078631', 'abnormal pyrimidine nucleobase metabolic process'),
(472065, 'HP:0034594', 'Elevated circulating dihydrothymine concentration', 'XPO:0141913', 'abnormal L-serine metabolic process', 0.4426229508196721, 8.366559792680423, 1.9243781810354827, 'UPHENO:0049618', 'abnormal small molecule metabolic process'),
(472066, 'HP:0034594', 'Elevated circulating dihydrothymine concentration', 'XPO:0141893', 'abnormal isoleucine metabolic process', 0.45, 8.366559792680423, 1.9403483982795953, 'UPHENO:0049618', 'abnormal small molecule metabolic process'),
(472067, 'HP:0034594', 'Elevated circulating dihydrothymine concentration', 'XPO:0141895', 'abnormal leucine metabolic process', 0.45, 8.366559792680423, 1.9403483982795953, 'UPHENO:0049618', 'abnormal small molecule metabolic process'),
(472068, 'HP:0034594', 'Elevated circulating dihydrothymine concentration', 'XPO:0141875', 'abnormal cytosine metabolic process', 0.45454545454545453, 14.30515924801628, 2.549969629767122, 'UPHENO:0078631', 'abnormal pyrimidine nucleobase metabolic process'),
(472069, 'HP:0034594', 'Elevated circulating dihydrothymine concentration', 'XPO:0141873', 'abnormal tricarboxylic acid metabolic process', 0.45454545454545453, 8.366559792680423, 1.9501235150486358, 'UPHENO:0049618', 'abnormal small molecule metabolic process'),
(472070, 'HP:0034594', 'Elevated circulating dihydrothymine concentration', 'XPO:0141916', 'abnormal thymine metabolic process', 0.45454545454545453, 14.30515924801628, 2.549969629767122, 'UPHENO:0078631', 'abnormal pyrimidine nucleobase metabolic process'),
(472071, 'HP:0034594', 'Elevated circulating dihydrothymine concentration', 'XPO:0141923', 'abnormal xanthine metabolic process', 0.4222222222222222, 12.92664762476255, 2.3362187153626808, 'UPHENO:0078592', 'abnormal nucleobase metabolic process'),
(472072, 'HP:0034594', 'Elevated circulating dihydrothymine concentration', 'XPO:0141887', 'abnormal histidine metabolic process', 0.45, 8.366559792680423, 1.9403483982795953, 'UPHENO:0049618', 'abnormal small molecule metabolic process'),
(472073, 'HP:0034594', 'Elevated circulating dihydrothymine concentration', 'XPO:0141853', 'abnormal glutamate metabolic process', 0.43548387096774194, 8.366559792680423, 1.908795915020655, 'UPHENO:0049618', 'abnormal small molecule metabolic process'),
(472074, 'HP:0034594', 'Elevated circulating dihydrothymine concentration', 'XPO:0141885', 'abnormal guanine metabolic process', 0.4222222222222222, 12.92664762476255, 2.3362187153626808, 'UPHENO:0078592', 'abnormal nucleobase metabolic process'),
(472075, 'HP:0034594', 'Elevated circulating dihydrothymine concentration', 'XPO:0141912', 'abnormal D-serine metabolic process', 0.4426229508196721, 8.366559792680423, 1.9243781810354827, 'UPHENO:0049618', 'abnormal small molecule metabolic process'),
(472076, 'HP:0034594', 'Elevated circulating dihydrothymine concentration', 'XPO:0141857', 'abnormal glycine metabolic process', 0.4426229508196721, 8.366559792680423, 1.9243781810354827, 'UPHENO:0049618', 'abnormal small molecule metabolic process'),
(472077, 'HP:0034594', 'Elevated circulating dihydrothymine concentration', 'XPO:0141922', 'abnormal valine metabolic process', 0.45, 8.366559792680423, 1.9403483982795953, 'UPHENO:0049618', 'abnormal small molecule metabolic process'),
(472078, 'HP:0034594', 'Elevated circulating dihydrothymine concentration', 'XPO:0141774', 'abnormal NADP metabolic process', 0.4090909090909091, 8.366559792680423, 1.8500496078622006, 'UPHENO:0049618', 'abnormal small molecule metabolic process'),
(472079, 'HP:0034594', 'Elevated circulating dihydrothymine concentration', 'XPO:0141847', 'abnormal arginine metabolic process', 0.45, 8.366559792680423, 1.9403483982795953, 'UPHENO:0049618', 'abnormal small molecule metabolic process'),
(472080, 'HP:0034594', 'Elevated circulating dihydrothymine concentration', 'XPO:0141889', 'abnormal homoserine metabolic process', 0.4426229508196721, 8.366559792680423, 1.9243781810354827, 'UPHENO:0049618', 'abnormal small molecule metabolic process'),
(472081, 'HP:0034594', 'Elevated circulating dihydrothymine concentration', 'XPO:0141896', 'abnormal lysine metabolic process', 0.45, 8.366559792680423, 1.9403483982795953, 'UPHENO:0049618', 'abnormal small molecule metabolic process'),
(472082, 'HP:0034594', 'Elevated circulating dihydrothymine concentration', 'XPO:0141780', 'abnormal NAD metabolic process', 0.4090909090909091, 8.366559792680423, 1.8500496078622006, 'UPHENO:0049618', 'abnormal small molecule metabolic process'),
(472083, 'HP:0034594', 'Elevated circulating dihydrothymine concentration', 'XPO:0141843', 'abnormal alanine metabolic process', 0.4576271186440678, 8.366559792680423, 1.95672293666928, 'UPHENO:0049618', 'abnormal small molecule metabolic process'),
(472084, 'HP:0034594', 'Elevated circulating dihydrothymine concentration', 'XPO:0141861', 'abnormal purine nucleoside metabolic process', 0.4090909090909091, 8.366559792680423, 1.8500496078622006, 'UPHENO:0049618', 'abnormal small molecule metabolic process'),
(472085, 'HP:0034594', 'Elevated circulating dihydrothymine concentration', 'XPO:0141905', 'abnormal ornithine metabolic process', 0.4576271186440678, 8.366559792680423, 1.95672293666928, 'UPHENO:0049618', 'abnormal small molecule metabolic process'),
(472086, 'HP:0034594', 'Elevated circulating dihydrothymine concentration', 'XPO:0141868', 'abnormal asparagine metabolic process', 0.45, 8.366559792680423, 1.9403483982795953, 'UPHENO:0049618', 'abnormal small molecule metabolic process'),
(472087, 'HP:0034594', 'Elevated circulating dihydrothymine concentration', 'XPO:0141888', 'abnormal threonine metabolic process', 0.45, 8.366559792680423, 1.9403483982795953, 'UPHENO:0049618', 'abnormal small molecule metabolic process'),
(472088, 'HP:0034594', 'Elevated circulating dihydrothymine concentration', 'XPO:0141858', 'abnormal serine family amino acid metabolic process', 0.4576271186440678, 8.366559792680423, 1.95672293666928, 'UPHENO:0049618', 'abnormal small molecule metabolic process'),
(472089, 'HP:0034594', 'Elevated circulating dihydrothymine concentration', 'XPO:0141865', 'abnormal adenine metabolic process', 0.4222222222222222, 12.92664762476255, 2.3362187153626808, 'UPHENO:0078592', 'abnormal nucleobase metabolic process'),
(472090, 'HP:0034594', 'Elevated circulating dihydrothymine concentration', 'XPO:0141848', 'abnormal proline metabolic process', 0.45, 8.366559792680423, 1.9403483982795953, 'UPHENO:0049618', 'abnormal small molecule metabolic process'),
(472091, 'HP:0034594', 'Elevated circulating dihydrothymine concentration', 'XPO:0141890', 'abnormal hypoxanthine metabolic process', 0.4222222222222222, 12.92664762476255, 2.3362187153626808, 'UPHENO:0078592', 'abnormal nucleobase metabolic process'),
(472092, 'HP:0034594', 'Elevated circulating dihydrothymine concentration', 'XPO:0141909', 'abnormal ribonucleoside metabolic process', 0.4090909090909091, 8.366559792680423, 1.8500496078622006, 'UPHENO:0049618', 'abnormal small molecule metabolic process'),
(472093, 'HP:0034594', 'Elevated circulating dihydrothymine concentration', 'XPO:0141882', 'abnormal gamma-aminobutyric acid metabolic process', 0.46551724137931033, 8.366559792680423, 1.9735191497737348, 'UPHENO:0049618', 'abnormal small molecule metabolic process'),
(472094, 'HP:0012325', 'Chronic myelomonocytic leukemia', 'XPO:0101450', 'abnormal myeloid cell', 0.40540540540540543, 5.574066539846944, 1.5032487170602729, 'UPHENO:0004459', 'abnormal hematopoietic system'),
(472095, 'HP:0012325', 'Chronic myelomonocytic leukemia', 'XPO:0100449', 'abnormal lymphocyte', 0.40540540540540543, 5.64885357140806, 1.5132996306721471, 'HP:0002715', 'Abnormality of the immune system'),
(472096, 'HP:0012325', 'Chronic myelomonocytic leukemia', 'XPO:0101587', 'abnormal hemangioblast', 0.40540540540540543, 5.574066539846944, 1.5032487170602729, 'HP:0001871', 'Abnormality of blood and blood-forming tissues'),
(472097, 'HP:0012325', 'Chronic myelomonocytic leukemia', 'XPO:0141497', 'abnormal lymphoblast', 0.40540540540540543, 5.64885357140806, 1.5132996306721471, 'HP:0002715', 'Abnormality of the immune system'),
(472098, 'HP:0012325', 'Chronic myelomonocytic leukemia', 'XPO:0101107', 'abnormal erythroid cell', 0.40540540540540543, 5.574066539846944, 1.5032487170602729, 'HP:0001871', 'Abnormality of blood and blood-forming tissues'),
(472099, 'HP:0001161', 'Hand polydactyly', 'XPO:0102787', 'abnormal forelimb digit 5 morphology', 0.44761904761904764, 7.492661022682715, 1.8313540867635612, 'HP:0001167', 'Abnormal finger morphology'),
(472100, 'HP:0001161', 'Hand polydactyly', 'XPO:0130624', 'increased size of the forelimb digit 4', 0.4051724137931034, 7.492661022682715, 1.7423603393941962, 'HP:0001167', 'Abnormal finger morphology'),
(472101, 'HP:0001161', 'Hand polydactyly', 'XPO:0133358', 'fused forelimb digits', 0.41964285714285715, 7.492661022682715, 1.7732009697610411, 'HP:0001167', 'Abnormal finger morphology'),
(472102, 'HP:0001161', 'Hand polydactyly', 'XPO:0102598', 'abnormal forelimb digit 3 morphology', 0.44761904761904764, 7.492661022682715, 1.8313540867635612, 'HP:0001167', 'Abnormal finger morphology'),
(472103, 'HP:0001161', 'Hand polydactyly', 'XPO:0115787', 'duplicated forelimb digit 3 in regenerating forelimb', 0.6428571428571429, 12.167655724266345, 2.7967953793889215, 'HP:0001161', 'Hand polydactyly'),
(472104, 'HP:0001161', 'Hand polydactyly', 'XPO:0103609', 'abnormally increased number of forelimb digit in the regenerating forelimb', 0.6728971962616822, 12.167655724266345, 2.8613950132647243, 'HP:0001161', 'Hand polydactyly'),
(472105, 'HP:0001161', 'Hand polydactyly', 'XPO:0103634', 'abnormally increased number of forelimb digit', 0.7128712871287128, 12.167655724266345, 2.945160844079114, 'HP:0001161', 'Hand polydactyly'),
(472106, 'HP:0001161', 'Hand polydactyly', 'XPO:0130664', 'increased size of the forelimb digit 2', 0.4051724137931034, 7.492661022682715, 1.7423603393941962, 'HP:0001167', 'Abnormal finger morphology'),
(472107, 'HP:0001161', 'Hand polydactyly', 'XPO:0141556', 'abnormal forelimb digit morphology in the regenerating forelimb', 0.43119266055045874, 7.492661022682715, 1.7974371869340195, 'HP:0001167', 'Abnormal finger morphology'),
(472108, 'HP:0001161', 'Hand polydactyly', 'XPO:0129652', 'increased size of the forelimb digit 3', 0.4051724137931034, 7.492661022682715, 1.7423603393941962, 'HP:0001167', 'Abnormal finger morphology'),
(472109, 'HP:0001161', 'Hand polydactyly', 'XPO:0102529', 'abnormal forelimb digit 4 morphology', 0.44761904761904764, 7.492661022682715, 1.8313540867635612, 'HP:0001167', 'Abnormal finger morphology'),
(472110, 'HP:0001161', 'Hand polydactyly', 'XPO:0115789', 'duplicated forelimb digit 5 in regenerating forelimb', 0.6428571428571429, 12.167655724266345, 2.7967953793889215, 'HP:0001161', 'Hand polydactyly'),
(472111, 'HP:0001161', 'Hand polydactyly', 'XPO:0140219', 'abnormally necrotic forelimb digit', 0.42342342342342343, 7.492661022682715, 1.781170452476563, 'HP:0001167', 'Abnormal finger morphology'),
(472112, 'HP:0001161', 'Hand polydactyly', 'XPO:0129148', 'decreased size of the forelimb digit 4', 0.4017094017094017, 7.492661022682715, 1.734898376457027, 'HP:0001167', 'Abnormal finger morphology'),
(472113, 'HP:0001161', 'Hand polydactyly', 'XPO:0129161', 'decreased size of the forelimb digit 5', 0.4017094017094017, 7.492661022682715, 1.734898376457027, 'HP:0001167', 'Abnormal finger morphology'),
(472114, 'HP:0001161', 'Hand polydactyly', 'XPO:0130637', 'increased size of the forelimb digit 5', 0.4051724137931034, 7.492661022682715, 1.7423603393941962, 'HP:0001167', 'Abnormal finger morphology'),
(472115, 'HP:0001161', 'Hand polydactyly', 'XPO:0140716', 'abnormally necrotic forelimb digit 4', 0.41228070175438597, 7.492661022682715, 1.7575777491876043, 'HP:0001167', 'Abnormal finger morphology'),
(472116, 'HP:0001161', 'Hand polydactyly', 'XPO:0103432', 'decreased size of the forelimb digit', 0.41228070175438597, 7.492661022682715, 1.7575777491876043, 'HP:0001167', 'Abnormal finger morphology'),
(472117, 'HP:0001161', 'Hand polydactyly', 'XPO:0102214', 'abnormal forelimb digit morphology', 0.4563106796116505, 7.492661022682715, 1.8490487401256015, 'HP:0001167', 'Abnormal finger morphology'),
(472118, 'HP:0001161', 'Hand polydactyly', 'XPO:0141108', 'abnormally necrotic forelimb digit 2', 0.41228070175438597, 7.492661022682715, 1.7575777491876043, 'HP:0001167', 'Abnormal finger morphology'),
(472119, 'HP:0001161', 'Hand polydactyly', 'XPO:0128172', 'decreased size of the forelimb digit 3', 0.4017094017094017, 7.492661022682715, 1.734898376457027, 'HP:0001167', 'Abnormal finger morphology'),
(472120, 'HP:0001161', 'Hand polydactyly', 'XPO:0129188', 'decreased size of the forelimb digit 2', 0.4017094017094017, 7.492661022682715, 1.734898376457027, 'HP:0001167', 'Abnormal finger morphology'),
(472121, 'HP:0001161', 'Hand polydactyly', 'XPO:0141143', 'abnormally necrotic forelimb digit 3', 0.41228070175438597, 7.492661022682715, 1.7575777491876043, 'HP:0001167', 'Abnormal finger morphology'),
(472122, 'HP:0001161', 'Hand polydactyly', 'XPO:0115786', 'duplicated forelimb digit 2 in regenerating forelimb', 0.6428571428571429, 12.167655724266345, 2.7967953793889215, 'HP:0001161', 'Hand polydactyly'),
(472123, 'HP:0001161', 'Hand polydactyly', 'XPO:0140898', 'abnormally necrotic forelimb digit 5', 0.41228070175438597, 7.492661022682715, 1.7575777491876043, 'HP:0001167', 'Abnormal finger morphology'),
(472124, 'HP:0001161', 'Hand polydactyly', 'XPO:0102746', 'abnormal forelimb digit 2 morphology', 0.44761904761904764, 7.492661022682715, 1.8313540867635612, 'HP:0001167', 'Abnormal finger morphology'),
(472125, 'HP:0001161', 'Hand polydactyly', 'XPO:0103632', 'abnormally increased number of digit', 0.4588235294117647, 11.404694921567193, 2.28751882522918, 'UPHENO:0056085', 'abnormally increased number of digit in the limb'),
(472126, 'HP:0001161', 'Hand polydactyly', 'XPO:0103755', 'increased size of the forelimb digit', 0.415929203539823, 7.492661022682715, 1.7653375120804229, 'HP:0001167', 'Abnormal finger morphology'),
(472127, 'HP:0001161', 'Hand polydactyly', 'XPO:0115788', 'duplicated forelimb digit 4 in regenerating forelimb', 0.6428571428571429, 12.167655724266345, 2.7967953793889215, 'HP:0001161', 'Hand polydactyly'),
(472128, 'HP:0030320', 'Increased intervertebral space', 'XPO:0100584', 'abnormal vertebral column', 0.44642857142857145, 8.05344015541032, 1.8961238840501222, 'UPHENO:0002813', 'abnormal vertebral column'),
(472129, 'HP:0030320', 'Increased intervertebral space', 'XPO:0102216', 'abnormal vertebral column morphology', 0.4262295081967213, 8.361863005979023, 1.8878751962581628, 'UPHENO:0076695', 'abnormal vertebral column morphology'),
(472130, 'HP:0030320', 'Increased intervertebral space', 'XPO:0100226', 'abnormal vertebral element', 0.4032258064516129, 8.05344015541032, 1.8020418700394085, 'UPHENO:0002813', 'abnormal vertebral column'),
(472131, 'HP:0030320', 'Increased intervertebral space', 'XPO:0129707', 'increased size of the vertebral column', 0.4393939393939394, 8.361863005979023, 1.9168077438464115, 'UPHENO:0076695', 'abnormal vertebral column morphology'),
(472132, 'HP:0009339', 'Fragmentation of the epiphysis of the distal phalanx of the 3rd finger', 'XPO:0115787', 'duplicated forelimb digit 3 in regenerating forelimb', 0.4014084507042254, 7.774297771301195, 1.7665414865468982, 'HP:0005918', 'Abnormal finger phalanx morphology'),
(472133, 'HP:0009339', 'Fragmentation of the epiphysis of the distal phalanx of the 3rd finger', 'XPO:0103634', 'abnormally increased number of forelimb digit', 0.4351145038167939, 7.774297771301195, 1.839214429391996, 'HP:0005918', 'Abnormal finger phalanx morphology'),
(472134, 'HP:0009339', 'Fragmentation of the epiphysis of the distal phalanx of the 3rd finger', 'XPO:0115788', 'duplicated forelimb digit 4 in regenerating forelimb', 0.4014084507042254, 7.774297771301195, 1.7665414865468982, 'HP:0005918', 'Abnormal finger phalanx morphology'),
(472135, 'HP:0009339', 'Fragmentation of the epiphysis of the distal phalanx of the 3rd finger', 'XPO:0115786', 'duplicated forelimb digit 2 in regenerating forelimb', 0.4014084507042254, 7.774297771301195, 1.7665414865468982, 'HP:0005918', 'Abnormal finger phalanx morphology'),
(472136, 'HP:0009339', 'Fragmentation of the epiphysis of the distal phalanx of the 3rd finger', 'XPO:0115789', 'duplicated forelimb digit 5 in regenerating forelimb', 0.4014084507042254, 7.774297771301195, 1.7665414865468982, 'HP:0005918', 'Abnormal finger phalanx morphology'),
(472137, 'HP:0009339', 'Fragmentation of the epiphysis of the distal phalanx of the 3rd finger', 'XPO:0103609', 'abnormally increased number of forelimb digit in the regenerating forelimb', 0.41605839416058393, 7.774297771301195, 1.7984887673971672, 'HP:0005918', 'Abnormal finger phalanx morphology'),
(472138, 'HP:0031286', 'Perifollicular erythema', 'XPO:0100205', 'abnormal limb segment', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(472139, 'HP:0031286', 'Perifollicular erythema', 'XPO:0100274', 'abnormal sensory system', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(472140, 'HP:0031286', 'Perifollicular erythema', 'XPO:0101157', 'abnormal female organism', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(472141, 'HP:0031286', 'Perifollicular erythema', 'XPO:0101535', 'abnormal absorptive cell', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(472142, 'HP:0031286', 'Perifollicular erythema', 'XPO:0101311', 'abnormal bottle cell', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(472143, 'HP:0031286', 'Perifollicular erythema', 'XPO:0100665', 'abnormal egg jelly', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(472144, 'HP:0031286', 'Perifollicular erythema', 'XPO:0100544', 'abnormal neuromast support cell', 0.4838709677419355, 6.8660902472206855, 1.8227182263109507, 'HP:0000951', 'Abnormality of the skin'),
(472145, 'HP:0031286', 'Perifollicular erythema', 'XPO:0100507', 'abnormal skin', 0.5555555555555556, 6.8660902472206855, 1.9530731122488143, 'HP:0000951', 'Abnormality of the skin'),
(472146, 'HP:0031286', 'Perifollicular erythema', 'XPO:0141315', 'abnormal anatomical region', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(472147, 'HP:0031286', 'Perifollicular erythema', 'XPO:0141499', 'abnormal tadpole', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(472148, 'HP:0031286', 'Perifollicular erythema', 'XPO:0100902', 'abnormal spermatocyte', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(472149, 'HP:0031286', 'Perifollicular erythema', 'XPO:0101547', 'abnormal lampbrush chromosome', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(472150, 'HP:0031286', 'Perifollicular erythema', 'XPO:0141776', 'abnormal metabolic process', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(472151, 'HP:0031286', 'Perifollicular erythema', 'XPO:0101366', 'abnormal morula cell', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(472152, 'HP:0031286', 'Perifollicular erythema', 'XPO:0101498', 'abnormal stage II oocyte', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(472153, 'HP:0031286', 'Perifollicular erythema', 'XPO:0101570', 'abnormal forelimb region', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(472154, 'HP:0031286', 'Perifollicular erythema', 'XPO:0101405', 'abnormal ring structure', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(472155, 'HP:0031286', 'Perifollicular erythema', 'XPO:0101497', 'abnormal ciliary axoneme', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(472156, 'HP:0031286', 'Perifollicular erythema', 'XPO:0100031', 'abnormal central nervous system', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(472157, 'HP:0031286', 'Perifollicular erythema', 'XPO:0100888', 'abnormal microtubule', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(472158, 'HP:0031286', 'Perifollicular erythema', 'XPO:0100004', 'abnormal cell', 0.4782608695652174, 1.8210412618256888, 0.9332377925239069, 'HP:0000118', 'Phenotypic abnormality'),
(472159, 'HP:0031286', 'Perifollicular erythema', 'XPO:0131725', 'abnormal phosphorylation of RNA polymerase II C-terminal domain', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(472160, 'HP:0031286', 'Perifollicular erythema', 'XPO:0107258', 'abnormal anatomical axis', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(472161, 'HP:0031286', 'Perifollicular erythema', 'XPO:0101591', 'abnormal xanthophore', 0.46875, 6.8660902472206855, 1.7940122082596586, 'HP:0000951', 'Abnormality of the skin'),
(472162, 'HP:0031286', 'Perifollicular erythema', 'XPO:0107339', 'abnormal yolk platelet', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(472163, 'HP:0031286', 'Perifollicular erythema', 'XPO:0100386', 'abnormal limb', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(472164, 'HP:0031286', 'Perifollicular erythema', 'XPO:0100784', 'abnormal left blastomere', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(472165, 'HP:0031286', 'Perifollicular erythema', 'XPO:0100307', 'abnormal blastomere', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(472166, 'HP:0031286', 'Perifollicular erythema', 'XPO:0141266', 'abnormal surface breathing', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(472167, 'HP:0031286', 'Perifollicular erythema', 'XPO:0100028', 'abnormal anatomical cluster', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(472168, 'HP:0031286', 'Perifollicular erythema', 'XPO:0115505', 'dead whole organism', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(472169, 'HP:0031286', 'Perifollicular erythema', 'XPO:0141784', 'abnormal cellular hormone metabolic process', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(472170, 'HP:0031286', 'Perifollicular erythema', 'XPO:0107253', 'abnormal enteric nervous system', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(472171, 'HP:0031286', 'Perifollicular erythema', 'XPO:0100104', 'abnormal embryonic structure', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(472172, 'HP:0031286', 'Perifollicular erythema', 'XPO:0107276', 'abnormal dorsal region', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(472173, 'HP:0031286', 'Perifollicular erythema', 'XPO:0100032', 'abnormal nervous system', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(472174, 'HP:0031286', 'Perifollicular erythema', 'XPO:0100481', 'abnormal anatomical line', 0.47368421052631576, 1.706362323152461, 0.8990422069704646, 'UPHENO:0002536', 'abnormal anatomical entity'),
(472175, 'HP:0031286', 'Perifollicular erythema', 'XPO:0100715', 'abnormal ciliated cell', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(472176, 'HP:0031286', 'Perifollicular erythema', 'XPO:0100545', 'abnormal male organism', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(472177, 'HP:0031286', 'Perifollicular erythema', 'XPO:0131723', 'abnormal pathway-restricted SMAD protein phosphorylation', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(472178, 'HP:0031286', 'Perifollicular erythema', 'XPO:0107284', 'abnormal migrating myoblast', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(472179, 'HP:0031286', 'Perifollicular erythema', 'XPO:0100587', 'abnormal vestibuloauditory system', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(472180, 'HP:0031286', 'Perifollicular erythema', 'XPO:0101113', 'abnormal stage IV oocyte', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(472181, 'HP:0031286', 'Perifollicular erythema', 'XPO:0100009', 'abnormal multi-tissue structure', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(472182, 'HP:0031286', 'Perifollicular erythema', 'XPO:0131666', 'abnormal adherens junction', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(472183, 'HP:0031286', 'Perifollicular erythema', 'XPO:0101004', 'abnormal acid secreting cell', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(472184, 'HP:0031286', 'Perifollicular erythema', 'XPO:0100006', 'abnormal anatomical structure', 0.47368421052631576, 1.706362323152461, 0.8990422069704646, 'UPHENO:0002536', 'abnormal anatomical entity'),
(472185, 'HP:0031286', 'Perifollicular erythema', 'XPO:0101061', 'abnormal plasma membrane', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(472186, 'HP:0031286', 'Perifollicular erythema', 'XPO:0101208', 'abnormal stratum spongiosum', 0.4838709677419355, 6.8660902472206855, 1.8227182263109507, 'HP:0000951', 'Abnormality of the skin'),
(472187, 'HP:0031286', 'Perifollicular erythema', 'XPO:0100239', 'abnormal acellular anatomical structure', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(472188, 'HP:0031286', 'Perifollicular erythema', 'XPO:0100704', 'abnormal Merkel cell', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(472189, 'HP:0031286', 'Perifollicular erythema', 'XPO:0101468', 'abnormal stage I oocyte', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(472190, 'HP:0031286', 'Perifollicular erythema', 'XPO:0100392', 'abnormal cilium', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(472191, 'HP:0031286', 'Perifollicular erythema', 'XPO:0100423', 'abnormal process', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(472192, 'HP:0031286', 'Perifollicular erythema', 'XPO:0131667', 'abnormal actin cytoskeleton', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(472193, 'HP:0031286', 'Perifollicular erythema', 'XPO:0101515', 'abnormal neuromast mantle cell', 0.4838709677419355, 6.8660902472206855, 1.8227182263109507, 'HP:0000951', 'Abnormality of the skin'),
(472194, 'HP:0031286', 'Perifollicular erythema', 'XPO:0100427', 'abnormal olfactory system', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(472195, 'HP:0031286', 'Perifollicular erythema', 'XPO:0100081', 'abnormal anatomical entity in vitro', 0.47368421052631576, 1.706362323152461, 0.8990422069704646, 'UPHENO:0002536', 'abnormal anatomical entity'),
(472196, 'HP:0031286', 'Perifollicular erythema', 'XPO:0100429', 'abnormal spermatid', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(472197, 'HP:0031286', 'Perifollicular erythema', 'XPO:0101110', 'abnormal cell-free extract', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(472198, 'HP:0031286', 'Perifollicular erythema', 'XPO:0101575', 'abnormal vitelline membrane', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(472199, 'HP:0031286', 'Perifollicular erythema', 'XPO:0100003', 'abnormal organism subdivision', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(472200, 'HP:0031286', 'Perifollicular erythema', 'XPO:0101529', 'abnormal skin mucous gland', 0.4838709677419355, 6.8660902472206855, 1.8227182263109507, 'HP:0000951', 'Abnormality of the skin'),
(472201, 'HP:0031286', 'Perifollicular erythema', 'XPO:0100802', 'abnormal exocrine cell', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(472202, 'HP:0031286', 'Perifollicular erythema', 'XPO:0141745', 'abnormal creatinine homeostasis', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(472203, 'HP:0031286', 'Perifollicular erythema', 'XPO:0100721', 'abnormal centromere', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(472204, 'HP:0031286', 'Perifollicular erythema', 'XPO:0100894', 'abnormal nucleus', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(472205, 'HP:0031286', 'Perifollicular erythema', 'XPO:0141272', 'absent surface breathing', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(472206, 'HP:0031286', 'Perifollicular erythema', 'XPO:0107278', 'abnormal medial region', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(472207, 'HP:0031286', 'Perifollicular erythema', 'XPO:0100344', 'abnormal portion of organism substance', 0.47368421052631576, 1.706362323152461, 0.8990422069704646, 'UPHENO:0002536', 'abnormal anatomical entity'),
(472208, 'HP:0031286', 'Perifollicular erythema', 'XPO:0100295', 'abnormal extracellular matrix', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(472209, 'HP:0031286', 'Perifollicular erythema', 'XPO:0131675', 'abnormal spindle microtubule', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(472210, 'HP:0031286', 'Perifollicular erythema', 'XPO:0100025', 'abnormal oocyte', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(472211, 'HP:0031286', 'Perifollicular erythema', 'XPO:0100994', 'abnormal granular gland', 0.5172413793103449, 6.8660902472206855, 1.8845227485869556, 'HP:0000951', 'Abnormality of the skin'),
(472212, 'HP:0031286', 'Perifollicular erythema', 'XPO:0100754', 'abnormal electrically active cell', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(472213, 'HP:0031286', 'Perifollicular erythema', 'XPO:0100533', 'abnormal melanoblast', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(472214, 'HP:0031286', 'Perifollicular erythema', 'XPO:0107271', 'abnormal apical region', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(472215, 'HP:0031286', 'Perifollicular erythema', 'XPO:0141264', 'abnormal schooling behavior', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(472216, 'HP:0031286', 'Perifollicular erythema', 'XPO:0141267', 'abnormal resting posture', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(472217, 'HP:0031286', 'Perifollicular erythema', 'XPO:0100574', 'abnormal gastrula cell', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(472218, 'HP:0031286', 'Perifollicular erythema', 'XPO:0100907', 'abnormal cytoplasm', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(472219, 'HP:0031286', 'Perifollicular erythema', 'XPO:0100653', 'abnormal myoblast', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(472220, 'HP:0031286', 'Perifollicular erythema', 'XPO:0115509', 'abnormally semi-viable whole organism', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(472221, 'HP:0031286', 'Perifollicular erythema', 'XPO:0100070', 'abnormal anatomical system', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(472222, 'HP:0031286', 'Perifollicular erythema', 'XPO:0101373', 'abnormal oxygen accumulating cell', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(472223, 'HP:0031286', 'Perifollicular erythema', 'XPO:0100691', 'abnormal keratin accumulating cell', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(472224, 'HP:0031286', 'Perifollicular erythema', 'XPO:0101448', 'abnormal myelin accumulating cell', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(472225, 'HP:0031286', 'Perifollicular erythema', 'XPO:0101072', 'abnormal mitochondrial cloud', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(472226, 'HP:0031286', 'Perifollicular erythema', 'XPO:0101278', 'abnormal pigment cell', 0.4838709677419355, 6.8660902472206855, 1.8227182263109507, 'HP:0000951', 'Abnormality of the skin'),
(472227, 'HP:0031286', 'Perifollicular erythema', 'XPO:0100218', 'abnormal epithelial cell', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(472228, 'HP:0031286', 'Perifollicular erythema', 'XPO:0100176', 'abnormal stage VI oocyte', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(472229, 'HP:0031286', 'Perifollicular erythema', 'XPO:0100317', 'abnormal respiratory system', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(472230, 'HP:0031286', 'Perifollicular erythema', 'XPO:0100501', 'abnormal urogenital system', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(472231, 'HP:0031286', 'Perifollicular erythema', 'XPO:0100917', 'abnormal stage III oocyte', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(472232, 'HP:0031286', 'Perifollicular erythema', 'XPO:0107270', 'abnormal proximal-distal axis', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(472233, 'HP:0031286', 'Perifollicular erythema', 'XPO:0103398', 'abnormally increased number of dense core granule in the goblet cell', 0.42857142857142855, 6.8660902472206855, 1.7154037734456928, 'HP:0000951', 'Abnormality of the skin'),
(472234, 'HP:0031286', 'Perifollicular erythema', 'XPO:0101302', 'abnormal subcortical cytoplasm', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(472235, 'HP:0031286', 'Perifollicular erythema', 'XPO:0100010', 'abnormal multicellular anatomical structure', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(472236, 'HP:0031286', 'Perifollicular erythema', 'XPO:0101322', 'abnormal iridophore', 0.46875, 6.8660902472206855, 1.7940122082596586, 'HP:0000951', 'Abnormality of the skin'),
(472237, 'HP:0031286', 'Perifollicular erythema', 'XPO:0100437', 'abnormal proepicardium', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(472238, 'HP:0031286', 'Perifollicular erythema', 'XPO:0100417', 'abnormal dense regular connective tissue', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(472239, 'HP:0031286', 'Perifollicular erythema', 'XPO:0101200', 'abnormal joint region', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(472240, 'HP:0031286', 'Perifollicular erythema', 'XPO:0101136', 'abnormal ooplasm', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(472241, 'HP:0031286', 'Perifollicular erythema', 'XPO:0100626', 'abnormal primordial germ cell', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(472242, 'HP:0031286', 'Perifollicular erythema', 'XPO:0101347', 'abnormal hindlimb region', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(472243, 'HP:0031286', 'Perifollicular erythema', 'XPO:0141743', 'abnormal chemical homeostasis within a tissue', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(472244, 'HP:0031286', 'Perifollicular erythema', 'XPO:0100062', 'abnormal anatomical space', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(472245, 'HP:0031286', 'Perifollicular erythema', 'XPO:0100551', 'abnormal oocyte cortex', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(472246, 'HP:0031286', 'Perifollicular erythema', 'XPO:0100643', 'abnormal thoracic region', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(472247, 'HP:0031286', 'Perifollicular erythema', 'XPO:0100983', 'abnormal skin gland', 0.5357142857142857, 6.8660902472206855, 1.917879723142109, 'HP:0000951', 'Abnormality of the skin'),
(472248, 'HP:0031286', 'Perifollicular erythema', 'XPO:0100929', 'abnormal dermis', 0.5172413793103449, 6.8660902472206855, 1.8845227485869556, 'HP:0000951', 'Abnormality of the skin'),
(472249, 'HP:0031286', 'Perifollicular erythema', 'XPO:0100546', 'abnormal whole organism', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(472250, 'HP:0031286', 'Perifollicular erythema', 'XPO:0100337', 'abnormal zygote', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(472251, 'HP:0031286', 'Perifollicular erythema', 'XPO:0101333', 'abnormal barrier epithelial cell', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(472252, 'HP:0031286', 'Perifollicular erythema', 'XPO:0101461', 'abnormal sperm entry point', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(472253, 'HP:0031286', 'Perifollicular erythema', 'XPO:0101467', 'abnormal alkali secreting cell', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(472254, 'HP:0031286', 'Perifollicular erythema', 'XPO:0142057', 'abnormal desmosome', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(472255, 'HP:0031286', 'Perifollicular erythema', 'XPO:0100273', 'abnormal visual system', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(472256, 'HP:0031286', 'Perifollicular erythema', 'XPO:0101228', 'abnormal mesenchymal stem cell', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(472257, 'HP:0031286', 'Perifollicular erythema', 'XPO:0100976', 'abnormal multiciliated cell', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(472258, 'HP:0031286', 'Perifollicular erythema', 'XPO:0101451', 'abnormal dorsal lymph space', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(472259, 'HP:0031286', 'Perifollicular erythema', 'XPO:0100887', 'abnormal right-dorsal blastomere', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(472260, 'HP:0031286', 'Perifollicular erythema', 'XPO:0100285', 'abnormal progenitor cell', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(472261, 'HP:0031286', 'Perifollicular erythema', 'XPO:0101387', 'abnormal melanophore', 0.46875, 6.8660902472206855, 1.7940122082596586, 'HP:0000951', 'Abnormality of the skin'),
(472262, 'HP:0031286', 'Perifollicular erythema', 'XPO:0101014', 'abnormal goblet cell', 0.4411764705882353, 6.8660902472206855, 1.740447489012273, 'HP:0000951', 'Abnormality of the skin'),
(472263, 'HP:0031286', 'Perifollicular erythema', 'XPO:0100232', 'abnormal lymphatic system', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(472264, 'HP:0031286', 'Perifollicular erythema', 'XPO:0100014', 'abnormal tissue', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(472265, 'HP:0031286', 'Perifollicular erythema', 'XPO:0141265', 'abnormal escape behavior', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(472266, 'HP:0031286', 'Perifollicular erythema', 'XPO:0101264', 'abnormal mitotic spindle', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(472267, 'HP:0031286', 'Perifollicular erythema', 'XPO:0126819', 'abnormally localised skin', 0.40540540540540543, 6.8660902472206855, 1.6683974647021622, 'HP:0000951', 'Abnormality of the skin'),
(472268, 'HP:0031286', 'Perifollicular erythema', 'XPO:0101435', 'abnormal paracrine cell', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(472269, 'HP:0031286', 'Perifollicular erythema', 'XPO:0100823', 'abnormal blood', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(472270, 'HP:0031286', 'Perifollicular erythema', 'XPO:0101326', 'abnormal cementoblast', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(472271, 'HP:0031286', 'Perifollicular erythema', 'XPO:0131687', 'abnormal astral microtubule', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(472272, 'HP:0031286', 'Perifollicular erythema', 'XPO:0107263', 'abnormal anatomical side', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(472273, 'HP:0031286', 'Perifollicular erythema', 'XPO:0101109', 'abnormal egg cell-free extract', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(472274, 'HP:0031286', 'Perifollicular erythema', 'XPO:0100749', 'abnormal mucociliary epithelium', 0.4166666666666667, 6.8660902472206855, 1.6914109306558096, 'HP:0000951', 'Abnormality of the skin'),
(472275, 'HP:0031286', 'Perifollicular erythema', 'XPO:0101569', 'abnormal activin-induced ectoderm', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(472276, 'HP:0031286', 'Perifollicular erythema', 'XPO:0100674', 'abnormal secondary oogonium', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(472277, 'HP:0031286', 'Perifollicular erythema', 'XPO:0131677', 'abnormal actin filament', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(472278, 'HP:0031286', 'Perifollicular erythema', 'XPO:0101095', 'abnormal skin seromucous gland', 0.5172413793103449, 6.8660902472206855, 1.8845227485869556, 'HP:0000951', 'Abnormality of the skin'),
(472279, 'HP:0031286', 'Perifollicular erythema', 'XPO:0100547', 'abnormal blastomere V2', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(472280, 'HP:0031286', 'Perifollicular erythema', 'XPO:0101389', 'abnormal wedge region', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(472281, 'HP:0031286', 'Perifollicular erythema', 'XPO:0100277', 'abnormal blastocoel', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(472282, 'HP:0031286', 'Perifollicular erythema', 'XPO:0101409', 'abnormal perivitelline space', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(472283, 'HP:0031286', 'Perifollicular erythema', 'XPO:0141771', 'abnormal urea homeostasis', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(472284, 'HP:0031286', 'Perifollicular erythema', 'XPO:0100477', 'abnormal pericyte', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(472285, 'HP:0031286', 'Perifollicular erythema', 'XPO:0101237', 'abnormal mucus secreting cell', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(472286, 'HP:0031286', 'Perifollicular erythema', 'XPO:0100642', 'abnormal gustatory system', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(472287, 'HP:0031286', 'Perifollicular erythema', 'XPO:0100108', 'abnormal cell part', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(472288, 'HP:0031286', 'Perifollicular erythema', 'XPO:0100432', 'abnormal epidermis inner layer', 0.4166666666666667, 6.8660902472206855, 1.6914109306558096, 'HP:0000951', 'Abnormality of the skin'),
(472289, 'HP:0031286', 'Perifollicular erythema', 'XPO:0100688', 'abnormal adipose tissue', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(472290, 'HP:0031286', 'Perifollicular erythema', 'XPO:0101240', 'abnormal ciliated non-epidermal cell', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(472291, 'HP:0031286', 'Perifollicular erythema', 'XPO:00000000', 'Xenopus phenotype', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(472292, 'HP:0031286', 'Perifollicular erythema', 'XPO:0100152', 'abnormal alimentary system', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(472293, 'HP:0031286', 'Perifollicular erythema', 'XPO:0101472', 'abnormal zygote cortex', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(472294, 'HP:0031286', 'Perifollicular erythema', 'XPO:0100225', 'abnormal endocrine system', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(472295, 'HP:0031286', 'Perifollicular erythema', 'XPO:0100581', 'abnormal immune system', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(472296, 'HP:0031286', 'Perifollicular erythema', 'XPO:0100862', 'abnormal blastomere V1', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(472297, 'HP:0031286', 'Perifollicular erythema', 'XPO:0141770', 'abnormal urate homeostasis', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(472298, 'HP:0031286', 'Perifollicular erythema', 'XPO:0101313', 'abnormal Eberth-Kastschenko layer', 0.4838709677419355, 6.8660902472206855, 1.8227182263109507, 'HP:0000951', 'Abnormality of the skin'),
(472299, 'HP:0031286', 'Perifollicular erythema', 'XPO:0101378', 'abnormal blastomere D1', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(472300, 'HP:0031286', 'Perifollicular erythema', 'XPO:0101411', 'abnormal marginal zone (sensu neural)', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(472301, 'HP:0031286', 'Perifollicular erythema', 'XPO:0101463', 'abnormal right-ventral blastomere', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(472302, 'HP:0031286', 'Perifollicular erythema', 'XPO:0107261', 'abnormal dorsal-ventral axis', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(472303, 'HP:0031286', 'Perifollicular erythema', 'XPO:0100008', 'abnormal epidermis', 0.42857142857142855, 6.8660902472206855, 1.7154037734456928, 'HP:0000951', 'Abnormality of the skin'),
(472304, 'HP:0031286', 'Perifollicular erythema', 'XPO:0100258', 'abnormal organ part', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(472305, 'HP:0031286', 'Perifollicular erythema', 'XPO:0101221', 'abnormal larval immune system', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(472306, 'HP:0031286', 'Perifollicular erythema', 'XPO:0100503', 'abnormal blastomere D2', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(472307, 'HP:0031286', 'Perifollicular erythema', 'XPO:0107273', 'abnormal basal region', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(472308, 'HP:0031286', 'Perifollicular erythema', 'XPO:0107259', 'abnormal animal-vegetal axis', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(472309, 'HP:0031286', 'Perifollicular erythema', 'XPO:0101241', 'abnormal nucleate erythrocyte', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(472310, 'HP:0031286', 'Perifollicular erythema', 'XPO:0101480', 'abnormal stage V oocyte', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(472311, 'HP:0031286', 'Perifollicular erythema', 'XPO:0100422', 'abnormal notochord', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(472312, 'HP:0031286', 'Perifollicular erythema', 'XPO:0100599', 'abnormal adult immune system', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(472313, 'HP:0031286', 'Perifollicular erythema', 'XPO:0101141', 'abnormal Keller explant', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(472314, 'HP:0031286', 'Perifollicular erythema', 'XPO:0131669', 'abnormal Roux spot', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(472315, 'HP:0031286', 'Perifollicular erythema', 'XPO:0100852', 'abnormal interdigital region', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(472316, 'HP:0031286', 'Perifollicular erythema', 'XPO:0100084', 'abnormal anatomical group', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(472317, 'HP:0031286', 'Perifollicular erythema', 'XPO:0101297', 'abnormal barrier cell', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(472318, 'HP:0031286', 'Perifollicular erythema', 'XPO:0100842', 'abnormal left-dorsal blastomere', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(472319, 'HP:0031286', 'Perifollicular erythema', 'XPO:0100172', 'abnormal stem cell', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(472320, 'HP:0031286', 'Perifollicular erythema', 'XPO:0107260', 'abnormal anterior-posterior axis', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(472321, 'HP:0031286', 'Perifollicular erythema', 'XPO:0141772', 'abnormal water homeostasis', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(472322, 'HP:0031286', 'Perifollicular erythema', 'XPO:0141263', 'abnormal visually guided collision avoidance behavior', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(472323, 'HP:0031286', 'Perifollicular erythema', 'XPO:0100899', 'abnormal secondary spermatogonium', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(472324, 'HP:0031286', 'Perifollicular erythema', 'XPO:0115508', 'abnormally peramorphic growth of whole organism', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(472325, 'HP:0031286', 'Perifollicular erythema', 'XPO:0100289', 'abnormal chondroblast', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(472326, 'HP:0031286', 'Perifollicular erythema', 'XPO:0101254', 'abnormal stratum compactum', 0.4838709677419355, 6.8660902472206855, 1.8227182263109507, 'HP:0000951', 'Abnormality of the skin'),
(472327, 'HP:0031286', 'Perifollicular erythema', 'XPO:0115512', 'abnormally semi-erect whole organism', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(472328, 'HP:0031286', 'Perifollicular erythema', 'XPO:0131685', 'abnormal cortical actin cytoskeleton', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(472329, 'HP:0031286', 'Perifollicular erythema', 'XPO:0100762', 'abnormal intersomitic region', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(472330, 'HP:0031286', 'Perifollicular erythema', 'XPO:0100377', 'abnormal connective tissue', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(472331, 'HP:0031286', 'Perifollicular erythema', 'XPO:0100465', 'abnormal skeletal system', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(472332, 'HP:0031286', 'Perifollicular erythema', 'XPO:0107262', 'abnormal left-right axis', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(472333, 'HP:0031286', 'Perifollicular erythema', 'XPO:0100638', 'abnormal polar body', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(472334, 'HP:0031286', 'Perifollicular erythema', 'XPO:0101071', 'abnormal endoplasmic reticulum', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(472335, 'HP:0031286', 'Perifollicular erythema', 'XPO:0100989', 'abnormal right blastomere', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(472336, 'HP:0031286', 'Perifollicular erythema', 'XPO:0101513', 'abnormal basal body', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(472337, 'HP:0031286', 'Perifollicular erythema', 'XPO:0100515', 'abnormal somatic stem cell', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(472338, 'HP:0031286', 'Perifollicular erythema', 'XPO:0107312', 'abnormal filopodium', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(472339, 'HP:0031286', 'Perifollicular erythema', 'XPO:0100573', 'abnormal extraembryonic structure', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(472340, 'HP:0031286', 'Perifollicular erythema', 'XPO:0100791', 'abnormal multiciliated cell precursor', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(472341, 'HP:0031286', 'Perifollicular erythema', 'XPO:0100956', 'abnormal centrosome', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(472342, 'HP:0031286', 'Perifollicular erythema', 'XPO:0100308', 'abnormal early embryonic cell', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(472343, 'HP:0031286', 'Perifollicular erythema', 'XPO:0100728', 'abnormal cell condensation', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(472344, 'HP:0031286', 'Perifollicular erythema', 'XPO:0101132', 'abnormal apoptotic cell', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(472345, 'HP:0031286', 'Perifollicular erythema', 'XPO:0100026', 'abnormal germ cell', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(472346, 'HP:0031286', 'Perifollicular erythema', 'XPO:0100549', 'abnormal mitotic cell', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(472347, 'HP:0031286', 'Perifollicular erythema', 'XPO:0101220', 'abnormal centriole', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(472348, 'HP:0031286', 'Perifollicular erythema', 'XPO:0100969', 'abnormal disaggregated/reaggregated ectoderm treated with activin', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(472349, 'HP:0031286', 'Perifollicular erythema', 'XPO:0141748', 'abnormal gas homeostasis', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(472350, 'HP:0031286', 'Perifollicular erythema', 'XPO:0141738', 'abnormal carbon dioxide homeostasis', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(472351, 'HP:0031286', 'Perifollicular erythema', 'XPO:0100585', 'abnormal elastica externa', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(472352, 'HP:0031286', 'Perifollicular erythema', 'XPO:0100372', 'abnormal hematological system', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(472353, 'HP:0031286', 'Perifollicular erythema', 'XPO:0100724', 'abnormal kinetochore', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(472354, 'HP:0031286', 'Perifollicular erythema', 'XPO:0101283', 'abnormal left-ventral blastomere', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(472355, 'HP:0031286', 'Perifollicular erythema', 'XPO:0107272', 'abnormal axial region', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(472356, 'HP:0031286', 'Perifollicular erythema', 'XPO:0100202', 'abnormal embryo', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(472357, 'HP:0031970', 'Abnormal blood urea nitrogen concentration', 'XPO:0141858', 'abnormal serine family amino acid metabolic process', 0.40350877192982454, 7.41682187759612, 1.729957423594889, 'HP:0430071', 'Abnormal circulating organic compound concentration'),
(472358, 'HP:0031970', 'Abnormal blood urea nitrogen concentration', 'XPO:0141873', 'abnormal tricarboxylic acid metabolic process', 0.45098039215686275, 7.41682187759612, 1.8288907126769214, 'HP:0430071', 'Abnormal circulating organic compound concentration'),
(472359, 'HP:0031970', 'Abnormal blood urea nitrogen concentration', 'XPO:0141869', 'abnormal alpha-amino acid metabolic process', 0.41818181818181815, 7.41682187759612, 1.7611303352971444, 'HP:0430071', 'Abnormal circulating organic compound concentration'),
(472360, 'HP:0031970', 'Abnormal blood urea nitrogen concentration', 'XPO:0141882', 'abnormal gamma-aminobutyric acid metabolic process', 0.4107142857142857, 7.41682187759612, 1.745335125334667, 'HP:0430071', 'Abnormal circulating organic compound concentration'),
(472361, 'HP:0031970', 'Abnormal blood urea nitrogen concentration', 'XPO:0141843', 'abnormal alanine metabolic process', 0.40350877192982454, 7.41682187759612, 1.729957423594889, 'HP:0430071', 'Abnormal circulating organic compound concentration'),
(472362, 'HP:0031970', 'Abnormal blood urea nitrogen concentration', 'XPO:0141905', 'abnormal ornithine metabolic process', 0.40350877192982454, 7.41682187759612, 1.729957423594889, 'HP:0430071', 'Abnormal circulating organic compound concentration'),
(472363, 'HP:0020127', 'Periarticular soft-tissue mass', 'XPO:0100344', 'abnormal portion of organism substance', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(472364, 'HP:0020127', 'Periarticular soft-tissue mass', 'XPO:0101448', 'abnormal myelin accumulating cell', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(472365, 'HP:0020127', 'Periarticular soft-tissue mass', 'XPO:0101333', 'abnormal barrier epithelial cell', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(472366, 'HP:0020127', 'Periarticular soft-tissue mass', 'XPO:0100350', 'abnormal appendicular skeleton', 0.45161290322580644, 4.3395673355180735, 1.399930213666808, 'UPHENO:0002964', 'abnormal skeletal system'),
(472367, 'HP:0020127', 'Periarticular soft-tissue mass', 'XPO:0102567', 'abnormal skeleton morphology', 0.4722222222222222, 4.638757693672553, 1.4800420488812078, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(472368, 'HP:0020127', 'Periarticular soft-tissue mass', 'XPO:0100791', 'abnormal multiciliated cell precursor', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(472369, 'HP:0020127', 'Periarticular soft-tissue mass', 'XPO:0139774', 'abnormally necrotic elastica externa', 0.4358974358974359, 4.638757693672553, 1.421978405047478, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(472370, 'HP:0020127', 'Periarticular soft-tissue mass', 'XPO:0101004', 'abnormal acid secreting cell', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(472371, 'HP:0020127', 'Periarticular soft-tissue mass', 'XPO:0139771', 'abnormally necrotic skeletal subdivision', 0.40476190476190477, 4.638757693672553, 1.3702526773627712, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(472372, 'HP:0020127', 'Periarticular soft-tissue mass', 'XPO:0101348', 'abnormal perichordal tissue', 0.45161290322580644, 4.3395673355180735, 1.399930213666808, 'UPHENO:0002964', 'abnormal skeletal system'),
(472373, 'HP:0020127', 'Periarticular soft-tissue mass', 'XPO:0100377', 'abnormal connective tissue', 0.42857142857142855, 3.9037819259951223, 1.293464107292913, 'HP:0033127', 'Abnormality of the musculoskeletal system'),
(472374, 'HP:0020127', 'Periarticular soft-tissue mass', 'XPO:0100325', 'abnormal axial skeleton', 0.45161290322580644, 4.3395673355180735, 1.399930213666808, 'UPHENO:0002964', 'abnormal skeletal system'),
(472375, 'HP:0020127', 'Periarticular soft-tissue mass', 'XPO:0101241', 'abnormal nucleate erythrocyte', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(472376, 'HP:0020127', 'Periarticular soft-tissue mass', 'XPO:0100829', 'abnormal postcranial axial skeleton', 0.4375, 4.3395673355180735, 1.3778826906849353, 'UPHENO:0002964', 'abnormal skeletal system'),
(472377, 'HP:0020127', 'Periarticular soft-tissue mass', 'XPO:0101586', 'abnormal joint', 0.4375, 4.3395673355180735, 1.3778826906849353, 'UPHENO:0002964', 'abnormal skeletal system'),
(472378, 'HP:0020127', 'Periarticular soft-tissue mass', 'XPO:0100477', 'abnormal pericyte', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(472379, 'HP:0020127', 'Periarticular soft-tissue mass', 'XPO:0128890', 'decreased size of the elastica externa', 0.4146341463414634, 4.638757693672553, 1.3868624071625903, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(472380, 'HP:0020127', 'Periarticular soft-tissue mass', 'XPO:0141714', 'abnormal anterior notochord', 0.5, 4.3395673355180735, 1.473018556488355, 'UPHENO:0002964', 'abnormal skeletal system'),
(472381, 'HP:0020127', 'Periarticular soft-tissue mass', 'XPO:0101237', 'abnormal mucus secreting cell', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(472382, 'HP:0020127', 'Periarticular soft-tissue mass', 'XPO:0100638', 'abnormal polar body', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(472383, 'HP:0020127', 'Periarticular soft-tissue mass', 'XPO:0141703', 'abnormally necrotic posterior notochord', 0.4146341463414634, 4.638757693672553, 1.3868624071625903, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(472384, 'HP:0020127', 'Periarticular soft-tissue mass', 'XPO:0100935', 'abnormal skeleton', 0.4827586206896552, 4.3395673355180735, 1.4473988881039626, 'UPHENO:0002964', 'abnormal skeletal system'),
(472385, 'HP:0020127', 'Periarticular soft-tissue mass', 'XPO:0102097', 'abnormal skeletal system morphology', 0.5, 4.638757693672553, 1.5229507040072823, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(472386, 'HP:0020127', 'Periarticular soft-tissue mass', 'XPO:0102217', 'abnormal elastica externa morphology', 0.5, 4.638757693672553, 1.5229507040072823, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(472387, 'HP:0020127', 'Periarticular soft-tissue mass', 'XPO:0102010', 'abnormal perichondrium morphology', 0.4594594594594595, 4.638757693672553, 1.4599044840325002, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(472388, 'HP:0020127', 'Periarticular soft-tissue mass', 'XPO:0100715', 'abnormal ciliated cell', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(472389, 'HP:0020127', 'Periarticular soft-tissue mass', 'XPO:0128352', 'decreased size of the skeletal system', 0.4146341463414634, 4.638757693672553, 1.3868624071625903, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(472390, 'HP:0020127', 'Periarticular soft-tissue mass', 'XPO:0107285', 'abnormal flexural organ', 0.5, 4.3395673355180735, 1.473018556488355, 'UPHENO:0002964', 'abnormal skeletal system'),
(472391, 'HP:0020127', 'Periarticular soft-tissue mass', 'XPO:0100026', 'abnormal germ cell', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(472392, 'HP:0020127', 'Periarticular soft-tissue mass', 'XPO:0100465', 'abnormal skeletal system', 0.5185185185185185, 4.3395673355180735, 1.5000486744849937, 'UPHENO:0002964', 'abnormal skeletal system'),
(472393, 'HP:0020127', 'Periarticular soft-tissue mass', 'XPO:0101535', 'abnormal absorptive cell', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(472394, 'HP:0020127', 'Periarticular soft-tissue mass', 'XPO:0101129', 'abnormal cartilaginous condensation', 0.4117647058823529, 4.3395673355180735, 1.3367425584480601, 'UPHENO:0002964', 'abnormal skeletal system'),
(472395, 'HP:0020127', 'Periarticular soft-tissue mass', 'XPO:0140559', 'abnormally necrotic articular system', 0.425, 4.638757693672553, 1.404091172186064, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(472396, 'HP:0020127', 'Periarticular soft-tissue mass', 'XPO:0101957', 'abnormal axial skeleton morphology', 0.425, 4.638757693672553, 1.404091172186064, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(472397, 'HP:0020127', 'Periarticular soft-tissue mass', 'XPO:0102806', 'abnormal articular system morphology', 0.4857142857142857, 4.638757693672553, 1.5010366017468766, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(472398, 'HP:0020127', 'Periarticular soft-tissue mass', 'XPO:0100004', 'abnormal cell', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(472399, 'HP:0020127', 'Periarticular soft-tissue mass', 'XPO:0140019', 'abnormally necrotic skeletal system', 0.4358974358974359, 4.638757693672553, 1.421978405047478, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(472400, 'HP:0020127', 'Periarticular soft-tissue mass', 'XPO:0100498', 'abnormal endoskeleton', 0.45161290322580644, 4.3395673355180735, 1.399930213666808, 'UPHENO:0002964', 'abnormal skeletal system'),
(472401, 'HP:0020127', 'Periarticular soft-tissue mass', 'XPO:0100461', 'abnormal craniofacial skeleton', 0.42424242424242425, 4.3395673355180735, 1.3568450783281876, 'UPHENO:0002964', 'abnormal skeletal system'),
(472402, 'HP:0020127', 'Periarticular soft-tissue mass', 'XPO:0100754', 'abnormal electrically active cell', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(472403, 'HP:0020127', 'Periarticular soft-tissue mass', 'XPO:0129427', 'decreased size of the joint', 0.40425531914893614, 8.100914173390091, 1.8096512494295556, 'UPHENO:0076767', 'abnormal skeletal joint morphology'),
(472404, 'HP:0020127', 'Periarticular soft-tissue mass', 'XPO:0140565', 'abnormally necrotic joint', 0.4222222222222222, 8.100914173390091, 1.8494285561546466, 'UPHENO:0076767', 'abnormal skeletal joint morphology'),
(472405, 'HP:0020127', 'Periarticular soft-tissue mass', 'XPO:0100802', 'abnormal exocrine cell', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(472406, 'HP:0020127', 'Periarticular soft-tissue mass', 'XPO:0101297', 'abnormal barrier cell', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(472407, 'HP:0020127', 'Periarticular soft-tissue mass', 'XPO:0100123', 'abnormal pelvic girdle', 0.4375, 4.3395673355180735, 1.3778826906849353, 'UPHENO:0002964', 'abnormal skeletal system'),
(472408, 'HP:0020127', 'Periarticular soft-tissue mass', 'XPO:0100973', 'abnormal dermal skeleton', 0.45161290322580644, 4.3395673355180735, 1.399930213666808, 'UPHENO:0002964', 'abnormal skeletal system'),
(472409, 'HP:0020127', 'Periarticular soft-tissue mass', 'XPO:0102054', 'abnormal notochord morphology', 0.4722222222222222, 4.638757693672553, 1.4800420488812078, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(472410, 'HP:0020127', 'Periarticular soft-tissue mass', 'XPO:0129786', 'increased size of the articular system', 0.40476190476190477, 4.638757693672553, 1.3702526773627712, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(472411, 'HP:0020127', 'Periarticular soft-tissue mass', 'XPO:0101326', 'abnormal cementoblast', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(472412, 'HP:0020127', 'Periarticular soft-tissue mass', 'XPO:0100006', 'abnormal anatomical structure', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(472413, 'HP:0020127', 'Periarticular soft-tissue mass', 'XPO:0100584', 'abnormal vertebral column', 0.4146341463414634, 4.638757693672553, 1.3868624071625903, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(472414, 'HP:0020127', 'Periarticular soft-tissue mass', 'XPO:0141718', 'abnormal posterior notochord', 0.5, 4.3395673355180735, 1.473018556488355, 'UPHENO:0002964', 'abnormal skeletal system'),
(472415, 'HP:0020127', 'Periarticular soft-tissue mass', 'XPO:0100585', 'abnormal elastica externa', 0.5384615384615384, 4.3395673355180735, 1.5286235977965605, 'UPHENO:0002964', 'abnormal skeletal system'),
(472416, 'HP:0020127', 'Periarticular soft-tissue mass', 'XPO:0100882', 'abnormal perichondrial cell', 0.42424242424242425, 4.3395673355180735, 1.3568450783281876, 'UPHENO:0002964', 'abnormal skeletal system'),
(472417, 'HP:0020127', 'Periarticular soft-tissue mass', 'XPO:0100852', 'abnormal interdigital region', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(472418, 'HP:0020127', 'Periarticular soft-tissue mass', 'XPO:0101484', 'abnormal bone marrow', 0.42424242424242425, 4.3395673355180735, 1.3568450783281876, 'UPHENO:0002964', 'abnormal skeletal system'),
(472419, 'HP:0020127', 'Periarticular soft-tissue mass', 'XPO:0102605', 'abnormal dermal skeleton morphology', 0.4358974358974359, 4.638757693672553, 1.421978405047478, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(472420, 'HP:0020127', 'Periarticular soft-tissue mass', 'XPO:0100640', 'abnormal notochordal sheath', 0.5, 4.3395673355180735, 1.473018556488355, 'UPHENO:0002964', 'abnormal skeletal system'),
(472421, 'HP:0020127', 'Periarticular soft-tissue mass', 'XPO:0100481', 'abnormal anatomical line', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(472422, 'HP:0020127', 'Periarticular soft-tissue mass', 'XPO:0102514', 'abnormal perichondrial cell morphology', 0.4146341463414634, 4.638757693672553, 1.3868624071625903, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(472423, 'HP:0020127', 'Periarticular soft-tissue mass', 'XPO:0141723', 'abnormal posterior notochord morphology', 0.4722222222222222, 4.638757693672553, 1.4800420488812078, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(472424, 'HP:0020127', 'Periarticular soft-tissue mass', 'XPO:0102130', 'abnormal endoskeleton morphology', 0.4358974358974359, 4.638757693672553, 1.421978405047478, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(472425, 'HP:0020127', 'Periarticular soft-tissue mass', 'XPO:0140432', 'abnormally necrotic skeleton', 0.4146341463414634, 4.638757693672553, 1.3868624071625903, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(472426, 'HP:0020127', 'Periarticular soft-tissue mass', 'XPO:0102728', 'abnormal tendon morphology', 0.40476190476190477, 4.638757693672553, 1.3702526773627712, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(472427, 'HP:0020127', 'Periarticular soft-tissue mass', 'XPO:0100172', 'abnormal stem cell', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(472428, 'HP:0020127', 'Periarticular soft-tissue mass', 'XPO:0141719', 'abnormal anterior notochord morphology', 0.4722222222222222, 4.638757693672553, 1.4800420488812078, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(472429, 'HP:0020127', 'Periarticular soft-tissue mass', 'XPO:0101467', 'abnormal alkali secreting cell', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(472430, 'HP:0020127', 'Periarticular soft-tissue mass', 'XPO:0102542', 'abnormal vacuolated notochordal tissue morphology', 0.425, 4.638757693672553, 1.404091172186064, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(472431, 'HP:0020127', 'Periarticular soft-tissue mass', 'XPO:0140683', 'abnormally necrotic flexural organ', 0.4146341463414634, 4.638757693672553, 1.3868624071625903, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(472432, 'HP:0020127', 'Periarticular soft-tissue mass', 'XPO:0100289', 'abnormal chondroblast', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(472433, 'HP:0020127', 'Periarticular soft-tissue mass', 'XPO:0102272', 'abnormal notochordal sheath morphology', 0.4722222222222222, 4.638757693672553, 1.4800420488812078, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(472434, 'HP:0020127', 'Periarticular soft-tissue mass', 'XPO:0102144', 'abnormal cranial skeleton morphology', 0.4146341463414634, 4.638757693672553, 1.3868624071625903, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(472435, 'HP:0020127', 'Periarticular soft-tissue mass', 'XPO:0100533', 'abnormal melanoblast', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(472436, 'HP:0020127', 'Periarticular soft-tissue mass', 'XPO:0101860', 'abnormal skeletal subdivision morphology', 0.4594594594594595, 4.638757693672553, 1.4599044840325002, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(472437, 'HP:0020127', 'Periarticular soft-tissue mass', 'XPO:0100653', 'abnormal myoblast', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(472438, 'HP:0020127', 'Periarticular soft-tissue mass', 'XPO:0100048', 'abnormal skeletal element', 0.4117647058823529, 4.3395673355180735, 1.3367425584480601, 'UPHENO:0002964', 'abnormal skeletal system'),
(472439, 'HP:0020127', 'Periarticular soft-tissue mass', 'XPO:0100910', 'abnormal vacuolated notochordal tissue', 0.45161290322580644, 4.3395673355180735, 1.399930213666808, 'UPHENO:0002964', 'abnormal skeletal system'),
(472440, 'HP:0020127', 'Periarticular soft-tissue mass', 'XPO:0102980', 'abnormal perichordal tissue morphology', 0.425, 4.638757693672553, 1.404091172186064, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(472441, 'HP:0020127', 'Periarticular soft-tissue mass', 'XPO:0100704', 'abnormal Merkel cell', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(472442, 'HP:0020127', 'Periarticular soft-tissue mass', 'XPO:0100417', 'abnormal dense regular connective tissue', 0.41379310344827586, 3.9037819259951223, 1.270967363209146, 'HP:0033127', 'Abnormality of the musculoskeletal system'),
(472443, 'HP:0020127', 'Periarticular soft-tissue mass', 'XPO:0100688', 'abnormal adipose tissue', 0.41379310344827586, 3.9037819259951223, 1.270967363209146, 'HP:0033127', 'Abnormality of the musculoskeletal system'),
(472444, 'HP:0020127', 'Periarticular soft-tissue mass', 'XPO:0101132', 'abnormal apoptotic cell', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(472445, 'HP:0020127', 'Periarticular soft-tissue mass', 'XPO:0101982', 'abnormal appendicular skeleton morphology', 0.4146341463414634, 4.638757693672553, 1.3868624071625903, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(472446, 'HP:0020127', 'Periarticular soft-tissue mass', 'XPO:0100108', 'abnormal cell part', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(472447, 'HP:0020127', 'Periarticular soft-tissue mass', 'XPO:0100285', 'abnormal progenitor cell', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(472448, 'HP:0020127', 'Periarticular soft-tissue mass', 'XPO:0107372', 'abnormal flexural organ morphology', 0.4722222222222222, 4.638757693672553, 1.4800420488812078, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(472449, 'HP:0020127', 'Periarticular soft-tissue mass', 'XPO:0100337', 'abnormal zygote', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(472450, 'HP:0020127', 'Periarticular soft-tissue mass', 'XPO:0100422', 'abnormal notochord', 0.5185185185185185, 4.3395673355180735, 1.5000486744849937, 'UPHENO:0002964', 'abnormal skeletal system'),
(472451, 'HP:0020127', 'Periarticular soft-tissue mass', 'XPO:0100378', 'abnormal perichondrium', 0.4827586206896552, 4.3395673355180735, 1.4473988881039626, 'UPHENO:0002964', 'abnormal skeletal system'),
(472452, 'HP:0020127', 'Periarticular soft-tissue mass', 'XPO:0140350', 'abnormally necrotic notochordal sheath', 0.4146341463414634, 4.638757693672553, 1.3868624071625903, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(472453, 'HP:0020127', 'Periarticular soft-tissue mass', 'XPO:0128306', 'decreased size of the articular system', 0.40476190476190477, 4.638757693672553, 1.3702526773627712, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(472454, 'HP:0020127', 'Periarticular soft-tissue mass', 'XPO:0100228', 'abnormal skeletal subdivision', 0.4666666666666667, 4.3395673355180735, 1.4230711237467255, 'UPHENO:0002964', 'abnormal skeletal system'),
(472455, 'HP:0020127', 'Periarticular soft-tissue mass', 'XPO:0100081', 'abnormal anatomical entity in vitro', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(472456, 'HP:0020127', 'Periarticular soft-tissue mass', 'XPO:0141699', 'abnormally necrotic anterior notochord', 0.4146341463414634, 4.638757693672553, 1.3868624071625903, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(472457, 'HP:0020127', 'Periarticular soft-tissue mass', 'XPO:0100512', 'abnormal cranial skeleton', 0.4375, 4.3395673355180735, 1.3778826906849353, 'UPHENO:0002964', 'abnormal skeletal system'),
(472458, 'HP:0020127', 'Periarticular soft-tissue mass', 'XPO:0130368', 'increased size of the elastica externa', 0.4146341463414634, 4.638757693672553, 1.3868624071625903, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(472459, 'HP:0020127', 'Periarticular soft-tissue mass', 'XPO:0101174', 'abnormal articular system', 0.5, 4.3395673355180735, 1.473018556488355, 'UPHENO:0002964', 'abnormal skeletal system'),
(472460, 'HP:0020127', 'Periarticular soft-tissue mass', 'XPO:0100549', 'abnormal mitotic cell', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(472461, 'HP:0020127', 'Periarticular soft-tissue mass', 'XPO:0103218', 'abnormal joint morphology', 0.475, 8.100914173390091, 1.9616152100654942, 'UPHENO:0076767', 'abnormal skeletal joint morphology'),
(472462, 'HP:0020127', 'Periarticular soft-tissue mass', 'XPO:0101435', 'abnormal paracrine cell', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(472463, 'HP:0020127', 'Periarticular soft-tissue mass', 'XPO:0101373', 'abnormal oxygen accumulating cell', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(472464, 'HP:0020127', 'Periarticular soft-tissue mass', 'XPO:0139917', 'abnormally necrotic notochord', 0.40476190476190477, 4.638757693672553, 1.3702526773627712, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(472465, 'HP:0020127', 'Periarticular soft-tissue mass', 'XPO:0129832', 'increased size of the skeletal system', 0.4146341463414634, 4.638757693672553, 1.3868624071625903, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(472466, 'HP:0020127', 'Periarticular soft-tissue mass', 'XPO:0100691', 'abnormal keratin accumulating cell', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(472467, 'HP:3000062', 'Abnormal internal carotid artery morphology', 'XPO:0101052', 'abnormal ophthalmic artery', 0.6825396825396826, 12.854497839006713, 2.9620440365130762, 'HP:3000062', 'Abnormal internal carotid artery morphology'),
(472468, 'HP:3000062', 'Abnormal internal carotid artery morphology', 'XPO:0130725', 'increased size of the facial vein', 0.42857142857142855, 8.976035651724713, 1.9613445444815998, 'HP:3000036', 'Abnormal head blood vessel morphology'),
(472469, 'HP:3000062', 'Abnormal internal carotid artery morphology', 'XPO:0102777', 'abnormal maxillary artery morphology', 0.5230769230769231, 9.01729298920255, 2.1718052102514123, 'UPHENO:0015290', 'abnormal artery morphology in the independent continuant'),
(472470, 'HP:3000062', 'Abnormal internal carotid artery morphology', 'XPO:0102695', 'abnormal metencephalic artery morphology', 0.43037974683544306, 9.01729298920255, 1.9699899171909507, 'UPHENO:0015290', 'abnormal artery morphology in the independent continuant'),
(472471, 'HP:3000062', 'Abnormal internal carotid artery morphology', 'XPO:0129254', 'decreased size of the anterior palatine artery', 0.56, 11.819732420846037, 2.5727514756916925, 'UPHENO:0087152', 'abnormal internal carotid artery morphology'),
(472472, 'HP:3000062', 'Abnormal internal carotid artery morphology', 'XPO:0103215', 'abnormal truncus arteriosus morphology', 0.4067796610169492, 6.974839882869777, 1.6844058309093048, 'UPHENO:0087186', 'abnormal blood vessel morphology'),
(472473, 'HP:3000062', 'Abnormal internal carotid artery morphology', 'XPO:0101685', 'abnormal head vasculature morphology', 0.47540983606557374, 6.65602285090012, 1.7788588286862843, 'HP:0025015', 'Abnormal vascular morphology'),
(472474, 'HP:3000062', 'Abnormal internal carotid artery morphology', 'XPO:0140107', 'abnormally necrotic internal carotid artery', 0.589041095890411, 12.854497839006713, 2.7516953854323036, 'HP:3000062', 'Abnormal internal carotid artery morphology'),
(472475, 'HP:3000062', 'Abnormal internal carotid artery morphology', 'XPO:0141139', 'abnormally necrotic ophthalmic artery', 0.5584415584415584, 12.854497839006713, 2.679269640442812, 'HP:3000062', 'Abnormal internal carotid artery morphology'),
(472476, 'HP:3000062', 'Abnormal internal carotid artery morphology', 'XPO:0140873', 'abnormally necrotic maxillary artery', 0.4722222222222222, 9.01729298920255, 2.0635324406924385, 'UPHENO:0015290', 'abnormal artery morphology in the independent continuant'),
(472477, 'HP:3000062', 'Abnormal internal carotid artery morphology', 'XPO:0140526', 'abnormally necrotic vena capitis lateralis', 0.44, 8.976035651724713, 1.9873237498603176, 'HP:3000036', 'Abnormal head blood vessel morphology'),
(472478, 'HP:3000062', 'Abnormal internal carotid artery morphology', 'XPO:0102786', 'abnormal external carotid artery morphology', 0.4177215189873418, 11.341685124041394, 2.176618004586636, 'UPHENO:0087623', 'abnormal carotid artery segment morphology'),
(472479, 'HP:3000062', 'Abnormal internal carotid artery morphology', 'XPO:0101774', 'abnormal paired dorsal aorta morphology', 0.44776119402985076, 9.08792853179561, 2.0172312040653027, 'UPHENO:0087334', 'abnormal systemic artery morphology'),
(472480, 'HP:3000062', 'Abnormal internal carotid artery morphology', 'XPO:0129796', 'increased size of the internal carotid artery', 0.5733333333333334, 12.854497839006713, 2.7147582018227423, 'HP:3000062', 'Abnormal internal carotid artery morphology'),
(472481, 'HP:3000062', 'Abnormal internal carotid artery morphology', 'XPO:0130730', 'increased size of the anterior palatine artery', 0.56, 11.819732420846037, 2.5727514756916925, 'UPHENO:0087152', 'abnormal internal carotid artery morphology'),
(472482, 'HP:3000062', 'Abnormal internal carotid artery morphology', 'XPO:0102424', 'abnormal capillary morphology', 0.4032258064516129, 7.803720102857406, 1.7738831223610367, 'HP:0033353', 'Abnormal blood vessel morphology'),
(472483, 'HP:3000062', 'Abnormal internal carotid artery morphology', 'XPO:0102619', 'abnormal larval aorta morphology', 0.4262295081967213, 9.01729298920255, 1.960468402207377, 'UPHENO:0015290', 'abnormal artery morphology in the independent continuant'),
(472484, 'HP:3000062', 'Abnormal internal carotid artery morphology', 'XPO:0127028', 'abnormally localised ophthalmic artery', 0.589041095890411, 12.854497839006713, 2.7516953854323036, 'HP:3000062', 'Abnormal internal carotid artery morphology'),
(472485, 'HP:3000062', 'Abnormal internal carotid artery morphology', 'XPO:0130030', 'increased size of the vena capitis medialis', 0.42857142857142855, 8.976035651724713, 1.9613445444815998, 'HP:3000036', 'Abnormal head blood vessel morphology'),
(472486, 'HP:3000062', 'Abnormal internal carotid artery morphology', 'XPO:0130057', 'increased size of the maxillary artery', 0.4594594594594595, 9.01729298920255, 2.035455861129535, 'UPHENO:0015290', 'abnormal artery morphology in the independent continuant'),
(472487, 'HP:3000062', 'Abnormal internal carotid artery morphology', 'XPO:0128577', 'decreased size of the maxillary artery', 0.4594594594594595, 9.01729298920255, 2.035455861129535, 'UPHENO:0015290', 'abnormal artery morphology in the independent continuant'),
(472488, 'HP:3000062', 'Abnormal internal carotid artery morphology', 'XPO:0102050', 'abnormal anterior palatine artery morphology', 0.6363636363636364, 11.819732420846037, 2.7425622881121132, 'UPHENO:0087152', 'abnormal internal carotid artery morphology'),
(472489, 'HP:3000062', 'Abnormal internal carotid artery morphology', 'XPO:0102329', 'abnormal caudal artery morphology', 0.4225352112676056, 9.08792853179561, 1.9595840890778735, 'UPHENO:0087334', 'abnormal systemic artery morphology'),
(472490, 'HP:3000062', 'Abnormal internal carotid artery morphology', 'XPO:0141174', 'abnormally necrotic retinal vein', 0.4074074074074074, 8.976035651724713, 1.9123031699146513, 'HP:3000036', 'Abnormal head blood vessel morphology'),
(472491, 'HP:3000062', 'Abnormal internal carotid artery morphology', 'XPO:0140751', 'abnormally necrotic ophthalmic vein', 0.4342105263157895, 8.976035651724713, 1.9742059579903708, 'HP:3000036', 'Abnormal head blood vessel morphology'),
(472492, 'HP:3000062', 'Abnormal internal carotid artery morphology', 'XPO:0101707', 'abnormal mandibular artery morphology', 0.5230769230769231, 9.01729298920255, 2.1718052102514123, 'UPHENO:0015290', 'abnormal artery morphology in the independent continuant'),
(472493, 'HP:3000062', 'Abnormal internal carotid artery morphology', 'XPO:0102684', 'abnormal ophthalmic artery morphology', 0.6142857142857143, 12.854497839006713, 2.8100417055300815, 'HP:3000062', 'Abnormal internal carotid artery morphology'),
(472494, 'HP:3000062', 'Abnormal internal carotid artery morphology', 'XPO:0129226', 'decreased size of the ophthalmic artery', 0.5443037974683544, 12.854497839006713, 2.6451374233336367, 'HP:3000062', 'Abnormal internal carotid artery morphology'),
(472495, 'HP:3000062', 'Abnormal internal carotid artery morphology', 'XPO:0125393', 'absent ophthalmic artery', 0.5733333333333334, 12.854497839006713, 2.7147582018227423, 'HP:3000062', 'Abnormal internal carotid artery morphology'),
(472496, 'HP:3000062', 'Abnormal internal carotid artery morphology', 'XPO:0102421', 'abnormal occipitovertebral artery morphology', 0.4262295081967213, 9.01729298920255, 1.960468402207377, 'UPHENO:0015290', 'abnormal artery morphology in the independent continuant'),
(472497, 'HP:3000062', 'Abnormal internal carotid artery morphology', 'XPO:0103001', 'abnormal nasociliary artery morphology', 0.5230769230769231, 9.01729298920255, 2.1718052102514123, 'UPHENO:0015290', 'abnormal artery morphology in the independent continuant'),
(472498, 'HP:3000062', 'Abnormal internal carotid artery morphology', 'XPO:0129509', 'increased size of the head vasculature', 0.4264705882352941, 6.65602285090012, 1.6848139305368215, 'HP:0025015', 'Abnormal vascular morphology'),
(472499, 'HP:3000062', 'Abnormal internal carotid artery morphology', 'XPO:0102417', 'abnormal mesencephalic artery morphology', 0.4146341463414634, 9.01729298920255, 1.9336177442526903, 'UPHENO:0015290', 'abnormal artery morphology in the independent continuant'),
(472500, 'HP:3000062', 'Abnormal internal carotid artery morphology', 'XPO:0140689', 'abnormally necrotic anterior palatine artery', 0.5753424657534246, 11.819732420846037, 2.6077565061859693, 'UPHENO:0087152', 'abnormal internal carotid artery morphology'),
(472501, 'HP:3000062', 'Abnormal internal carotid artery morphology', 'XPO:0102503', 'abnormal posterior palatine artery morphology', 0.6363636363636364, 11.819732420846037, 2.7425622881121132, 'UPHENO:0087152', 'abnormal internal carotid artery morphology'),
(472502, 'HP:3000062', 'Abnormal internal carotid artery morphology', 'XPO:0102875', 'abnormal vertebral artery morphology', 0.4262295081967213, 9.01729298920255, 1.960468402207377, 'UPHENO:0015290', 'abnormal artery morphology in the independent continuant'),
(472503, 'HP:3000062', 'Abnormal internal carotid artery morphology', 'XPO:0130365', 'increased size of the ophthalmic vein', 0.4230769230769231, 8.976035651724713, 1.9487312654546434, 'HP:3000036', 'Abnormal head blood vessel morphology'),
(472504, 'HP:3000062', 'Abnormal internal carotid artery morphology', 'XPO:0139747', 'abnormally necrotic head vasculature', 0.4393939393939394, 6.65602285090012, 1.7101509001117658, 'HP:0025015', 'Abnormal vascular morphology'),
(472505, 'HP:3000062', 'Abnormal internal carotid artery morphology', 'XPO:0101675', 'abnormal vein morphology', 0.4032258064516129, 7.803720102857406, 1.7738831223610367, 'HP:0033353', 'Abnormal blood vessel morphology'),
(472506, 'HP:3000062', 'Abnormal internal carotid artery morphology', 'XPO:0141032', 'abnormally necrotic cerebral artery', 0.47191011235955055, 11.819732420846037, 2.361747500217006, 'UPHENO:0087152', 'abnormal internal carotid artery morphology'),
(472507, 'HP:3000062', 'Abnormal internal carotid artery morphology', 'XPO:0128316', 'decreased size of the internal carotid artery', 0.5733333333333334, 12.854497839006713, 2.7147582018227423, 'HP:3000062', 'Abnormal internal carotid artery morphology'),
(472508, 'HP:3000062', 'Abnormal internal carotid artery morphology', 'XPO:0139803', 'abnormally necrotic aorta', 0.4166666666666667, 9.08792853179561, 1.945928284456591, 'UPHENO:0087334', 'abnormal systemic artery morphology'),
(472509, 'HP:3000062', 'Abnormal internal carotid artery morphology', 'XPO:0102003', 'abnormal hyaloid blood vessel morphology', 0.42105263157894735, 8.976035651724713, 1.9440636389545334, 'HP:3000036', 'Abnormal head blood vessel morphology'),
(472510, 'HP:3000062', 'Abnormal internal carotid artery morphology', 'XPO:0127366', 'abnormally localised external carotid artery', 0.40789473684210525, 11.135234246573967, 2.1311976545317157, 'UPHENO:0076798', 'abnormal common carotid artery plus branches morphology'),
(472511, 'HP:3000062', 'Abnormal internal carotid artery morphology', 'XPO:0102846', 'abnormal ophthalmic vein morphology', 0.4782608695652174, 8.976035651724713, 2.0719282362191636, 'HP:3000036', 'Abnormal head blood vessel morphology'),
(472512, 'HP:3000062', 'Abnormal internal carotid artery morphology', 'XPO:0139729', 'abnormally necrotic vena capitis medialis', 0.44, 8.976035651724713, 1.9873237498603176, 'HP:3000036', 'Abnormal head blood vessel morphology'),
(472513, 'HP:3000062', 'Abnormal internal carotid artery morphology', 'XPO:0102120', 'abnormal external jugular vein morphology', 0.4342105263157895, 8.976035651724713, 1.9742059579903708, 'HP:3000036', 'Abnormal head blood vessel morphology'),
(472514, 'HP:3000062', 'Abnormal internal carotid artery morphology', 'XPO:0103063', 'abnormal ischiadic artery morphology', 0.4262295081967213, 9.01729298920255, 1.960468402207377, 'UPHENO:0015290', 'abnormal artery morphology in the independent continuant'),
(472515, 'HP:3000062', 'Abnormal internal carotid artery morphology', 'XPO:0103003', 'abnormal facial vein morphology', 0.4852941176470588, 8.976035651724713, 2.0871074005839487, 'HP:3000036', 'Abnormal head blood vessel morphology'),
(472516, 'HP:3000062', 'Abnormal internal carotid artery morphology', 'XPO:0102225', 'abnormal cerebral artery morphology', 0.5121951219512195, 11.819732420846037, 2.4604896441005435, 'UPHENO:0087152', 'abnormal internal carotid artery morphology'),
(472517, 'HP:3000062', 'Abnormal internal carotid artery morphology', 'XPO:0128093', 'decreased size of the aorta', 0.40540540540540543, 9.08792853179561, 1.9194518360010886, 'UPHENO:0087334', 'abnormal systemic artery morphology'),
(472518, 'HP:3000062', 'Abnormal internal carotid artery morphology', 'XPO:0130196', 'increased size of the nasociliary artery', 0.4594594594594595, 9.01729298920255, 2.035455861129535, 'UPHENO:0015290', 'abnormal artery morphology in the independent continuant'),
(472519, 'HP:3000062', 'Abnormal internal carotid artery morphology', 'XPO:0101840', 'abnormal ventral aorta morphology', 0.4166666666666667, 9.08792853179561, 1.945928284456591, 'UPHENO:0087334', 'abnormal systemic artery morphology'),
(472520, 'HP:3000062', 'Abnormal internal carotid artery morphology', 'XPO:0128550', 'decreased size of the vena capitis medialis', 0.42857142857142855, 8.976035651724713, 1.9613445444815998, 'HP:3000036', 'Abnormal head blood vessel morphology'),
(472521, 'HP:3000062', 'Abnormal internal carotid artery morphology', 'XPO:0102802', 'abnormal arteria subclavia morphology', 0.40298507462686567, 9.08792853179561, 1.9137135516030803, 'UPHENO:0087334', 'abnormal systemic artery morphology'),
(472522, 'HP:3000062', 'Abnormal internal carotid artery morphology', 'XPO:0129044', 'decreased size of the posterior palatine artery', 0.56, 11.819732420846037, 2.5727514756916925, 'UPHENO:0087152', 'abnormal internal carotid artery morphology'),
(472523, 'HP:3000062', 'Abnormal internal carotid artery morphology', 'XPO:0103091', 'abnormal arteria iliaca communis morphology', 0.42857142857142855, 9.08792853179561, 1.973531482806061, 'UPHENO:0087334', 'abnormal systemic artery morphology'),
(472524, 'HP:3000062', 'Abnormal internal carotid artery morphology', 'XPO:0101154', 'abnormal external carotid artery', 0.4696969696969697, 11.135234246573967, 2.286959943348749, 'UPHENO:0076798', 'abnormal common carotid artery plus branches morphology'),
(472525, 'HP:3000062', 'Abnormal internal carotid artery morphology', 'XPO:0102443', 'abnormal vena capitis medialis morphology', 0.4852941176470588, 8.976035651724713, 2.0871074005839487, 'HP:3000036', 'Abnormal head blood vessel morphology'),
(472526, 'HP:3000062', 'Abnormal internal carotid artery morphology', 'XPO:0129573', 'increased size of the aorta', 0.40540540540540543, 9.08792853179561, 1.9194518360010886, 'UPHENO:0087334', 'abnormal systemic artery morphology'),
(472527, 'HP:3000062', 'Abnormal internal carotid artery morphology', 'XPO:0141310', 'abnormal retinal vein morphology', 0.44594594594594594, 8.976035651724713, 2.0007065525840897, 'HP:3000036', 'Abnormal head blood vessel morphology'),
(472528, 'HP:3000062', 'Abnormal internal carotid artery morphology', 'XPO:0102273', 'abnormal metencephalic vein morphology', 0.4024390243902439, 8.976035651724713, 1.9006070163429738, 'HP:3000036', 'Abnormal head blood vessel morphology'),
(472529, 'HP:3000062', 'Abnormal internal carotid artery morphology', 'XPO:0102587', 'abnormal internal jugular vein morphology', 0.4230769230769231, 8.976035651724713, 1.9487312654546434, 'HP:3000036', 'Abnormal head blood vessel morphology'),
(472530, 'HP:3000062', 'Abnormal internal carotid artery morphology', 'XPO:0128717', 'decreased size of the nasociliary artery', 0.4594594594594595, 9.01729298920255, 2.035455861129535, 'UPHENO:0015290', 'abnormal artery morphology in the independent continuant'),
(472531, 'HP:3000062', 'Abnormal internal carotid artery morphology', 'XPO:0129249', 'decreased size of the facial vein', 0.42857142857142855, 8.976035651724713, 1.9613445444815998, 'HP:3000036', 'Abnormal head blood vessel morphology'),
(472532, 'HP:3000062', 'Abnormal internal carotid artery morphology', 'XPO:0141159', 'abnormally necrotic posterior palatine artery', 0.5753424657534246, 11.819732420846037, 2.6077565061859693, 'UPHENO:0087152', 'abnormal internal carotid artery morphology'),
(472533, 'HP:3000062', 'Abnormal internal carotid artery morphology', 'XPO:0102613', 'abnormal dorsal longitudinal anastomosing vessel morphology', 0.4067796610169492, 6.974839882869777, 1.6844058309093048, 'UPHENO:0087186', 'abnormal blood vessel morphology'),
(472534, 'HP:3000062', 'Abnormal internal carotid artery morphology', 'XPO:0102433', 'abnormal vena capitis lateralis morphology', 0.4852941176470588, 8.976035651724713, 2.0871074005839487, 'HP:3000036', 'Abnormal head blood vessel morphology'),
(472535, 'HP:3000062', 'Abnormal internal carotid artery morphology', 'XPO:0129336', 'decreased size of the cerebral artery', 0.46153846153846156, 11.819732420846037, 2.3356500417043553, 'UPHENO:0087152', 'abnormal internal carotid artery morphology'),
(472536, 'HP:3000062', 'Abnormal internal carotid artery morphology', 'XPO:0128029', 'decreased size of the head vasculature', 0.4264705882352941, 6.65602285090012, 1.6848139305368215, 'HP:0025015', 'Abnormal vascular morphology'),
(472537, 'HP:3000062', 'Abnormal internal carotid artery morphology', 'XPO:0130521', 'increased size of the posterior palatine artery', 0.56, 11.819732420846037, 2.5727514756916925, 'UPHENO:0087152', 'abnormal internal carotid artery morphology'),
(472538, 'HP:3000062', 'Abnormal internal carotid artery morphology', 'XPO:0101780', 'abnormal arteria mesenterica posterior morphology', 0.4166666666666667, 9.08792853179561, 1.945928284456591, 'UPHENO:0087334', 'abnormal systemic artery morphology'),
(472539, 'HP:3000062', 'Abnormal internal carotid artery morphology', 'XPO:0128887', 'decreased size of the ophthalmic vein', 0.4230769230769231, 8.976035651724713, 1.9487312654546434, 'HP:3000036', 'Abnormal head blood vessel morphology'),
(472540, 'HP:3000062', 'Abnormal internal carotid artery morphology', 'XPO:0141130', 'abnormally necrotic mandibular artery', 0.4722222222222222, 9.01729298920255, 2.0635324406924385, 'UPHENO:0015290', 'abnormal artery morphology in the independent continuant'),
(472541, 'HP:3000062', 'Abnormal internal carotid artery morphology', 'XPO:0140255', 'abnormally necrotic nasociliary artery', 0.4722222222222222, 9.01729298920255, 2.0635324406924385, 'UPHENO:0015290', 'abnormal artery morphology in the independent continuant'),
(472542, 'HP:3000062', 'Abnormal internal carotid artery morphology', 'XPO:0130579', 'increased size of the vena capitis lateralis', 0.42857142857142855, 8.976035651724713, 1.9613445444815998, 'HP:3000036', 'Abnormal head blood vessel morphology'),
(472543, 'HP:3000062', 'Abnormal internal carotid artery morphology', 'XPO:0102074', 'abnormal internal carotid artery morphology', 0.6515151515151515, 12.854497839006713, 2.8939419668043875, 'HP:3000062', 'Abnormal internal carotid artery morphology'),
(472544, 'HP:3000062', 'Abnormal internal carotid artery morphology', 'XPO:0129102', 'decreased size of the vena capitis lateralis', 0.42857142857142855, 8.976035651724713, 1.9613445444815998, 'HP:3000036', 'Abnormal head blood vessel morphology'),
(472545, 'HP:3000062', 'Abnormal internal carotid artery morphology', 'XPO:0140299', 'abnormally necrotic facial vein', 0.44, 8.976035651724713, 1.9873237498603176, 'HP:3000036', 'Abnormal head blood vessel morphology'),
(472546, 'HP:3000062', 'Abnormal internal carotid artery morphology', 'XPO:0101686', 'abnormal blood vessel morphology', 0.42105263157894735, 6.974839882869777, 1.7137020416408788, 'UPHENO:0087186', 'abnormal blood vessel morphology'),
(472547, 'HP:3000062', 'Abnormal internal carotid artery morphology', 'XPO:0100955', 'abnormal internal jugular vein', 0.4027777777777778, 7.803720102857406, 1.77289735783792, 'HP:0033353', 'Abnormal blood vessel morphology'),
(472548, 'HP:3000062', 'Abnormal internal carotid artery morphology', 'XPO:0130702', 'increased size of the ophthalmic artery', 0.5443037974683544, 12.854497839006713, 2.6451374233336367, 'HP:3000062', 'Abnormal internal carotid artery morphology'),
(472549, 'HP:3000062', 'Abnormal internal carotid artery morphology', 'XPO:0101708', 'abnormal artery morphology', 0.4406779661016949, 9.01729298920255, 1.9934197586621973, 'UPHENO:0015290', 'abnormal artery morphology in the independent continuant'),
(472550, 'HP:3000062', 'Abnormal internal carotid artery morphology', 'XPO:0130811', 'increased size of the cerebral artery', 0.46153846153846156, 11.819732420846037, 2.3356500417043553, 'UPHENO:0087152', 'abnormal internal carotid artery morphology'),
(472551, 'HP:3000062', 'Abnormal internal carotid artery morphology', 'XPO:0101711', 'abnormal dorsal aorta morphology', 0.4166666666666667, 9.08792853179561, 1.945928284456591, 'UPHENO:0087334', 'abnormal systemic artery morphology'),
(472552, 'HP:3000062', 'Abnormal internal carotid artery morphology', 'XPO:0129111', 'decreased size of the mandibular artery', 0.4594594594594595, 9.01729298920255, 2.035455861129535, 'UPHENO:0015290', 'abnormal artery morphology in the independent continuant'),
(472553, 'HP:3000062', 'Abnormal internal carotid artery morphology', 'XPO:0130587', 'increased size of the mandibular artery', 0.4594594594594595, 9.01729298920255, 2.035455861129535, 'UPHENO:0015290', 'abnormal artery morphology in the independent continuant'),
(472554, 'HP:3000062', 'Abnormal internal carotid artery morphology', 'XPO:0101712', 'abnormal aorta morphology', 0.46153846153846156, 9.08792853179561, 2.0480304082548275, 'UPHENO:0087334', 'abnormal systemic artery morphology'),
(472555, 'HP:0010900', 'Abnormal circulating threonine concentration', 'XPO:0141896', 'abnormal lysine metabolic process', 0.6176470588235294, 12.511610125483706, 2.779884744940283, 'UPHENO:0050388', 'abnormal aspartate family amino acid metabolic process'),
(472556, 'HP:0010900', 'Abnormal circulating threonine concentration', 'XPO:0141882', 'abnormal gamma-aminobutyric acid metabolic process', 0.5882352941176471, 10.007478699375595, 2.4262630063748842, 'UPHENO:0051195', 'abnormal amino acid metabolic process'),
(472557, 'HP:0010900', 'Abnormal circulating threonine concentration', 'XPO:0141853', 'abnormal glutamate metabolic process', 0.5774647887323944, 10.156767408123608, 2.4218124505287704, 'UPHENO:0050249', 'abnormal alpha-amino acid metabolic process'),
(472558, 'HP:0010900', 'Abnormal circulating threonine concentration', 'XPO:0141888', 'abnormal threonine metabolic process', 0.6417910447761194, 14.7526182249875, 3.077027504556621, 'UPHENO:0078634', 'abnormal threonine metabolic process'),
(472559, 'HP:0010900', 'Abnormal circulating threonine concentration', 'XPO:0141869', 'abnormal alpha-amino acid metabolic process', 0.6212121212121212, 10.156767408123608, 2.511873210625609, 'UPHENO:0050249', 'abnormal alpha-amino acid metabolic process'),
(472560, 'HP:0010900', 'Abnormal circulating threonine concentration', 'XPO:0141887', 'abnormal histidine metabolic process', 0.5942028985507246, 10.156767408123608, 2.456660463680844, 'UPHENO:0050249', 'abnormal alpha-amino acid metabolic process'),
(472561, 'HP:0010900', 'Abnormal circulating threonine concentration', 'XPO:0141857', 'abnormal glycine metabolic process', 0.5857142857142857, 10.156767408123608, 2.4390497673510594, 'UPHENO:0050249', 'abnormal alpha-amino acid metabolic process'),
(472562, 'HP:0010900', 'Abnormal circulating threonine concentration', 'XPO:0141873', 'abnormal tricarboxylic acid metabolic process', 0.5147058823529411, 9.119292702704945, 2.1665072344629928, 'HP:0004354', 'Abnormal circulating carboxylic acid concentration'),
(472563, 'HP:0010900', 'Abnormal circulating threonine concentration', 'XPO:0141893', 'abnormal isoleucine metabolic process', 0.5942028985507246, 10.156767408123608, 2.456660463680844, 'UPHENO:0050249', 'abnormal alpha-amino acid metabolic process'),
(472564, 'HP:0010900', 'Abnormal circulating threonine concentration', 'XPO:0141858', 'abnormal serine family amino acid metabolic process', 0.6029411764705882, 10.156767408123608, 2.474658216843727, 'UPHENO:0050249', 'abnormal alpha-amino acid metabolic process'),
(472565, 'HP:0010900', 'Abnormal circulating threonine concentration', 'XPO:0141895', 'abnormal leucine metabolic process', 0.5942028985507246, 10.156767408123608, 2.456660463680844, 'UPHENO:0050249', 'abnormal alpha-amino acid metabolic process'),
(472566, 'HP:0010900', 'Abnormal circulating threonine concentration', 'XPO:0141922', 'abnormal valine metabolic process', 0.5942028985507246, 10.156767408123608, 2.456660463680844, 'UPHENO:0050249', 'abnormal alpha-amino acid metabolic process'),
(472567, 'HP:0010900', 'Abnormal circulating threonine concentration', 'XPO:0141912', 'abnormal D-serine metabolic process', 0.5857142857142857, 10.156767408123608, 2.4390497673510594, 'UPHENO:0050249', 'abnormal alpha-amino acid metabolic process'),
(472568, 'HP:0010900', 'Abnormal circulating threonine concentration', 'XPO:0141913', 'abnormal L-serine metabolic process', 0.5857142857142857, 10.156767408123608, 2.4390497673510594, 'UPHENO:0050249', 'abnormal alpha-amino acid metabolic process'),
(472569, 'HP:0010900', 'Abnormal circulating threonine concentration', 'XPO:0141843', 'abnormal alanine metabolic process', 0.6029411764705882, 10.156767408123608, 2.474658216843727, 'UPHENO:0050249', 'abnormal alpha-amino acid metabolic process'),
(472570, 'HP:0010900', 'Abnormal circulating threonine concentration', 'XPO:0141868', 'abnormal asparagine metabolic process', 0.6176470588235294, 12.511610125483706, 2.779884744940283, 'UPHENO:0050388', 'abnormal aspartate family amino acid metabolic process'),
(472571, 'HP:0010900', 'Abnormal circulating threonine concentration', 'XPO:0141917', 'abnormal tryptophan metabolic process', 0.5942028985507246, 10.156767408123608, 2.456660463680844, 'UPHENO:0050249', 'abnormal alpha-amino acid metabolic process'),
(472572, 'HP:0010900', 'Abnormal circulating threonine concentration', 'XPO:0141847', 'abnormal arginine metabolic process', 0.5942028985507246, 10.156767408123608, 2.456660463680844, 'UPHENO:0050249', 'abnormal alpha-amino acid metabolic process'),
(472573, 'HP:0010900', 'Abnormal circulating threonine concentration', 'XPO:0141848', 'abnormal proline metabolic process', 0.5942028985507246, 10.156767408123608, 2.456660463680844, 'UPHENO:0050249', 'abnormal alpha-amino acid metabolic process'),
(472574, 'HP:0010900', 'Abnormal circulating threonine concentration', 'XPO:0141905', 'abnormal ornithine metabolic process', 0.6029411764705882, 10.156767408123608, 2.474658216843727, 'UPHENO:0050249', 'abnormal alpha-amino acid metabolic process'),
(472575, 'HP:0010900', 'Abnormal circulating threonine concentration', 'XPO:0141889', 'abnormal homoserine metabolic process', 0.5857142857142857, 10.156767408123608, 2.4390497673510594, 'UPHENO:0050249', 'abnormal alpha-amino acid metabolic process'),
(472576, 'HP:0010900', 'Abnormal circulating threonine concentration', 'XPO:0141918', 'abnormal tyrosine metabolic process', 0.5942028985507246, 10.156767408123608, 2.456660463680844, 'UPHENO:0050249', 'abnormal alpha-amino acid metabolic process'),
(472577, 'HP:0012479', 'Temporomandibular joint crepitus', 'XPO:0102337', 'abnormal processus retroarticularis of Meckels cartilage morphology', 0.4845360824742268, 8.608423498638606, 2.0423250961366137, 'UPHENO:0088116', 'abnormal jaw skeleton morphology'),
(472578, 'HP:0012479', 'Temporomandibular joint crepitus', 'XPO:0101659', 'abnormal lower jaw morphology', 0.6527777777777778, 8.608423498638606, 2.370524743935678, 'UPHENO:0088116', 'abnormal jaw skeleton morphology'),
(472579, 'HP:0012479', 'Temporomandibular joint crepitus', 'XPO:0103350', 'decreased size of the Meckels cartilage', 0.4392523364485981, 8.608423498638606, 1.9445488255418075, 'UPHENO:0088116', 'abnormal jaw skeleton morphology'),
(472580, 'HP:0012479', 'Temporomandibular joint crepitus', 'XPO:0130324', 'increased size of the choana', 0.4146341463414634, 7.024697770424301, 1.7066574241325239, 'HP:0000929', 'Abnormal skull morphology'),
(472581, 'HP:0012479', 'Temporomandibular joint crepitus', 'XPO:0130701', 'increased size of the upper jaw', 0.5802469135802469, 8.608423498638606, 2.2349521618765626, 'UPHENO:0088116', 'abnormal jaw skeleton morphology'),
(472582, 'HP:0012479', 'Temporomandibular joint crepitus', 'XPO:0102052', 'abnormal choana morphology', 0.4473684210526316, 7.024697770424301, 1.7727458785530037, 'HP:0000929', 'Abnormal skull morphology'),
(472583, 'HP:0012479', 'Temporomandibular joint crepitus', 'XPO:0129225', 'decreased size of the upper jaw', 0.5802469135802469, 8.608423498638606, 2.2349521618765626, 'UPHENO:0088116', 'abnormal jaw skeleton morphology'),
(472584, 'HP:0012479', 'Temporomandibular joint crepitus', 'XPO:0140789', 'abnormally necrotic roof of mouth', 0.4177215189873418, 7.312692920701687, 1.7477611949930372, 'UPHENO:0076800', 'abnormal mouth morphology'),
(472585, 'HP:0012479', 'Temporomandibular joint crepitus', 'XPO:0140560', 'abnormally necrotic orbital region', 0.4444444444444444, 8.057231734572694, 1.8923508876612467, 'UPHENO:0084457', 'abnormal facial skeleton morphology'),
(472586, 'HP:0012479', 'Temporomandibular joint crepitus', 'XPO:0129291', 'decreased size of the orbital region', 0.4235294117647059, 8.057231734572694, 1.847288449862526, 'UPHENO:0084457', 'abnormal facial skeleton morphology'),
(472587, 'HP:0012479', 'Temporomandibular joint crepitus', 'XPO:0130431', 'increased size of the processus retroarticularis of Meckels cartilage', 0.4351851851851852, 8.608423498638606, 1.9355253484280543, 'UPHENO:0088116', 'abnormal jaw skeleton morphology'),
(472588, 'HP:0012479', 'Temporomandibular joint crepitus', 'XPO:0128953', 'decreased size of the processus retroarticularis of Meckels cartilage', 0.4351851851851852, 8.608423498638606, 1.9355253484280543, 'UPHENO:0088116', 'abnormal jaw skeleton morphology'),
(472589, 'HP:0012479', 'Temporomandibular joint crepitus', 'XPO:0101816', 'abnormal tooth morphology', 0.4367816091954023, 7.312692920701687, 1.7871904715099365, 'UPHENO:0076800', 'abnormal mouth morphology'),
(472590, 'HP:0012479', 'Temporomandibular joint crepitus', 'XPO:0102401', 'abnormal neurocranium morphology', 0.4189189189189189, 7.024697770424301, 1.7154529418548001, 'HP:0000929', 'Abnormal skull morphology'),
(472591, 'HP:0012479', 'Temporomandibular joint crepitus', 'XPO:0131573', 'decreased size of the roof of mouth', 0.4074074074074074, 7.312692920701687, 1.7260490329042149, 'UPHENO:0076800', 'abnormal mouth morphology'),
(472592, 'HP:0012479', 'Temporomandibular joint crepitus', 'XPO:0130767', 'increased size of the orbital region', 0.4235294117647059, 8.057231734572694, 1.847288449862526, 'UPHENO:0084457', 'abnormal facial skeleton morphology'),
(472593, 'HP:0012479', 'Temporomandibular joint crepitus', 'XPO:0140897', 'abnormally necrotic lower jaw', 0.6103896103896104, 8.608423498638606, 2.2922679305445044, 'UPHENO:0088116', 'abnormal jaw skeleton morphology'),
(472594, 'HP:0012479', 'Temporomandibular joint crepitus', 'XPO:0102279', 'abnormal mouth morphology', 0.4647887323943662, 7.312692920701687, 1.8435990000545652, 'UPHENO:0076800', 'abnormal mouth morphology'),
(472595, 'HP:0012479', 'Temporomandibular joint crepitus', 'XPO:0141311', 'abnormal roof of mouth morphology', 0.44594594594594594, 7.312692920701687, 1.8058421198805104, 'UPHENO:0076800', 'abnormal mouth morphology'),
(472596, 'HP:0012479', 'Temporomandibular joint crepitus', 'XPO:0103352', 'decreased size of the mouth', 0.4024390243902439, 7.312692920701687, 1.7154920590526295, 'UPHENO:0076800', 'abnormal mouth morphology'),
(472597, 'HP:0012479', 'Temporomandibular joint crepitus', 'XPO:0103138', 'abnormal upper jaw morphology', 0.6351351351351351, 8.608423498638606, 2.3382712037119013, 'UPHENO:0088116', 'abnormal jaw skeleton morphology'),
(472598, 'HP:0012479', 'Temporomandibular joint crepitus', 'XPO:0103381', 'increased size of the head', 0.4025974025974026, 7.024697770424301, 1.6817030286006471, 'HP:0000929', 'Abnormal skull morphology'),
(472599, 'HP:0012479', 'Temporomandibular joint crepitus', 'XPO:0102960', 'abnormal oral epithelium morphology', 0.4125, 7.312692920701687, 1.7368033365322182, 'UPHENO:0076800', 'abnormal mouth morphology'),
(472600, 'HP:0012479', 'Temporomandibular joint crepitus', 'XPO:0102564', 'abnormal olfactory region morphology', 0.4189189189189189, 7.024697770424301, 1.7154529418548001, 'HP:0000929', 'Abnormal skull morphology'),
(472601, 'HP:0012479', 'Temporomandibular joint crepitus', 'XPO:0115558', 'abnormally incomplete structure of mouth', 0.4583333333333333, 7.312692920701687, 1.830751463740579, 'UPHENO:0076800', 'abnormal mouth morphology'),
(472602, 'HP:0012479', 'Temporomandibular joint crepitus', 'XPO:0127750', 'abnormally localised tongue', 0.4025974025974026, 7.312692920701687, 1.7158295882362307, 'UPHENO:0076800', 'abnormal mouth morphology'),
(472603, 'HP:0012479', 'Temporomandibular joint crepitus', 'XPO:0103735', 'increased size of the mouth', 0.4024390243902439, 7.312692920701687, 1.7154920590526295, 'UPHENO:0076800', 'abnormal mouth morphology'),
(472604, 'HP:0012479', 'Temporomandibular joint crepitus', 'XPO:0101567', 'abnormal tongue', 0.44776119402985076, 7.312692920701687, 1.8095137782694621, 'UPHENO:0076800', 'abnormal mouth morphology'),
(472605, 'HP:0012479', 'Temporomandibular joint crepitus', 'XPO:0140665', 'abnormally necrotic processus retroarticularis of Meckels cartilage', 0.44339622641509435, 8.608423498638606, 1.9536996940879583, 'UPHENO:0088116', 'abnormal jaw skeleton morphology'),
(472606, 'HP:0012479', 'Temporomandibular joint crepitus', 'XPO:0102921', 'abnormal orbital region morphology', 0.47368421052631576, 8.057231734572694, 1.9536078043503626, 'UPHENO:0084457', 'abnormal facial skeleton morphology'),
(472607, 'HP:0012479', 'Temporomandibular joint crepitus', 'XPO:0140639', 'abnormally necrotic upper jaw', 0.5949367088607594, 8.608423498638606, 2.263065872828203, 'UPHENO:0088116', 'abnormal jaw skeleton morphology'),
(472608, 'HP:0012479', 'Temporomandibular joint crepitus', 'XPO:0140626', 'abnormally necrotic tongue', 0.4230769230769231, 7.312692920701687, 1.7589291117884391, 'UPHENO:0076800', 'abnormal mouth morphology'),
(472609, 'HP:0012479', 'Temporomandibular joint crepitus', 'XPO:0102828', 'abnormal occipital region morphology', 0.4246575342465753, 7.024697770424301, 1.727162654186281, 'HP:0000929', 'Abnormal skull morphology'),
(472610, 'HP:0012479', 'Temporomandibular joint crepitus', 'XPO:0128880', 'decreased size of the lower jaw', 0.5949367088607594, 8.608423498638606, 2.263065872828203, 'UPHENO:0088116', 'abnormal jaw skeleton morphology'),
(472611, 'HP:0012479', 'Temporomandibular joint crepitus', 'XPO:0103733', 'increased size of the Meckels cartilage', 0.4392523364485981, 8.608423498638606, 1.9445488255418075, 'UPHENO:0088116', 'abnormal jaw skeleton morphology'),
(472612, 'HP:0012479', 'Temporomandibular joint crepitus', 'XPO:0131611', 'increased size of the roof of mouth', 0.4074074074074074, 7.312692920701687, 1.7260490329042149, 'UPHENO:0076800', 'abnormal mouth morphology'),
(472613, 'HP:0012479', 'Temporomandibular joint crepitus', 'XPO:0102398', 'abnormal Meckels cartilage morphology', 0.49473684210526314, 8.608423498638606, 2.0637112824281414, 'UPHENO:0088116', 'abnormal jaw skeleton morphology'),
(472614, 'HP:0012479', 'Temporomandibular joint crepitus', 'XPO:0130628', 'increased size of the oral cavity', 0.4230769230769231, 7.312692920701687, 1.7589291117884391, 'UPHENO:0076800', 'abnormal mouth morphology'),
(472615, 'HP:0012479', 'Temporomandibular joint crepitus', 'XPO:0115393', 'abnormally decreased volume of oral cavity', 0.4125, 7.312692920701687, 1.7368033365322182, 'UPHENO:0076800', 'abnormal mouth morphology'),
(472616, 'HP:0012479', 'Temporomandibular joint crepitus', 'XPO:0103096', 'abnormal oral cavity morphology', 0.4520547945205479, 7.312692920701687, 1.8181688303509294, 'UPHENO:0076800', 'abnormal mouth morphology'),
(472617, 'HP:0012479', 'Temporomandibular joint crepitus', 'XPO:0128846', 'decreased size of the choana', 0.4146341463414634, 7.024697770424301, 1.7066574241325239, 'HP:0000929', 'Abnormal skull morphology'),
(472618, 'HP:0012479', 'Temporomandibular joint crepitus', 'XPO:0103152', 'abnormal otic region morphology', 0.4189189189189189, 7.024697770424301, 1.7154529418548001, 'HP:0000929', 'Abnormal skull morphology'),
(472619, 'HP:0012479', 'Temporomandibular joint crepitus', 'XPO:0102351', 'abnormal sphenoid region morphology', 0.4189189189189189, 7.024697770424301, 1.7154529418548001, 'HP:0000929', 'Abnormal skull morphology'),
(472620, 'HP:0012479', 'Temporomandibular joint crepitus', 'XPO:0140524', 'abnormally necrotic Meckels cartilage', 0.4519230769230769, 8.608423498638606, 1.9723958109268225, 'UPHENO:0088116', 'abnormal jaw skeleton morphology'),
(472621, 'HP:0012479', 'Temporomandibular joint crepitus', 'XPO:0103199', 'abnormal tongue morphology', 0.4520547945205479, 7.312692920701687, 1.8181688303509294, 'UPHENO:0076800', 'abnormal mouth morphology'),
(472622, 'HP:0012479', 'Temporomandibular joint crepitus', 'XPO:0130358', 'increased size of the lower jaw', 0.5949367088607594, 8.608423498638606, 2.263065872828203, 'UPHENO:0088116', 'abnormal jaw skeleton morphology'),
(472623, 'HP:0012479', 'Temporomandibular joint crepitus', 'XPO:0129152', 'decreased size of the oral cavity', 0.4230769230769231, 7.312692920701687, 1.7589291117884391, 'UPHENO:0076800', 'abnormal mouth morphology'),
(472624, 'HP:0012506', 'Small pituitary gland', 'XPO:0140253', 'abnormally necrotic hypophysis', 0.5465116279069767, 9.837010412277873, 2.318629029006551, 'UPHENO:0087940', 'abnormal pituitary gland morphology'),
(472625, 'HP:0012506', 'Small pituitary gland', 'XPO:0100914', 'abnormal pars intermedia', 0.4025974025974026, 7.431510076152836, 1.7297128819649685, 'UPHENO:0004618', 'abnormal diencephalon'),
(472626, 'HP:0012506', 'Small pituitary gland', 'XPO:0140316', 'abnormally necrotic pars distalis', 0.5340909090909091, 9.837010412277873, 2.29212954124112, 'UPHENO:0087940', 'abnormal pituitary gland morphology'),
(472627, 'HP:0012506', 'Small pituitary gland', 'XPO:0100491', 'abnormal pars distalis', 0.4025974025974026, 7.431510076152836, 1.7297128819649685, 'UPHENO:0004618', 'abnormal diencephalon'),
(472628, 'HP:0012506', 'Small pituitary gland', 'XPO:0100315', 'abnormal neurohypophysis', 0.40789473684210525, 7.431510076152836, 1.741055383051273, 'UPHENO:0004618', 'abnormal diencephalon'),
(472629, 'HP:0012506', 'Small pituitary gland', 'XPO:0102123', 'abnormal pars distalis morphology', 0.5662650602409639, 9.837010412277873, 2.360160014426886, 'UPHENO:0087940', 'abnormal pituitary gland morphology'),
(472630, 'HP:0012506', 'Small pituitary gland', 'XPO:0101526', 'abnormal infundibulum', 0.41333333333333333, 7.431510076152836, 1.7526239846232008, 'UPHENO:0004618', 'abnormal diencephalon'),
(472631, 'HP:0012506', 'Small pituitary gland', 'XPO:0140341', 'abnormally necrotic neurohypophysis', 0.5402298850574713, 9.837010412277873, 2.3052650616217703, 'UPHENO:0087940', 'abnormal pituitary gland morphology'),
(472632, 'HP:0012506', 'Small pituitary gland', 'XPO:0128362', 'decreased size of the pineal gland', 0.40404040404040403, 9.57542522308115, 1.9669414521007949, 'UPHENO:0086771', 'abnormal neuroendocrine gland morphology'),
(472633, 'HP:0012506', 'Small pituitary gland', 'XPO:0100611', 'abnormal hypophysis', 0.41333333333333333, 7.431510076152836, 1.7526239846232008, 'UPHENO:0004618', 'abnormal diencephalon'),
(472634, 'HP:0012506', 'Small pituitary gland', 'XPO:0100951', 'abnormal adenohypophysis', 0.40789473684210525, 7.431510076152836, 1.741055383051273, 'UPHENO:0004618', 'abnormal diencephalon'),
(472635, 'HP:0012506', 'Small pituitary gland', 'XPO:0140782', 'abnormally necrotic melanotrope', 0.5222222222222223, 9.837010412277873, 2.266518351463956, 'UPHENO:0087940', 'abnormal pituitary gland morphology'),
(472636, 'HP:0012506', 'Small pituitary gland', 'XPO:0140394', 'abnormally necrotic pars nervosa', 0.5340909090909091, 9.837010412277873, 2.29212954124112, 'UPHENO:0087940', 'abnormal pituitary gland morphology'),
(472637, 'HP:0012506', 'Small pituitary gland', 'XPO:0129041', 'decreased size of the pars distalis', 0.5747126436781609, 9.837010412277873, 2.3776993628147802, 'UPHENO:0087940', 'abnormal pituitary gland morphology'),
(472638, 'HP:0012506', 'Small pituitary gland', 'XPO:0130435', 'increased size of the neurohypophysis', 0.5454545454545454, 9.837010412277873, 2.3163855557874338, 'UPHENO:0087940', 'abnormal pituitary gland morphology'),
(472639, 'HP:0012506', 'Small pituitary gland', 'XPO:0128489', 'decreased size of the hypophysis', 0.6162790697674418, 15.042124842182485, 3.0446915615651364, 'HP:0012506', 'Small pituitary gland'),
(472640, 'HP:0012506', 'Small pituitary gland', 'XPO:0102578', 'abnormal melanotrope morphology', 0.5465116279069767, 9.837010412277873, 2.318629029006551, 'UPHENO:0087940', 'abnormal pituitary gland morphology'),
(472641, 'HP:0012506', 'Small pituitary gland', 'XPO:0128957', 'decreased size of the neurohypophysis', 0.5813953488372093, 9.837010412277873, 2.3914832427097528, 'UPHENO:0087940', 'abnormal pituitary gland morphology'),
(472642, 'HP:0012506', 'Small pituitary gland', 'XPO:0129970', 'increased size of the infundibulum', 0.5217391304347826, 9.837010412277873, 2.26546976554086, 'UPHENO:0087940', 'abnormal pituitary gland morphology'),
(472643, 'HP:0012506', 'Small pituitary gland', 'XPO:0102243', 'abnormal hypophysis morphology', 0.5802469135802469, 9.837010412277873, 2.389120116398711, 'UPHENO:0087940', 'abnormal pituitary gland morphology'),
(472644, 'HP:0012506', 'Small pituitary gland', 'XPO:0103158', 'abnormal infundibulum morphology', 0.5465116279069767, 9.837010412277873, 2.318629029006551, 'UPHENO:0087940', 'abnormal pituitary gland morphology'),
(472645, 'HP:0012506', 'Small pituitary gland', 'XPO:0140405', 'abnormally necrotic adenohypophysis', 0.5402298850574713, 9.837010412277873, 2.3052650616217703, 'UPHENO:0087940', 'abnormal pituitary gland morphology'),
(472646, 'HP:0012506', 'Small pituitary gland', 'XPO:0101865', 'abnormal pars nervosa morphology', 0.5662650602409639, 9.837010412277873, 2.360160014426886, 'UPHENO:0087940', 'abnormal pituitary gland morphology'),
(472647, 'HP:0012506', 'Small pituitary gland', 'XPO:0130794', 'increased size of the pars intermedia', 0.5517241379310345, 9.837010412277873, 2.329660080254761, 'UPHENO:0087940', 'abnormal pituitary gland morphology'),
(472648, 'HP:0012506', 'Small pituitary gland', 'XPO:0100233', 'abnormal pars nervosa', 0.4025974025974026, 7.431510076152836, 1.7297128819649685, 'UPHENO:0004618', 'abnormal diencephalon'),
(472649, 'HP:0012506', 'Small pituitary gland', 'XPO:0129694', 'increased size of the adenohypophysis', 0.5454545454545454, 9.837010412277873, 2.3163855557874338, 'UPHENO:0087940', 'abnormal pituitary gland morphology'),
(472650, 'HP:0012506', 'Small pituitary gland', 'XPO:0128958', 'decreased size of the pars nervosa', 0.5747126436781609, 9.837010412277873, 2.3776993628147802, 'UPHENO:0087940', 'abnormal pituitary gland morphology'),
(472651, 'HP:0012506', 'Small pituitary gland', 'XPO:0101947', 'abnormal neurohypophysis morphology', 0.573170731707317, 9.837010412277873, 2.374507623870221, 'UPHENO:0087940', 'abnormal pituitary gland morphology'),
(472652, 'HP:0012506', 'Small pituitary gland', 'XPO:0130518', 'increased size of the pars distalis', 0.5393258426966292, 9.837010412277873, 2.303335392472681, 'UPHENO:0087940', 'abnormal pituitary gland morphology'),
(472653, 'HP:0012506', 'Small pituitary gland', 'XPO:0128837', 'decreased size of the melanotrope', 0.5263157894736842, 9.837010412277873, 2.2753843414242967, 'UPHENO:0087940', 'abnormal pituitary gland morphology'),
(472654, 'HP:0012506', 'Small pituitary gland', 'XPO:0128214', 'decreased size of the adenohypophysis', 0.5813953488372093, 9.837010412277873, 2.3914832427097528, 'UPHENO:0087940', 'abnormal pituitary gland morphology'),
(472655, 'HP:0012506', 'Small pituitary gland', 'XPO:0130315', 'increased size of the melanotrope', 0.4948453608247423, 9.837010412277873, 2.2063089010608627, 'UPHENO:0087940', 'abnormal pituitary gland morphology'),
(472656, 'HP:0012506', 'Small pituitary gland', 'XPO:0129969', 'increased size of the hypophysis', 0.5617977528089888, 13.568193653850074, 2.7609021540811898, 'HP:0012504', 'Abnormal size of pituitary gland'),
(472657, 'HP:0012506', 'Small pituitary gland', 'XPO:0102546', 'abnormal pars intermedia morphology', 0.573170731707317, 9.837010412277873, 2.374507623870221, 'UPHENO:0087940', 'abnormal pituitary gland morphology'),
(472658, 'HP:0012506', 'Small pituitary gland', 'XPO:0140252', 'abnormally necrotic infundibulum', 0.5164835164835165, 9.837010412277873, 2.2540305520152657, 'UPHENO:0087940', 'abnormal pituitary gland morphology'),
(472659, 'HP:0012506', 'Small pituitary gland', 'XPO:0126921', 'abnormally localised hypophysis', 0.4166666666666667, 7.431510076152836, 1.7596768259343385, 'UPHENO:0004618', 'abnormal diencephalon'),
(472660, 'HP:0012506', 'Small pituitary gland', 'XPO:0128490', 'decreased size of the infundibulum', 0.5555555555555556, 9.837010412277873, 2.3377351827353796, 'UPHENO:0087940', 'abnormal pituitary gland morphology'),
(472661, 'HP:0012506', 'Small pituitary gland', 'XPO:0102583', 'abnormal adenohypophysis morphology', 0.573170731707317, 9.837010412277873, 2.374507623870221, 'UPHENO:0087940', 'abnormal pituitary gland morphology'),
(472662, 'HP:0012506', 'Small pituitary gland', 'XPO:0129318', 'decreased size of the pars intermedia', 0.5882352941176471, 9.837010412277873, 2.405509657661892, 'UPHENO:0087940', 'abnormal pituitary gland morphology'),
(472663, 'HP:0012506', 'Small pituitary gland', 'XPO:0130436', 'increased size of the pars nervosa', 0.5393258426966292, 9.837010412277873, 2.303335392472681, 'UPHENO:0087940', 'abnormal pituitary gland morphology'),
(472664, 'HP:0012506', 'Small pituitary gland', 'XPO:0141184', 'abnormally necrotic pars intermedia', 0.5465116279069767, 9.837010412277873, 2.318629029006551, 'UPHENO:0087940', 'abnormal pituitary gland morphology'),
(472665, 'HP:0009408', 'Aplasia/Hypoplasia of the phalanges of the 4th finger', 'XPO:0103280', 'absent forelimb digit 3', 0.44537815126050423, 10.200822588201543, 2.1314838741284428, 'HP:0005927', 'Aplasia/hypoplasia involving bones of the hand'),
(472666, 'HP:0009408', 'Aplasia/Hypoplasia of the phalanges of the 4th finger', 'XPO:0140219', 'abnormally necrotic forelimb digit', 0.42727272727272725, 7.492661022682715, 1.7892483644513149, 'HP:0001167', 'Abnormal finger morphology'),
(472667, 'HP:0009408', 'Aplasia/Hypoplasia of the phalanges of the 4th finger', 'XPO:0103824', 'decreased length of forelimb digit 5 in regenerating forelimb', 0.40601503759398494, 10.200822588201543, 2.0351136004258388, 'HP:0005927', 'Aplasia/hypoplasia involving bones of the hand'),
(472668, 'HP:0009408', 'Aplasia/Hypoplasia of the phalanges of the 4th finger', 'XPO:0102214', 'abnormal forelimb digit morphology', 0.46078431372549017, 7.492661022682715, 1.8580905971761936, 'HP:0001167', 'Abnormal finger morphology'),
(472669, 'HP:0009408', 'Aplasia/Hypoplasia of the phalanges of the 4th finger', 'XPO:0103432', 'decreased size of the forelimb digit', 0.415929203539823, 7.492661022682715, 1.7653375120804229, 'HP:0001167', 'Abnormal finger morphology'),
(472670, 'HP:0009408', 'Aplasia/Hypoplasia of the phalanges of the 4th finger', 'XPO:0102598', 'abnormal forelimb digit 3 morphology', 0.4519230769230769, 7.492661022682715, 1.8401376099934432, 'HP:0001167', 'Abnormal finger morphology'),
(472671, 'HP:0009408', 'Aplasia/Hypoplasia of the phalanges of the 4th finger', 'XPO:0103279', 'absent forelimb digit 2', 0.44537815126050423, 10.200822588201543, 2.1314838741284428, 'HP:0005927', 'Aplasia/hypoplasia involving bones of the hand'),
(472672, 'HP:0009408', 'Aplasia/Hypoplasia of the phalanges of the 4th finger', 'XPO:0103634', 'abnormally increased number of forelimb digit', 0.4956521739130435, 7.774297771301195, 1.9629945468576235, 'HP:0005918', 'Abnormal finger phalanx morphology'),
(472673, 'HP:0009408', 'Aplasia/Hypoplasia of the phalanges of the 4th finger', 'XPO:0140716', 'abnormally necrotic forelimb digit 4', 0.415929203539823, 7.492661022682715, 1.7653375120804229, 'HP:0001167', 'Abnormal finger morphology'),
(472674, 'HP:0009408', 'Aplasia/Hypoplasia of the phalanges of the 4th finger', 'XPO:0129652', 'increased size of the forelimb digit 3', 0.40869565217391307, 7.492661022682715, 1.7499194219115835, 'HP:0001167', 'Abnormal finger morphology'),
(472675, 'HP:0009408', 'Aplasia/Hypoplasia of the phalanges of the 4th finger', 'XPO:0129148', 'decreased size of the forelimb digit 4', 0.4051724137931034, 7.492661022682715, 1.7423603393941962, 'HP:0001167', 'Abnormal finger morphology'),
(472676, 'HP:0009408', 'Aplasia/Hypoplasia of the phalanges of the 4th finger', 'XPO:0129188', 'decreased size of the forelimb digit 2', 0.4051724137931034, 7.492661022682715, 1.7423603393941962, 'HP:0001167', 'Abnormal finger morphology'),
(472677, 'HP:0009408', 'Aplasia/Hypoplasia of the phalanges of the 4th finger', 'XPO:0102787', 'abnormal forelimb digit 5 morphology', 0.4519230769230769, 7.492661022682715, 1.8401376099934432, 'HP:0001167', 'Abnormal finger morphology'),
(472678, 'HP:0009408', 'Aplasia/Hypoplasia of the phalanges of the 4th finger', 'XPO:0103821', 'decreased length of forelimb digit 2 in regenerating forelimb', 0.40601503759398494, 10.200822588201543, 2.0351136004258388, 'HP:0005927', 'Aplasia/hypoplasia involving bones of the hand'),
(472679, 'HP:0009408', 'Aplasia/Hypoplasia of the phalanges of the 4th finger', 'XPO:0141143', 'abnormally necrotic forelimb digit 3', 0.415929203539823, 7.492661022682715, 1.7653375120804229, 'HP:0001167', 'Abnormal finger morphology'),
(472680, 'HP:0009408', 'Aplasia/Hypoplasia of the phalanges of the 4th finger', 'XPO:0115788', 'duplicated forelimb digit 4 in regenerating forelimb', 0.4523809523809524, 7.774297771301195, 1.875351761636827, 'HP:0005918', 'Abnormal finger phalanx morphology'),
(472681, 'HP:0009408', 'Aplasia/Hypoplasia of the phalanges of the 4th finger', 'XPO:0103282', 'absent forelimb digit 5', 0.44537815126050423, 10.200822588201543, 2.1314838741284428, 'HP:0005927', 'Aplasia/hypoplasia involving bones of the hand'),
(472682, 'HP:0009408', 'Aplasia/Hypoplasia of the phalanges of the 4th finger', 'XPO:0103281', 'absent forelimb digit 4', 0.44537815126050423, 10.200822588201543, 2.1314838741284428, 'HP:0005927', 'Aplasia/hypoplasia involving bones of the hand'),
(472683, 'HP:0009408', 'Aplasia/Hypoplasia of the phalanges of the 4th finger', 'XPO:0133358', 'fused forelimb digits', 0.42342342342342343, 7.492661022682715, 1.781170452476563, 'HP:0001167', 'Abnormal finger morphology'),
(472684, 'HP:0009408', 'Aplasia/Hypoplasia of the phalanges of the 4th finger', 'XPO:0130664', 'increased size of the forelimb digit 2', 0.40869565217391307, 7.492661022682715, 1.7499194219115835, 'HP:0001167', 'Abnormal finger morphology'),
(472685, 'HP:0009408', 'Aplasia/Hypoplasia of the phalanges of the 4th finger', 'XPO:0141108', 'abnormally necrotic forelimb digit 2', 0.415929203539823, 7.492661022682715, 1.7653375120804229, 'HP:0001167', 'Abnormal finger morphology'),
(472686, 'HP:0009408', 'Aplasia/Hypoplasia of the phalanges of the 4th finger', 'XPO:0128172', 'decreased size of the forelimb digit 3', 0.4051724137931034, 7.492661022682715, 1.7423603393941962, 'HP:0001167', 'Abnormal finger morphology'),
(472687, 'HP:0009408', 'Aplasia/Hypoplasia of the phalanges of the 4th finger', 'XPO:0102746', 'abnormal forelimb digit 2 morphology', 0.4519230769230769, 7.492661022682715, 1.8401376099934432, 'HP:0001167', 'Abnormal finger morphology'),
(472688, 'HP:0009408', 'Aplasia/Hypoplasia of the phalanges of the 4th finger', 'XPO:0129161', 'decreased size of the forelimb digit 5', 0.4051724137931034, 7.492661022682715, 1.7423603393941962, 'HP:0001167', 'Abnormal finger morphology'),
(472689, 'HP:0009408', 'Aplasia/Hypoplasia of the phalanges of the 4th finger', 'XPO:0115786', 'duplicated forelimb digit 2 in regenerating forelimb', 0.4523809523809524, 7.774297771301195, 1.875351761636827, 'HP:0005918', 'Abnormal finger phalanx morphology'),
(472690, 'HP:0009408', 'Aplasia/Hypoplasia of the phalanges of the 4th finger', 'XPO:0115787', 'duplicated forelimb digit 3 in regenerating forelimb', 0.4523809523809524, 7.774297771301195, 1.875351761636827, 'HP:0005918', 'Abnormal finger phalanx morphology'),
(472691, 'HP:0009408', 'Aplasia/Hypoplasia of the phalanges of the 4th finger', 'XPO:0103823', 'decreased length of forelimb digit 4 in regenerating forelimb', 0.40601503759398494, 10.200822588201543, 2.0351136004258388, 'HP:0005927', 'Aplasia/hypoplasia involving bones of the hand'),
(472692, 'HP:0009408', 'Aplasia/Hypoplasia of the phalanges of the 4th finger', 'XPO:0125257', 'absent forelimb digit', 0.45689655172413796, 10.200822588201543, 2.1588702289158053, 'HP:0005927', 'Aplasia/hypoplasia involving bones of the hand'),
(472693, 'HP:0009408', 'Aplasia/Hypoplasia of the phalanges of the 4th finger', 'XPO:0103609', 'abnormally increased number of forelimb digit in the regenerating forelimb', 0.47107438016528924, 7.774297771301195, 1.9137064831985338, 'HP:0005918', 'Abnormal finger phalanx morphology'),
(472694, 'HP:0009408', 'Aplasia/Hypoplasia of the phalanges of the 4th finger', 'XPO:0103755', 'increased size of the forelimb digit', 0.41964285714285715, 7.492661022682715, 1.7732009697610411, 'HP:0001167', 'Abnormal finger morphology'),
(472695, 'HP:0009408', 'Aplasia/Hypoplasia of the phalanges of the 4th finger', 'XPO:0140898', 'abnormally necrotic forelimb digit 5', 0.415929203539823, 7.492661022682715, 1.7653375120804229, 'HP:0001167', 'Abnormal finger morphology'),
(472696, 'HP:0009408', 'Aplasia/Hypoplasia of the phalanges of the 4th finger', 'XPO:0130637', 'increased size of the forelimb digit 5', 0.40869565217391307, 7.492661022682715, 1.7499194219115835, 'HP:0001167', 'Abnormal finger morphology'),
(472697, 'HP:0009408', 'Aplasia/Hypoplasia of the phalanges of the 4th finger', 'XPO:0141556', 'abnormal forelimb digit morphology in the regenerating forelimb', 0.4351851851851852, 7.492661022682715, 1.8057394813997938, 'HP:0001167', 'Abnormal finger morphology'),
(472698, 'HP:0009408', 'Aplasia/Hypoplasia of the phalanges of the 4th finger', 'XPO:0130624', 'increased size of the forelimb digit 4', 0.40869565217391307, 7.492661022682715, 1.7499194219115835, 'HP:0001167', 'Abnormal finger morphology'),
(472699, 'HP:0009408', 'Aplasia/Hypoplasia of the phalanges of the 4th finger', 'XPO:0103822', 'decreased length of forelimb digit 3 in regenerating forelimb', 0.40601503759398494, 10.200822588201543, 2.0351136004258388, 'HP:0005927', 'Aplasia/hypoplasia involving bones of the hand'),
(472700, 'HP:0009408', 'Aplasia/Hypoplasia of the phalanges of the 4th finger', 'XPO:0115789', 'duplicated forelimb digit 5 in regenerating forelimb', 0.4523809523809524, 7.774297771301195, 1.875351761636827, 'HP:0005918', 'Abnormal finger phalanx morphology'),
(472701, 'HP:0009408', 'Aplasia/Hypoplasia of the phalanges of the 4th finger', 'XPO:0102529', 'abnormal forelimb digit 4 morphology', 0.4519230769230769, 7.492661022682715, 1.8401376099934432, 'HP:0001167', 'Abnormal finger morphology'),
(472702, 'HP:0009506', 'Fragmentation of the epiphysis of the distal phalanx of the 2nd finger', 'XPO:0102214', 'abnormal forelimb digit morphology', 0.4017094017094017, 7.492661022682715, 1.734898376457027, 'HP:0001167', 'Abnormal finger morphology'),
(472703, 'HP:0009506', 'Fragmentation of the epiphysis of the distal phalanx of the 2nd finger', 'XPO:0115789', 'duplicated forelimb digit 5 in regenerating forelimb', 0.40425531914893614, 7.774297771301195, 1.7727947503014068, 'HP:0005918', 'Abnormal finger phalanx morphology'),
(472704, 'HP:0009506', 'Fragmentation of the epiphysis of the distal phalanx of the 2nd finger', 'XPO:0115787', 'duplicated forelimb digit 3 in regenerating forelimb', 0.40425531914893614, 7.774297771301195, 1.7727947503014068, 'HP:0005918', 'Abnormal finger phalanx morphology'),
(472705, 'HP:0009506', 'Fragmentation of the epiphysis of the distal phalanx of the 2nd finger', 'XPO:0103609', 'abnormally increased number of forelimb digit in the regenerating forelimb', 0.41911764705882354, 7.774297771301195, 1.805088748356272, 'HP:0005918', 'Abnormal finger phalanx morphology'),
(472706, 'HP:0009506', 'Fragmentation of the epiphysis of the distal phalanx of the 2nd finger', 'XPO:0103634', 'abnormally increased number of forelimb digit', 0.43846153846153846, 7.774297771301195, 1.8462747794580392, 'HP:0005918', 'Abnormal finger phalanx morphology'),
(472707, 'HP:0009506', 'Fragmentation of the epiphysis of the distal phalanx of the 2nd finger', 'XPO:0115788', 'duplicated forelimb digit 4 in regenerating forelimb', 0.40425531914893614, 7.774297771301195, 1.7727947503014068, 'HP:0005918', 'Abnormal finger phalanx morphology'),
(472708, 'HP:0009506', 'Fragmentation of the epiphysis of the distal phalanx of the 2nd finger', 'XPO:0115786', 'duplicated forelimb digit 2 in regenerating forelimb', 0.40425531914893614, 7.774297771301195, 1.7727947503014068, 'HP:0005918', 'Abnormal finger phalanx morphology'),
(472709, 'HP:0004302', 'Functional motor deficit', 'XPO:0100417', 'abnormal dense regular connective tissue', 0.41379310344827586, 3.9037819259951223, 1.270967363209146, 'HP:0033127', 'Abnormality of the musculoskeletal system'),
(472710, 'HP:0004302', 'Functional motor deficit', 'XPO:0100549', 'abnormal mitotic cell', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(472711, 'HP:0004302', 'Functional motor deficit', 'XPO:0101435', 'abnormal paracrine cell', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(472712, 'HP:0004302', 'Functional motor deficit', 'XPO:0101466', 'abnormal secondary myofiber', 0.4117647058823529, 5.968280811662945, 1.5676502776568768, 'UPHENO:0002816', 'abnormal musculature'),
(472713, 'HP:0004302', 'Functional motor deficit', 'XPO:0101132', 'abnormal apoptotic cell', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(472714, 'HP:0004302', 'Functional motor deficit', 'XPO:0100108', 'abnormal cell part', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(472715, 'HP:0004302', 'Functional motor deficit', 'XPO:0100691', 'abnormal keratin accumulating cell', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(472716, 'HP:0004302', 'Functional motor deficit', 'XPO:0100172', 'abnormal stem cell', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(472717, 'HP:0004302', 'Functional motor deficit', 'XPO:0101241', 'abnormal nucleate erythrocyte', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(472718, 'HP:0004302', 'Functional motor deficit', 'XPO:0100791', 'abnormal multiciliated cell precursor', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(472719, 'HP:0004302', 'Functional motor deficit', 'XPO:0100585', 'abnormal elastica externa', 0.42857142857142855, 3.9037819259951223, 1.293464107292913, 'HP:0033127', 'Abnormality of the musculoskeletal system'),
(472720, 'HP:0004302', 'Functional motor deficit', 'XPO:0100337', 'abnormal zygote', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(472721, 'HP:0004302', 'Functional motor deficit', 'XPO:0100688', 'abnormal adipose tissue', 0.41379310344827586, 3.9037819259951223, 1.270967363209146, 'HP:0033127', 'Abnormality of the musculoskeletal system'),
(472722, 'HP:0004302', 'Functional motor deficit', 'XPO:0100465', 'abnormal skeletal system', 0.41379310344827586, 3.9037819259951223, 1.270967363209146, 'HP:0033127', 'Abnormality of the musculoskeletal system'),
(472723, 'HP:0004302', 'Functional motor deficit', 'XPO:0100377', 'abnormal connective tissue', 0.42857142857142855, 3.9037819259951223, 1.293464107292913, 'HP:0033127', 'Abnormality of the musculoskeletal system'),
(472724, 'HP:0004302', 'Functional motor deficit', 'XPO:0100704', 'abnormal Merkel cell', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(472725, 'HP:0004302', 'Functional motor deficit', 'XPO:0100481', 'abnormal anatomical line', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(472726, 'HP:0004302', 'Functional motor deficit', 'XPO:0100596', 'abnormal myocyte', 0.4117647058823529, 5.968280811662945, 1.5676502776568768, 'UPHENO:0002816', 'abnormal musculature'),
(472727, 'HP:0004302', 'Functional motor deficit', 'XPO:0101448', 'abnormal myelin accumulating cell', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(472728, 'HP:0004302', 'Functional motor deficit', 'XPO:0100081', 'abnormal anatomical entity in vitro', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(472729, 'HP:0004302', 'Functional motor deficit', 'XPO:0100004', 'abnormal cell', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(472730, 'HP:0004302', 'Functional motor deficit', 'XPO:0101326', 'abnormal cementoblast', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(472731, 'HP:0004302', 'Functional motor deficit', 'XPO:0101004', 'abnormal acid secreting cell', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(472732, 'HP:0004302', 'Functional motor deficit', 'XPO:0100746', 'abnormal smooth muscle', 0.45161290322580644, 5.968280811662945, 1.6417529121710048, 'UPHENO:0002816', 'abnormal musculature'),
(472733, 'HP:0004302', 'Functional motor deficit', 'XPO:0100344', 'abnormal portion of organism substance', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(472734, 'HP:0004302', 'Functional motor deficit', 'XPO:0100653', 'abnormal myoblast', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(472735, 'HP:0004302', 'Functional motor deficit', 'XPO:0101237', 'abnormal mucus secreting cell', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(472736, 'HP:0004302', 'Functional motor deficit', 'XPO:0101535', 'abnormal absorptive cell', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(472737, 'HP:0004302', 'Functional motor deficit', 'XPO:0100477', 'abnormal pericyte', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(472738, 'HP:0004302', 'Functional motor deficit', 'XPO:0101333', 'abnormal barrier epithelial cell', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(472739, 'HP:0004302', 'Functional motor deficit', 'XPO:0100533', 'abnormal melanoblast', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(472740, 'HP:0004302', 'Functional motor deficit', 'XPO:0100100', 'abnormal muscle', 0.4666666666666667, 5.968280811662945, 1.6688911624516964, 'UPHENO:0002816', 'abnormal musculature'),
(472741, 'HP:0004302', 'Functional motor deficit', 'XPO:0100852', 'abnormal interdigital region', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(472742, 'HP:0004302', 'Functional motor deficit', 'XPO:0101467', 'abnormal alkali secreting cell', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(472743, 'HP:0004302', 'Functional motor deficit', 'XPO:0100638', 'abnormal polar body', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(472744, 'HP:0004302', 'Functional motor deficit', 'XPO:0100006', 'abnormal anatomical structure', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(472745, 'HP:0004302', 'Functional motor deficit', 'XPO:0100275', 'abnormal skeletal muscle', 0.45161290322580644, 5.968280811662945, 1.6417529121710048, 'UPHENO:0002816', 'abnormal musculature'),
(472746, 'HP:0004302', 'Functional motor deficit', 'XPO:0100422', 'abnormal notochord', 0.41379310344827586, 3.9037819259951223, 1.270967363209146, 'HP:0033127', 'Abnormality of the musculoskeletal system'),
(472747, 'HP:0004302', 'Functional motor deficit', 'XPO:0100285', 'abnormal progenitor cell', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(472748, 'HP:0004302', 'Functional motor deficit', 'XPO:0100715', 'abnormal ciliated cell', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(472749, 'HP:0004302', 'Functional motor deficit', 'XPO:0101373', 'abnormal oxygen accumulating cell', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(472750, 'HP:0004302', 'Functional motor deficit', 'XPO:0100802', 'abnormal exocrine cell', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(472751, 'HP:0004302', 'Functional motor deficit', 'XPO:0100026', 'abnormal germ cell', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(472752, 'HP:0004302', 'Functional motor deficit', 'XPO:0100289', 'abnormal chondroblast', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(472753, 'HP:0004302', 'Functional motor deficit', 'XPO:0100754', 'abnormal electrically active cell', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(472754, 'HP:0004302', 'Functional motor deficit', 'XPO:0101297', 'abnormal barrier cell', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(472755, 'HP:0012333', 'Abnormal sudomotor regulation', 'XPO:0100273', 'abnormal visual system', 0.41935483870967744, 3.94131651835137, 1.2856166430382838, 'UPHENO:0004523', 'abnormal nervous system'),
(472756, 'HP:0012333', 'Abnormal sudomotor regulation', 'XPO:0100834', 'abnormal ventral lateral line', 0.4166666666666667, 6.642668884102504, 1.6636642394754348, 'HP:0410008', 'Abnormality of the peripheral nervous system'),
(472757, 'HP:0012333', 'Abnormal sudomotor regulation', 'XPO:0126426', 'abnormally localised peripheral nervous system', 0.41025641025641024, 6.642668884102504, 1.650817219111143, 'HP:0410008', 'Abnormality of the peripheral nervous system'),
(472758, 'HP:0012333', 'Abnormal sudomotor regulation', 'XPO:0100587', 'abnormal vestibuloauditory system', 0.41935483870967744, 3.94131651835137, 1.2856166430382838, 'UPHENO:0004523', 'abnormal nervous system'),
(472759, 'HP:0012333', 'Abnormal sudomotor regulation', 'XPO:0101270', 'abnormal caudal lateral line', 0.4166666666666667, 6.642668884102504, 1.6636642394754348, 'HP:0410008', 'Abnormality of the peripheral nervous system'),
(472760, 'HP:0012333', 'Abnormal sudomotor regulation', 'XPO:0107257', 'abnormal peripheral ganglion', 0.4411764705882353, 6.642668884102504, 1.7118963793333504, 'HP:0410008', 'Abnormality of the peripheral nervous system'),
(472761, 'HP:0012333', 'Abnormal sudomotor regulation', 'XPO:0100114', 'abnormal peripheral nervous system', 0.5, 6.642668884102504, 1.8224528641507445, 'HP:0410008', 'Abnormality of the peripheral nervous system'),
(472762, 'HP:0012333', 'Abnormal sudomotor regulation', 'XPO:0100328', 'abnormal supraorbital lateral line', 0.4166666666666667, 6.642668884102504, 1.6636642394754348, 'HP:0410008', 'Abnormality of the peripheral nervous system'),
(472763, 'HP:0012333', 'Abnormal sudomotor regulation', 'XPO:0100164', 'abnormal neural nucleus', 0.40625, 3.94131651835137, 1.2653694462805098, 'UPHENO:0004523', 'abnormal nervous system'),
(472764, 'HP:0012333', 'Abnormal sudomotor regulation', 'XPO:0101115', 'abnormal trunk lateral line', 0.4166666666666667, 6.642668884102504, 1.6636642394754348, 'HP:0410008', 'Abnormality of the peripheral nervous system'),
(472765, 'HP:0012333', 'Abnormal sudomotor regulation', 'XPO:0101231', 'abnormal taste bud', 0.4166666666666667, 6.642668884102504, 1.6636642394754348, 'HP:0410008', 'Abnormality of the peripheral nervous system'),
(472766, 'HP:0012333', 'Abnormal sudomotor regulation', 'XPO:0100445', 'abnormal spinal ganglion', 0.4411764705882353, 6.642668884102504, 1.7118963793333504, 'HP:0410008', 'Abnormality of the peripheral nervous system'),
(472767, 'HP:0012333', 'Abnormal sudomotor regulation', 'XPO:0101363', 'abnormal infraorbital lateral line', 0.4166666666666667, 6.642668884102504, 1.6636642394754348, 'HP:0410008', 'Abnormality of the peripheral nervous system'),
(472768, 'HP:0012333', 'Abnormal sudomotor regulation', 'XPO:0142051', 'abnormal cerebrospinal fluid', 0.40625, 3.94131651835137, 1.2653694462805098, 'UPHENO:0004523', 'abnormal nervous system'),
(472769, 'HP:0012333', 'Abnormal sudomotor regulation', 'XPO:0101038', 'abnormal hyomandibular lateral line', 0.4166666666666667, 6.642668884102504, 1.6636642394754348, 'HP:0410008', 'Abnormality of the peripheral nervous system'),
(472770, 'HP:0012333', 'Abnormal sudomotor regulation', 'XPO:0100427', 'abnormal olfactory system', 0.41935483870967744, 3.94131651835137, 1.2856166430382838, 'UPHENO:0004523', 'abnormal nervous system'),
(472771, 'HP:0012333', 'Abnormal sudomotor regulation', 'XPO:0100032', 'abnormal nervous system', 0.4482758620689655, 3.94131651835137, 1.3292091859262085, 'UPHENO:0004523', 'abnormal nervous system'),
(472772, 'HP:0012333', 'Abnormal sudomotor regulation', 'XPO:0100319', 'abnormal middle lateral line', 0.4166666666666667, 6.642668884102504, 1.6636642394754348, 'HP:0410008', 'Abnormality of the peripheral nervous system'),
(472773, 'HP:0012333', 'Abnormal sudomotor regulation', 'XPO:0100694', 'abnormal lateral line primordium', 0.4166666666666667, 6.642668884102504, 1.6636642394754348, 'HP:0410008', 'Abnormality of the peripheral nervous system'),
(472774, 'HP:0012333', 'Abnormal sudomotor regulation', 'XPO:0100358', 'abnormal ganglion', 0.45454545454545453, 6.642668884102504, 1.7376406266312143, 'HP:0410008', 'Abnormality of the peripheral nervous system'),
(472775, 'HP:0012333', 'Abnormal sudomotor regulation', 'XPO:0101566', 'abnormal posterior lateral line', 0.4166666666666667, 6.642668884102504, 1.6636642394754348, 'HP:0410008', 'Abnormality of the peripheral nervous system'),
(472776, 'HP:0012333', 'Abnormal sudomotor regulation', 'XPO:0100891', 'abnormal dorsal lateral line', 0.4166666666666667, 6.642668884102504, 1.6636642394754348, 'HP:0410008', 'Abnormality of the peripheral nervous system'),
(472777, 'HP:0012333', 'Abnormal sudomotor regulation', 'XPO:0107253', 'abnormal enteric nervous system', 0.43333333333333335, 3.94131651835137, 1.3068679445984308, 'UPHENO:0004523', 'abnormal nervous system'),
(472778, 'HP:0012333', 'Abnormal sudomotor regulation', 'XPO:0100734', 'abnormal lateral line system', 0.46875, 6.642668884102504, 1.7645823980259603, 'HP:0410008', 'Abnormality of the peripheral nervous system'),
(472779, 'HP:0012333', 'Abnormal sudomotor regulation', 'XPO:0100851', 'abnormal infraorbital lateral line primordium', 0.40540540540540543, 6.642668884102504, 1.6410282971153933, 'HP:0410008', 'Abnormality of the peripheral nervous system'),
(472780, 'HP:0012333', 'Abnormal sudomotor regulation', 'XPO:0100274', 'abnormal sensory system', 0.43333333333333335, 3.94131651835137, 1.3068679445984308, 'UPHENO:0004523', 'abnormal nervous system'),
(472781, 'HP:0012333', 'Abnormal sudomotor regulation', 'XPO:0100773', 'abnormal profundus ganglion', 0.4411764705882353, 6.642668884102504, 1.7118963793333504, 'HP:0410008', 'Abnormality of the peripheral nervous system'),
(472782, 'HP:0012333', 'Abnormal sudomotor regulation', 'XPO:0100642', 'abnormal gustatory system', 0.41935483870967744, 3.94131651835137, 1.2856166430382838, 'UPHENO:0004523', 'abnormal nervous system'),
(472783, 'HP:0012333', 'Abnormal sudomotor regulation', 'XPO:0100320', 'abnormal lateral line', 0.42857142857142855, 6.642668884102504, 1.6872634925188144, 'HP:0410008', 'Abnormality of the peripheral nervous system'),
(472784, 'HP:0012333', 'Abnormal sudomotor regulation', 'XPO:0100031', 'abnormal central nervous system', 0.43333333333333335, 3.94131651835137, 1.3068679445984308, 'UPHENO:0004523', 'abnormal nervous system'),
(472785, 'HP:0012333', 'Abnormal sudomotor regulation', 'XPO:0100874', 'abnormal occipital lateral line', 0.4166666666666667, 6.642668884102504, 1.6636642394754348, 'HP:0410008', 'Abnormality of the peripheral nervous system'),
(472786, 'HP:0031518', 'Absent posterior alpha rhythm', 'XPO:0100031', 'abnormal central nervous system', 0.43333333333333335, 3.94131651835137, 1.3068679445984308, 'UPHENO:0004523', 'abnormal nervous system'),
(472787, 'HP:0031518', 'Absent posterior alpha rhythm', 'XPO:0142051', 'abnormal cerebrospinal fluid', 0.40625, 3.94131651835137, 1.2653694462805098, 'UPHENO:0004523', 'abnormal nervous system'),
(472788, 'HP:0031518', 'Absent posterior alpha rhythm', 'XPO:0100273', 'abnormal visual system', 0.41935483870967744, 3.94131651835137, 1.2856166430382838, 'UPHENO:0004523', 'abnormal nervous system'),
(472789, 'HP:0031518', 'Absent posterior alpha rhythm', 'XPO:0100642', 'abnormal gustatory system', 0.41935483870967744, 3.94131651835137, 1.2856166430382838, 'UPHENO:0004523', 'abnormal nervous system'),
(472790, 'HP:0031518', 'Absent posterior alpha rhythm', 'XPO:0100164', 'abnormal neural nucleus', 0.40625, 3.94131651835137, 1.2653694462805098, 'UPHENO:0004523', 'abnormal nervous system'),
(472791, 'HP:0031518', 'Absent posterior alpha rhythm', 'XPO:0100587', 'abnormal vestibuloauditory system', 0.41935483870967744, 3.94131651835137, 1.2856166430382838, 'UPHENO:0004523', 'abnormal nervous system'),
(472792, 'HP:0031518', 'Absent posterior alpha rhythm', 'XPO:0107253', 'abnormal enteric nervous system', 0.43333333333333335, 3.94131651835137, 1.3068679445984308, 'UPHENO:0004523', 'abnormal nervous system'),
(472793, 'HP:0031518', 'Absent posterior alpha rhythm', 'XPO:0100114', 'abnormal peripheral nervous system', 0.40625, 3.94131651835137, 1.2653694462805098, 'UPHENO:0004523', 'abnormal nervous system'),
(472794, 'HP:0031518', 'Absent posterior alpha rhythm', 'XPO:0100274', 'abnormal sensory system', 0.43333333333333335, 3.94131651835137, 1.3068679445984308, 'UPHENO:0004523', 'abnormal nervous system'),
(472795, 'HP:0031518', 'Absent posterior alpha rhythm', 'XPO:0100427', 'abnormal olfactory system', 0.41935483870967744, 3.94131651835137, 1.2856166430382838, 'UPHENO:0004523', 'abnormal nervous system'),
(472796, 'HP:0031518', 'Absent posterior alpha rhythm', 'XPO:0100032', 'abnormal nervous system', 0.4482758620689655, 3.94131651835137, 1.3292091859262085, 'UPHENO:0004523', 'abnormal nervous system'),
(472797, 'HP:0001325', 'Hypoglycemic coma', 'XPO:0100196', 'abnormal neuron', 0.40625, 3.94131651835137, 1.2653694462805098, 'UPHENO:0004523', 'abnormal nervous system'),
(472798, 'HP:0001325', 'Hypoglycemic coma', 'XPO:0100274', 'abnormal sensory system', 0.4482758620689655, 3.94131651835137, 1.3292091859262085, 'UPHENO:0004523', 'abnormal nervous system'),
(472799, 'HP:0001325', 'Hypoglycemic coma', 'XPO:0107253', 'abnormal enteric nervous system', 0.4482758620689655, 3.94131651835137, 1.3292091859262085, 'UPHENO:0004523', 'abnormal nervous system'),
(472800, 'HP:0001325', 'Hypoglycemic coma', 'XPO:0100702', 'abnormal glial cell', 0.40625, 3.94131651835137, 1.2653694462805098, 'UPHENO:0004523', 'abnormal nervous system'),
(472801, 'HP:0001325', 'Hypoglycemic coma', 'XPO:0100114', 'abnormal peripheral nervous system', 0.41935483870967744, 3.94131651835137, 1.2856166430382838, 'UPHENO:0004523', 'abnormal nervous system'),
(472802, 'HP:0001325', 'Hypoglycemic coma', 'XPO:0100031', 'abnormal central nervous system', 0.4482758620689655, 3.94131651835137, 1.3292091859262085, 'UPHENO:0004523', 'abnormal nervous system'),
(472803, 'HP:0001325', 'Hypoglycemic coma', 'XPO:0100164', 'abnormal neural nucleus', 0.41935483870967744, 3.94131651835137, 1.2856166430382838, 'UPHENO:0004523', 'abnormal nervous system'),
(472804, 'HP:0001325', 'Hypoglycemic coma', 'XPO:0100032', 'abnormal nervous system', 0.4642857142857143, 3.94131651835137, 1.3527368387638634, 'UPHENO:0004523', 'abnormal nervous system'),
(472805, 'HP:0001325', 'Hypoglycemic coma', 'XPO:0100175', 'abnormal migrating neuroblast', 0.40625, 3.94131651835137, 1.2653694462805098, 'UPHENO:0004523', 'abnormal nervous system'),
(472806, 'HP:0001325', 'Hypoglycemic coma', 'XPO:0100858', 'abnormal presumptive midbrain-hindbrain boundary', 0.40625, 3.94131651835137, 1.2653694462805098, 'UPHENO:0004523', 'abnormal nervous system'),
(472807, 'HP:0001325', 'Hypoglycemic coma', 'XPO:0142051', 'abnormal cerebrospinal fluid', 0.41935483870967744, 3.94131651835137, 1.2856166430382838, 'UPHENO:0004523', 'abnormal nervous system'),
(472808, 'HP:0001325', 'Hypoglycemic coma', 'XPO:0100158', 'abnormal neuromere', 0.40625, 3.94131651835137, 1.2653694462805098, 'UPHENO:0004523', 'abnormal nervous system'),
(472809, 'HP:0001325', 'Hypoglycemic coma', 'XPO:0100587', 'abnormal vestibuloauditory system', 0.43333333333333335, 3.94131651835137, 1.3068679445984308, 'UPHENO:0004523', 'abnormal nervous system'),
(472810, 'HP:0001325', 'Hypoglycemic coma', 'XPO:0100916', 'abnormal principal cavity', 0.40625, 3.94131651835137, 1.2653694462805098, 'UPHENO:0004523', 'abnormal nervous system'),
(472811, 'HP:0001325', 'Hypoglycemic coma', 'XPO:0100273', 'abnormal visual system', 0.43333333333333335, 3.94131651835137, 1.3068679445984308, 'UPHENO:0004523', 'abnormal nervous system'),
(472812, 'HP:0001325', 'Hypoglycemic coma', 'XPO:0100537', 'abnormal medium cavity', 0.40625, 3.94131651835137, 1.2653694462805098, 'UPHENO:0004523', 'abnormal nervous system'),
(472813, 'HP:0001325', 'Hypoglycemic coma', 'XPO:0101501', 'abnormal parabrachial area', 0.40625, 3.94131651835137, 1.2653694462805098, 'UPHENO:0004523', 'abnormal nervous system'),
(472814, 'HP:0001325', 'Hypoglycemic coma', 'XPO:0100642', 'abnormal gustatory system', 0.43333333333333335, 3.94131651835137, 1.3068679445984308, 'UPHENO:0004523', 'abnormal nervous system'),
(472815, 'HP:0001325', 'Hypoglycemic coma', 'XPO:0100427', 'abnormal olfactory system', 0.43333333333333335, 3.94131651835137, 1.3068679445984308, 'UPHENO:0004523', 'abnormal nervous system'),
(472816, 'HP:0007354', 'Amyotrophic lateral sclerosis', 'XPO:0128096', 'decreased size of the glial cell', 0.5614035087719298, 9.529055259943116, 2.312929972613455, 'UPHENO:0080059', 'decreased size of the cell'),
(472817, 'HP:0007354', 'Amyotrophic lateral sclerosis', 'XPO:0128525', 'decreased size of the neural stem cell', 0.4358974358974359, 9.529055259943116, 2.0380605374556904, 'UPHENO:0080059', 'decreased size of the cell'),
(472818, 'HP:0007354', 'Amyotrophic lateral sclerosis', 'XPO:0128836', 'decreased size of the acid secreting cell', 0.5185185185185185, 9.529055259943116, 2.22283414052124, 'UPHENO:0080059', 'decreased size of the cell'),
(472819, 'HP:0007354', 'Amyotrophic lateral sclerosis', 'XPO:0128211', 'decreased size of the progenitor cell', 0.5185185185185185, 9.529055259943116, 2.22283414052124, 'UPHENO:0080059', 'decreased size of the cell'),
(472820, 'HP:0007354', 'Amyotrophic lateral sclerosis', 'XPO:0128548', 'decreased size of the dorsal vegetal hemisphere blastomere', 0.4117647058823529, 9.529055259943116, 1.9808403864135962, 'UPHENO:0080059', 'decreased size of the cell'),
(472821, 'HP:0007354', 'Amyotrophic lateral sclerosis', 'XPO:0128267', 'decreased size of the zygote', 0.5185185185185185, 9.529055259943116, 2.22283414052124, 'UPHENO:0080059', 'decreased size of the cell'),
(472822, 'HP:0007354', 'Amyotrophic lateral sclerosis', 'XPO:0129862', 'increased size of the myoblast', 0.41379310344827586, 8.042124842182485, 1.8242192293595543, 'UPHENO:0077801', 'abnormal size of cell'),
(472823, 'HP:0007354', 'Amyotrophic lateral sclerosis', 'XPO:0102765', 'abnormal motor neuron morphology', 0.4107142857142857, 5.43643956286526, 1.4942634947997255, 'HP:0025461', 'Abnormal cell morphology'),
(472824, 'HP:0007354', 'Amyotrophic lateral sclerosis', 'XPO:0131576', 'decreased size of the neuron projection', 0.4067796610169492, 5.653868323764771, 1.5165350771332327, 'UPHENO:0012541', 'decreased size of the anatomical entity in the independent continuant'),
(472825, 'HP:0007354', 'Amyotrophic lateral sclerosis', 'XPO:0128903', 'decreased size of the multiciliated cell', 0.49122807017543857, 9.529055259943116, 2.1635478792799963, 'UPHENO:0080059', 'decreased size of the cell'),
(472826, 'HP:0007354', 'Amyotrophic lateral sclerosis', 'XPO:0129380', 'decreased size of the natural killer cell', 0.42424242424242425, 9.529055259943116, 2.01062913144575, 'UPHENO:0080059', 'decreased size of the cell'),
(472827, 'HP:0007354', 'Amyotrophic lateral sclerosis', 'XPO:0129545', 'increased size of the neuron', 0.45901639344262296, 8.042124842182485, 1.921319114742246, 'UPHENO:0077801', 'abnormal size of cell'),
(472828, 'HP:0007354', 'Amyotrophic lateral sclerosis', 'XPO:0101968', 'abnormal interneuron morphology', 0.40350877192982454, 5.43643956286526, 1.4810979210310415, 'HP:0025461', 'Abnormal cell morphology'),
(472829, 'HP:0007354', 'Amyotrophic lateral sclerosis', 'XPO:0129015', 'decreased size of the spermatid', 0.49122807017543857, 9.529055259943116, 2.1635478792799963, 'UPHENO:0080059', 'decreased size of the cell'),
(472830, 'HP:0007354', 'Amyotrophic lateral sclerosis', 'XPO:0128375', 'decreased size of the stage I oocyte', 0.4666666666666667, 9.529055259943116, 2.1087656234489693, 'UPHENO:0080059', 'decreased size of the cell'),
(472831, 'HP:0007354', 'Amyotrophic lateral sclerosis', 'XPO:0128775', 'decreased size of the stage II oocyte', 0.4666666666666667, 9.529055259943116, 2.1087656234489693, 'UPHENO:0080059', 'decreased size of the cell'),
(472832, 'HP:0007354', 'Amyotrophic lateral sclerosis', 'XPO:0128916', 'decreased size of the left blastomere', 0.45161290322580644, 9.529055259943116, 2.0744744662063335, 'UPHENO:0080059', 'decreased size of the cell'),
(472833, 'HP:0007354', 'Amyotrophic lateral sclerosis', 'XPO:0129352', 'decreased size of the olfactory epithelial support cell', 0.5333333333333333, 9.529055259943116, 2.254365277700798, 'UPHENO:0080059', 'decreased size of the cell'),
(472834, 'HP:0007354', 'Amyotrophic lateral sclerosis', 'XPO:0103433', 'decreased size of the germ cell', 0.5185185185185185, 9.529055259943116, 2.22283414052124, 'UPHENO:0080059', 'decreased size of the cell'),
(472835, 'HP:0007354', 'Amyotrophic lateral sclerosis', 'XPO:0129620', 'increased size of the electrically active cell', 0.41379310344827586, 8.042124842182485, 1.8242192293595543, 'UPHENO:0077801', 'abnormal size of cell'),
(472836, 'HP:0007354', 'Amyotrophic lateral sclerosis', 'XPO:0128382', 'decreased size of the myoblast', 0.5185185185185185, 9.529055259943116, 2.22283414052124, 'UPHENO:0080059', 'decreased size of the cell'),
(472837, 'HP:0007354', 'Amyotrophic lateral sclerosis', 'XPO:0128588', 'decreased size of the intersomitic neuron', 0.5079365079365079, 9.529055259943116, 2.2000352389608486, 'UPHENO:0080059', 'decreased size of the cell'),
(472838, 'HP:0007354', 'Amyotrophic lateral sclerosis', 'XPO:0128924', 'decreased size of the oligodendrocyte', 0.41975308641975306, 9.529055259943116, 1.999962588656474, 'UPHENO:0080059', 'decreased size of the cell'),
(472839, 'HP:0007354', 'Amyotrophic lateral sclerosis', 'XPO:0128908', 'decreased size of the endodermal cell', 0.4375, 9.529055259943116, 2.04180353516814, 'UPHENO:0080059', 'decreased size of the cell'),
(472840, 'HP:0007354', 'Amyotrophic lateral sclerosis', 'XPO:0129623', 'increased size of the stem cell', 0.41379310344827586, 8.042124842182485, 1.8242192293595543, 'UPHENO:0077801', 'abnormal size of cell'),
(472841, 'HP:0007354', 'Amyotrophic lateral sclerosis', 'XPO:0128988', 'decreased size of the migrating myoblast', 0.49122807017543857, 9.529055259943116, 2.1635478792799963, 'UPHENO:0080059', 'decreased size of the cell'),
(472842, 'HP:0007354', 'Amyotrophic lateral sclerosis', 'XPO:0130258', 'increased size of the keratin accumulating cell', 0.41379310344827586, 8.042124842182485, 1.8242192293595543, 'UPHENO:0077801', 'abnormal size of cell'),
(472843, 'HP:0007354', 'Amyotrophic lateral sclerosis', 'XPO:0128154', 'decreased size of the somatic stem cell', 0.49122807017543857, 9.529055259943116, 2.1635478792799963, 'UPHENO:0080059', 'decreased size of the cell'),
(472844, 'HP:0007354', 'Amyotrophic lateral sclerosis', 'XPO:0128370', 'decreased size of the ascending interneuron', 0.5, 9.529055259943116, 2.182779794200862, 'UPHENO:0080059', 'decreased size of the cell'),
(472845, 'HP:0007354', 'Amyotrophic lateral sclerosis', 'XPO:0130090', 'increased size of the afferent neuron', 0.4307692307692308, 8.042124842182485, 1.8612629937805862, 'UPHENO:0077801', 'abnormal size of cell'),
(472846, 'HP:0007354', 'Amyotrophic lateral sclerosis', 'XPO:0128156', 'decreased size of the chondroblast', 0.5185185185185185, 9.529055259943116, 2.22283414052124, 'UPHENO:0080059', 'decreased size of the cell'),
(472847, 'HP:0007354', 'Amyotrophic lateral sclerosis', 'XPO:0130314', 'increased size of the acid secreting cell', 0.41379310344827586, 8.042124842182485, 1.8242192293595543, 'UPHENO:0077801', 'abnormal size of cell'),
(472848, 'HP:0007354', 'Amyotrophic lateral sclerosis', 'XPO:0130890', 'increased size of the microglial cell', 0.4375, 8.042124842182485, 1.8757477491536108, 'UPHENO:0077801', 'abnormal size of cell'),
(472849, 'HP:0007354', 'Amyotrophic lateral sclerosis', 'XPO:0128450', 'decreased size of the postmigratory neural crest cell', 0.417910447761194, 9.529055259943116, 1.9955680270098508, 'UPHENO:0080059', 'decreased size of the cell'),
(472850, 'HP:0007354', 'Amyotrophic lateral sclerosis', 'XPO:0129879', 'increased size of the pericyte', 0.41379310344827586, 8.042124842182485, 1.8242192293595543, 'UPHENO:0077801', 'abnormal size of cell'),
(472851, 'HP:0007354', 'Amyotrophic lateral sclerosis', 'XPO:0128408', 'decreased size of the animal blastomere', 0.4307692307692308, 9.529055259943116, 2.0260364765431023, 'UPHENO:0080059', 'decreased size of the cell'),
(472852, 'HP:0007354', 'Amyotrophic lateral sclerosis', 'XPO:0129097', 'decreased size of the spinal neuron', 0.5, 9.529055259943116, 2.182779794200862, 'UPHENO:0080059', 'decreased size of the cell'),
(472853, 'HP:0007354', 'Amyotrophic lateral sclerosis', 'XPO:0128106', 'decreased size of the endocrine cell', 0.45901639344262296, 9.529055259943116, 2.091409232631085, 'UPHENO:0080059', 'decreased size of the cell'),
(472854, 'HP:0007354', 'Amyotrophic lateral sclerosis', 'XPO:0102586', 'abnormal neural progenitor cell morphology', 0.4107142857142857, 5.43643956286526, 1.4942634947997255, 'HP:0025461', 'Abnormal cell morphology'),
(472855, 'HP:0007354', 'Amyotrophic lateral sclerosis', 'XPO:0128006', 'decreased size of the cell', 0.5490196078431373, 9.529055259943116, 2.2872774606351443, 'UPHENO:0080059', 'decreased size of the cell'),
(472856, 'HP:0007354', 'Amyotrophic lateral sclerosis', 'XPO:0102496', 'abnormal dorsolateral ascending neuron morphology', 0.4107142857142857, 5.43643956286526, 1.4942634947997255, 'HP:0025461', 'Abnormal cell morphology'),
(472857, 'HP:0007354', 'Amyotrophic lateral sclerosis', 'XPO:0129070', 'decreased size of the paracrine cell', 0.5185185185185185, 9.529055259943116, 2.22283414052124, 'UPHENO:0080059', 'decreased size of the cell'),
(472858, 'HP:0007354', 'Amyotrophic lateral sclerosis', 'XPO:0142037', 'decreased size of the cerebrospinal fluid', 0.42857142857142855, 5.653868323764771, 1.5566266169093397, 'UPHENO:0012541', 'decreased size of the anatomical entity in the independent continuant'),
(472859, 'HP:0007354', 'Amyotrophic lateral sclerosis', 'XPO:0129397', 'decreased size of the alkali secreting cell', 0.5185185185185185, 9.529055259943116, 2.22283414052124, 'UPHENO:0080059', 'decreased size of the cell'),
(472860, 'HP:0007354', 'Amyotrophic lateral sclerosis', 'XPO:0129087', 'decreased size of the ciliated non-epidermal cell', 0.49122807017543857, 9.529055259943116, 2.1635478792799963, 'UPHENO:0080059', 'decreased size of the cell'),
(472861, 'HP:0007354', 'Amyotrophic lateral sclerosis', 'XPO:0102871', 'abnormal olfactory epithelial support cell morphology', 0.40350877192982454, 5.43643956286526, 1.4810979210310415, 'HP:0025461', 'Abnormal cell morphology'),
(472862, 'HP:0007354', 'Amyotrophic lateral sclerosis', 'XPO:0130574', 'increased size of the spinal neuron', 0.4166666666666667, 8.042124842182485, 1.8305423652320558, 'UPHENO:0077801', 'abnormal size of cell'),
(472863, 'HP:0007354', 'Amyotrophic lateral sclerosis', 'XPO:0128143', 'decreased size of the stem cell', 0.5185185185185185, 9.529055259943116, 2.22283414052124, 'UPHENO:0080059', 'decreased size of the cell'),
(472864, 'HP:0007354', 'Amyotrophic lateral sclerosis', 'XPO:0128140', 'decreased size of the electrically active cell', 0.5185185185185185, 9.529055259943116, 2.22283414052124, 'UPHENO:0080059', 'decreased size of the cell'),
(472865, 'HP:0007354', 'Amyotrophic lateral sclerosis', 'XPO:0128405', 'decreased size of the stromal cell', 0.4666666666666667, 9.529055259943116, 2.1087656234489693, 'UPHENO:0080059', 'decreased size of the cell'),
(472866, 'HP:0007354', 'Amyotrophic lateral sclerosis', 'XPO:0129445', 'decreased size of the dorsolateral commissural neuron', 0.5333333333333333, 9.529055259943116, 2.254365277700798, 'UPHENO:0080059', 'decreased size of the cell'),
(472867, 'HP:0007354', 'Amyotrophic lateral sclerosis', 'XPO:0128422', 'decreased size of the vegetal blastomere', 0.4307692307692308, 9.529055259943116, 2.0260364765431023, 'UPHENO:0080059', 'decreased size of the cell'),
(472868, 'HP:0007354', 'Amyotrophic lateral sclerosis', 'XPO:0128637', 'decreased size of the secondary spermatogonium', 0.49122807017543857, 9.529055259943116, 2.1635478792799963, 'UPHENO:0080059', 'decreased size of the cell'),
(472869, 'HP:0007354', 'Amyotrophic lateral sclerosis', 'XPO:0129435', 'decreased size of the secretory epithelial cell', 0.4666666666666667, 9.529055259943116, 2.1087656234489693, 'UPHENO:0080059', 'decreased size of the cell'),
(472870, 'HP:0007354', 'Amyotrophic lateral sclerosis', 'XPO:0128937', 'decreased size of the hatching gland cell', 0.42424242424242425, 9.529055259943116, 2.01062913144575, 'UPHENO:0080059', 'decreased size of the cell'),
(472871, 'HP:0007354', 'Amyotrophic lateral sclerosis', 'XPO:0129438', 'decreased size of the mitotic cell', 0.5185185185185185, 9.529055259943116, 2.22283414052124, 'UPHENO:0080059', 'decreased size of the cell'),
(472872, 'HP:0007354', 'Amyotrophic lateral sclerosis', 'XPO:0130867', 'increased size of the barrier epithelial cell', 0.41379310344827586, 8.042124842182485, 1.8242192293595543, 'UPHENO:0077801', 'abnormal size of cell'),
(472873, 'HP:0007354', 'Amyotrophic lateral sclerosis', 'XPO:0129416', 'decreased size of the microglial cell', 0.5333333333333333, 9.529055259943116, 2.254365277700798, 'UPHENO:0080059', 'decreased size of the cell'),
(472874, 'HP:0007354', 'Amyotrophic lateral sclerosis', 'XPO:0128806', 'decreased size of the migrating neuroblast', 0.5614035087719298, 9.529055259943116, 2.312929972613455, 'UPHENO:0080059', 'decreased size of the cell'),
(472875, 'HP:0007354', 'Amyotrophic lateral sclerosis', 'XPO:0130068', 'increased size of the intersomitic neuron', 0.417910447761194, 8.042124842182485, 1.8332724821334945, 'UPHENO:0077801', 'abnormal size of cell'),
(472876, 'HP:0007354', 'Amyotrophic lateral sclerosis', 'XPO:0130231', 'increased size of the melanoblast', 0.41379310344827586, 8.042124842182485, 1.8242192293595543, 'UPHENO:0077801', 'abnormal size of cell'),
(472877, 'HP:0007354', 'Amyotrophic lateral sclerosis', 'XPO:0129408', 'decreased size of the exocrine cell', 0.5185185185185185, 9.529055259943116, 2.22283414052124, 'UPHENO:0080059', 'decreased size of the cell'),
(472878, 'HP:0007354', 'Amyotrophic lateral sclerosis', 'XPO:0130907', 'increased size of the mucus secreting cell', 0.41379310344827586, 8.042124842182485, 1.8242192293595543, 'UPHENO:0077801', 'abnormal size of cell'),
(472879, 'HP:0007354', 'Amyotrophic lateral sclerosis', 'XPO:0130919', 'increased size of the dorsolateral commissural neuron', 0.4375, 8.042124842182485, 1.8757477491536108, 'UPHENO:0077801', 'abnormal size of cell'),
(472880, 'HP:0007354', 'Amyotrophic lateral sclerosis', 'XPO:0130074', 'increased size of the ciliated cell', 0.41379310344827586, 8.042124842182485, 1.8242192293595543, 'UPHENO:0077801', 'abnormal size of cell'),
(472881, 'HP:0007354', 'Amyotrophic lateral sclerosis', 'XPO:0129365', 'decreased size of the absorptive cell', 0.5185185185185185, 9.529055259943116, 2.22283414052124, 'UPHENO:0080059', 'decreased size of the cell'),
(472882, 'HP:0007354', 'Amyotrophic lateral sclerosis', 'XPO:0102333', 'abnormal microglial cell morphology', 0.4107142857142857, 5.43643956286526, 1.4942634947997255, 'HP:0025461', 'Abnormal cell morphology'),
(472883, 'HP:0007354', 'Amyotrophic lateral sclerosis', 'XPO:0129218', 'decreased size of the left-ventral blastomere', 0.45161290322580644, 9.529055259943116, 2.0744744662063335, 'UPHENO:0080059', 'decreased size of the cell'),
(472884, 'HP:0007354', 'Amyotrophic lateral sclerosis', 'XPO:0128898', 'decreased size of the apoptotic cell', 0.5185185185185185, 9.529055259943116, 2.22283414052124, 'UPHENO:0080059', 'decreased size of the cell'),
(472885, 'HP:0007354', 'Amyotrophic lateral sclerosis', 'XPO:0141584', 'decreased length of neuron in regenerating tail', 0.47761194029850745, 9.529055259943116, 2.1333519568775166, 'UPHENO:0080059', 'decreased size of the cell'),
(472886, 'HP:0007354', 'Amyotrophic lateral sclerosis', 'XPO:0128249', 'decreased size of the erythroid cell', 0.4666666666666667, 9.529055259943116, 2.1087656234489693, 'UPHENO:0080059', 'decreased size of the cell'),
(472887, 'HP:0007354', 'Amyotrophic lateral sclerosis', 'XPO:0129636', 'increased size of the chondroblast', 0.41379310344827586, 8.042124842182485, 1.8242192293595543, 'UPHENO:0077801', 'abnormal size of cell'),
(472888, 'HP:0007354', 'Amyotrophic lateral sclerosis', 'XPO:0128558', 'decreased size of the mesodermal cell', 0.4375, 9.529055259943116, 2.04180353516814, 'UPHENO:0080059', 'decreased size of the cell'),
(472889, 'HP:0007354', 'Amyotrophic lateral sclerosis', 'XPO:0129409', 'decreased size of the hemangioblast', 0.4666666666666667, 9.529055259943116, 2.1087656234489693, 'UPHENO:0080059', 'decreased size of the cell'),
(472890, 'HP:0007354', 'Amyotrophic lateral sclerosis', 'XPO:0101828', 'abnormal neuron morphology', 0.42592592592592593, 5.43643956286526, 1.521683460695332, 'HP:0025461', 'Abnormal cell morphology'),
(472891, 'HP:0007354', 'Amyotrophic lateral sclerosis', 'XPO:0128814', 'decreased size of the gastrula cell', 0.4745762711864407, 9.529055259943116, 2.1265614294426913, 'UPHENO:0080059', 'decreased size of the cell'),
(472892, 'HP:0007354', 'Amyotrophic lateral sclerosis', 'XPO:0128734', 'decreased size of the spermatocyte', 0.49122807017543857, 9.529055259943116, 2.1635478792799963, 'UPHENO:0080059', 'decreased size of the cell'),
(472893, 'HP:0007354', 'Amyotrophic lateral sclerosis', 'XPO:0129361', 'decreased size of the right-dorsal blastomere', 0.45161290322580644, 9.529055259943116, 2.0744744662063335, 'UPHENO:0080059', 'decreased size of the cell'),
(472894, 'HP:0007354', 'Amyotrophic lateral sclerosis', 'XPO:0128027', 'decreased size of the circulating cell', 0.45161290322580644, 9.529055259943116, 2.0744744662063335, 'UPHENO:0080059', 'decreased size of the cell'),
(472895, 'HP:0007354', 'Amyotrophic lateral sclerosis', 'XPO:0128584', 'decreased size of the blastomere D1', 0.45161290322580644, 9.529055259943116, 2.0744744662063335, 'UPHENO:0080059', 'decreased size of the cell'),
(472896, 'HP:0007354', 'Amyotrophic lateral sclerosis', 'XPO:0130632', 'increased size of the oxygen accumulating cell', 0.41379310344827586, 8.042124842182485, 1.8242192293595543, 'UPHENO:0077801', 'abnormal size of cell'),
(472897, 'HP:0007354', 'Amyotrophic lateral sclerosis', 'XPO:0128171', 'decreased size of the gamete', 0.42424242424242425, 9.529055259943116, 2.01062913144575, 'UPHENO:0080059', 'decreased size of the cell'),
(472898, 'HP:0007354', 'Amyotrophic lateral sclerosis', 'XPO:0128529', 'decreased size of the blastomere V1', 0.45161290322580644, 9.529055259943116, 2.0744744662063335, 'UPHENO:0080059', 'decreased size of the cell'),
(472899, 'HP:0007354', 'Amyotrophic lateral sclerosis', 'XPO:0128371', 'decreased size of the interneuron', 0.5245901639344263, 9.529055259943116, 2.2358105154403773, 'UPHENO:0080059', 'decreased size of the cell'),
(472900, 'HP:0007354', 'Amyotrophic lateral sclerosis', 'XPO:0130547', 'increased size of the paracrine cell', 0.41379310344827586, 8.042124842182485, 1.8242192293595543, 'UPHENO:0077801', 'abnormal size of cell'),
(472901, 'HP:0007354', 'Amyotrophic lateral sclerosis', 'XPO:0129266', 'decreased size of the neuromast mantle cell', 0.417910447761194, 9.529055259943116, 1.9955680270098508, 'UPHENO:0080059', 'decreased size of the cell'),
(472902, 'HP:0007354', 'Amyotrophic lateral sclerosis', 'XPO:0128694', 'decreased size of the ventral animal hemisphere blastomere', 0.4117647058823529, 9.529055259943116, 1.9808403864135962, 'UPHENO:0080059', 'decreased size of the cell'),
(472903, 'HP:0007354', 'Amyotrophic lateral sclerosis', 'XPO:0128361', 'decreased size of the ectodermal cell', 0.4375, 9.529055259943116, 2.04180353516814, 'UPHENO:0080059', 'decreased size of the cell'),
(472904, 'HP:0007354', 'Amyotrophic lateral sclerosis', 'XPO:0129576', 'increased size of the glial cell', 0.45901639344262296, 8.042124842182485, 1.921319114742246, 'UPHENO:0077801', 'abnormal size of cell'),
(472905, 'HP:0007354', 'Amyotrophic lateral sclerosis', 'XPO:0129455', 'decreased size of the polar body', 0.4307692307692308, 9.529055259943116, 2.0260364765431023, 'UPHENO:0080059', 'decreased size of the cell'),
(472906, 'HP:0007354', 'Amyotrophic lateral sclerosis', 'XPO:0128893', 'decreased size of the spermatozoon', 0.4057971014492754, 9.529055259943116, 1.966434083318047, 'UPHENO:0080059', 'decreased size of the cell'),
(472907, 'HP:0007354', 'Amyotrophic lateral sclerosis', 'XPO:0128606', 'decreased size of the right blastomere', 0.45161290322580644, 9.529055259943116, 2.0744744662063335, 'UPHENO:0080059', 'decreased size of the cell'),
(472908, 'HP:0007354', 'Amyotrophic lateral sclerosis', 'XPO:0131596', 'decreased size of the pial cell', 0.44155844155844154, 9.529055259943116, 2.051252005509014, 'UPHENO:0080059', 'decreased size of the cell'),
(472909, 'HP:0007354', 'Amyotrophic lateral sclerosis', 'XPO:0128907', 'decreased size of the right-ventral blastomere', 0.45161290322580644, 9.529055259943116, 2.0744744662063335, 'UPHENO:0080059', 'decreased size of the cell'),
(472910, 'HP:0007354', 'Amyotrophic lateral sclerosis', 'XPO:0128744', 'decreased size of the nucleate erythrocyte', 0.5185185185185185, 9.529055259943116, 2.22283414052124, 'UPHENO:0080059', 'decreased size of the cell'),
(472911, 'HP:0007354', 'Amyotrophic lateral sclerosis', 'XPO:0130647', 'increased size of the descending interneuron', 0.4117647058823529, 8.042124842182485, 1.8197426110058628, 'UPHENO:0077801', 'abnormal size of cell'),
(472912, 'HP:0007354', 'Amyotrophic lateral sclerosis', 'XPO:0129319', 'decreased size of the left-dorsal blastomere', 0.45161290322580644, 9.529055259943116, 2.0744744662063335, 'UPHENO:0080059', 'decreased size of the cell'),
(472913, 'HP:0007354', 'Amyotrophic lateral sclerosis', 'XPO:0128395', 'decreased size of the T cell', 0.4444444444444444, 9.529055259943116, 2.0579445257552083, 'UPHENO:0080059', 'decreased size of the cell'),
(472914, 'HP:0007354', 'Amyotrophic lateral sclerosis', 'XPO:0115702', 'abnormally decreased thickness of motor neuron', 0.5079365079365079, 9.529055259943116, 2.2000352389608486, 'UPHENO:0080059', 'decreased size of the cell'),
(472915, 'HP:0007354', 'Amyotrophic lateral sclerosis', 'XPO:0129386', 'decreased size of the efferent neuron', 0.5245901639344263, 9.529055259943116, 2.2358105154403773, 'UPHENO:0080059', 'decreased size of the cell'),
(472916, 'HP:0007354', 'Amyotrophic lateral sclerosis', 'XPO:0129316', 'decreased size of the Rohon-Beard neuron', 0.43243243243243246, 9.529055259943116, 2.02994397578856, 'UPHENO:0080059', 'decreased size of the cell'),
(472917, 'HP:0007354', 'Amyotrophic lateral sclerosis', 'XPO:0130714', 'increased size of the neural progenitor cell', 0.4375, 8.042124842182485, 1.8757477491536108, 'UPHENO:0077801', 'abnormal size of cell'),
(472918, 'HP:0007354', 'Amyotrophic lateral sclerosis', 'XPO:0130861', 'increased size of the efferent neuron', 0.4307692307692308, 8.042124842182485, 1.8612629937805862, 'UPHENO:0077801', 'abnormal size of cell'),
(472919, 'HP:0007354', 'Amyotrophic lateral sclerosis', 'XPO:0128780', 'decreased size of the keratin accumulating cell', 0.5185185185185185, 9.529055259943116, 2.22283414052124, 'UPHENO:0080059', 'decreased size of the cell'),
(472920, 'HP:0007354', 'Amyotrophic lateral sclerosis', 'XPO:0128065', 'decreased size of the neuron', 0.5614035087719298, 9.529055259943116, 2.312929972613455, 'UPHENO:0080059', 'decreased size of the cell'),
(472921, 'HP:0007354', 'Amyotrophic lateral sclerosis', 'XPO:0130895', 'increased size of the cementoblast', 0.41379310344827586, 8.042124842182485, 1.8242192293595543, 'UPHENO:0077801', 'abnormal size of cell'),
(472922, 'HP:0007354', 'Amyotrophic lateral sclerosis', 'XPO:0128505', 'decreased size of the myocyte', 0.42424242424242425, 9.529055259943116, 2.01062913144575, 'UPHENO:0080059', 'decreased size of the cell'),
(472923, 'HP:0007354', 'Amyotrophic lateral sclerosis', 'XPO:0128506', 'decreased size of the non-ciliated epithelial cell', 0.4666666666666667, 9.529055259943116, 2.1087656234489693, 'UPHENO:0080059', 'decreased size of the cell'),
(472924, 'HP:0007354', 'Amyotrophic lateral sclerosis', 'XPO:0103756', 'increased size of the germ cell', 0.41379310344827586, 8.042124842182485, 1.8242192293595543, 'UPHENO:0077801', 'abnormal size of cell'),
(472925, 'HP:0007354', 'Amyotrophic lateral sclerosis', 'XPO:0130222', 'increased size of the nucleate erythrocyte', 0.41379310344827586, 8.042124842182485, 1.8242192293595543, 'UPHENO:0077801', 'abnormal size of cell'),
(472926, 'HP:0007354', 'Amyotrophic lateral sclerosis', 'XPO:0128687', 'decreased size of the morula cell', 0.4745762711864407, 9.529055259943116, 2.1265614294426913, 'UPHENO:0080059', 'decreased size of the cell'),
(472927, 'HP:0007354', 'Amyotrophic lateral sclerosis', 'XPO:0128563', 'decreased size of the primordial germ cell', 0.49122807017543857, 9.529055259943116, 2.1635478792799963, 'UPHENO:0080059', 'decreased size of the cell'),
(472928, 'HP:0007354', 'Amyotrophic lateral sclerosis', 'XPO:0129238', 'decreased size of the neural progenitor cell', 0.5333333333333333, 9.529055259943116, 2.254365277700798, 'UPHENO:0080059', 'decreased size of the cell'),
(472929, 'HP:0007354', 'Amyotrophic lateral sclerosis', 'XPO:0128610', 'decreased size of the afferent neuron', 0.5245901639344263, 9.529055259943116, 2.2358105154403773, 'UPHENO:0080059', 'decreased size of the cell'),
(472930, 'HP:0007354', 'Amyotrophic lateral sclerosis', 'XPO:0129294', 'decreased size of the Schwann cell', 0.4155844155844156, 9.529055259943116, 1.9900067490526412, 'UPHENO:0080059', 'decreased size of the cell'),
(472931, 'HP:0007354', 'Amyotrophic lateral sclerosis', 'XPO:0129421', 'decreased size of the cementoblast', 0.5185185185185185, 9.529055259943116, 2.22283414052124, 'UPHENO:0080059', 'decreased size of the cell'),
(472932, 'HP:0007354', 'Amyotrophic lateral sclerosis', 'XPO:0130376', 'increased size of the apoptotic cell', 0.41379310344827586, 8.042124842182485, 1.8242192293595543, 'UPHENO:0077801', 'abnormal size of cell'),
(472933, 'HP:0007354', 'Amyotrophic lateral sclerosis', 'XPO:0141483', 'decreased size of the lymphoblast', 0.4666666666666667, 9.529055259943116, 2.1087656234489693, 'UPHENO:0080059', 'decreased size of the cell'),
(472934, 'HP:0007354', 'Amyotrophic lateral sclerosis', 'XPO:0128207', 'decreased size of the ligament cell', 0.4444444444444444, 9.529055259943116, 2.0579445257552083, 'UPHENO:0080059', 'decreased size of the cell'),
(472935, 'HP:0007354', 'Amyotrophic lateral sclerosis', 'XPO:0128136', 'decreased size of the enteroendocrine cell', 0.4375, 9.529055259943116, 2.04180353516814, 'UPHENO:0080059', 'decreased size of the cell'),
(472936, 'HP:0007354', 'Amyotrophic lateral sclerosis', 'XPO:0128723', 'decreased size of the pigment cell', 0.417910447761194, 9.529055259943116, 1.9955680270098508, 'UPHENO:0080059', 'decreased size of the cell'),
(472937, 'HP:0007354', 'Amyotrophic lateral sclerosis', 'XPO:0107373', 'abnormal efferent neuron morphology', 0.40350877192982454, 5.43643956286526, 1.4810979210310415, 'HP:0025461', 'Abnormal cell morphology'),
(472938, 'HP:0007354', 'Amyotrophic lateral sclerosis', 'XPO:0129171', 'decreased size of the descending interneuron', 0.5, 9.529055259943116, 2.182779794200862, 'UPHENO:0080059', 'decreased size of the cell'),
(472939, 'HP:0007354', 'Amyotrophic lateral sclerosis', 'XPO:0129229', 'decreased size of the endothelial cell', 0.4117647058823529, 9.529055259943116, 1.9808403864135962, 'UPHENO:0080059', 'decreased size of the cell'),
(472940, 'HP:0007354', 'Amyotrophic lateral sclerosis', 'XPO:0128402', 'decreased size of the thrombocyte', 0.4117647058823529, 9.529055259943116, 1.9808403864135962, 'UPHENO:0080059', 'decreased size of the cell'),
(472941, 'HP:0007354', 'Amyotrophic lateral sclerosis', 'XPO:0129950', 'increased size of the dorsolateral ascending neuron', 0.4375, 8.042124842182485, 1.8757477491536108, 'UPHENO:0077801', 'abnormal size of cell'),
(472942, 'HP:0007354', 'Amyotrophic lateral sclerosis', 'XPO:0128336', 'decreased size of the proepicardium', 0.49122807017543857, 9.529055259943116, 2.1635478792799963, 'UPHENO:0080059', 'decreased size of the cell'),
(472943, 'HP:0007354', 'Amyotrophic lateral sclerosis', 'XPO:0102334', 'abnormal glial cell morphology', 0.42592592592592593, 5.43643956286526, 1.521683460695332, 'HP:0025461', 'Abnormal cell morphology'),
(472944, 'HP:0007354', 'Amyotrophic lateral sclerosis', 'XPO:0128181', 'decreased size of the motor neuron', 0.5333333333333333, 9.529055259943116, 2.254365277700798, 'UPHENO:0080059', 'decreased size of the cell'),
(472945, 'HP:0007354', 'Amyotrophic lateral sclerosis', 'XPO:0129661', 'increased size of the motor neuron', 0.4375, 8.042124842182485, 1.8757477491536108, 'UPHENO:0077801', 'abnormal size of cell'),
(472946, 'HP:0007354', 'Amyotrophic lateral sclerosis', 'XPO:0130827', 'increased size of the olfactory epithelial support cell', 0.4375, 8.042124842182485, 1.8757477491536108, 'UPHENO:0077801', 'abnormal size of cell'),
(472947, 'HP:0007354', 'Amyotrophic lateral sclerosis', 'XPO:0130912', 'increased size of the mitotic cell', 0.41379310344827586, 8.042124842182485, 1.8242192293595543, 'UPHENO:0077801', 'abnormal size of cell'),
(472948, 'HP:0007354', 'Amyotrophic lateral sclerosis', 'XPO:0129320', 'decreased size of the skeletal muscle satellite cell', 0.417910447761194, 9.529055259943116, 1.9955680270098508, 'UPHENO:0080059', 'decreased size of the cell'),
(472949, 'HP:0007354', 'Amyotrophic lateral sclerosis', 'XPO:0129222', 'decreased size of the fibroblast', 0.417910447761194, 9.529055259943116, 1.9955680270098508, 'UPHENO:0080059', 'decreased size of the cell'),
(472950, 'HP:0007354', 'Amyotrophic lateral sclerosis', 'XPO:0128399', 'decreased size of the pericyte', 0.5185185185185185, 9.529055259943116, 2.22283414052124, 'UPHENO:0080059', 'decreased size of the cell'),
(472951, 'HP:0007354', 'Amyotrophic lateral sclerosis', 'XPO:0129851', 'increased size of the interneuron', 0.4307692307692308, 8.042124842182485, 1.8612629937805862, 'UPHENO:0077801', 'abnormal size of cell'),
(472952, 'HP:0007354', 'Amyotrophic lateral sclerosis', 'XPO:0130483', 'increased size of the myelin accumulating cell', 0.41379310344827586, 8.042124842182485, 1.8242192293595543, 'UPHENO:0077801', 'abnormal size of cell'),
(472953, 'HP:0007354', 'Amyotrophic lateral sclerosis', 'XPO:0129182', 'decreased size of the neuromast support cell', 0.417910447761194, 9.529055259943116, 1.9955680270098508, 'UPHENO:0080059', 'decreased size of the cell'),
(472954, 'HP:0007354', 'Amyotrophic lateral sclerosis', 'XPO:0128228', 'decreased size of the blastomere', 0.4745762711864407, 9.529055259943116, 2.1265614294426913, 'UPHENO:0080059', 'decreased size of the cell'),
(472955, 'HP:0007354', 'Amyotrophic lateral sclerosis', 'XPO:0129691', 'increased size of the progenitor cell', 0.41379310344827586, 8.042124842182485, 1.8242192293595543, 'UPHENO:0077801', 'abnormal size of cell'),
(472956, 'HP:0007354', 'Amyotrophic lateral sclerosis', 'XPO:0128435', 'decreased size of the blastomere V2', 0.45161290322580644, 9.529055259943116, 2.0744744662063335, 'UPHENO:0080059', 'decreased size of the cell'),
(472957, 'HP:0007354', 'Amyotrophic lateral sclerosis', 'XPO:0128470', 'decreased size of the dorsolateral ascending neuron', 0.5333333333333333, 9.529055259943116, 2.254365277700798, 'UPHENO:0080059', 'decreased size of the cell'),
(472958, 'HP:0007354', 'Amyotrophic lateral sclerosis', 'XPO:0128170', 'decreased size of the egg', 0.4057971014492754, 9.529055259943116, 1.966434083318047, 'UPHENO:0080059', 'decreased size of the cell'),
(472959, 'HP:0007354', 'Amyotrophic lateral sclerosis', 'XPO:0129006', 'decreased size of the myelin accumulating cell', 0.5185185185185185, 9.529055259943116, 2.22283414052124, 'UPHENO:0080059', 'decreased size of the cell'),
(472960, 'HP:0007354', 'Amyotrophic lateral sclerosis', 'XPO:0128955', 'decreased size of the secondary myofiber', 0.42424242424242425, 9.529055259943116, 2.01062913144575, 'UPHENO:0080059', 'decreased size of the cell'),
(472961, 'HP:0007354', 'Amyotrophic lateral sclerosis', 'XPO:0129486', 'increased size of the cell', 0.43636363636363634, 8.042124842182485, 1.873310129216485, 'UPHENO:0077801', 'abnormal size of cell'),
(472962, 'HP:0007354', 'Amyotrophic lateral sclerosis', 'XPO:0128961', 'decreased size of the Merkel cell', 0.5185185185185185, 9.529055259943116, 2.22283414052124, 'UPHENO:0080059', 'decreased size of the cell'),
(472963, 'HP:0007354', 'Amyotrophic lateral sclerosis', 'XPO:0129286', 'decreased size of the perichondrial cell', 0.4307692307692308, 9.529055259943116, 2.0260364765431023, 'UPHENO:0080059', 'decreased size of the cell'),
(472964, 'HP:0007354', 'Amyotrophic lateral sclerosis', 'XPO:0128557', 'decreased size of the secondary oogonium', 0.49122807017543857, 9.529055259943116, 2.1635478792799963, 'UPHENO:0080059', 'decreased size of the cell'),
(472965, 'HP:0007354', 'Amyotrophic lateral sclerosis', 'XPO:0128412', 'decreased size of the premigratory neural crest cell', 0.417910447761194, 9.529055259943116, 1.9955680270098508, 'UPHENO:0080059', 'decreased size of the cell'),
(472966, 'HP:0007354', 'Amyotrophic lateral sclerosis', 'XPO:0130389', 'increased size of the barrier cell', 0.41379310344827586, 8.042124842182485, 1.8242192293595543, 'UPHENO:0077801', 'abnormal size of cell'),
(472967, 'HP:0007354', 'Amyotrophic lateral sclerosis', 'XPO:0128427', 'decreased size of the commissural interneuron', 0.5, 9.529055259943116, 2.182779794200862, 'UPHENO:0080059', 'decreased size of the cell'),
(472968, 'HP:0007354', 'Amyotrophic lateral sclerosis', 'XPO:0128236', 'decreased size of the dorsal animal hemisphere blastomere', 0.4117647058823529, 9.529055259943116, 1.9808403864135962, 'UPHENO:0080059', 'decreased size of the cell'),
(472969, 'HP:0007354', 'Amyotrophic lateral sclerosis', 'XPO:0128753', 'decreased size of the melanoblast', 0.5185185185185185, 9.529055259943116, 2.22283414052124, 'UPHENO:0080059', 'decreased size of the cell'),
(472970, 'HP:0007354', 'Amyotrophic lateral sclerosis', 'XPO:0130558', 'increased size of the multiciliated cell precursor', 0.41379310344827586, 8.042124842182485, 1.8242192293595543, 'UPHENO:0077801', 'abnormal size of cell'),
(472971, 'HP:0007354', 'Amyotrophic lateral sclerosis', 'XPO:0115704', 'abnormally defasciculated motor neuron', 0.40350877192982454, 5.43643956286526, 1.4810979210310415, 'HP:0025461', 'Abnormal cell morphology'),
(472972, 'HP:0007354', 'Amyotrophic lateral sclerosis', 'XPO:0128562', 'decreased size of the mesenchymal stem cell', 0.49122807017543857, 9.529055259943116, 2.1635478792799963, 'UPHENO:0080059', 'decreased size of the cell'),
(472973, 'HP:0007354', 'Amyotrophic lateral sclerosis', 'XPO:0128590', 'decreased size of the stage III oocyte', 0.4666666666666667, 9.529055259943116, 2.1087656234489693, 'UPHENO:0080059', 'decreased size of the cell'),
(472974, 'HP:0007354', 'Amyotrophic lateral sclerosis', 'XPO:0128396', 'decreased size of the lymphocyte', 0.4666666666666667, 9.529055259943116, 2.1087656234489693, 'UPHENO:0080059', 'decreased size of the cell'),
(472975, 'HP:0007354', 'Amyotrophic lateral sclerosis', 'XPO:0128317', 'decreased size of the epithelial cell', 0.49122807017543857, 9.529055259943116, 2.1635478792799963, 'UPHENO:0080059', 'decreased size of the cell'),
(472976, 'HP:0007354', 'Amyotrophic lateral sclerosis', 'XPO:0129156', 'decreased size of the oxygen accumulating cell', 0.5185185185185185, 9.529055259943116, 2.22283414052124, 'UPHENO:0080059', 'decreased size of the cell'),
(472977, 'HP:0007354', 'Amyotrophic lateral sclerosis', 'XPO:0130839', 'increased size of the absorptive cell', 0.41379310344827586, 8.042124842182485, 1.8242192293595543, 'UPHENO:0077801', 'abnormal size of cell'),
(472978, 'HP:0007354', 'Amyotrophic lateral sclerosis', 'XPO:0128597', 'decreased size of the blastomere D2', 0.45161290322580644, 9.529055259943116, 2.0744744662063335, 'UPHENO:0080059', 'decreased size of the cell'),
(472979, 'HP:0007354', 'Amyotrophic lateral sclerosis', 'XPO:0130439', 'increased size of the Merkel cell', 0.41379310344827586, 8.042124842182485, 1.8242192293595543, 'UPHENO:0077801', 'abnormal size of cell'),
(472980, 'HP:0007354', 'Amyotrophic lateral sclerosis', 'XPO:0129098', 'decreased size of the olfactory sensory neuron', 0.47761194029850745, 9.529055259943116, 2.1333519568775166, 'UPHENO:0080059', 'decreased size of the cell'),
(472981, 'HP:0007354', 'Amyotrophic lateral sclerosis', 'XPO:0128403', 'decreased size of the Mauthner cell', 0.425, 9.529055259943116, 2.0124235353115467, 'UPHENO:0080059', 'decreased size of the cell'),
(472982, 'HP:0007354', 'Amyotrophic lateral sclerosis', 'XPO:0129433', 'decreased size of the mucus secreting cell', 0.5185185185185185, 9.529055259943116, 2.22283414052124, 'UPHENO:0080059', 'decreased size of the cell'),
(472983, 'HP:0007354', 'Amyotrophic lateral sclerosis', 'XPO:0128601', 'decreased size of the stage IV oocyte', 0.4666666666666667, 9.529055259943116, 2.1087656234489693, 'UPHENO:0080059', 'decreased size of the cell'),
(472984, 'HP:0007354', 'Amyotrophic lateral sclerosis', 'XPO:0129850', 'increased size of the ascending interneuron', 0.4117647058823529, 8.042124842182485, 1.8197426110058628, 'UPHENO:0077801', 'abnormal size of cell'),
(472985, 'HP:0007354', 'Amyotrophic lateral sclerosis', 'XPO:0128761', 'decreased size of the angioblast', 0.45161290322580644, 9.529055259943116, 2.0744744662063335, 'UPHENO:0080059', 'decreased size of the cell'),
(472986, 'HP:0007354', 'Amyotrophic lateral sclerosis', 'XPO:0128543', 'decreased size of the sensory epithelial cell', 0.4666666666666667, 9.529055259943116, 2.1087656234489693, 'UPHENO:0080059', 'decreased size of the cell'),
(472987, 'HP:0007354', 'Amyotrophic lateral sclerosis', 'XPO:0130871', 'increased size of the alkali secreting cell', 0.41379310344827586, 8.042124842182485, 1.8242192293595543, 'UPHENO:0077801', 'abnormal size of cell'),
(472988, 'HP:0007354', 'Amyotrophic lateral sclerosis', 'XPO:0107374', 'abnormal afferent neuron morphology', 0.40350877192982454, 5.43643956286526, 1.4810979210310415, 'HP:0025461', 'Abnormal cell morphology'),
(472989, 'HP:0007354', 'Amyotrophic lateral sclerosis', 'XPO:0128359', 'decreased size of the myeloid cell', 0.4666666666666667, 9.529055259943116, 2.1087656234489693, 'UPHENO:0080059', 'decreased size of the cell'),
(472990, 'HP:0007354', 'Amyotrophic lateral sclerosis', 'XPO:0128895', 'decreased size of the stage V oocyte', 0.4666666666666667, 9.529055259943116, 2.1087656234489693, 'UPHENO:0080059', 'decreased size of the cell'),
(472991, 'HP:0007354', 'Amyotrophic lateral sclerosis', 'XPO:0128751', 'decreased size of the B cell', 0.4444444444444444, 9.529055259943116, 2.0579445257552083, 'UPHENO:0080059', 'decreased size of the cell'),
(472992, 'HP:0007354', 'Amyotrophic lateral sclerosis', 'XPO:0129907', 'increased size of the commissural interneuron', 0.4117647058823529, 8.042124842182485, 1.8197426110058628, 'UPHENO:0077801', 'abnormal size of cell'),
(472993, 'HP:0007354', 'Amyotrophic lateral sclerosis', 'XPO:0129392', 'decreased size of the barrier epithelial cell', 0.5185185185185185, 9.529055259943116, 2.22283414052124, 'UPHENO:0080059', 'decreased size of the cell'),
(472994, 'HP:0007354', 'Amyotrophic lateral sclerosis', 'XPO:0128594', 'decreased size of the ciliated cell', 0.5185185185185185, 9.529055259943116, 2.22283414052124, 'UPHENO:0080059', 'decreased size of the cell'),
(472995, 'HP:0007354', 'Amyotrophic lateral sclerosis', 'XPO:0128911', 'decreased size of the barrier cell', 0.5185185185185185, 9.529055259943116, 2.22283414052124, 'UPHENO:0080059', 'decreased size of the cell'),
(472996, 'HP:0007354', 'Amyotrophic lateral sclerosis', 'XPO:0128614', 'decreased size of the migratory neural crest cell', 0.417910447761194, 9.529055259943116, 1.9955680270098508, 'UPHENO:0080059', 'decreased size of the cell'),
(472997, 'HP:0007354', 'Amyotrophic lateral sclerosis', 'XPO:0128307', 'decreased size of the oocyte', 0.49122807017543857, 9.529055259943116, 2.1635478792799963, 'UPHENO:0080059', 'decreased size of the cell'),
(472998, 'HP:0007354', 'Amyotrophic lateral sclerosis', 'XPO:0129405', 'decreased size of the digestive enzyme secreting cell', 0.4307692307692308, 9.529055259943116, 2.0260364765431023, 'UPHENO:0080059', 'decreased size of the cell'),
(472999, 'HP:0007354', 'Amyotrophic lateral sclerosis', 'XPO:0128356', 'decreased size of the astrocyte', 0.41975308641975306, 9.529055259943116, 1.999962588656474, 'UPHENO:0080059', 'decreased size of the cell'),
(473000, 'HP:0007354', 'Amyotrophic lateral sclerosis', 'XPO:0101807', 'abnormal migrating neuroblast morphology', 0.42592592592592593, 5.43643956286526, 1.521683460695332, 'HP:0025461', 'Abnormal cell morphology'),
(473001, 'HP:0007354', 'Amyotrophic lateral sclerosis', 'XPO:0129351', 'decreased size of the stage VI oocyte', 0.4666666666666667, 9.529055259943116, 2.1087656234489693, 'UPHENO:0080059', 'decreased size of the cell'),
(473002, 'HP:0007354', 'Amyotrophic lateral sclerosis', 'XPO:0102819', 'abnormal dorsolateral commissural neuron morphology', 0.4107142857142857, 5.43643956286526, 1.4942634947997255, 'HP:0025461', 'Abnormal cell morphology'),
(473003, 'HP:0007354', 'Amyotrophic lateral sclerosis', 'XPO:0129207', 'decreased size of the neuroendocrine cell', 0.4375, 9.529055259943116, 2.04180353516814, 'UPHENO:0080059', 'decreased size of the cell'),
(473004, 'HP:0007354', 'Amyotrophic lateral sclerosis', 'XPO:0129747', 'increased size of the zygote', 0.41379310344827586, 8.042124842182485, 1.8242192293595543, 'UPHENO:0077801', 'abnormal size of cell'),
(473005, 'HP:0007354', 'Amyotrophic lateral sclerosis', 'XPO:0130882', 'increased size of the exocrine cell', 0.41379310344827586, 8.042124842182485, 1.8242192293595543, 'UPHENO:0077801', 'abnormal size of cell'),
(473006, 'HP:0007354', 'Amyotrophic lateral sclerosis', 'XPO:0129081', 'decreased size of the multiciliated cell precursor', 0.5185185185185185, 9.529055259943116, 2.22283414052124, 'UPHENO:0080059', 'decreased size of the cell'),
(473007, 'HP:0007354', 'Amyotrophic lateral sclerosis', 'XPO:0128229', 'decreased size of the early embryonic cell', 0.5, 9.529055259943116, 2.182779794200862, 'UPHENO:0080059', 'decreased size of the cell'),
(473008, 'HP:0007354', 'Amyotrophic lateral sclerosis', 'XPO:0130284', 'increased size of the migrating neuroblast', 0.45901639344262296, 8.042124842182485, 1.921319114742246, 'UPHENO:0077801', 'abnormal size of cell'),
(473009, 'HP:0007354', 'Amyotrophic lateral sclerosis', 'XPO:0128434', 'decreased size of the ventral vegetal hemisphere blastomere', 0.4117647058823529, 9.529055259943116, 1.9808403864135962, 'UPHENO:0080059', 'decreased size of the cell'),
(473010, 'HP:0007354', 'Amyotrophic lateral sclerosis', 'XPO:0128632', 'decreased size of the bottle cell', 0.45161290322580644, 9.529055259943116, 2.0744744662063335, 'UPHENO:0080059', 'decreased size of the cell'),
(473011, 'HP:0031488', 'Arteriovenous malformation of the lip', 'XPO:0130132', 'increased size of the oral epithelium', 0.4342105263157895, 7.312692920701687, 1.7819226251113227, 'UPHENO:0076800', 'abnormal mouth morphology'),
(473012, 'HP:0031488', 'Arteriovenous malformation of the lip', 'XPO:0140430', 'abnormally necrotic hyoid arch', 0.40298507462686567, 5.725717590856133, 1.5190058362769763, 'UPHENO:0076803', 'abnormal digestive system morphology'),
(473013, 'HP:0031488', 'Arteriovenous malformation of the lip', 'XPO:0101567', 'abnormal tongue', 0.6153846153846154, 7.884497199543557, 2.202725193173717, 'UPHENO:0076786', 'abnormal oral cavity morphology'),
(473014, 'HP:0031488', 'Arteriovenous malformation of the lip', 'XPO:0101634', 'abnormal head morphology', 0.40384615384615385, 4.5318002188002176, 1.3528303989641963, 'UPHENO:0087907', 'abnormal head morphology'),
(473015, 'HP:0031488', 'Arteriovenous malformation of the lip', 'XPO:0101464', 'abnormal oral cavity', 0.4107142857142857, 7.0866363731414825, 1.7060430229369012, 'HP:0000153', 'Abnormality of the mouth'),
(473016, 'HP:0031488', 'Arteriovenous malformation of the lip', 'XPO:0102522', 'abnormal pharyngeal cavity morphology', 0.4117647058823529, 5.725717590856133, 1.5354635846428564, 'UPHENO:0076803', 'abnormal digestive system morphology'),
(473017, 'HP:0031488', 'Arteriovenous malformation of the lip', 'XPO:0140897', 'abnormally necrotic lower jaw', 0.44155844155844154, 7.312692920701687, 1.7969366404134801, 'UPHENO:0076800', 'abnormal mouth morphology'),
(473018, 'HP:0031488', 'Arteriovenous malformation of the lip', 'XPO:0131651', 'abnormal roof of mouth', 0.40350877192982454, 7.0866363731414825, 1.6910115138695967, 'HP:0000153', 'Abnormality of the mouth'),
(473019, 'HP:0031488', 'Arteriovenous malformation of the lip', 'XPO:0130701', 'increased size of the upper jaw', 0.41975308641975306, 7.312692920701687, 1.752006114003148, 'UPHENO:0076800', 'abnormal mouth morphology'),
(473020, 'HP:0031488', 'Arteriovenous malformation of the lip', 'XPO:0100647', 'abnormal mouth', 0.41818181818181815, 7.0866363731414825, 1.721482641014341, 'HP:0000153', 'Abnormality of the mouth'),
(473021, 'HP:0031488', 'Arteriovenous malformation of the lip', 'XPO:0129225', 'decreased size of the upper jaw', 0.41975308641975306, 7.312692920701687, 1.752006114003148, 'UPHENO:0076800', 'abnormal mouth morphology'),
(473022, 'HP:0031488', 'Arteriovenous malformation of the lip', 'XPO:0115558', 'abnormally incomplete structure of mouth', 0.559322033898305, 7.312692920701687, 2.022411995039736, 'UPHENO:0076800', 'abnormal mouth morphology'),
(473023, 'HP:0031488', 'Arteriovenous malformation of the lip', 'XPO:0139736', 'abnormally necrotic tooth', 0.4117647058823529, 7.884497199543557, 1.8018206543383524, 'UPHENO:0076786', 'abnormal oral cavity morphology'),
(473024, 'HP:0031488', 'Arteriovenous malformation of the lip', 'XPO:0101816', 'abnormal tooth morphology', 0.45454545454545453, 7.884497199543557, 1.8931091789510952, 'UPHENO:0076786', 'abnormal oral cavity morphology'),
(473025, 'HP:0031488', 'Arteriovenous malformation of the lip', 'XPO:0127750', 'abnormally localised tongue', 0.532258064516129, 7.884497199543557, 2.0485573507011936, 'UPHENO:0076786', 'abnormal oral cavity morphology'),
(473026, 'HP:0031488', 'Arteriovenous malformation of the lip', 'XPO:0102525', 'abnormal hyoid arch morphology', 0.4426229508196721, 5.725717590856133, 1.5919591752381232, 'UPHENO:0076803', 'abnormal digestive system morphology'),
(473027, 'HP:0031488', 'Arteriovenous malformation of the lip', 'XPO:0141830', 'increased width of mouth', 0.4861111111111111, 7.884497199543557, 1.9577389239177327, 'UPHENO:0076786', 'abnormal oral cavity morphology'),
(473028, 'HP:0031488', 'Arteriovenous malformation of the lip', 'XPO:0102204', 'abnormal branchial arch morphology', 0.45, 5.725717590856133, 1.6051706812315194, 'UPHENO:0076803', 'abnormal digestive system morphology'),
(473029, 'HP:0031488', 'Arteriovenous malformation of the lip', 'XPO:0140789', 'abnormally necrotic roof of mouth', 0.5, 7.312692920701687, 1.9121575406725366, 'UPHENO:0076800', 'abnormal mouth morphology'),
(473030, 'HP:0031488', 'Arteriovenous malformation of the lip', 'XPO:0101483', 'abnormal nostril', 0.41379310344827586, 5.788671267106304, 1.5476796336638217, 'UPHENO:0087472', 'abnormal face morphology'),
(473031, 'HP:0031488', 'Arteriovenous malformation of the lip', 'XPO:0129585', 'increased size of the tongue', 0.4605263157894737, 7.884497199543557, 1.9055231426456665, 'UPHENO:0076786', 'abnormal oral cavity morphology'),
(473032, 'HP:0031488', 'Arteriovenous malformation of the lip', 'XPO:0140626', 'abnormally necrotic tongue', 0.5555555555555556, 7.884497199543557, 2.0929109445861864, 'UPHENO:0076786', 'abnormal oral cavity morphology'),
(473033, 'HP:0031488', 'Arteriovenous malformation of the lip', 'XPO:0115392', 'abnormally incomplete structure of alimentary system', 0.40384615384615385, 5.725717590856133, 1.520627839767678, 'UPHENO:0076803', 'abnormal digestive system morphology'),
(473034, 'HP:0031488', 'Arteriovenous malformation of the lip', 'XPO:0139987', 'abnormally necrotic branchial arch', 0.4090909090909091, 5.725717590856133, 1.5304701939081158, 'UPHENO:0076803', 'abnormal digestive system morphology'),
(473035, 'HP:0031488', 'Arteriovenous malformation of the lip', 'XPO:0102259', 'abnormal pharyngeal region morphology', 0.4117647058823529, 4.5318002188002176, 1.3660290568695288, 'UPHENO:0087907', 'abnormal head morphology'),
(473036, 'HP:0031488', 'Arteriovenous malformation of the lip', 'XPO:0128653', 'decreased size of the oral epithelium', 0.4342105263157895, 7.312692920701687, 1.7819226251113227, 'UPHENO:0076800', 'abnormal mouth morphology'),
(473037, 'HP:0031488', 'Arteriovenous malformation of the lip', 'XPO:0103199', 'abnormal tongue morphology', 0.603448275862069, 7.884497199543557, 2.181257949235686, 'UPHENO:0076786', 'abnormal oral cavity morphology'),
(473038, 'HP:0031488', 'Arteriovenous malformation of the lip', 'XPO:0103352', 'decreased size of the mouth', 0.5223880597014925, 7.884497199543557, 2.0294746102849897, 'UPHENO:0076786', 'abnormal oral cavity morphology'),
(473039, 'HP:0031488', 'Arteriovenous malformation of the lip', 'XPO:0103828', 'decreased width of the mouth', 0.4861111111111111, 7.884497199543557, 1.9577389239177327, 'UPHENO:0076786', 'abnormal oral cavity morphology'),
(473040, 'HP:0031488', 'Arteriovenous malformation of the lip', 'XPO:0101784', 'abnormal alimentary system morphology', 0.4117647058823529, 5.725717590856133, 1.5354635846428564, 'UPHENO:0076803', 'abnormal digestive system morphology'),
(473041, 'HP:0031488', 'Arteriovenous malformation of the lip', 'XPO:0101659', 'abnormal lower jaw morphology', 0.4722222222222222, 7.312692920701687, 1.8582831058378761, 'UPHENO:0076800', 'abnormal mouth morphology'),
(473042, 'HP:0031488', 'Arteriovenous malformation of the lip', 'XPO:0103357', 'decreased size of the pharyngeal arch', 0.4090909090909091, 5.725717590856133, 1.5304701939081158, 'UPHENO:0076803', 'abnormal digestive system morphology'),
(473043, 'HP:0031488', 'Arteriovenous malformation of the lip', 'XPO:0102223', 'abnormal pharyngeal arch morphology', 0.46551724137931033, 5.725717590856133, 1.6326114840378705, 'UPHENO:0076803', 'abnormal digestive system morphology'),
(473044, 'HP:0031488', 'Arteriovenous malformation of the lip', 'XPO:0102960', 'abnormal oral epithelium morphology', 0.4925373134328358, 7.312692920701687, 1.8978340615348135, 'UPHENO:0076800', 'abnormal mouth morphology'),
(473045, 'HP:0031488', 'Arteriovenous malformation of the lip', 'XPO:0102261', 'abnormal branchial arch 2 morphology', 0.42857142857142855, 5.725717590856133, 1.5664861849086864, 'UPHENO:0076803', 'abnormal digestive system morphology'),
(473046, 'HP:0031488', 'Arteriovenous malformation of the lip', 'XPO:0102420', 'abnormal branchial arch 4 morphology', 0.42857142857142855, 5.725717590856133, 1.5664861849086864, 'UPHENO:0076803', 'abnormal digestive system morphology'),
(473047, 'HP:0031488', 'Arteriovenous malformation of the lip', 'XPO:0129152', 'decreased size of the oral cavity', 0.5555555555555556, 7.884497199543557, 2.0929109445861864, 'UPHENO:0076786', 'abnormal oral cavity morphology'),
(473048, 'HP:0031488', 'Arteriovenous malformation of the lip', 'XPO:0126089', 'absent tongue', 0.515625, 7.884497199543557, 2.016294588723247, 'UPHENO:0076786', 'abnormal oral cavity morphology'),
(473049, 'HP:0031488', 'Arteriovenous malformation of the lip', 'XPO:0130358', 'increased size of the lower jaw', 0.43037974683544306, 7.312692920701687, 1.7740447930920258, 'UPHENO:0076800', 'abnormal mouth morphology'),
(473050, 'HP:0031488', 'Arteriovenous malformation of the lip', 'XPO:0131573', 'decreased size of the roof of mouth', 0.4852941176470588, 7.312692920701687, 1.8838277146745184, 'UPHENO:0076800', 'abnormal mouth morphology'),
(473051, 'HP:0031488', 'Arteriovenous malformation of the lip', 'XPO:0141311', 'abnormal roof of mouth morphology', 0.5409836065573771, 7.312692920701687, 1.9889813950582338, 'UPHENO:0076800', 'abnormal mouth morphology'),
(473052, 'HP:0031488', 'Arteriovenous malformation of the lip', 'XPO:0140639', 'abnormally necrotic upper jaw', 0.43037974683544306, 7.312692920701687, 1.7740447930920258, 'UPHENO:0076800', 'abnormal mouth morphology'),
(473053, 'HP:0031488', 'Arteriovenous malformation of the lip', 'XPO:0102735', 'abnormal pharyngeal mesenchyme morphology', 0.43548387096774194, 5.725717590856133, 1.5790686053918375, 'UPHENO:0076803', 'abnormal digestive system morphology'),
(473054, 'HP:0031488', 'Arteriovenous malformation of the lip', 'XPO:0115393', 'abnormally decreased volume of oral cavity', 0.5384615384615384, 7.884497199543557, 2.060460747517874, 'UPHENO:0076786', 'abnormal oral cavity morphology'),
(473055, 'HP:0031488', 'Arteriovenous malformation of the lip', 'XPO:0102861', 'abnormal cementum morphology', 0.4069767441860465, 7.884497199543557, 1.791314321891677, 'UPHENO:0076786', 'abnormal oral cavity morphology'),
(473056, 'HP:0031488', 'Arteriovenous malformation of the lip', 'XPO:0128105', 'decreased size of the tongue', 0.49295774647887325, 7.884497199543557, 1.971477611236298, 'UPHENO:0076786', 'abnormal oral cavity morphology'),
(473057, 'HP:0031488', 'Arteriovenous malformation of the lip', 'XPO:0103735', 'increased size of the mouth', 0.5223880597014925, 7.884497199543557, 2.0294746102849897, 'UPHENO:0076786', 'abnormal oral cavity morphology'),
(473058, 'HP:0031488', 'Arteriovenous malformation of the lip', 'XPO:0130628', 'increased size of the oral cavity', 0.5555555555555556, 7.884497199543557, 2.0929109445861864, 'UPHENO:0076786', 'abnormal oral cavity morphology'),
(473059, 'HP:0031488', 'Arteriovenous malformation of the lip', 'XPO:0102445', 'abnormal branchial arch 3 morphology', 0.43548387096774194, 5.725717590856133, 1.5790686053918375, 'UPHENO:0076803', 'abnormal digestive system morphology'),
(473060, 'HP:0031488', 'Arteriovenous malformation of the lip', 'XPO:0103138', 'abnormal upper jaw morphology', 0.4594594594594595, 7.312692920701687, 1.8329991643584056, 'UPHENO:0076800', 'abnormal mouth morphology'),
(473061, 'HP:0031488', 'Arteriovenous malformation of the lip', 'XPO:0128880', 'decreased size of the lower jaw', 0.43037974683544306, 7.312692920701687, 1.7740447930920258, 'UPHENO:0076800', 'abnormal mouth morphology'),
(473062, 'HP:0031488', 'Arteriovenous malformation of the lip', 'XPO:0131611', 'increased size of the roof of mouth', 0.4852941176470588, 7.312692920701687, 1.8838277146745184, 'UPHENO:0076800', 'abnormal mouth morphology'),
(473063, 'HP:0031488', 'Arteriovenous malformation of the lip', 'XPO:0103096', 'abnormal oral cavity morphology', 0.603448275862069, 7.884497199543557, 2.181257949235686, 'UPHENO:0076786', 'abnormal oral cavity morphology'),
(473064, 'HP:0031488', 'Arteriovenous malformation of the lip', 'XPO:0102203', 'abnormal branchial arch 1 morphology', 0.42857142857142855, 5.725717590856133, 1.5664861849086864, 'UPHENO:0076803', 'abnormal digestive system morphology'),
(473065, 'HP:0031488', 'Arteriovenous malformation of the lip', 'XPO:0139863', 'abnormally necrotic pharyngeal arch', 0.42857142857142855, 5.725717590856133, 1.5664861849086864, 'UPHENO:0076803', 'abnormal digestive system morphology'),
(473066, 'HP:0031488', 'Arteriovenous malformation of the lip', 'XPO:0102279', 'abnormal mouth morphology', 0.5689655172413793, 7.312692920701687, 2.039772073064637, 'UPHENO:0076800', 'abnormal mouth morphology'),
(473067, 'HP:0031488', 'Arteriovenous malformation of the lip', 'XPO:0141009', 'abnormally necrotic oral epithelium', 0.44594594594594594, 7.312692920701687, 1.8058421198805104, 'UPHENO:0076800', 'abnormal mouth morphology'),
(473068, 'HP:0031488', 'Arteriovenous malformation of the lip', 'XPO:0103738', 'increased size of the pharyngeal arch', 0.4090909090909091, 5.725717590856133, 1.5304701939081158, 'UPHENO:0076803', 'abnormal digestive system morphology'),
(473069, 'HP:0025231', 'Abnormal synovial bursa morphology', 'XPO:0100969', 'abnormal disaggregated/reaggregated ectoderm treated with activin', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(473070, 'HP:0025231', 'Abnormal synovial bursa morphology', 'XPO:0102761', 'abnormal cartilaginous condensation morphology', 0.40476190476190477, 4.638757693672553, 1.3702526773627712, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(473071, 'HP:0025231', 'Abnormal synovial bursa morphology', 'XPO:0100350', 'abnormal appendicular skeleton', 0.4827586206896552, 4.3395673355180735, 1.4473988881039626, 'UPHENO:0002964', 'abnormal skeletal system'),
(473072, 'HP:0025231', 'Abnormal synovial bursa morphology', 'XPO:0100386', 'abnormal limb', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(473073, 'HP:0025231', 'Abnormal synovial bursa morphology', 'XPO:0100176', 'abnormal stage VI oocyte', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(473074, 'HP:0025231', 'Abnormal synovial bursa morphology', 'XPO:0128158', 'decreased size of the skeletal subdivision', 0.40476190476190477, 4.638757693672553, 1.3702526773627712, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(473075, 'HP:0025231', 'Abnormal synovial bursa morphology', 'XPO:0140432', 'abnormally necrotic skeleton', 0.4358974358974359, 4.638757693672553, 1.421978405047478, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(473076, 'HP:0025231', 'Abnormal synovial bursa morphology', 'XPO:0100545', 'abnormal male organism', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(473077, 'HP:0025231', 'Abnormal synovial bursa morphology', 'XPO:0100829', 'abnormal postcranial axial skeleton', 0.4666666666666667, 4.3395673355180735, 1.4230711237467255, 'UPHENO:0002964', 'abnormal skeletal system'),
(473078, 'HP:0025231', 'Abnormal synovial bursa morphology', 'XPO:0101020', 'abnormal subocular cartilage', 0.4117647058823529, 4.3395673355180735, 1.3367425584480601, 'UPHENO:0002964', 'abnormal skeletal system'),
(473079, 'HP:0025231', 'Abnormal synovial bursa morphology', 'XPO:0100724', 'abnormal kinetochore', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(473080, 'HP:0025231', 'Abnormal synovial bursa morphology', 'XPO:0102567', 'abnormal skeleton morphology', 0.5, 4.638757693672553, 1.5229507040072823, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(473081, 'HP:0025231', 'Abnormal synovial bursa morphology', 'XPO:0100416', 'abnormal ligament', 0.42857142857142855, 3.9037819259951223, 1.293464107292913, 'HP:0033127', 'Abnormality of the musculoskeletal system'),
(473082, 'HP:0025231', 'Abnormal synovial bursa morphology', 'XPO:0140683', 'abnormally necrotic flexural organ', 0.4358974358974359, 4.638757693672553, 1.421978405047478, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(473083, 'HP:0025231', 'Abnormal synovial bursa morphology', 'XPO:0101373', 'abnormal oxygen accumulating cell', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(473084, 'HP:0025231', 'Abnormal synovial bursa morphology', 'XPO:0100802', 'abnormal exocrine cell', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(473085, 'HP:0025231', 'Abnormal synovial bursa morphology', 'XPO:0100754', 'abnormal electrically active cell', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(473086, 'HP:0025231', 'Abnormal synovial bursa morphology', 'XPO:0103116', 'abnormal bone marrow morphology', 0.4146341463414634, 4.638757693672553, 1.3868624071625903, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(473087, 'HP:0025231', 'Abnormal synovial bursa morphology', 'XPO:0100307', 'abnormal blastomere', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(473088, 'HP:0025231', 'Abnormal synovial bursa morphology', 'XPO:0131677', 'abnormal actin filament', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(473089, 'HP:0025231', 'Abnormal synovial bursa morphology', 'XPO:0100581', 'abnormal immune system', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(473090, 'HP:0025231', 'Abnormal synovial bursa morphology', 'XPO:0100232', 'abnormal lymphatic system', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(473091, 'HP:0025231', 'Abnormal synovial bursa morphology', 'XPO:0102113', 'abnormal anatomical line morphology', 0.4166666666666667, 2.485033483301678, 1.0175611126818702, 'UPHENO:0076692', 'abnormal anatomical entity morphology'),
(473092, 'HP:0025231', 'Abnormal synovial bursa morphology', 'XPO:0100532', 'abnormal mandibular mesenchyme', 0.4117647058823529, 4.3395673355180735, 1.3367425584480601, 'UPHENO:0002964', 'abnormal skeletal system'),
(473093, 'HP:0025231', 'Abnormal synovial bursa morphology', 'XPO:0115505', 'dead whole organism', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(473094, 'HP:0025231', 'Abnormal synovial bursa morphology', 'XPO:0102806', 'abnormal articular system morphology', 0.5151515151515151, 4.638757693672553, 1.545853503510654, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(473095, 'HP:0025231', 'Abnormal synovial bursa morphology', 'XPO:0102728', 'abnormal tendon morphology', 0.425, 4.638757693672553, 1.404091172186064, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(473096, 'HP:0025231', 'Abnormal synovial bursa morphology', 'XPO:0100025', 'abnormal oocyte', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(473097, 'HP:0025231', 'Abnormal synovial bursa morphology', 'XPO:0100533', 'abnormal melanoblast', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(473098, 'HP:0025231', 'Abnormal synovial bursa morphology', 'XPO:0101237', 'abnormal mucus secreting cell', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(473099, 'HP:0025231', 'Abnormal synovial bursa morphology', 'XPO:0100852', 'abnormal interdigital region', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(473100, 'HP:0025231', 'Abnormal synovial bursa morphology', 'XPO:0101713', 'abnormal anatomical entity in vitro morphology', 0.4166666666666667, 2.485033483301678, 1.0175611126818702, 'UPHENO:0076692', 'abnormal anatomical entity morphology'),
(473101, 'HP:0025231', 'Abnormal synovial bursa morphology', 'XPO:0102097', 'abnormal skeletal system morphology', 0.53125, 4.638757693672553, 1.5698216538077006, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(473102, 'HP:0025231', 'Abnormal synovial bursa morphology', 'XPO:0140350', 'abnormally necrotic notochordal sheath', 0.4358974358974359, 4.638757693672553, 1.421978405047478, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(473103, 'HP:0025231', 'Abnormal synovial bursa morphology', 'XPO:0100515', 'abnormal somatic stem cell', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(473104, 'HP:0025231', 'Abnormal synovial bursa morphology', 'XPO:0128890', 'decreased size of the elastica externa', 0.4358974358974359, 4.638757693672553, 1.421978405047478, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(473105, 'HP:0025231', 'Abnormal synovial bursa morphology', 'XPO:0100791', 'abnormal multiciliated cell precursor', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(473106, 'HP:0025231', 'Abnormal synovial bursa morphology', 'XPO:0101467', 'abnormal alkali secreting cell', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(473107, 'HP:0025231', 'Abnormal synovial bursa morphology', 'XPO:0101461', 'abnormal sperm entry point', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(473108, 'HP:0025231', 'Abnormal synovial bursa morphology', 'XPO:0101241', 'abnormal nucleate erythrocyte', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(473109, 'HP:0025231', 'Abnormal synovial bursa morphology', 'XPO:0102217', 'abnormal elastica externa morphology', 0.53125, 4.638757693672553, 1.5698216538077006, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(473110, 'HP:0025231', 'Abnormal synovial bursa morphology', 'XPO:0100512', 'abnormal cranial skeleton', 0.4666666666666667, 4.3395673355180735, 1.4230711237467255, 'UPHENO:0002964', 'abnormal skeletal system'),
(473111, 'HP:0025231', 'Abnormal synovial bursa morphology', 'XPO:0100899', 'abnormal secondary spermatogonium', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(473112, 'HP:0025231', 'Abnormal synovial bursa morphology', 'XPO:0101174', 'abnormal articular system', 0.5384615384615384, 4.3395673355180735, 1.5286235977965605, 'UPHENO:0002964', 'abnormal skeletal system'),
(473113, 'HP:0025231', 'Abnormal synovial bursa morphology', 'XPO:0141315', 'abnormal anatomical region', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(473114, 'HP:0025231', 'Abnormal synovial bursa morphology', 'XPO:0101860', 'abnormal skeletal subdivision morphology', 0.4857142857142857, 4.638757693672553, 1.5010366017468766, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(473115, 'HP:0025231', 'Abnormal synovial bursa morphology', 'XPO:0100976', 'abnormal multiciliated cell', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(473116, 'HP:0025231', 'Abnormal synovial bursa morphology', 'XPO:0101110', 'abnormal cell-free extract', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(473117, 'HP:0025231', 'Abnormal synovial bursa morphology', 'XPO:0102054', 'abnormal notochord morphology', 0.5, 4.638757693672553, 1.5229507040072823, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(473118, 'HP:0025231', 'Abnormal synovial bursa morphology', 'XPO:0100477', 'abnormal pericyte', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(473119, 'HP:0025231', 'Abnormal synovial bursa morphology', 'XPO:0101547', 'abnormal lampbrush chromosome', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(473120, 'HP:0025231', 'Abnormal synovial bursa morphology', 'XPO:0101976', 'abnormal portion of organism substance morphology', 0.4166666666666667, 2.485033483301678, 1.0175611126818702, 'UPHENO:0076692', 'abnormal anatomical entity morphology'),
(473121, 'HP:0025231', 'Abnormal synovial bursa morphology', 'XPO:0128306', 'decreased size of the articular system', 0.425, 4.638757693672553, 1.404091172186064, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(473122, 'HP:0025231', 'Abnormal synovial bursa morphology', 'XPO:0100688', 'abnormal adipose tissue', 0.4444444444444444, 3.9037819259951223, 1.3171993734173904, 'HP:0033127', 'Abnormality of the musculoskeletal system'),
(473123, 'HP:0025231', 'Abnormal synovial bursa morphology', 'XPO:0126722', 'abnormally localised elastica externa', 0.4117647058823529, 4.3395673355180735, 1.3367425584480601, 'UPHENO:0002964', 'abnormal skeletal system'),
(473124, 'HP:0025231', 'Abnormal synovial bursa morphology', 'XPO:0140019', 'abnormally necrotic skeletal system', 0.4594594594594595, 4.638757693672553, 1.4599044840325002, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(473125, 'HP:0025231', 'Abnormal synovial bursa morphology', 'XPO:0100178', 'abnormal digit', 0.4146341463414634, 4.638757693672553, 1.3868624071625903, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(473126, 'HP:0025231', 'Abnormal synovial bursa morphology', 'XPO:0101535', 'abnormal absorptive cell', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(473127, 'HP:0025231', 'Abnormal synovial bursa morphology', 'XPO:0100546', 'abnormal whole organism', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(473128, 'HP:0025231', 'Abnormal synovial bursa morphology', 'XPO:0100423', 'abnormal process', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(473129, 'HP:0025231', 'Abnormal synovial bursa morphology', 'XPO:0107284', 'abnormal migrating myoblast', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(473130, 'HP:0025231', 'Abnormal synovial bursa morphology', 'XPO:0100289', 'abnormal chondroblast', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(473131, 'HP:0025231', 'Abnormal synovial bursa morphology', 'XPO:0100377', 'abnormal connective tissue', 0.46153846153846156, 3.9037819259951223, 1.3422911399191462, 'HP:0033127', 'Abnormality of the musculoskeletal system'),
(473132, 'HP:0025231', 'Abnormal synovial bursa morphology', 'XPO:0100239', 'abnormal acellular anatomical structure', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(473133, 'HP:0025231', 'Abnormal synovial bursa morphology', 'XPO:0107259', 'abnormal animal-vegetal axis', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(473134, 'HP:0025231', 'Abnormal synovial bursa morphology', 'XPO:0128709', 'decreased size of the flexural organ', 0.4146341463414634, 4.638757693672553, 1.3868624071625903, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(473135, 'HP:0025231', 'Abnormal synovial bursa morphology', 'XPO:0100715', 'abnormal ciliated cell', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(473136, 'HP:0025231', 'Abnormal synovial bursa morphology', 'XPO:0101638', 'abnormal anatomical structure morphology', 0.4166666666666667, 2.485033483301678, 1.0175611126818702, 'UPHENO:0076692', 'abnormal anatomical entity morphology'),
(473137, 'HP:0025231', 'Abnormal synovial bursa morphology', 'XPO:0141713', 'increased size of the posterior notochord', 0.4146341463414634, 4.638757693672553, 1.3868624071625903, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(473138, 'HP:0025231', 'Abnormal synovial bursa morphology', 'XPO:0140043', 'abnormally necrotic perichondrium', 0.4146341463414634, 4.638757693672553, 1.3868624071625903, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(473139, 'HP:0025231', 'Abnormal synovial bursa morphology', 'XPO:0100973', 'abnormal dermal skeleton', 0.4827586206896552, 4.3395673355180735, 1.4473988881039626, 'UPHENO:0002964', 'abnormal skeletal system'),
(473140, 'HP:0025231', 'Abnormal synovial bursa morphology', 'XPO:0131667', 'abnormal actin cytoskeleton', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(473141, 'HP:0025231', 'Abnormal synovial bursa morphology', 'XPO:0101096', 'abnormal tendon', 0.42857142857142855, 3.9037819259951223, 1.293464107292913, 'HP:0033127', 'Abnormality of the musculoskeletal system'),
(473142, 'HP:0025231', 'Abnormal synovial bursa morphology', 'XPO:0100481', 'abnormal anatomical line', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(473143, 'HP:0025231', 'Abnormal synovial bursa morphology', 'XPO:0130188', 'increased size of the flexural organ', 0.4146341463414634, 4.638757693672553, 1.3868624071625903, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(473144, 'HP:0025231', 'Abnormal synovial bursa morphology', 'XPO:0103737', 'increased size of the notochord', 0.40476190476190477, 4.638757693672553, 1.3702526773627712, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(473145, 'HP:0025231', 'Abnormal synovial bursa morphology', 'XPO:0102461', 'abnormal postcranial axial skeleton morphology', 0.4146341463414634, 4.638757693672553, 1.3868624071625903, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(473146, 'HP:0025231', 'Abnormal synovial bursa morphology', 'XPO:0100344', 'abnormal portion of organism substance', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(473147, 'HP:0025231', 'Abnormal synovial bursa morphology', 'XPO:0100372', 'abnormal hematological system', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(473148, 'HP:0025231', 'Abnormal synovial bursa morphology', 'XPO:0100378', 'abnormal perichondrium', 0.5185185185185185, 4.3395673355180735, 1.5000486744849937, 'UPHENO:0002964', 'abnormal skeletal system'),
(473149, 'HP:0025231', 'Abnormal synovial bursa morphology', 'XPO:0141709', 'increased size of the anterior notochord', 0.4146341463414634, 4.638757693672553, 1.3868624071625903, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(473150, 'HP:0025231', 'Abnormal synovial bursa morphology', 'XPO:0100172', 'abnormal stem cell', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(473151, 'HP:0025231', 'Abnormal synovial bursa morphology', 'XPO:0100894', 'abnormal nucleus', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(473152, 'HP:0025231', 'Abnormal synovial bursa morphology', 'XPO:0101326', 'abnormal cementoblast', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(473153, 'HP:0025231', 'Abnormal synovial bursa morphology', 'XPO:0141499', 'abnormal tadpole', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(473154, 'HP:0025231', 'Abnormal synovial bursa morphology', 'XPO:0129638', 'increased size of the skeletal subdivision', 0.40476190476190477, 4.638757693672553, 1.3702526773627712, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(473155, 'HP:0025231', 'Abnormal synovial bursa morphology', 'XPO:0129786', 'increased size of the articular system', 0.425, 4.638757693672553, 1.404091172186064, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(473156, 'HP:0025231', 'Abnormal synovial bursa morphology', 'XPO:0101141', 'abnormal Keller explant', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(473157, 'HP:0025231', 'Abnormal synovial bursa morphology', 'XPO:0107285', 'abnormal flexural organ', 0.5384615384615384, 4.3395673355180735, 1.5286235977965605, 'UPHENO:0002964', 'abnormal skeletal system'),
(473158, 'HP:0025231', 'Abnormal synovial bursa morphology', 'XPO:0100902', 'abnormal spermatocyte', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(473159, 'HP:0025231', 'Abnormal synovial bursa morphology', 'XPO:0100285', 'abnormal progenitor cell', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(473160, 'HP:0025231', 'Abnormal synovial bursa morphology', 'XPO:0101157', 'abnormal female organism', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(473161, 'HP:0025231', 'Abnormal synovial bursa morphology', 'XPO:0115508', 'abnormally peramorphic growth of whole organism', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(473162, 'HP:0025231', 'Abnormal synovial bursa morphology', 'XPO:0107258', 'abnormal anatomical axis', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(473163, 'HP:0025231', 'Abnormal synovial bursa morphology', 'XPO:0100585', 'abnormal elastica externa', 0.5833333333333334, 4.3395673355180735, 1.5910418847573466, 'UPHENO:0002964', 'abnormal skeletal system'),
(473164, 'HP:0025231', 'Abnormal synovial bursa morphology', 'XPO:0100653', 'abnormal myoblast', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(473165, 'HP:0025231', 'Abnormal synovial bursa morphology', 'XPO:0101071', 'abnormal endoplasmic reticulum', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(473166, 'HP:0025231', 'Abnormal synovial bursa morphology', 'XPO:0100123', 'abnormal pelvic girdle', 0.4666666666666667, 4.3395673355180735, 1.4230711237467255, 'UPHENO:0002964', 'abnormal skeletal system'),
(473167, 'HP:0025231', 'Abnormal synovial bursa morphology', 'XPO:0100888', 'abnormal microtubule', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(473168, 'HP:0025231', 'Abnormal synovial bursa morphology', 'XPO:0141704', 'decreased size of the anterior notochord', 0.4146341463414634, 4.638757693672553, 1.3868624071625903, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(473169, 'HP:0025231', 'Abnormal synovial bursa morphology', 'XPO:0100392', 'abnormal cilium', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(473170, 'HP:0025231', 'Abnormal synovial bursa morphology', 'XPO:0129832', 'increased size of the skeletal system', 0.4358974358974359, 4.638757693672553, 1.421978405047478, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(473171, 'HP:0025231', 'Abnormal synovial bursa morphology', 'XPO:0102130', 'abnormal endoskeleton morphology', 0.4594594594594595, 4.638757693672553, 1.4599044840325002, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(473172, 'HP:0025231', 'Abnormal synovial bursa morphology', 'XPO:0100674', 'abnormal secondary oogonium', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(473173, 'HP:0025231', 'Abnormal synovial bursa morphology', 'XPO:0130368', 'increased size of the elastica externa', 0.4358974358974359, 4.638757693672553, 1.421978405047478, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(473174, 'HP:0025231', 'Abnormal synovial bursa morphology', 'XPO:0101569', 'abnormal activin-induced ectoderm', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(473175, 'HP:0025231', 'Abnormal synovial bursa morphology', 'XPO:0101435', 'abnormal paracrine cell', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(473176, 'HP:0025231', 'Abnormal synovial bursa morphology', 'XPO:0101586', 'abnormal joint', 0.4666666666666667, 4.3395673355180735, 1.4230711237467255, 'UPHENO:0002964', 'abnormal skeletal system'),
(473177, 'HP:0025231', 'Abnormal synovial bursa morphology', 'XPO:0101480', 'abnormal stage V oocyte', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(473178, 'HP:0025231', 'Abnormal synovial bursa morphology', 'XPO:0107372', 'abnormal flexural organ morphology', 0.5, 4.638757693672553, 1.5229507040072823, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(473179, 'HP:0025231', 'Abnormal synovial bursa morphology', 'XPO:0100417', 'abnormal dense regular connective tissue', 0.4444444444444444, 3.9037819259951223, 1.3171993734173904, 'HP:0033127', 'Abnormality of the musculoskeletal system'),
(473180, 'HP:0025231', 'Abnormal synovial bursa morphology', 'XPO:0100222', 'abnormal bone element', 0.42424242424242425, 4.3395673355180735, 1.3568450783281876, 'UPHENO:0002964', 'abnormal skeletal system'),
(473181, 'HP:0025231', 'Abnormal synovial bursa morphology', 'XPO:0101228', 'abnormal mesenchymal stem cell', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(473182, 'HP:0025231', 'Abnormal synovial bursa morphology', 'XPO:0141718', 'abnormal posterior notochord', 0.5384615384615384, 4.3395673355180735, 1.5286235977965605, 'UPHENO:0002964', 'abnormal skeletal system'),
(473183, 'HP:0025231', 'Abnormal synovial bursa morphology', 'XPO:0100325', 'abnormal axial skeleton', 0.4827586206896552, 4.3395673355180735, 1.4473988881039626, 'UPHENO:0002964', 'abnormal skeletal system'),
(473184, 'HP:0025231', 'Abnormal synovial bursa morphology', 'XPO:0100429', 'abnormal spermatid', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(473185, 'HP:0025231', 'Abnormal synovial bursa morphology', 'XPO:0100031', 'abnormal central nervous system', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(473186, 'HP:0025231', 'Abnormal synovial bursa morphology', 'XPO:0140559', 'abnormally necrotic articular system', 0.4473684210526316, 4.638757693672553, 1.4405671470167702, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(473187, 'HP:0025231', 'Abnormal synovial bursa morphology', 'XPO:0102093', 'abnormal craniofacial skeleton morphology', 0.4146341463414634, 4.638757693672553, 1.3868624071625903, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(473188, 'HP:0025231', 'Abnormal synovial bursa morphology', 'XPO:0101468', 'abnormal stage I oocyte', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(473189, 'HP:0025231', 'Abnormal synovial bursa morphology', 'XPO:0131685', 'abnormal cortical actin cytoskeleton', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(473190, 'HP:0025231', 'Abnormal synovial bursa morphology', 'XPO:0129434', 'decreased size of the notochordal sheath', 0.4146341463414634, 4.638757693672553, 1.3868624071625903, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(473191, 'HP:0025231', 'Abnormal synovial bursa morphology', 'XPO:0101484', 'abnormal bone marrow', 0.45161290322580644, 4.3395673355180735, 1.399930213666808, 'UPHENO:0002964', 'abnormal skeletal system'),
(473192, 'HP:0025231', 'Abnormal synovial bursa morphology', 'XPO:0103218', 'abnormal joint morphology', 0.425, 4.638757693672553, 1.404091172186064, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(473193, 'HP:0025231', 'Abnormal synovial bursa morphology', 'XPO:0100317', 'abnormal respiratory system', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(473194, 'HP:0025231', 'Abnormal synovial bursa morphology', 'XPO:0101448', 'abnormal myelin accumulating cell', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(473195, 'HP:0025231', 'Abnormal synovial bursa morphology', 'XPO:0100228', 'abnormal skeletal subdivision', 0.5, 4.3395673355180735, 1.473018556488355, 'UPHENO:0002964', 'abnormal skeletal system'),
(473196, 'HP:0025231', 'Abnormal synovial bursa morphology', 'XPO:0100437', 'abnormal proepicardium', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(473197, 'HP:0025231', 'Abnormal synovial bursa morphology', 'XPO:0100349', 'abnormal ossicle', 0.42424242424242425, 4.3395673355180735, 1.3568450783281876, 'UPHENO:0002964', 'abnormal skeletal system'),
(473198, 'HP:0025231', 'Abnormal synovial bursa morphology', 'XPO:0102010', 'abnormal perichondrium morphology', 0.4857142857142857, 4.638757693672553, 1.5010366017468766, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(473199, 'HP:0025231', 'Abnormal synovial bursa morphology', 'XPO:0100584', 'abnormal vertebral column', 0.4358974358974359, 4.638757693672553, 1.421978405047478, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(473200, 'HP:0025231', 'Abnormal synovial bursa morphology', 'XPO:0100704', 'abnormal Merkel cell', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(473201, 'HP:0025231', 'Abnormal synovial bursa morphology', 'XPO:0100026', 'abnormal germ cell', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(473202, 'HP:0025231', 'Abnormal synovial bursa morphology', 'XPO:0100062', 'abnormal anatomical space', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(473203, 'HP:0025231', 'Abnormal synovial bursa morphology', 'XPO:0141703', 'abnormally necrotic posterior notochord', 0.4358974358974359, 4.638757693672553, 1.421978405047478, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(473204, 'HP:0025231', 'Abnormal synovial bursa morphology', 'XPO:0142057', 'abnormal desmosome', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(473205, 'HP:0025231', 'Abnormal synovial bursa morphology', 'XPO:0100465', 'abnormal skeletal system', 0.56, 4.3395673355180735, 1.5588963108206144, 'UPHENO:0002964', 'abnormal skeletal system'),
(473206, 'HP:0025231', 'Abnormal synovial bursa morphology', 'XPO:0107270', 'abnormal proximal-distal axis', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(473207, 'HP:0025231', 'Abnormal synovial bursa morphology', 'XPO:0100728', 'abnormal cell condensation', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(473208, 'HP:0025231', 'Abnormal synovial bursa morphology', 'XPO:0101297', 'abnormal barrier cell', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(473209, 'HP:0025231', 'Abnormal synovial bursa morphology', 'XPO:0101409', 'abnormal perivitelline space', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(473210, 'HP:0025231', 'Abnormal synovial bursa morphology', 'XPO:0107253', 'abnormal enteric nervous system', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(473211, 'HP:0025231', 'Abnormal synovial bursa morphology', 'XPO:0101513', 'abnormal basal body', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(473212, 'HP:0025231', 'Abnormal synovial bursa morphology', 'XPO:0107262', 'abnormal left-right axis', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(473213, 'HP:0025231', 'Abnormal synovial bursa morphology', 'XPO:0100574', 'abnormal gastrula cell', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(473214, 'HP:0025231', 'Abnormal synovial bursa morphology', 'XPO:0131666', 'abnormal adherens junction', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(473215, 'HP:0025231', 'Abnormal synovial bursa morphology', 'XPO:0115512', 'abnormally semi-erect whole organism', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(473216, 'HP:0025231', 'Abnormal synovial bursa morphology', 'XPO:0100422', 'abnormal notochord', 0.56, 4.3395673355180735, 1.5588963108206144, 'UPHENO:0002964', 'abnormal skeletal system'),
(473217, 'HP:0025231', 'Abnormal synovial bursa morphology', 'XPO:0100337', 'abnormal zygote', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(473218, 'HP:0025231', 'Abnormal synovial bursa morphology', 'XPO:0102542', 'abnormal vacuolated notochordal tissue morphology', 0.4473684210526316, 4.638757693672553, 1.4405671470167702, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(473219, 'HP:0025231', 'Abnormal synovial bursa morphology', 'XPO:0100274', 'abnormal sensory system', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(473220, 'HP:0025231', 'Abnormal synovial bursa morphology', 'XPO:0102980', 'abnormal perichordal tissue morphology', 0.4473684210526316, 4.638757693672553, 1.4405671470167702, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(473221, 'HP:0025231', 'Abnormal synovial bursa morphology', 'XPO:0141708', 'decreased size of the posterior notochord', 0.4146341463414634, 4.638757693672553, 1.3868624071625903, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(473222, 'HP:0025231', 'Abnormal synovial bursa morphology', 'XPO:0101109', 'abnormal egg cell-free extract', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(473223, 'HP:0025231', 'Abnormal synovial bursa morphology', 'XPO:0100638', 'abnormal polar body', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(473224, 'HP:0025231', 'Abnormal synovial bursa morphology', 'XPO:0100225', 'abnormal endocrine system', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(473225, 'HP:0025231', 'Abnormal synovial bursa morphology', 'XPO:0100047', 'abnormal cartilage element', 0.42424242424242425, 4.3395673355180735, 1.3568450783281876, 'UPHENO:0002964', 'abnormal skeletal system'),
(473226, 'HP:0025231', 'Abnormal synovial bursa morphology', 'XPO:0131675', 'abnormal spindle microtubule', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(473227, 'HP:0025231', 'Abnormal synovial bursa morphology', 'XPO:0100721', 'abnormal centromere', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(473228, 'HP:0025231', 'Abnormal synovial bursa morphology', 'XPO:0100258', 'abnormal organ part', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(473229, 'HP:0025231', 'Abnormal synovial bursa morphology', 'XPO:0101498', 'abnormal stage II oocyte', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(473230, 'HP:0025231', 'Abnormal synovial bursa morphology', 'XPO:0101982', 'abnormal appendicular skeleton morphology', 0.4358974358974359, 4.638757693672553, 1.421978405047478, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(473231, 'HP:0025231', 'Abnormal synovial bursa morphology', 'XPO:0101129', 'abnormal cartilaginous condensation', 0.4375, 4.3395673355180735, 1.3778826906849353, 'UPHENO:0002964', 'abnormal skeletal system'),
(473232, 'HP:0025231', 'Abnormal synovial bursa morphology', 'XPO:0128184', 'decreased size of the skeleton', 0.4146341463414634, 4.638757693672553, 1.3868624071625903, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(473233, 'HP:0025231', 'Abnormal synovial bursa morphology', 'XPO:0100108', 'abnormal cell part', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(473234, 'HP:0025231', 'Abnormal synovial bursa morphology', 'XPO:0115509', 'abnormally semi-viable whole organism', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(473235, 'HP:0025231', 'Abnormal synovial bursa morphology', 'XPO:0102272', 'abnormal notochordal sheath morphology', 0.5, 4.638757693672553, 1.5229507040072823, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(473236, 'HP:0025231', 'Abnormal synovial bursa morphology', 'XPO:0101680', 'abnormal skeletal element morphology', 0.4146341463414634, 4.638757693672553, 1.3868624071625903, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(473237, 'HP:0025231', 'Abnormal synovial bursa morphology', 'XPO:0139917', 'abnormally necrotic notochord', 0.425, 4.638757693672553, 1.404091172186064, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(473238, 'HP:0025231', 'Abnormal synovial bursa morphology', 'XPO:0100935', 'abnormal skeleton', 0.5185185185185185, 4.3395673355180735, 1.5000486744849937, 'UPHENO:0002964', 'abnormal skeletal system'),
(473239, 'HP:0025231', 'Abnormal synovial bursa morphology', 'XPO:0107312', 'abnormal filopodium', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(473240, 'HP:0025231', 'Abnormal synovial bursa morphology', 'XPO:0141723', 'abnormal posterior notochord morphology', 0.5, 4.638757693672553, 1.5229507040072823, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(473241, 'HP:0025231', 'Abnormal synovial bursa morphology', 'XPO:0100573', 'abnormal extraembryonic structure', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(473242, 'HP:0025231', 'Abnormal synovial bursa morphology', 'XPO:0100084', 'abnormal anatomical group', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(473243, 'HP:0025231', 'Abnormal synovial bursa morphology', 'XPO:0139774', 'abnormally necrotic elastica externa', 0.4594594594594595, 4.638757693672553, 1.4599044840325002, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(473244, 'HP:0025231', 'Abnormal synovial bursa morphology', 'XPO:0100081', 'abnormal anatomical entity in vitro', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(473245, 'HP:0025231', 'Abnormal synovial bursa morphology', 'XPO:0100910', 'abnormal vacuolated notochordal tissue', 0.4827586206896552, 4.3395673355180735, 1.4473988881039626, 'UPHENO:0002964', 'abnormal skeletal system'),
(473246, 'HP:0025231', 'Abnormal synovial bursa morphology', 'XPO:0127013', 'abnormally localised skeletal system', 0.4117647058823529, 4.3395673355180735, 1.3367425584480601, 'UPHENO:0002964', 'abnormal skeletal system'),
(473247, 'HP:0025231', 'Abnormal synovial bursa morphology', 'XPO:0100048', 'abnormal skeletal element', 0.4375, 4.3395673355180735, 1.3778826906849353, 'UPHENO:0002964', 'abnormal skeletal system'),
(473248, 'HP:0025231', 'Abnormal synovial bursa morphology', 'XPO:0100626', 'abnormal primordial germ cell', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(473249, 'HP:0025231', 'Abnormal synovial bursa morphology', 'XPO:0101195', 'abnormal femur rudiment', 0.4117647058823529, 4.3395673355180735, 1.3367425584480601, 'UPHENO:0002964', 'abnormal skeletal system'),
(473250, 'HP:0025231', 'Abnormal synovial bursa morphology', 'XPO:0100202', 'abnormal embryo', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(473251, 'HP:0025231', 'Abnormal synovial bursa morphology', 'XPO:0130908', 'increased size of the notochordal sheath', 0.4146341463414634, 4.638757693672553, 1.3868624071625903, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(473252, 'HP:0025231', 'Abnormal synovial bursa morphology', 'XPO:0100956', 'abnormal centrosome', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(473253, 'HP:0025231', 'Abnormal synovial bursa morphology', 'XPO:0101333', 'abnormal barrier epithelial cell', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(473254, 'HP:0025231', 'Abnormal synovial bursa morphology', 'XPO:0100640', 'abnormal notochordal sheath', 0.5384615384615384, 4.3395673355180735, 1.5286235977965605, 'UPHENO:0002964', 'abnormal skeletal system'),
(473255, 'HP:0025231', 'Abnormal synovial bursa morphology', 'XPO:0107260', 'abnormal anterior-posterior axis', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(473256, 'HP:0025231', 'Abnormal synovial bursa morphology', 'XPO:0102144', 'abnormal cranial skeleton morphology', 0.4358974358974359, 4.638757693672553, 1.421978405047478, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(473257, 'HP:0025231', 'Abnormal synovial bursa morphology', 'XPO:0101061', 'abnormal plasma membrane', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(473258, 'HP:0025231', 'Abnormal synovial bursa morphology', 'XPO:0100882', 'abnormal perichondrial cell', 0.45161290322580644, 4.3395673355180735, 1.399930213666808, 'UPHENO:0002964', 'abnormal skeletal system'),
(473259, 'HP:0025231', 'Abnormal synovial bursa morphology', 'XPO:0139771', 'abnormally necrotic skeletal subdivision', 0.425, 4.638757693672553, 1.404091172186064, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(473260, 'HP:0025231', 'Abnormal synovial bursa morphology', 'XPO:0129664', 'increased size of the skeleton', 0.4146341463414634, 4.638757693672553, 1.3868624071625903, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(473261, 'HP:0025231', 'Abnormal synovial bursa morphology', 'XPO:0100907', 'abnormal cytoplasm', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(473262, 'HP:0025231', 'Abnormal synovial bursa morphology', 'XPO:0101348', 'abnormal perichordal tissue', 0.4827586206896552, 4.3395673355180735, 1.4473988881039626, 'UPHENO:0002964', 'abnormal skeletal system'),
(473263, 'HP:0025231', 'Abnormal synovial bursa morphology', 'XPO:0102605', 'abnormal dermal skeleton morphology', 0.4594594594594595, 4.638757693672553, 1.4599044840325002, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(473264, 'HP:0025231', 'Abnormal synovial bursa morphology', 'XPO:0100308', 'abnormal early embryonic cell', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(473265, 'HP:0025231', 'Abnormal synovial bursa morphology', 'XPO:0100006', 'abnormal anatomical structure', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(473266, 'HP:0025231', 'Abnormal synovial bursa morphology', 'XPO:0141699', 'abnormally necrotic anterior notochord', 0.4358974358974359, 4.638757693672553, 1.421978405047478, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(473267, 'HP:0025231', 'Abnormal synovial bursa morphology', 'XPO:0101366', 'abnormal morula cell', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(473268, 'HP:0025231', 'Abnormal synovial bursa morphology', 'XPO:00000000', 'Xenopus phenotype', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(473269, 'HP:0025231', 'Abnormal synovial bursa morphology', 'XPO:0141719', 'abnormal anterior notochord morphology', 0.5, 4.638757693672553, 1.5229507040072823, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(473270, 'HP:0025231', 'Abnormal synovial bursa morphology', 'XPO:0100461', 'abnormal craniofacial skeleton', 0.45161290322580644, 4.3395673355180735, 1.399930213666808, 'UPHENO:0002964', 'abnormal skeletal system'),
(473271, 'HP:0025231', 'Abnormal synovial bursa morphology', 'XPO:0102514', 'abnormal perichondrial cell morphology', 0.4358974358974359, 4.638757693672553, 1.421978405047478, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(473272, 'HP:0025231', 'Abnormal synovial bursa morphology', 'XPO:0100004', 'abnormal cell', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(473273, 'HP:0025231', 'Abnormal synovial bursa morphology', 'XPO:0101240', 'abnormal ciliated non-epidermal cell', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(473274, 'HP:0025231', 'Abnormal synovial bursa morphology', 'XPO:0101472', 'abnormal zygote cortex', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(473275, 'HP:0025231', 'Abnormal synovial bursa morphology', 'XPO:0128352', 'decreased size of the skeletal system', 0.4358974358974359, 4.638757693672553, 1.421978405047478, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(473276, 'HP:0025231', 'Abnormal synovial bursa morphology', 'XPO:0100501', 'abnormal urogenital system', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(473277, 'HP:0025231', 'Abnormal synovial bursa morphology', 'XPO:0101004', 'abnormal acid secreting cell', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(473278, 'HP:0025231', 'Abnormal synovial bursa morphology', 'XPO:0100691', 'abnormal keratin accumulating cell', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(473279, 'HP:0025231', 'Abnormal synovial bursa morphology', 'XPO:0101113', 'abnormal stage IV oocyte', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(473280, 'HP:0025231', 'Abnormal synovial bursa morphology', 'XPO:0100917', 'abnormal stage III oocyte', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(473281, 'HP:0025231', 'Abnormal synovial bursa morphology', 'XPO:0100599', 'abnormal adult immune system', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(473282, 'HP:0025231', 'Abnormal synovial bursa morphology', 'XPO:0100032', 'abnormal nervous system', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(473283, 'HP:0025231', 'Abnormal synovial bursa morphology', 'XPO:0101221', 'abnormal larval immune system', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(473284, 'HP:0025231', 'Abnormal synovial bursa morphology', 'XPO:0101264', 'abnormal mitotic spindle', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(473285, 'HP:0025231', 'Abnormal synovial bursa morphology', 'XPO:0107261', 'abnormal dorsal-ventral axis', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(473286, 'HP:0025231', 'Abnormal synovial bursa morphology', 'XPO:0101132', 'abnormal apoptotic cell', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(473287, 'HP:0025231', 'Abnormal synovial bursa morphology', 'XPO:0141776', 'abnormal metabolic process', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(473288, 'HP:0025231', 'Abnormal synovial bursa morphology', 'XPO:0100696', 'abnormal sesamoid', 0.4117647058823529, 4.3395673355180735, 1.3367425584480601, 'UPHENO:0002964', 'abnormal skeletal system'),
(473289, 'HP:0025231', 'Abnormal synovial bursa morphology', 'XPO:0101220', 'abnormal centriole', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(473290, 'HP:0025231', 'Abnormal synovial bursa morphology', 'XPO:0101957', 'abnormal axial skeleton morphology', 0.4473684210526316, 4.638757693672553, 1.4405671470167702, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(473291, 'HP:0025231', 'Abnormal synovial bursa morphology', 'XPO:0100010', 'abnormal multicellular anatomical structure', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(473292, 'HP:0025231', 'Abnormal synovial bursa morphology', 'XPO:0100549', 'abnormal mitotic cell', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(473293, 'HP:0025231', 'Abnormal synovial bursa morphology', 'XPO:0100498', 'abnormal endoskeleton', 0.4827586206896552, 4.3395673355180735, 1.4473988881039626, 'UPHENO:0002964', 'abnormal skeletal system'),
(473294, 'HP:0025231', 'Abnormal synovial bursa morphology', 'XPO:0141714', 'abnormal anterior notochord', 0.5384615384615384, 4.3395673355180735, 1.5286235977965605, 'UPHENO:0002964', 'abnormal skeletal system'),
(473295, 'HP:0012150', 'Single lineage myelodysplasia', 'XPO:0100907', 'abnormal cytoplasm', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(473296, 'HP:0012150', 'Single lineage myelodysplasia', 'XPO:0107262', 'abnormal left-right axis', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(473297, 'HP:0012150', 'Single lineage myelodysplasia', 'XPO:0107270', 'abnormal proximal-distal axis', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(473298, 'HP:0012150', 'Single lineage myelodysplasia', 'XPO:0100754', 'abnormal electrically active cell', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(473299, 'HP:0012150', 'Single lineage myelodysplasia', 'XPO:0101461', 'abnormal sperm entry point', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(473300, 'HP:0012150', 'Single lineage myelodysplasia', 'XPO:0101169', 'abnormal hepato-pancreatic duct', 0.41935483870967744, 4.970960464763942, 1.4438131194629262, 'HP:0011793', 'Neoplasm by anatomical site'),
(473301, 'HP:0012150', 'Single lineage myelodysplasia', 'XPO:0100285', 'abnormal progenitor cell', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(473302, 'HP:0012150', 'Single lineage myelodysplasia', 'XPO:0100437', 'abnormal proepicardium', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(473303, 'HP:0012150', 'Single lineage myelodysplasia', 'XPO:0115505', 'dead whole organism', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(473304, 'HP:0012150', 'Single lineage myelodysplasia', 'XPO:0100721', 'abnormal centromere', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(473305, 'HP:0012150', 'Single lineage myelodysplasia', 'XPO:0100501', 'abnormal urogenital system', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(473306, 'HP:0012150', 'Single lineage myelodysplasia', 'XPO:0100704', 'abnormal Merkel cell', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(473307, 'HP:0012150', 'Single lineage myelodysplasia', 'XPO:0101237', 'abnormal mucus secreting cell', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(473308, 'HP:0012150', 'Single lineage myelodysplasia', 'XPO:0100025', 'abnormal oocyte', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(473309, 'HP:0012150', 'Single lineage myelodysplasia', 'XPO:0100574', 'abnormal gastrula cell', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(473310, 'HP:0012150', 'Single lineage myelodysplasia', 'XPO:0100026', 'abnormal germ cell', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(473311, 'HP:0012150', 'Single lineage myelodysplasia', 'XPO:0101004', 'abnormal acid secreting cell', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(473312, 'HP:0012150', 'Single lineage myelodysplasia', 'XPO:0115509', 'abnormally semi-viable whole organism', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(473313, 'HP:0012150', 'Single lineage myelodysplasia', 'XPO:0101132', 'abnormal apoptotic cell', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(473314, 'HP:0012150', 'Single lineage myelodysplasia', 'XPO:0100791', 'abnormal multiciliated cell precursor', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(473315, 'HP:0012150', 'Single lineage myelodysplasia', 'XPO:0131685', 'abnormal cortical actin cytoskeleton', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(473316, 'HP:0012150', 'Single lineage myelodysplasia', 'XPO:0107261', 'abnormal dorsal-ventral axis', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(473317, 'HP:0012150', 'Single lineage myelodysplasia', 'XPO:0101450', 'abnormal myeloid cell', 0.4642857142857143, 5.574066539846944, 1.6087136056268494, 'UPHENO:0004459', 'abnormal hematopoietic system'),
(473318, 'HP:0012150', 'Single lineage myelodysplasia', 'XPO:0100344', 'abnormal portion of organism substance', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(473319, 'HP:0012150', 'Single lineage myelodysplasia', 'XPO:0101056', 'abnormal anterior ventral blood island', 0.43333333333333335, 5.574066539846944, 1.5541649957239663, 'HP:0001871', 'Abnormality of blood and blood-forming tissues'),
(473320, 'HP:0012150', 'Single lineage myelodysplasia', 'XPO:0101326', 'abnormal cementoblast', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(473321, 'HP:0012150', 'Single lineage myelodysplasia', 'XPO:0115508', 'abnormally peramorphic growth of whole organism', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(473322, 'HP:0012150', 'Single lineage myelodysplasia', 'XPO:0100486', 'abnormal oral evagination', 0.4482758620689655, 4.970960464763942, 1.4927697704779535, 'HP:0011793', 'Neoplasm by anatomical site'),
(473323, 'HP:0012150', 'Single lineage myelodysplasia', 'XPO:0100545', 'abnormal male organism', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(473324, 'HP:0012150', 'Single lineage myelodysplasia', 'XPO:0100894', 'abnormal nucleus', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(473325, 'HP:0012150', 'Single lineage myelodysplasia', 'XPO:0100225', 'abnormal endocrine system', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(473326, 'HP:0012150', 'Single lineage myelodysplasia', 'XPO:0100585', 'abnormal elastica externa', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(473327, 'HP:0012150', 'Single lineage myelodysplasia', 'XPO:0107258', 'abnormal anatomical axis', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(473328, 'HP:0012150', 'Single lineage myelodysplasia', 'XPO:0100289', 'abnormal chondroblast', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(473329, 'HP:0012150', 'Single lineage myelodysplasia', 'XPO:0101333', 'abnormal barrier epithelial cell', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(473330, 'HP:0012150', 'Single lineage myelodysplasia', 'XPO:0101569', 'abnormal activin-induced ectoderm', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(473331, 'HP:0012150', 'Single lineage myelodysplasia', 'XPO:0141776', 'abnormal metabolic process', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(473332, 'HP:0012150', 'Single lineage myelodysplasia', 'XPO:0100581', 'abnormal immune system', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(473333, 'HP:0012150', 'Single lineage myelodysplasia', 'XPO:0101109', 'abnormal egg cell-free extract', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(473334, 'HP:0012150', 'Single lineage myelodysplasia', 'XPO:0100956', 'abnormal centrosome', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(473335, 'HP:0012150', 'Single lineage myelodysplasia', 'XPO:0100004', 'abnormal cell', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(473336, 'HP:0012150', 'Single lineage myelodysplasia', 'XPO:0100202', 'abnormal embryo', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(473337, 'HP:0012150', 'Single lineage myelodysplasia', 'XPO:0101297', 'abnormal barrier cell', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(473338, 'HP:0012150', 'Single lineage myelodysplasia', 'XPO:0100429', 'abnormal spermatid', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(473339, 'HP:0012150', 'Single lineage myelodysplasia', 'XPO:0100239', 'abnormal acellular anatomical structure', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(473340, 'HP:0012150', 'Single lineage myelodysplasia', 'XPO:0107304', 'abnormal hindgut endoderm', 0.40625, 4.970960464763942, 1.4210744839065794, 'HP:0011793', 'Neoplasm by anatomical site'),
(473341, 'HP:0012150', 'Single lineage myelodysplasia', 'XPO:0100317', 'abnormal respiratory system', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(473342, 'HP:0012150', 'Single lineage myelodysplasia', 'XPO:0100156', 'abnormal foregut', 0.4482758620689655, 4.970960464763942, 1.4927697704779535, 'HP:0011793', 'Neoplasm by anatomical site'),
(473343, 'HP:0012150', 'Single lineage myelodysplasia', 'XPO:0100477', 'abnormal pericyte', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(473344, 'HP:0012150', 'Single lineage myelodysplasia', 'XPO:0107323', 'abnormal thrombocyte', 0.40625, 5.574066539846944, 1.5048137864243607, 'HP:0001871', 'Abnormality of blood and blood-forming tissues'),
(473345, 'HP:0012150', 'Single lineage myelodysplasia', 'XPO:0100258', 'abnormal organ part', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(473346, 'HP:0012150', 'Single lineage myelodysplasia', 'XPO:0100616', 'abnormal ventral blood island', 0.4482758620689655, 5.574066539846944, 1.5807338433081215, 'HP:0001871', 'Abnormality of blood and blood-forming tissues'),
(473347, 'HP:0012150', 'Single lineage myelodysplasia', 'XPO:0101101', 'abnormal posterior foregut', 0.43333333333333335, 4.970960464763942, 1.4676794159707953, 'HP:0011793', 'Neoplasm by anatomical site'),
(473348, 'HP:0012150', 'Single lineage myelodysplasia', 'XPO:0101409', 'abnormal perivitelline space', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(473349, 'HP:0012150', 'Single lineage myelodysplasia', 'XPO:0107312', 'abnormal filopodium', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(473350, 'HP:0012150', 'Single lineage myelodysplasia', 'XPO:0100888', 'abnormal microtubule', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(473351, 'HP:0012150', 'Single lineage myelodysplasia', 'XPO:0100152', 'abnormal alimentary system', 0.5, 4.970960464763942, 1.5765405901472918, 'HP:0011793', 'Neoplasm by anatomical site'),
(473352, 'HP:0012150', 'Single lineage myelodysplasia', 'XPO:0101240', 'abnormal ciliated non-epidermal cell', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(473353, 'HP:0012150', 'Single lineage myelodysplasia', 'XPO:0100492', 'abnormal gall bladder primordium', 0.40625, 4.970960464763942, 1.4210744839065794, 'HP:0011793', 'Neoplasm by anatomical site'),
(473354, 'HP:0012150', 'Single lineage myelodysplasia', 'XPO:0101241', 'abnormal nucleate erythrocyte', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(473355, 'HP:0012150', 'Single lineage myelodysplasia', 'XPO:0100899', 'abnormal secondary spermatogonium', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(473356, 'HP:0012150', 'Single lineage myelodysplasia', 'XPO:00000000', 'Xenopus phenotype', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(473357, 'HP:0012150', 'Single lineage myelodysplasia', 'XPO:0100728', 'abnormal cell condensation', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(473358, 'HP:0012150', 'Single lineage myelodysplasia', 'XPO:0101601', 'abnormal proctodeum', 0.41935483870967744, 4.970960464763942, 1.4438131194629262, 'HP:0011793', 'Neoplasm by anatomical site'),
(473359, 'HP:0012150', 'Single lineage myelodysplasia', 'XPO:0100599', 'abnormal adult immune system', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(473360, 'HP:0012150', 'Single lineage myelodysplasia', 'XPO:0101448', 'abnormal myelin accumulating cell', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(473361, 'HP:0012150', 'Single lineage myelodysplasia', 'XPO:0101113', 'abnormal stage IV oocyte', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(473362, 'HP:0012150', 'Single lineage myelodysplasia', 'XPO:0101264', 'abnormal mitotic spindle', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(473363, 'HP:0012150', 'Single lineage myelodysplasia', 'XPO:0101472', 'abnormal zygote cortex', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(473364, 'HP:0012150', 'Single lineage myelodysplasia', 'XPO:0100638', 'abnormal polar body', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(473365, 'HP:0012150', 'Single lineage myelodysplasia', 'XPO:0100377', 'abnormal connective tissue', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(473366, 'HP:0012150', 'Single lineage myelodysplasia', 'XPO:0100493', 'abnormal liver and biliary system', 0.48148148148148145, 4.970960464763942, 1.5470699431378068, 'HP:0011793', 'Neoplasm by anatomical site'),
(473367, 'HP:0012150', 'Single lineage myelodysplasia', 'XPO:0100546', 'abnormal whole organism', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(473368, 'HP:0012150', 'Single lineage myelodysplasia', 'XPO:0101480', 'abnormal stage V oocyte', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(473369, 'HP:0012150', 'Single lineage myelodysplasia', 'XPO:0101071', 'abnormal endoplasmic reticulum', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(473370, 'HP:0012150', 'Single lineage myelodysplasia', 'XPO:0100976', 'abnormal multiciliated cell', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(473371, 'HP:0012150', 'Single lineage myelodysplasia', 'XPO:0115391', 'abnormally undifferentiated alimentary system', 0.48148148148148145, 4.970960464763942, 1.5470699431378068, 'HP:0011793', 'Neoplasm by anatomical site'),
(473372, 'HP:0012150', 'Single lineage myelodysplasia', 'XPO:0101467', 'abnormal alkali secreting cell', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(473373, 'HP:0012150', 'Single lineage myelodysplasia', 'XPO:0142057', 'abnormal desmosome', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(473374, 'HP:0012150', 'Single lineage myelodysplasia', 'XPO:0100215', 'abnormal first pancreatic bud', 0.40625, 4.970960464763942, 1.4210744839065794, 'HP:0011793', 'Neoplasm by anatomical site'),
(473375, 'HP:0012150', 'Single lineage myelodysplasia', 'XPO:0101366', 'abnormal morula cell', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(473376, 'HP:0012150', 'Single lineage myelodysplasia', 'XPO:0100392', 'abnormal cilium', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(473377, 'HP:0012150', 'Single lineage myelodysplasia', 'XPO:0101435', 'abnormal paracrine cell', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(473378, 'HP:0012150', 'Single lineage myelodysplasia', 'XPO:0115512', 'abnormally semi-erect whole organism', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(473379, 'HP:0012150', 'Single lineage myelodysplasia', 'XPO:0100549', 'abnormal mitotic cell', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(473380, 'HP:0012150', 'Single lineage myelodysplasia', 'XPO:0100852', 'abnormal interdigital region', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(473381, 'HP:0012150', 'Single lineage myelodysplasia', 'XPO:0131677', 'abnormal actin filament', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(473382, 'HP:0012150', 'Single lineage myelodysplasia', 'XPO:0100006', 'abnormal anatomical structure', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(473383, 'HP:0012150', 'Single lineage myelodysplasia', 'XPO:0100386', 'abnormal limb', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(473384, 'HP:0012150', 'Single lineage myelodysplasia', 'XPO:0100062', 'abnormal anatomical space', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(473385, 'HP:0012150', 'Single lineage myelodysplasia', 'XPO:0100337', 'abnormal zygote', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(473386, 'HP:0012150', 'Single lineage myelodysplasia', 'XPO:0101198', 'abnormal digestive enzyme secreting cell', 0.40625, 4.970960464763942, 1.4210744839065794, 'HP:0011793', 'Neoplasm by anatomical site'),
(473387, 'HP:0012150', 'Single lineage myelodysplasia', 'XPO:0101587', 'abnormal hemangioblast', 0.4642857142857143, 5.574066539846944, 1.6087136056268494, 'HP:0001871', 'Abnormality of blood and blood-forming tissues'),
(473388, 'HP:0012150', 'Single lineage myelodysplasia', 'XPO:0101188', 'abnormal posterior ventral blood island', 0.43333333333333335, 5.574066539846944, 1.5541649957239663, 'HP:0001871', 'Abnormality of blood and blood-forming tissues'),
(473389, 'HP:0012150', 'Single lineage myelodysplasia', 'XPO:0100986', 'abnormal gut epithelium', 0.43333333333333335, 4.970960464763942, 1.4676794159707953, 'HP:0011793', 'Neoplasm by anatomical site'),
(473390, 'HP:0012150', 'Single lineage myelodysplasia', 'XPO:0100523', 'abnormal midgut', 0.4482758620689655, 4.970960464763942, 1.4927697704779535, 'HP:0011793', 'Neoplasm by anatomical site'),
(473391, 'HP:0012150', 'Single lineage myelodysplasia', 'XPO:0101377', 'abnormal manicotto glandulare', 0.4482758620689655, 4.970960464763942, 1.4927697704779535, 'HP:0011793', 'Neoplasm by anatomical site'),
(473392, 'HP:0012150', 'Single lineage myelodysplasia', 'XPO:0131675', 'abnormal spindle microtubule', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(473393, 'HP:0012150', 'Single lineage myelodysplasia', 'XPO:0101373', 'abnormal oxygen accumulating cell', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(473394, 'HP:0012150', 'Single lineage myelodysplasia', 'XPO:0142054', 'abnormal digestive tract', 0.4642857142857143, 4.970960464763942, 1.51919252567572, 'HP:0011793', 'Neoplasm by anatomical site'),
(473395, 'HP:0012150', 'Single lineage myelodysplasia', 'XPO:0100462', 'abnormal anterior foregut', 0.43333333333333335, 4.970960464763942, 1.4676794159707953, 'HP:0011793', 'Neoplasm by anatomical site'),
(473396, 'HP:0012150', 'Single lineage myelodysplasia', 'XPO:0107284', 'abnormal migrating myoblast', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(473397, 'HP:0012150', 'Single lineage myelodysplasia', 'XPO:0107253', 'abnormal enteric nervous system', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(473398, 'HP:0012150', 'Single lineage myelodysplasia', 'XPO:0100890', 'abnormal pharyngeal cavity', 0.4642857142857143, 4.970960464763942, 1.51919252567572, 'HP:0011793', 'Neoplasm by anatomical site'),
(473399, 'HP:0012150', 'Single lineage myelodysplasia', 'XPO:0101141', 'abnormal Keller explant', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(473400, 'HP:0012150', 'Single lineage myelodysplasia', 'XPO:0107260', 'abnormal anterior-posterior axis', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(473401, 'HP:0012150', 'Single lineage myelodysplasia', 'XPO:0101107', 'abnormal erythroid cell', 0.4642857142857143, 5.574066539846944, 1.6087136056268494, 'HP:0001871', 'Abnormality of blood and blood-forming tissues'),
(473402, 'HP:0012150', 'Single lineage myelodysplasia', 'XPO:0100108', 'abnormal cell part', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(473403, 'HP:0012150', 'Single lineage myelodysplasia', 'XPO:0100573', 'abnormal extraembryonic structure', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(473404, 'HP:0012150', 'Single lineage myelodysplasia', 'XPO:0131666', 'abnormal adherens junction', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(473405, 'HP:0012150', 'Single lineage myelodysplasia', 'XPO:0101535', 'abnormal absorptive cell', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(473406, 'HP:0012150', 'Single lineage myelodysplasia', 'XPO:0100232', 'abnormal lymphatic system', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(473407, 'HP:0012150', 'Single lineage myelodysplasia', 'XPO:0107259', 'abnormal animal-vegetal axis', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(473408, 'HP:0012150', 'Single lineage myelodysplasia', 'XPO:0100032', 'abnormal nervous system', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(473409, 'HP:0012150', 'Single lineage myelodysplasia', 'XPO:0100802', 'abnormal exocrine cell', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(473410, 'HP:0012150', 'Single lineage myelodysplasia', 'XPO:0100917', 'abnormal stage III oocyte', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(473411, 'HP:0012150', 'Single lineage myelodysplasia', 'XPO:0100718', 'abnormal ventral pancreatic bud', 0.41935483870967744, 4.970960464763942, 1.4438131194629262, 'HP:0011793', 'Neoplasm by anatomical site'),
(473412, 'HP:0012150', 'Single lineage myelodysplasia', 'XPO:0100031', 'abnormal central nervous system', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(473413, 'HP:0012150', 'Single lineage myelodysplasia', 'XPO:0100176', 'abnormal stage VI oocyte', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(473414, 'HP:0012150', 'Single lineage myelodysplasia', 'XPO:0101220', 'abnormal centriole', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(473415, 'HP:0012150', 'Single lineage myelodysplasia', 'XPO:0107288', 'abnormal larval alimentary system', 0.48148148148148145, 4.970960464763942, 1.5470699431378068, 'HP:0011793', 'Neoplasm by anatomical site'),
(473416, 'HP:0012150', 'Single lineage myelodysplasia', 'XPO:0100372', 'abnormal hematological system', 0.5416666666666666, 5.574066539846944, 1.737609289344729, 'HP:0001871', 'Abnormality of blood and blood-forming tissues'),
(473417, 'HP:0012150', 'Single lineage myelodysplasia', 'XPO:0100307', 'abnormal blastomere', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(473418, 'HP:0012150', 'Single lineage myelodysplasia', 'XPO:0101498', 'abnormal stage II oocyte', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(473419, 'HP:0012150', 'Single lineage myelodysplasia', 'XPO:0100653', 'abnormal myoblast', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(473420, 'HP:0012150', 'Single lineage myelodysplasia', 'XPO:0100481', 'abnormal anatomical line', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(473421, 'HP:0012150', 'Single lineage myelodysplasia', 'XPO:0100274', 'abnormal sensory system', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(473422, 'HP:0012150', 'Single lineage myelodysplasia', 'XPO:0101221', 'abnormal larval immune system', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(473423, 'HP:0012150', 'Single lineage myelodysplasia', 'XPO:0101228', 'abnormal mesenchymal stem cell', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(473424, 'HP:0012150', 'Single lineage myelodysplasia', 'XPO:0101547', 'abnormal lampbrush chromosome', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(473425, 'HP:0012150', 'Single lineage myelodysplasia', 'XPO:0101513', 'abnormal basal body', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(473426, 'HP:0012150', 'Single lineage myelodysplasia', 'XPO:0101484', 'abnormal bone marrow', 0.40625, 5.574066539846944, 1.5048137864243607, 'UPHENO:0004459', 'abnormal hematopoietic system'),
(473427, 'HP:0012150', 'Single lineage myelodysplasia', 'XPO:0141499', 'abnormal tadpole', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(473428, 'HP:0012150', 'Single lineage myelodysplasia', 'XPO:0100626', 'abnormal primordial germ cell', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(473429, 'HP:0012150', 'Single lineage myelodysplasia', 'XPO:0100823', 'abnormal blood', 0.5, 5.574066539846944, 1.6694410052240456, 'HP:0001871', 'Abnormality of blood and blood-forming tissues'),
(473430, 'HP:0012150', 'Single lineage myelodysplasia', 'XPO:0100621', 'abnormal peritoneum', 0.40625, 4.970960464763942, 1.4210744839065794, 'HP:0011793', 'Neoplasm by anatomical site'),
(473431, 'HP:0012150', 'Single lineage myelodysplasia', 'XPO:0101381', 'abnormal ventral foregut', 0.43333333333333335, 4.970960464763942, 1.4676794159707953, 'HP:0011793', 'Neoplasm by anatomical site'),
(473432, 'HP:0012150', 'Single lineage myelodysplasia', 'XPO:0101021', 'abnormal dorsal foregut', 0.43333333333333335, 4.970960464763942, 1.4676794159707953, 'HP:0011793', 'Neoplasm by anatomical site'),
(473433, 'HP:0012150', 'Single lineage myelodysplasia', 'XPO:0100515', 'abnormal somatic stem cell', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(473434, 'HP:0012150', 'Single lineage myelodysplasia', 'XPO:0100172', 'abnormal stem cell', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(473435, 'HP:0012150', 'Single lineage myelodysplasia', 'XPO:0100691', 'abnormal keratin accumulating cell', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(473436, 'HP:0012150', 'Single lineage myelodysplasia', 'XPO:0100423', 'abnormal process', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(473437, 'HP:0012150', 'Single lineage myelodysplasia', 'XPO:0100902', 'abnormal spermatocyte', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(473438, 'HP:0012150', 'Single lineage myelodysplasia', 'XPO:0100084', 'abnormal anatomical group', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(473439, 'HP:0012150', 'Single lineage myelodysplasia', 'XPO:0100010', 'abnormal multicellular anatomical structure', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(473440, 'HP:0012150', 'Single lineage myelodysplasia', 'XPO:0101061', 'abnormal plasma membrane', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(473441, 'HP:0012150', 'Single lineage myelodysplasia', 'XPO:0100735', 'abnormal hindgut', 0.4482758620689655, 4.970960464763942, 1.4927697704779535, 'HP:0011793', 'Neoplasm by anatomical site'),
(473442, 'HP:0012150', 'Single lineage myelodysplasia', 'XPO:0100533', 'abnormal melanoblast', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(473443, 'HP:0012150', 'Single lineage myelodysplasia', 'XPO:0101468', 'abnormal stage I oocyte', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(473444, 'HP:0012150', 'Single lineage myelodysplasia', 'XPO:0100081', 'abnormal anatomical entity in vitro', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(473445, 'HP:0012150', 'Single lineage myelodysplasia', 'XPO:0101157', 'abnormal female organism', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(473446, 'HP:0012150', 'Single lineage myelodysplasia', 'XPO:0100715', 'abnormal ciliated cell', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(473447, 'HP:0012150', 'Single lineage myelodysplasia', 'XPO:0141315', 'abnormal anatomical region', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(473448, 'HP:0012150', 'Single lineage myelodysplasia', 'XPO:0101110', 'abnormal cell-free extract', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(473449, 'HP:0012150', 'Single lineage myelodysplasia', 'XPO:0100674', 'abnormal secondary oogonium', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(473450, 'HP:0012150', 'Single lineage myelodysplasia', 'XPO:0100308', 'abnormal early embryonic cell', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(473451, 'HP:0012150', 'Single lineage myelodysplasia', 'XPO:0131667', 'abnormal actin cytoskeleton', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(473452, 'HP:0012150', 'Single lineage myelodysplasia', 'XPO:0100969', 'abnormal disaggregated/reaggregated ectoderm treated with activin', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(473453, 'HP:0012150', 'Single lineage myelodysplasia', 'XPO:0100724', 'abnormal kinetochore', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(473454, 'HP:0030853', 'Heterotaxy', 'XPO:0132044', 'abnormal development of marginal zone', 0.4090909090909091, 3.334430194052109, 1.1679405290445888, 'UPHENO:0049587', 'abnormal biological_process'),
(473455, 'HP:0030853', 'Heterotaxy', 'XPO:0132547', 'abnormal development of pial cell', 0.4090909090909091, 3.334430194052109, 1.1679405290445888, 'UPHENO:0049587', 'abnormal biological_process'),
(473456, 'HP:0030853', 'Heterotaxy', 'XPO:0132583', 'abnormal development of mitotic cell', 0.4090909090909091, 3.334430194052109, 1.1679405290445888, 'UPHENO:0049587', 'abnormal biological_process'),
(473457, 'HP:0030853', 'Heterotaxy', 'XPO:0132558', 'abnormal development of dorsal-ventral axis', 0.4090909090909091, 3.334430194052109, 1.1679405290445888, 'UPHENO:0049587', 'abnormal biological_process'),
(473458, 'HP:0030853', 'Heterotaxy', 'XPO:0132962', 'abnormal development of female organism', 0.4090909090909091, 3.334430194052109, 1.1679405290445888, 'UPHENO:0049587', 'abnormal biological_process'),
(473459, 'HP:0030853', 'Heterotaxy', 'XPO:0133148', 'abnormal development of hindlimb region', 0.42857142857142855, 3.334430194052109, 1.195425243056469, 'UPHENO:0049587', 'abnormal biological_process'),
(473460, 'HP:0030853', 'Heterotaxy', 'XPO:0141798', 'abnormal lipid metabolic process', 0.4782608695652174, 3.334430194052109, 1.2628251993494104, 'UPHENO:0049587', 'abnormal biological_process'),
(473461, 'HP:0030853', 'Heterotaxy', 'XPO:0100894', 'abnormal nucleus', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(473462, 'HP:0030853', 'Heterotaxy', 'XPO:0132996', 'abnormal development of ventricular zone', 0.42857142857142855, 3.334430194052109, 1.195425243056469, 'UPHENO:0049587', 'abnormal biological_process'),
(473463, 'HP:0030853', 'Heterotaxy', 'XPO:0101513', 'abnormal basal body', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(473464, 'HP:0030853', 'Heterotaxy', 'XPO:0100004', 'abnormal cell', 0.47619047619047616, 1.8210412618256888, 0.9312156064152277, 'HP:0000118', 'Phenotypic abnormality'),
(473465, 'HP:0030853', 'Heterotaxy', 'XPO:0141767', 'abnormal temperature homeostasis', 0.44, 3.334430194052109, 1.2112593798947144, 'UPHENO:0049587', 'abnormal biological_process'),
(473466, 'HP:0030853', 'Heterotaxy', 'XPO:0141786', 'abnormal pigment metabolic process', 0.5238095238095238, 3.334430194052109, 1.3215923320459049, 'UPHENO:0049587', 'abnormal biological_process'),
(473467, 'HP:0030853', 'Heterotaxy', 'XPO:0100704', 'abnormal Merkel cell', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(473468, 'HP:0030853', 'Heterotaxy', 'XPO:0131741', 'abnormal convergent extension', 0.42857142857142855, 3.334430194052109, 1.195425243056469, 'UPHENO:0049587', 'abnormal biological_process'),
(473469, 'HP:0030853', 'Heterotaxy', 'XPO:0132439', 'abnormal development of lower blastopore lip', 0.4090909090909091, 3.334430194052109, 1.1679405290445888, 'UPHENO:0049587', 'abnormal biological_process'),
(473470, 'HP:0030853', 'Heterotaxy', 'XPO:0141880', 'abnormal ethanolamine metabolic process', 0.44, 3.334430194052109, 1.2112593798947144, 'UPHENO:0049587', 'abnormal biological_process'),
(473471, 'HP:0030853', 'Heterotaxy', 'XPO:0132839', 'abnormal development of perichondrial cell', 0.4090909090909091, 3.334430194052109, 1.1679405290445888, 'UPHENO:0049587', 'abnormal biological_process'),
(473472, 'HP:0030853', 'Heterotaxy', 'XPO:0141746', 'abnormal energy homeostasis', 0.4090909090909091, 3.334430194052109, 1.1679405290445888, 'UPHENO:0049587', 'abnormal biological_process'),
(473473, 'HP:0030853', 'Heterotaxy', 'XPO:0131833', 'abnormal development of cell part', 0.42857142857142855, 3.334430194052109, 1.195425243056469, 'UPHENO:0049587', 'abnormal biological_process'),
(473474, 'HP:0030853', 'Heterotaxy', 'XPO:0131942', 'abnormal development of dorsal endoderm', 0.4090909090909091, 3.334430194052109, 1.1679405290445888, 'UPHENO:0049587', 'abnormal biological_process'),
(473475, 'HP:0030853', 'Heterotaxy', 'XPO:0141841', 'abnormality of whole organism mass', 0.5652173913043478, 8.819732420846037, 2.232726170159023, 'HP:0001507', 'Growth abnormality'),
(473476, 'HP:0030853', 'Heterotaxy', 'XPO:0133049', 'abnormal development of anterior entopeduncular region', 0.42857142857142855, 3.334430194052109, 1.195425243056469, 'UPHENO:0049587', 'abnormal biological_process'),
(473477, 'HP:0030853', 'Heterotaxy', 'XPO:0100546', 'abnormal whole organism', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(473478, 'HP:0030853', 'Heterotaxy', 'XPO:0132150', 'abnormal development of lampbrush chromosome', 0.4090909090909091, 3.334430194052109, 1.1679405290445888, 'UPHENO:0049587', 'abnormal biological_process'),
(473479, 'HP:0030853', 'Heterotaxy', 'XPO:0101468', 'abnormal stage I oocyte', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(473480, 'HP:0030853', 'Heterotaxy', 'XPO:0132496', 'abnormal development of left-right organizer', 0.42857142857142855, 3.334430194052109, 1.195425243056469, 'UPHENO:0049587', 'abnormal biological_process'),
(473481, 'HP:0030853', 'Heterotaxy', 'XPO:0131908', 'abnormal development of zygote', 0.4090909090909091, 3.334430194052109, 1.1679405290445888, 'UPHENO:0049587', 'abnormal biological_process'),
(473482, 'HP:0030853', 'Heterotaxy', 'XPO:0100081', 'abnormal anatomical entity in vitro', 0.47058823529411764, 1.4755025719078136, 0.8332791557971614, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(473483, 'HP:0030853', 'Heterotaxy', 'XPO:0133074', 'abnormal development of ciliary axoneme', 0.4090909090909091, 3.334430194052109, 1.1679405290445888, 'UPHENO:0049587', 'abnormal biological_process'),
(473484, 'HP:0030853', 'Heterotaxy', 'XPO:0141272', 'absent surface breathing', 0.5, 1.4755025719078136, 0.8589244937443028, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(473485, 'HP:0030853', 'Heterotaxy', 'XPO:0131691', 'abnormal molecular function', 0.47058823529411764, 1.4755025719078136, 0.8332791557971614, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(473486, 'HP:0030853', 'Heterotaxy', 'XPO:0141784', 'abnormal cellular hormone metabolic process', 0.5, 1.4755025719078136, 0.8589244937443028, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(473487, 'HP:0030853', 'Heterotaxy', 'XPO:0133246', 'abnormal development of myocoelic slit', 0.42857142857142855, 3.334430194052109, 1.195425243056469, 'UPHENO:0049587', 'abnormal biological_process'),
(473488, 'HP:0030853', 'Heterotaxy', 'XPO:0100515', 'abnormal somatic stem cell', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(473489, 'HP:0030853', 'Heterotaxy', 'XPO:0132056', 'abnormal development of eye photoreceptor cell', 0.4090909090909091, 3.334430194052109, 1.1679405290445888, 'UPHENO:0049587', 'abnormal biological_process'),
(473490, 'HP:0030853', 'Heterotaxy', 'XPO:0133241', 'abnormal development of choroid fissure', 0.4090909090909091, 3.334430194052109, 1.1679405290445888, 'UPHENO:0049587', 'abnormal biological_process'),
(473491, 'HP:0030853', 'Heterotaxy', 'XPO:0100372', 'abnormal hematological system', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(473492, 'HP:0030853', 'Heterotaxy', 'XPO:0131739', 'abnormal wound healing', 0.42857142857142855, 3.334430194052109, 1.195425243056469, 'UPHENO:0049587', 'abnormal biological_process'),
(473493, 'HP:0030853', 'Heterotaxy', 'XPO:0116433', 'abnormal axis specification', 0.47368421052631576, 3.334430194052109, 1.2567684488499395, 'UPHENO:0049587', 'abnormal biological_process'),
(473494, 'HP:0030853', 'Heterotaxy', 'XPO:0141724', 'abnormal prevention of polyspermy', 0.47368421052631576, 3.334430194052109, 1.2567684488499395, 'UPHENO:0049587', 'abnormal biological_process'),
(473495, 'HP:0030853', 'Heterotaxy', 'XPO:0100549', 'abnormal mitotic cell', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(473496, 'HP:0030853', 'Heterotaxy', 'XPO:0132376', 'abnormal development of third ventricle', 0.4090909090909091, 3.334430194052109, 1.1679405290445888, 'UPHENO:0049587', 'abnormal biological_process'),
(473497, 'HP:0030853', 'Heterotaxy', 'XPO:0131731', 'abnormal pigment accumulation in tissues', 0.4090909090909091, 3.334430194052109, 1.1679405290445888, 'UPHENO:0049587', 'abnormal biological_process'),
(473498, 'HP:0030853', 'Heterotaxy', 'XPO:0133305', 'abnormal development of small secretory cell', 0.4090909090909091, 3.334430194052109, 1.1679405290445888, 'UPHENO:0049587', 'abnormal biological_process'),
(473499, 'HP:0030853', 'Heterotaxy', 'XPO:0132117', 'abnormal development of process', 0.42857142857142855, 3.334430194052109, 1.195425243056469, 'UPHENO:0049587', 'abnormal biological_process'),
(473500, 'HP:0030853', 'Heterotaxy', 'XPO:0141276', 'decreased surface breathing', 0.47058823529411764, 1.4755025719078136, 0.8332791557971614, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(473501, 'HP:0030853', 'Heterotaxy', 'XPO:0132658', 'abnormal development of ventral endoderm', 0.42857142857142855, 3.334430194052109, 1.195425243056469, 'UPHENO:0049587', 'abnormal biological_process'),
(473502, 'HP:0030853', 'Heterotaxy', 'XPO:0100176', 'abnormal stage VI oocyte', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(473503, 'HP:0030853', 'Heterotaxy', 'XPO:0132765', 'abnormal development of hypobranchial placode', 0.4090909090909091, 3.334430194052109, 1.1679405290445888, 'UPHENO:0049587', 'abnormal biological_process'),
(473504, 'HP:0030853', 'Heterotaxy', 'XPO:0131859', 'abnormal development of ventrolateral neural tube', 0.4090909090909091, 3.334430194052109, 1.1679405290445888, 'UPHENO:0049587', 'abnormal biological_process'),
(473505, 'HP:0030853', 'Heterotaxy', 'XPO:0131993', 'abnormal development of stem cell', 0.4090909090909091, 3.334430194052109, 1.1679405290445888, 'UPHENO:0049587', 'abnormal biological_process'),
(473506, 'HP:0030853', 'Heterotaxy', 'XPO:0132836', 'abnormal development of transverse process', 0.4090909090909091, 3.334430194052109, 1.1679405290445888, 'UPHENO:0049587', 'abnormal biological_process'),
(473507, 'HP:0030853', 'Heterotaxy', 'XPO:0131827', 'abnormal development of neuron', 0.4090909090909091, 3.334430194052109, 1.1679405290445888, 'UPHENO:0049587', 'abnormal biological_process'),
(473508, 'HP:0030853', 'Heterotaxy', 'XPO:0131406', 'abnormal social behavior', 0.42857142857142855, 3.334430194052109, 1.195425243056469, 'UPHENO:0049587', 'abnormal biological_process'),
(473509, 'HP:0030853', 'Heterotaxy', 'XPO:0133213', 'abnormal development of fenestra basicranialis', 0.42857142857142855, 3.334430194052109, 1.195425243056469, 'UPHENO:0049587', 'abnormal biological_process'),
(473510, 'HP:0030853', 'Heterotaxy', 'XPO:0101221', 'abnormal larval immune system', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(473511, 'HP:0030853', 'Heterotaxy', 'XPO:0132453', 'abnormal development of myoblast', 0.4090909090909091, 3.334430194052109, 1.1679405290445888, 'UPHENO:0049587', 'abnormal biological_process'),
(473512, 'HP:0030853', 'Heterotaxy', 'XPO:0101109', 'abnormal egg cell-free extract', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(473513, 'HP:0030853', 'Heterotaxy', 'XPO:0132559', 'abnormal development of anatomical axis', 0.42857142857142855, 3.334430194052109, 1.195425243056469, 'UPHENO:0049587', 'abnormal biological_process'),
(473514, 'HP:0030853', 'Heterotaxy', 'XPO:0131862', 'abnormal development of pharyngeal region', 0.42857142857142855, 3.334430194052109, 1.195425243056469, 'UPHENO:0049587', 'abnormal biological_process'),
(473515, 'HP:0030853', 'Heterotaxy', 'XPO:0132635', 'abnormal development of medial nasal prominence', 0.4090909090909091, 3.334430194052109, 1.1679405290445888, 'UPHENO:0049587', 'abnormal biological_process'),
(473516, 'HP:0030853', 'Heterotaxy', 'XPO:0100581', 'abnormal immune system', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(473517, 'HP:0030853', 'Heterotaxy', 'XPO:0133090', 'abnormal development of fenestra subocularis', 0.42857142857142855, 3.334430194052109, 1.195425243056469, 'UPHENO:0049587', 'abnormal biological_process'),
(473518, 'HP:0030853', 'Heterotaxy', 'XPO:0131409', 'abnormal locomotory behavior', 0.42857142857142855, 3.334430194052109, 1.195425243056469, 'UPHENO:0049587', 'abnormal biological_process'),
(473519, 'HP:0030853', 'Heterotaxy', 'XPO:0142010', 'abnormal development of cerebrospinal fluid', 0.42857142857142855, 3.334430194052109, 1.195425243056469, 'UPHENO:0049587', 'abnormal biological_process'),
(473520, 'HP:0030853', 'Heterotaxy', 'XPO:0131778', 'abnormal development of primordium', 0.4090909090909091, 3.334430194052109, 1.1679405290445888, 'UPHENO:0049587', 'abnormal biological_process'),
(473521, 'HP:0030853', 'Heterotaxy', 'XPO:0131804', 'abnormal development of central vegetal yolk mass', 0.4090909090909091, 3.334430194052109, 1.1679405290445888, 'UPHENO:0049587', 'abnormal biological_process'),
(473522, 'HP:0030853', 'Heterotaxy', 'XPO:0131904', 'abnormal development of lymphocyte', 0.4090909090909091, 3.334430194052109, 1.1679405290445888, 'UPHENO:0049587', 'abnormal biological_process'),
(473523, 'HP:0030853', 'Heterotaxy', 'XPO:0107262', 'abnormal left-right axis', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(473524, 'HP:0030853', 'Heterotaxy', 'XPO:0132599', 'abnormal development of mesodermal cell', 0.4090909090909091, 3.334430194052109, 1.1679405290445888, 'UPHENO:0049587', 'abnormal biological_process'),
(473525, 'HP:0030853', 'Heterotaxy', 'XPO:0133087', 'abnormal development of neuromast support cell', 0.4090909090909091, 3.334430194052109, 1.1679405290445888, 'UPHENO:0049587', 'abnormal biological_process'),
(473526, 'HP:0030853', 'Heterotaxy', 'XPO:0107270', 'abnormal proximal-distal axis', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(473527, 'HP:0030853', 'Heterotaxy', 'XPO:0100481', 'abnormal anatomical line', 0.47058823529411764, 1.4755025719078136, 0.8332791557971614, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(473528, 'HP:0030853', 'Heterotaxy', 'XPO:0131921', 'abnormal development of endocrine cell', 0.4090909090909091, 3.334430194052109, 1.1679405290445888, 'UPHENO:0049587', 'abnormal biological_process'),
(473529, 'HP:0030853', 'Heterotaxy', 'XPO:0101333', 'abnormal barrier epithelial cell', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(473530, 'HP:0030853', 'Heterotaxy', 'XPO:0131725', 'abnormal phosphorylation of RNA polymerase II C-terminal domain', 0.5, 1.4755025719078136, 0.8589244937443028, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(473531, 'HP:0030853', 'Heterotaxy', 'XPO:0131814', 'abnormal development of lateral ventricle', 0.4090909090909091, 3.334430194052109, 1.1679405290445888, 'UPHENO:0049587', 'abnormal biological_process'),
(473532, 'HP:0030853', 'Heterotaxy', 'XPO:0131940', 'abnormal development of acellular anatomical structure', 0.42857142857142855, 3.334430194052109, 1.195425243056469, 'UPHENO:0049587', 'abnormal biological_process'),
(473533, 'HP:0030853', 'Heterotaxy', 'XPO:0132550', 'abnormal development of interdigital region', 0.4090909090909091, 3.334430194052109, 1.1679405290445888, 'UPHENO:0049587', 'abnormal biological_process'),
(473534, 'HP:0030853', 'Heterotaxy', 'XPO:0132091', 'abnormal development of intersomitic region', 0.4090909090909091, 3.334430194052109, 1.1679405290445888, 'UPHENO:0049587', 'abnormal biological_process'),
(473535, 'HP:0030853', 'Heterotaxy', 'XPO:0132847', 'abnormal development of perivitelline space', 0.4090909090909091, 3.334430194052109, 1.1679405290445888, 'UPHENO:0049587', 'abnormal biological_process'),
(473536, 'HP:0030853', 'Heterotaxy', 'XPO:0133261', 'abnormal development of pronephric sinus', 0.42857142857142855, 3.334430194052109, 1.195425243056469, 'UPHENO:0049587', 'abnormal biological_process'),
(473537, 'HP:0030853', 'Heterotaxy', 'XPO:0132986', 'abnormal development of vegetal pole', 0.42857142857142855, 3.334430194052109, 1.195425243056469, 'UPHENO:0049587', 'abnormal biological_process'),
(473538, 'HP:0030853', 'Heterotaxy', 'XPO:0133129', 'abnormal development of neurocoel', 0.42857142857142855, 3.334430194052109, 1.195425243056469, 'UPHENO:0049587', 'abnormal biological_process'),
(473539, 'HP:0030853', 'Heterotaxy', 'XPO:0132435', 'abnormal development of pupil', 0.42857142857142855, 3.334430194052109, 1.195425243056469, 'UPHENO:0049587', 'abnormal biological_process'),
(473540, 'HP:0030853', 'Heterotaxy', 'XPO:0132007', 'abnormal development of extracellular matrix', 0.4090909090909091, 3.334430194052109, 1.1679405290445888, 'UPHENO:0049587', 'abnormal biological_process'),
(473541, 'HP:0030853', 'Heterotaxy', 'XPO:0133037', 'abnormal development of dorsal region', 0.42857142857142855, 3.334430194052109, 1.195425243056469, 'UPHENO:0049587', 'abnormal biological_process'),
(473542, 'HP:0030853', 'Heterotaxy', 'XPO:0131760', 'abnormal development of anatomical structure', 0.45, 3.334430194052109, 1.2249463609984925, 'UPHENO:0049587', 'abnormal biological_process'),
(473543, 'HP:0030853', 'Heterotaxy', 'XPO:0141910', 'abnormal D-ribose metabolic process', 0.4230769230769231, 3.334430194052109, 1.187737541174124, 'UPHENO:0049587', 'abnormal biological_process'),
(473544, 'HP:0030853', 'Heterotaxy', 'XPO:0133228', 'abnormal development of dorsolateral neural tube', 0.4090909090909091, 3.334430194052109, 1.1679405290445888, 'UPHENO:0049587', 'abnormal biological_process'),
(473545, 'HP:0030853', 'Heterotaxy', 'XPO:0131782', 'abnormal development of organism subdivision', 0.4090909090909091, 3.334430194052109, 1.1679405290445888, 'UPHENO:0049587', 'abnormal biological_process'),
(473546, 'HP:0030853', 'Heterotaxy', 'XPO:0100728', 'abnormal cell condensation', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(473547, 'HP:0030853', 'Heterotaxy', 'XPO:0132280', 'abnormal development of chondroblast', 0.4090909090909091, 3.334430194052109, 1.1679405290445888, 'UPHENO:0049587', 'abnormal biological_process'),
(473548, 'HP:0030853', 'Heterotaxy', 'XPO:0132231', 'abnormal development of actin cytoskeleton', 0.4090909090909091, 3.334430194052109, 1.1679405290445888, 'UPHENO:0049587', 'abnormal biological_process'),
(473549, 'HP:0030853', 'Heterotaxy', 'XPO:0133299', 'abnormal development of centromere', 0.4090909090909091, 3.334430194052109, 1.1679405290445888, 'UPHENO:0049587', 'abnormal biological_process'),
(473550, 'HP:0030853', 'Heterotaxy', 'XPO:0131764', 'abnormal development of retinal progenitor cell region', 0.42857142857142855, 3.334430194052109, 1.195425243056469, 'UPHENO:0049587', 'abnormal biological_process'),
(473551, 'HP:0030853', 'Heterotaxy', 'XPO:0101297', 'abnormal barrier cell', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(473552, 'HP:0030853', 'Heterotaxy', 'XPO:0141745', 'abnormal creatinine homeostasis', 0.5, 1.4755025719078136, 0.8589244937443028, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(473553, 'HP:0030853', 'Heterotaxy', 'XPO:0133335', 'abnormal development of postero-ventral region', 0.42857142857142855, 3.334430194052109, 1.195425243056469, 'UPHENO:0049587', 'abnormal biological_process'),
(473554, 'HP:0030853', 'Heterotaxy', 'XPO:0132892', 'abnormal development of M band', 0.4090909090909091, 3.334430194052109, 1.1679405290445888, 'UPHENO:0049587', 'abnormal biological_process'),
(473555, 'HP:0030853', 'Heterotaxy', 'XPO:0141783', 'abnormal collagen metabolic process', 0.5238095238095238, 3.334430194052109, 1.3215923320459049, 'UPHENO:0049587', 'abnormal biological_process'),
(473556, 'HP:0030853', 'Heterotaxy', 'XPO:0132052', 'abnormal development of trunk placode', 0.4090909090909091, 3.334430194052109, 1.1679405290445888, 'UPHENO:0049587', 'abnormal biological_process'),
(473557, 'HP:0030853', 'Heterotaxy', 'XPO:0132400', 'abnormal development of oval window', 0.42857142857142855, 3.334430194052109, 1.195425243056469, 'UPHENO:0049587', 'abnormal biological_process'),
(473558, 'HP:0030853', 'Heterotaxy', 'XPO:0100721', 'abnormal centromere', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(473559, 'HP:0030853', 'Heterotaxy', 'XPO:0141791', 'abnormal primary metabolic process', 0.5238095238095238, 3.334430194052109, 1.3215923320459049, 'UPHENO:0049587', 'abnormal biological_process'),
(473560, 'HP:0030853', 'Heterotaxy', 'XPO:0132607', 'abnormal development of microtubule', 0.4090909090909091, 3.334430194052109, 1.1679405290445888, 'UPHENO:0049587', 'abnormal biological_process'),
(473561, 'HP:0030853', 'Heterotaxy', 'XPO:0132372', 'abnormal development of cleavage furrow', 0.4090909090909091, 3.334430194052109, 1.1679405290445888, 'UPHENO:0049587', 'abnormal biological_process'),
(473562, 'HP:0030853', 'Heterotaxy', 'XPO:0101240', 'abnormal ciliated non-epidermal cell', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(473563, 'HP:0030853', 'Heterotaxy', 'XPO:0131861', 'abnormal development of thrombocyte', 0.4090909090909091, 3.334430194052109, 1.1679405290445888, 'UPHENO:0049587', 'abnormal biological_process'),
(473564, 'HP:0030853', 'Heterotaxy', 'XPO:0132861', 'abnormal development of pericyte', 0.4090909090909091, 3.334430194052109, 1.1679405290445888, 'UPHENO:0049587', 'abnormal biological_process'),
(473565, 'HP:0030853', 'Heterotaxy', 'XPO:0133254', 'abnormal development of ligament cell', 0.4090909090909091, 3.334430194052109, 1.1679405290445888, 'UPHENO:0049587', 'abnormal biological_process'),
(473566, 'HP:0030853', 'Heterotaxy', 'XPO:0100239', 'abnormal acellular anatomical structure', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(473567, 'HP:0030853', 'Heterotaxy', 'XPO:0101061', 'abnormal plasma membrane', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(473568, 'HP:0030853', 'Heterotaxy', 'XPO:0131723', 'abnormal pathway-restricted SMAD protein phosphorylation', 0.5, 1.4755025719078136, 0.8589244937443028, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(473569, 'HP:0030853', 'Heterotaxy', 'XPO:0100501', 'abnormal urogenital system', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(473570, 'HP:0030853', 'Heterotaxy', 'XPO:0131756', 'abnormal development of vegetal yolk mass', 0.4090909090909091, 3.334430194052109, 1.1679405290445888, 'UPHENO:0049587', 'abnormal biological_process'),
(473571, 'HP:0030853', 'Heterotaxy', 'XPO:0100084', 'abnormal anatomical group', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(473572, 'HP:0030853', 'Heterotaxy', 'XPO:0141907', 'abnormal putrescine metabolic process', 0.4782608695652174, 3.334430194052109, 1.2628251993494104, 'UPHENO:0049587', 'abnormal biological_process'),
(473573, 'HP:0030853', 'Heterotaxy', 'XPO:0115505', 'dead whole organism', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(473574, 'HP:0030853', 'Heterotaxy', 'XPO:0131740', 'abnormal detection of nodal flow', 0.47368421052631576, 3.334430194052109, 1.2567684488499395, 'UPHENO:0049587', 'abnormal biological_process'),
(473575, 'HP:0030853', 'Heterotaxy', 'XPO:0131667', 'abnormal actin cytoskeleton', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(473576, 'HP:0030853', 'Heterotaxy', 'XPO:0133263', 'abnormal development of yolk platelet', 0.4090909090909091, 3.334430194052109, 1.1679405290445888, 'UPHENO:0049587', 'abnormal biological_process'),
(473577, 'HP:0030853', 'Heterotaxy', 'XPO:0133388', 'absent insulin receptor signaling pathway', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(473578, 'HP:0030853', 'Heterotaxy', 'XPO:0132485', 'abnormal development of ring structure', 0.4090909090909091, 3.334430194052109, 1.1679405290445888, 'UPHENO:0049587', 'abnormal biological_process'),
(473579, 'HP:0030853', 'Heterotaxy', 'XPO:0107259', 'abnormal animal-vegetal axis', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(473580, 'HP:0030853', 'Heterotaxy', 'XPO:0131807', 'abnormal development of anatomical group', 0.42857142857142855, 3.334430194052109, 1.195425243056469, 'UPHENO:0049587', 'abnormal biological_process'),
(473581, 'HP:0030853', 'Heterotaxy', 'XPO:0132321', 'abnormal development of epiphysis', 0.4090909090909091, 3.334430194052109, 1.1679405290445888, 'UPHENO:0049587', 'abnormal biological_process'),
(473582, 'HP:0030853', 'Heterotaxy', 'XPO:0141871', 'abnormal cadaverine transport', 0.45, 3.334430194052109, 1.2249463609984925, 'UPHENO:0049587', 'abnormal biological_process'),
(473583, 'HP:0030853', 'Heterotaxy', 'XPO:0141770', 'abnormal urate homeostasis', 0.5, 1.4755025719078136, 0.8589244937443028, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(473584, 'HP:0030853', 'Heterotaxy', 'XPO:0141265', 'abnormal escape behavior', 0.5, 1.4755025719078136, 0.8589244937443028, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(473585, 'HP:0030853', 'Heterotaxy', 'XPO:0132979', 'abnormal development of presumptive paraxial mesoderm', 0.4090909090909091, 3.334430194052109, 1.1679405290445888, 'UPHENO:0049587', 'abnormal biological_process'),
(473586, 'HP:0030853', 'Heterotaxy', 'XPO:0107253', 'abnormal enteric nervous system', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(473587, 'HP:0030853', 'Heterotaxy', 'XPO:0141795', 'abnormal glycosylation', 0.4782608695652174, 3.334430194052109, 1.2628251993494104, 'UPHENO:0049587', 'abnormal biological_process'),
(473588, 'HP:0030853', 'Heterotaxy', 'XPO:0132943', 'abnormal development of left-right axis', 0.4090909090909091, 3.334430194052109, 1.1679405290445888, 'UPHENO:0049587', 'abnormal biological_process'),
(473589, 'HP:0030853', 'Heterotaxy', 'XPO:0141787', 'abnormal hormone metabolic process', 0.5238095238095238, 3.334430194052109, 1.3215923320459049, 'UPHENO:0049587', 'abnormal biological_process'),
(473590, 'HP:0030853', 'Heterotaxy', 'XPO:0132787', 'abnormal development of apical region', 0.42857142857142855, 3.334430194052109, 1.195425243056469, 'UPHENO:0049587', 'abnormal biological_process'),
(473591, 'HP:0030853', 'Heterotaxy', 'XPO:0132668', 'abnormal development of anterior endoderm', 0.42857142857142855, 3.334430194052109, 1.195425243056469, 'UPHENO:0049587', 'abnormal biological_process'),
(473592, 'HP:0030853', 'Heterotaxy', 'XPO:0132911', 'abnormal development of posterior foregut', 0.4090909090909091, 3.334430194052109, 1.1679405290445888, 'UPHENO:0049587', 'abnormal biological_process'),
(473593, 'HP:0030853', 'Heterotaxy', 'XPO:0107312', 'abnormal filopodium', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(473594, 'HP:0030853', 'Heterotaxy', 'XPO:0107258', 'abnormal anatomical axis', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(473595, 'HP:0030853', 'Heterotaxy', 'XPO:0141738', 'abnormal carbon dioxide homeostasis', 0.5, 1.4755025719078136, 0.8589244937443028, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(473596, 'HP:0030853', 'Heterotaxy', 'XPO:0101113', 'abnormal stage IV oocyte', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(473597, 'HP:0030853', 'Heterotaxy', 'XPO:0132858', 'abnormal development of rib', 0.4090909090909091, 3.334430194052109, 1.1679405290445888, 'UPHENO:0049587', 'abnormal biological_process'),
(473598, 'HP:0030853', 'Heterotaxy', 'XPO:0100969', 'abnormal disaggregated/reaggregated ectoderm treated with activin', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(473599, 'HP:0030853', 'Heterotaxy', 'XPO:0132876', 'abnormal development of endodermal cell', 0.4090909090909091, 3.334430194052109, 1.1679405290445888, 'UPHENO:0049587', 'abnormal biological_process'),
(473600, 'HP:0030853', 'Heterotaxy', 'XPO:0131721', 'abnormal nodal signaling pathway', 0.45, 3.334430194052109, 1.2249463609984925, 'UPHENO:0049587', 'abnormal biological_process'),
(473601, 'HP:0030853', 'Heterotaxy', 'XPO:0100585', 'abnormal elastica externa', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(473602, 'HP:0030853', 'Heterotaxy', 'XPO:0133069', 'abnormal development of astrocyte end-foot', 0.4090909090909091, 3.334430194052109, 1.1679405290445888, 'UPHENO:0049587', 'abnormal biological_process'),
(473603, 'HP:0030853', 'Heterotaxy', 'XPO:0100308', 'abnormal early embryonic cell', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(473604, 'HP:0030853', 'Heterotaxy', 'XPO:0133206', 'abnormal development of hemangioblast', 0.4090909090909091, 3.334430194052109, 1.1679405290445888, 'UPHENO:0049587', 'abnormal biological_process'),
(473605, 'HP:0030853', 'Heterotaxy', 'XPO:0141790', 'abnormal cellular metabolic process', 0.5, 3.334430194052109, 1.2912068374300278, 'UPHENO:0049587', 'abnormal biological_process'),
(473606, 'HP:0030853', 'Heterotaxy', 'XPO:0101467', 'abnormal alkali secreting cell', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(473607, 'HP:0030853', 'Heterotaxy', 'XPO:0131719', 'abnormal activation of meiosis', 0.47368421052631576, 3.334430194052109, 1.2567684488499395, 'UPHENO:0049587', 'abnormal biological_process'),
(473608, 'HP:0030853', 'Heterotaxy', 'XPO:0141744', 'abnormal chemical homeostasis', 0.45, 3.334430194052109, 1.2249463609984925, 'UPHENO:0049587', 'abnormal biological_process'),
(473609, 'HP:0030853', 'Heterotaxy', 'XPO:0101132', 'abnormal apoptotic cell', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(473610, 'HP:0030853', 'Heterotaxy', 'XPO:0100545', 'abnormal male organism', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(473611, 'HP:0030853', 'Heterotaxy', 'XPO:0116434', 'abnormal biological process', 0.5625, 3.334430194052109, 1.369531665991813, 'UPHENO:0049587', 'abnormal biological_process'),
(473612, 'HP:0030853', 'Heterotaxy', 'XPO:0101157', 'abnormal female organism', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(473613, 'HP:0030853', 'Heterotaxy', 'XPO:0132920', 'abnormal development of olfactory epithelial support cell', 0.4090909090909091, 3.334430194052109, 1.1679405290445888, 'UPHENO:0049587', 'abnormal biological_process'),
(473614, 'HP:0030853', 'Heterotaxy', 'XPO:0132678', 'abnormal development of proximal tubule branch', 0.42857142857142855, 3.334430194052109, 1.195425243056469, 'UPHENO:0049587', 'abnormal biological_process'),
(473615, 'HP:0030853', 'Heterotaxy', 'XPO:0131798', 'abnormal development of anatomical space', 0.45, 3.334430194052109, 1.2249463609984925, 'UPHENO:0049587', 'abnormal biological_process'),
(473616, 'HP:0030853', 'Heterotaxy', 'XPO:0141748', 'abnormal gas homeostasis', 0.5, 1.4755025719078136, 0.8589244937443028, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(473617, 'HP:0030853', 'Heterotaxy', 'XPO:0116494', 'absent biological process', 0.47058823529411764, 1.4755025719078136, 0.8332791557971614, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(473618, 'HP:0030853', 'Heterotaxy', 'XPO:0141776', 'abnormal metabolic process', 0.5789473684210527, 3.334430194052109, 1.3894097977307374, 'UPHENO:0049587', 'abnormal biological_process'),
(473619, 'HP:0030853', 'Heterotaxy', 'XPO:0133304', 'abnormal development of digit-joint region', 0.4090909090909091, 3.334430194052109, 1.1679405290445888, 'UPHENO:0049587', 'abnormal biological_process'),
(473620, 'HP:0030853', 'Heterotaxy', 'XPO:0132317', 'abnormal development of cilium', 0.4090909090909091, 3.334430194052109, 1.1679405290445888, 'UPHENO:0049587', 'abnormal biological_process'),
(473621, 'HP:0030853', 'Heterotaxy', 'XPO:0132865', 'abnormal development of lateral nasal prominence', 0.4090909090909091, 3.334430194052109, 1.1679405290445888, 'UPHENO:0049587', 'abnormal biological_process'),
(473622, 'HP:0030853', 'Heterotaxy', 'XPO:0141883', 'abnormal glycerol metabolic process', 0.4230769230769231, 3.334430194052109, 1.187737541174124, 'UPHENO:0049587', 'abnormal biological_process'),
(473623, 'HP:0030853', 'Heterotaxy', 'XPO:0100802', 'abnormal exocrine cell', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(473624, 'HP:0030853', 'Heterotaxy', 'XPO:0131909', 'abnormal development of blastopore lip', 0.4090909090909091, 3.334430194052109, 1.1679405290445888, 'UPHENO:0049587', 'abnormal biological_process'),
(473625, 'HP:0030853', 'Heterotaxy', 'XPO:0132536', 'abnormal development of choana', 0.4090909090909091, 3.334430194052109, 1.1679405290445888, 'UPHENO:0049587', 'abnormal biological_process'),
(473626, 'HP:0030853', 'Heterotaxy', 'XPO:0132181', 'abnormal development of germ plasm', 0.4090909090909091, 3.334430194052109, 1.1679405290445888, 'UPHENO:0049587', 'abnormal biological_process'),
(473627, 'HP:0030853', 'Heterotaxy', 'XPO:0101237', 'abnormal mucus secreting cell', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(473628, 'HP:0030853', 'Heterotaxy', 'XPO:0141736', 'abnormal anatomical structure homeostasis', 0.4090909090909091, 3.334430194052109, 1.1679405290445888, 'UPHENO:0049587', 'abnormal biological_process'),
(473629, 'HP:0030853', 'Heterotaxy', 'XPO:0132935', 'abnormal development of circumpharyngeal ridge', 0.4090909090909091, 3.334430194052109, 1.1679405290445888, 'UPHENO:0049587', 'abnormal biological_process'),
(473630, 'HP:0030853', 'Heterotaxy', 'XPO:0100172', 'abnormal stem cell', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(473631, 'HP:0030853', 'Heterotaxy', 'XPO:0101326', 'abnormal cementoblast', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(473632, 'HP:0030853', 'Heterotaxy', 'XPO:0141781', 'abnormal secondary metabolic process', 0.5238095238095238, 3.334430194052109, 1.3215923320459049, 'UPHENO:0049587', 'abnormal biological_process'),
(473633, 'HP:0030853', 'Heterotaxy', 'XPO:0133325', 'abnormal development of postero-dorsal region', 0.42857142857142855, 3.334430194052109, 1.195425243056469, 'UPHENO:0049587', 'abnormal biological_process'),
(473634, 'HP:0030853', 'Heterotaxy', 'XPO:0131469', 'abnormal heart process', 0.5, 3.334430194052109, 1.2912068374300278, 'UPHENO:0049587', 'abnormal biological_process'),
(473635, 'HP:0030853', 'Heterotaxy', 'XPO:0133300', 'abnormal development of skeletal muscle satellite cell', 0.4090909090909091, 3.334430194052109, 1.1679405290445888, 'UPHENO:0049587', 'abnormal biological_process'),
(473636, 'HP:0030853', 'Heterotaxy', 'XPO:0132587', 'abnormal development of keratin accumulating cell', 0.4090909090909091, 3.334430194052109, 1.1679405290445888, 'UPHENO:0049587', 'abnormal biological_process'),
(473637, 'HP:0030853', 'Heterotaxy', 'XPO:0131880', 'abnormal development of presumptive rhombomere', 0.4090909090909091, 3.334430194052109, 1.1679405290445888, 'UPHENO:0049587', 'abnormal biological_process'),
(473638, 'HP:0030853', 'Heterotaxy', 'XPO:0133184', 'abnormal development of ventro-lateral region', 0.42857142857142855, 3.334430194052109, 1.195425243056469, 'UPHENO:0049587', 'abnormal biological_process'),
(473639, 'HP:0030853', 'Heterotaxy', 'XPO:0100344', 'abnormal portion of organism substance', 0.47058823529411764, 1.4755025719078136, 0.8332791557971614, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(473640, 'HP:0030853', 'Heterotaxy', 'XPO:0131403', 'abnormal mechanosensory behavior', 0.42857142857142855, 3.334430194052109, 1.195425243056469, 'UPHENO:0049587', 'abnormal biological_process'),
(473641, 'HP:0030853', 'Heterotaxy', 'XPO:0100392', 'abnormal cilium', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(473642, 'HP:0030853', 'Heterotaxy', 'XPO:0132823', 'abnormal development of basal region', 0.42857142857142855, 3.334430194052109, 1.195425243056469, 'UPHENO:0049587', 'abnormal biological_process'),
(473643, 'HP:0030853', 'Heterotaxy', 'XPO:0131755', 'abnormal development of tissue', 0.4090909090909091, 3.334430194052109, 1.1679405290445888, 'UPHENO:0049587', 'abnormal biological_process'),
(473644, 'HP:0030853', 'Heterotaxy', 'XPO:0131685', 'abnormal cortical actin cytoskeleton', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(473645, 'HP:0030853', 'Heterotaxy', 'XPO:0100377', 'abnormal connective tissue', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(473646, 'HP:0030853', 'Heterotaxy', 'XPO:0132927', 'abnormal development of central retina', 0.42857142857142855, 3.334430194052109, 1.195425243056469, 'UPHENO:0049587', 'abnormal biological_process'),
(473647, 'HP:0030853', 'Heterotaxy', 'XPO:0100031', 'abnormal central nervous system', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(473648, 'HP:0030853', 'Heterotaxy', 'XPO:0131704', 'abnormal cell migration', 0.42857142857142855, 3.334430194052109, 1.195425243056469, 'UPHENO:0049587', 'abnormal biological_process'),
(473649, 'HP:0030853', 'Heterotaxy', 'XPO:0133001', 'abnormal development of wedge region', 0.4090909090909091, 3.334430194052109, 1.1679405290445888, 'UPHENO:0049587', 'abnormal biological_process'),
(473650, 'HP:0030853', 'Heterotaxy', 'XPO:0116429', 'abnormal behavior', 0.47368421052631576, 3.334430194052109, 1.2567684488499395, 'UPHENO:0049587', 'abnormal biological_process'),
(473651, 'HP:0030853', 'Heterotaxy', 'XPO:0100423', 'abnormal process', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(473652, 'HP:0030853', 'Heterotaxy', 'XPO:0132192', 'abnormal development of prechordal plate', 0.4090909090909091, 3.334430194052109, 1.1679405290445888, 'UPHENO:0049587', 'abnormal biological_process'),
(473653, 'HP:0030853', 'Heterotaxy', 'XPO:0132808', 'abnormal development of medium cavity', 0.42857142857142855, 3.334430194052109, 1.195425243056469, 'UPHENO:0049587', 'abnormal biological_process'),
(473654, 'HP:0030853', 'Heterotaxy', 'XPO:0132695', 'abnormal development of posterior endomesoderm', 0.42857142857142855, 3.334430194052109, 1.195425243056469, 'UPHENO:0049587', 'abnormal biological_process'),
(473655, 'HP:0030853', 'Heterotaxy', 'XPO:0131745', 'abnormal axis elongation', 0.6190476190476191, 8.819732420846037, 2.336628844245879, 'HP:0001507', 'Growth abnormality'),
(473656, 'HP:0030853', 'Heterotaxy', 'XPO:0101569', 'abnormal activin-induced ectoderm', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(473657, 'HP:0030853', 'Heterotaxy', 'XPO:0132382', 'abnormal development of presumptive midbrain-hindbrain boundary', 0.4090909090909091, 3.334430194052109, 1.1679405290445888, 'UPHENO:0049587', 'abnormal biological_process'),
(473658, 'HP:0030853', 'Heterotaxy', 'XPO:0141771', 'abnormal urea homeostasis', 0.5, 1.4755025719078136, 0.8589244937443028, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(473659, 'HP:0030853', 'Heterotaxy', 'XPO:0133215', 'abnormal development of adherens junction', 0.4090909090909091, 3.334430194052109, 1.1679405290445888, 'UPHENO:0049587', 'abnormal biological_process'),
(473660, 'HP:0030853', 'Heterotaxy', 'XPO:0133140', 'abnormal development of basal lamina', 0.4090909090909091, 3.334430194052109, 1.1679405290445888, 'UPHENO:0049587', 'abnormal biological_process'),
(473661, 'HP:0030853', 'Heterotaxy', 'XPO:0131726', 'abnormal Wnt signaling pathway, planar cell polarity pathway', 0.4090909090909091, 3.334430194052109, 1.1679405290445888, 'UPHENO:0049587', 'abnormal biological_process'),
(473662, 'HP:0030853', 'Heterotaxy', 'XPO:0132611', 'abnormal development of intercanthal region', 0.42857142857142855, 3.334430194052109, 1.195425243056469, 'UPHENO:0049587', 'abnormal biological_process'),
(473663, 'HP:0030853', 'Heterotaxy', 'XPO:0132785', 'abnormal development of oocyte cortex', 0.4090909090909091, 3.334430194052109, 1.1679405290445888, 'UPHENO:0049587', 'abnormal biological_process'),
(473664, 'HP:0030853', 'Heterotaxy', 'XPO:0141864', 'abnormal 5-methylcytosine metabolic process', 0.4230769230769231, 3.334430194052109, 1.187737541174124, 'UPHENO:0049587', 'abnormal biological_process'),
(473665, 'HP:0030853', 'Heterotaxy', 'XPO:0101472', 'abnormal zygote cortex', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(473666, 'HP:0030853', 'Heterotaxy', 'XPO:0132446', 'abnormal development of midbrain-hindbrain boundary', 0.4090909090909091, 3.334430194052109, 1.1679405290445888, 'UPHENO:0049587', 'abnormal biological_process'),
(473667, 'HP:0030853', 'Heterotaxy', 'XPO:0132585', 'abnormal development of pharyngeal cavity', 0.42857142857142855, 3.334430194052109, 1.195425243056469, 'UPHENO:0049587', 'abnormal biological_process'),
(473668, 'HP:0030853', 'Heterotaxy', 'XPO:0131774', 'abnormal development of anatomical cluster', 0.4090909090909091, 3.334430194052109, 1.1679405290445888, 'UPHENO:0049587', 'abnormal biological_process'),
(473669, 'HP:0030853', 'Heterotaxy', 'XPO:0141794', 'abnormal prosthetic group metabolic process', 0.5238095238095238, 3.334430194052109, 1.3215923320459049, 'UPHENO:0049587', 'abnormal biological_process'),
(473670, 'HP:0030853', 'Heterotaxy', 'XPO:0133026', 'abnormal development of forebrain-midbrain boundary', 0.42857142857142855, 3.334430194052109, 1.195425243056469, 'UPHENO:0049587', 'abnormal biological_process'),
(473671, 'HP:0030853', 'Heterotaxy', 'XPO:0132528', 'abnormal development of sarcomere', 0.4090909090909091, 3.334430194052109, 1.1679405290445888, 'UPHENO:0049587', 'abnormal biological_process'),
(473672, 'HP:0030853', 'Heterotaxy', 'XPO:0141877', 'abnormal 2-deoxyribose 1-phosphate metabolic process', 0.4583333333333333, 3.334430194052109, 1.2362364278758398, 'UPHENO:0049587', 'abnormal biological_process'),
(473673, 'HP:0030853', 'Heterotaxy', 'XPO:0141911', 'abnormal ribose phosphate metabolic process', 0.4583333333333333, 3.334430194052109, 1.2362364278758398, 'UPHENO:0049587', 'abnormal biological_process'),
(473674, 'HP:0030853', 'Heterotaxy', 'XPO:0131983', 'abnormal development of upper blastopore lip', 0.4090909090909091, 3.334430194052109, 1.1679405290445888, 'UPHENO:0049587', 'abnormal biological_process'),
(473675, 'HP:0030853', 'Heterotaxy', 'XPO:0132403', 'abnormal development of cell condensation', 0.42857142857142855, 3.334430194052109, 1.195425243056469, 'UPHENO:0049587', 'abnormal biological_process'),
(473676, 'HP:0030853', 'Heterotaxy', 'XPO:0141842', 'increased whole organism mass', 0.48148148148148145, 8.819732420846037, 2.0607129427116244, 'HP:0001507', 'Growth abnormality'),
(473677, 'HP:0030853', 'Heterotaxy', 'XPO:0101547', 'abnormal lampbrush chromosome', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(473678, 'HP:0030853', 'Heterotaxy', 'XPO:0101366', 'abnormal morula cell', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(473679, 'HP:0030853', 'Heterotaxy', 'XPO:0100032', 'abnormal nervous system', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(473680, 'HP:0030853', 'Heterotaxy', 'XPO:0101480', 'abnormal stage V oocyte', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(473681, 'HP:0030853', 'Heterotaxy', 'XPO:0133109', 'abnormal development of plasma membrane', 0.4090909090909091, 3.334430194052109, 1.1679405290445888, 'UPHENO:0049587', 'abnormal biological_process'),
(473682, 'HP:0030853', 'Heterotaxy', 'XPO:0100638', 'abnormal polar body', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(473683, 'HP:0030853', 'Heterotaxy', 'XPO:0100899', 'abnormal secondary spermatogonium', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(473684, 'HP:0030853', 'Heterotaxy', 'XPO:0133179', 'abnormal development of mucus secreting cell', 0.4090909090909091, 3.334430194052109, 1.1679405290445888, 'UPHENO:0049587', 'abnormal biological_process'),
(473685, 'HP:0030853', 'Heterotaxy', 'XPO:0100026', 'abnormal germ cell', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(473686, 'HP:0030853', 'Heterotaxy', 'XPO:0100258', 'abnormal organ part', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(473687, 'HP:0030853', 'Heterotaxy', 'XPO:0131730', 'abnormal regulation of protein folding', 0.5, 3.334430194052109, 1.2912068374300278, 'UPHENO:0049587', 'abnormal biological_process'),
(473688, 'HP:0030853', 'Heterotaxy', 'XPO:0141775', 'abnormal nitrogen compound metabolic process', 0.5238095238095238, 3.334430194052109, 1.3215923320459049, 'UPHENO:0049587', 'abnormal biological_process'),
(473689, 'HP:0030853', 'Heterotaxy', 'XPO:0132456', 'abnormal development of prime meridian', 0.42857142857142855, 3.334430194052109, 1.195425243056469, 'UPHENO:0049587', 'abnormal biological_process'),
(473690, 'HP:0030853', 'Heterotaxy', 'XPO:0131705', 'abnormal chemotaxis', 0.45, 3.334430194052109, 1.2249463609984925, 'UPHENO:0049587', 'abnormal biological_process'),
(473691, 'HP:0030853', 'Heterotaxy', 'XPO:0141600', 'absent metamorphosis', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(473692, 'HP:0030853', 'Heterotaxy', 'XPO:0131701', 'abnormal calcium ion transport', 0.42857142857142855, 3.334430194052109, 1.195425243056469, 'UPHENO:0049587', 'abnormal biological_process'),
(473693, 'HP:0030853', 'Heterotaxy', 'XPO:0141597', 'abnormal metamorphosis', 0.42857142857142855, 3.334430194052109, 1.195425243056469, 'UPHENO:0049587', 'abnormal biological_process'),
(473694, 'HP:0030853', 'Heterotaxy', 'XPO:0131806', 'abnormal development of anatomical system', 0.4090909090909091, 3.334430194052109, 1.1679405290445888, 'UPHENO:0049587', 'abnormal biological_process'),
(473695, 'HP:0030853', 'Heterotaxy', 'XPO:0101461', 'abnormal sperm entry point', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(473696, 'HP:0030853', 'Heterotaxy', 'XPO:0133302', 'abnormal development of growth cone', 0.4090909090909091, 3.334430194052109, 1.1679405290445888, 'UPHENO:0049587', 'abnormal biological_process'),
(473697, 'HP:0030853', 'Heterotaxy', 'XPO:0132851', 'abnormal development of angioblast', 0.4090909090909091, 3.334430194052109, 1.1679405290445888, 'UPHENO:0049587', 'abnormal biological_process'),
(473698, 'HP:0030853', 'Heterotaxy', 'XPO:0131401', 'abnormal behavioral response to pain', 0.42857142857142855, 3.334430194052109, 1.195425243056469, 'UPHENO:0049587', 'abnormal biological_process'),
(473699, 'HP:0030853', 'Heterotaxy', 'XPO:0131761', 'abnormal development of multi-tissue structure', 0.4090909090909091, 3.334430194052109, 1.1679405290445888, 'UPHENO:0049587', 'abnormal biological_process'),
(473700, 'HP:0030853', 'Heterotaxy', 'XPO:0141854', 'abnormal glutathione metabolic process', 0.4230769230769231, 3.334430194052109, 1.187737541174124, 'UPHENO:0049587', 'abnormal biological_process'),
(473701, 'HP:0030853', 'Heterotaxy', 'XPO:0131757', 'abnormal development of multicellular anatomical structure', 0.42857142857142855, 3.334430194052109, 1.195425243056469, 'UPHENO:0049587', 'abnormal biological_process'),
(473702, 'HP:0030853', 'Heterotaxy', 'XPO:0133394', 'abnormal determination of left/right symmetry in lateral plate mesoderm', 0.4090909090909091, 3.334430194052109, 1.1679405290445888, 'UPHENO:0049587', 'abnormal biological_process'),
(473703, 'HP:0030853', 'Heterotaxy', 'XPO:0141263', 'abnormal visually guided collision avoidance behavior', 0.5, 1.4755025719078136, 0.8589244937443028, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(473704, 'HP:0030853', 'Heterotaxy', 'XPO:0132804', 'abnormal development of alkali secreting cell', 0.4090909090909091, 3.334430194052109, 1.1679405290445888, 'UPHENO:0049587', 'abnormal biological_process'),
(473705, 'HP:0030853', 'Heterotaxy', 'XPO:0100225', 'abnormal endocrine system', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(473706, 'HP:0030853', 'Heterotaxy', 'XPO:0133403', 'abnormal developmental process', 0.5, 3.334430194052109, 1.2912068374300278, 'UPHENO:0049587', 'abnormal biological_process'),
(473707, 'HP:0030853', 'Heterotaxy', 'XPO:0131912', 'abnormal development of premigratory neural crest cell', 0.4090909090909091, 3.334430194052109, 1.1679405290445888, 'UPHENO:0049587', 'abnormal biological_process'),
(473708, 'HP:0030853', 'Heterotaxy', 'XPO:0133112', 'abnormal development of vegetal cortex', 0.4090909090909091, 3.334430194052109, 1.1679405290445888, 'UPHENO:0049587', 'abnormal biological_process'),
(473709, 'HP:0030853', 'Heterotaxy', 'XPO:0131871', 'abnormal development of embryo', 0.4090909090909091, 3.334430194052109, 1.1679405290445888, 'UPHENO:0049587', 'abnormal biological_process'),
(473710, 'HP:0030853', 'Heterotaxy', 'XPO:0133149', 'abnormal development of dorsal foregut', 0.4090909090909091, 3.334430194052109, 1.1679405290445888, 'UPHENO:0049587', 'abnormal biological_process'),
(473711, 'HP:0030853', 'Heterotaxy', 'XPO:0133336', 'abnormal development of anterior-posterior axis', 0.4090909090909091, 3.334430194052109, 1.1679405290445888, 'UPHENO:0049587', 'abnormal biological_process'),
(473712, 'HP:0030853', 'Heterotaxy', 'XPO:0132567', 'abnormal development of retinal stem cell region', 0.42857142857142855, 3.334430194052109, 1.195425243056469, 'UPHENO:0049587', 'abnormal biological_process'),
(473713, 'HP:0030853', 'Heterotaxy', 'XPO:0133007', 'abnormal development of acinar cell', 0.4090909090909091, 3.334430194052109, 1.1679405290445888, 'UPHENO:0049587', 'abnormal biological_process'),
(473714, 'HP:0030853', 'Heterotaxy', 'XPO:0133137', 'abnormal development of posterior endoderm', 0.42857142857142855, 3.334430194052109, 1.195425243056469, 'UPHENO:0049587', 'abnormal biological_process'),
(473715, 'HP:0030853', 'Heterotaxy', 'XPO:0132999', 'abnormal development of secondary myofiber', 0.4090909090909091, 3.334430194052109, 1.1679405290445888, 'UPHENO:0049587', 'abnormal biological_process'),
(473716, 'HP:0030853', 'Heterotaxy', 'XPO:0141315', 'abnormal anatomical region', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(473717, 'HP:0030853', 'Heterotaxy', 'XPO:0133216', 'abnormal development of barrier cell', 0.4090909090909091, 3.334430194052109, 1.1679405290445888, 'UPHENO:0049587', 'abnormal biological_process'),
(473718, 'HP:0030853', 'Heterotaxy', 'XPO:0131990', 'abnormal development of progenitor cell', 0.4090909090909091, 3.334430194052109, 1.1679405290445888, 'UPHENO:0049587', 'abnormal biological_process'),
(473719, 'HP:0030853', 'Heterotaxy', 'XPO:0132098', 'abnormal development of organ part', 0.42857142857142855, 3.334430194052109, 1.195425243056469, 'UPHENO:0049587', 'abnormal biological_process'),
(473720, 'HP:0030853', 'Heterotaxy', 'XPO:0132316', 'abnormal development of migratory neural crest cell', 0.4090909090909091, 3.334430194052109, 1.1679405290445888, 'UPHENO:0049587', 'abnormal biological_process'),
(473721, 'HP:0030853', 'Heterotaxy', 'XPO:0133060', 'abnormal development of zygote cortex', 0.4090909090909091, 3.334430194052109, 1.1679405290445888, 'UPHENO:0049587', 'abnormal biological_process'),
(473722, 'HP:0030853', 'Heterotaxy', 'XPO:0141859', 'abnormal lactose catabolic process', 0.4230769230769231, 3.334430194052109, 1.187737541174124, 'UPHENO:0049587', 'abnormal biological_process'),
(473723, 'HP:0030853', 'Heterotaxy', 'XPO:0103444', 'abnormal gastrulation', 0.42857142857142855, 3.334430194052109, 1.195425243056469, 'UPHENO:0049587', 'abnormal biological_process'),
(473724, 'HP:0030853', 'Heterotaxy', 'XPO:0100386', 'abnormal limb', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(473725, 'HP:0030853', 'Heterotaxy', 'XPO:0132347', 'abnormal development of myeloid cell', 0.4090909090909091, 3.334430194052109, 1.1679405290445888, 'UPHENO:0049587', 'abnormal biological_process'),
(473726, 'HP:0030853', 'Heterotaxy', 'XPO:0100289', 'abnormal chondroblast', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(473727, 'HP:0030853', 'Heterotaxy', 'XPO:0100791', 'abnormal multiciliated cell precursor', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(473728, 'HP:0030853', 'Heterotaxy', 'XPO:0115512', 'abnormally semi-erect whole organism', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(473729, 'HP:0030853', 'Heterotaxy', 'XPO:0100006', 'abnormal anatomical structure', 0.47058823529411764, 1.4755025719078136, 0.8332791557971614, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(473730, 'HP:0030853', 'Heterotaxy', 'XPO:0132250', 'abnormal development of male organism', 0.4090909090909091, 3.334430194052109, 1.1679405290445888, 'UPHENO:0049587', 'abnormal biological_process'),
(473731, 'HP:0030853', 'Heterotaxy', 'XPO:0100653', 'abnormal myoblast', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(473732, 'HP:0030853', 'Heterotaxy', 'XPO:0141904', 'abnormal glucosamine metabolic process', 0.5238095238095238, 3.334430194052109, 1.3215923320459049, 'UPHENO:0049587', 'abnormal biological_process'),
(473733, 'HP:0030853', 'Heterotaxy', 'XPO:0100010', 'abnormal multicellular anatomical structure', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(473734, 'HP:0030853', 'Heterotaxy', 'XPO:0132932', 'abnormal development of endothelial cell', 0.4090909090909091, 3.334430194052109, 1.1679405290445888, 'UPHENO:0049587', 'abnormal biological_process'),
(473735, 'HP:0030853', 'Heterotaxy', 'XPO:0133153', 'abnormal development of exocrine cell', 0.4090909090909091, 3.334430194052109, 1.1679405290445888, 'UPHENO:0049587', 'abnormal biological_process'),
(473736, 'HP:0030853', 'Heterotaxy', 'XPO:0141902', 'abnormal D-methionine transport', 0.4090909090909091, 3.334430194052109, 1.1679405290445888, 'UPHENO:0049587', 'abnormal biological_process'),
(473737, 'HP:0030853', 'Heterotaxy', 'XPO:0131786', 'abnormal development of chondrocyte', 0.4090909090909091, 3.334430194052109, 1.1679405290445888, 'UPHENO:0049587', 'abnormal biological_process'),
(473738, 'HP:0030853', 'Heterotaxy', 'XPO:0132624', 'abnormal development of migrating neuroblast', 0.4090909090909091, 3.334430194052109, 1.1679405290445888, 'UPHENO:0049587', 'abnormal biological_process'),
(473739, 'HP:0030853', 'Heterotaxy', 'XPO:0132906', 'abnormal development of optic disc', 0.42857142857142855, 3.334430194052109, 1.195425243056469, 'UPHENO:0049587', 'abnormal biological_process'),
(473740, 'HP:0030853', 'Heterotaxy', 'XPO:0132211', 'abnormal development of myofibril', 0.4090909090909091, 3.334430194052109, 1.1679405290445888, 'UPHENO:0049587', 'abnormal biological_process'),
(473741, 'HP:0030853', 'Heterotaxy', 'XPO:0141266', 'abnormal surface breathing', 0.5, 1.4755025719078136, 0.8589244937443028, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(473742, 'HP:0030853', 'Heterotaxy', 'XPO:0100956', 'abnormal centrosome', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(473743, 'HP:0030853', 'Heterotaxy', 'XPO:0100724', 'abnormal kinetochore', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(473744, 'HP:0030853', 'Heterotaxy', 'XPO:0131864', 'abnormal development of coelom', 0.42857142857142855, 3.334430194052109, 1.195425243056469, 'UPHENO:0049587', 'abnormal biological_process'),
(473745, 'HP:0030853', 'Heterotaxy', 'XPO:0132484', 'abnormal development of posterior neural tube', 0.4090909090909091, 3.334430194052109, 1.1679405290445888, 'UPHENO:0049587', 'abnormal biological_process'),
(473746, 'HP:0030853', 'Heterotaxy', 'XPO:0132373', 'abnormal development of axial mesoderm', 0.4090909090909091, 3.334430194052109, 1.1679405290445888, 'UPHENO:0049587', 'abnormal biological_process'),
(473747, 'HP:0030853', 'Heterotaxy', 'XPO:0131891', 'abnormal development of anterior neural tube', 0.4090909090909091, 3.334430194052109, 1.1679405290445888, 'UPHENO:0049587', 'abnormal biological_process'),
(473748, 'HP:0030853', 'Heterotaxy', 'XPO:0132205', 'abnormal development of somatic layer of lateral plate mesoderm', 0.4090909090909091, 3.334430194052109, 1.1679405290445888, 'UPHENO:0049587', 'abnormal biological_process'),
(473749, 'HP:0030853', 'Heterotaxy', 'XPO:0132054', 'abnormal development of portion of organism substance', 0.45, 3.334430194052109, 1.2249463609984925, 'UPHENO:0049587', 'abnormal biological_process'),
(473750, 'HP:0030853', 'Heterotaxy', 'XPO:0132557', 'abnormal development of filopodium', 0.4090909090909091, 3.334430194052109, 1.1679405290445888, 'UPHENO:0049587', 'abnormal biological_process'),
(473751, 'HP:0030853', 'Heterotaxy', 'XPO:0131818', 'abnormal development of mesonephric sinus', 0.42857142857142855, 3.334430194052109, 1.195425243056469, 'UPHENO:0049587', 'abnormal biological_process'),
(473752, 'HP:0030853', 'Heterotaxy', 'XPO:0132361', 'abnormal development of dorsal lateral plate mesoderm', 0.4090909090909091, 3.334430194052109, 1.1679405290445888, 'UPHENO:0049587', 'abnormal biological_process'),
(473753, 'HP:0030853', 'Heterotaxy', 'XPO:0133331', 'abnormal development of osteoblast', 0.4090909090909091, 3.334430194052109, 1.1679405290445888, 'UPHENO:0049587', 'abnormal biological_process'),
(473754, 'HP:0030853', 'Heterotaxy', 'XPO:0133139', 'abnormal development of apical junction complex', 0.4090909090909091, 3.334430194052109, 1.1679405290445888, 'UPHENO:0049587', 'abnormal biological_process'),
(473755, 'HP:0030853', 'Heterotaxy', 'XPO:0133210', 'abnormal development of animal-vegetal axis', 0.4090909090909091, 3.334430194052109, 1.1679405290445888, 'UPHENO:0049587', 'abnormal biological_process'),
(473756, 'HP:0030853', 'Heterotaxy', 'XPO:0141840', 'decreased whole organism mass', 0.4482758620689655, 8.819732420846037, 1.9883845589252502, 'HP:0001507', 'Growth abnormality'),
(473757, 'HP:0030853', 'Heterotaxy', 'XPO:0132688', 'abnormal development of nucleus', 0.4090909090909091, 3.334430194052109, 1.1679405290445888, 'UPHENO:0049587', 'abnormal biological_process'),
(473758, 'HP:0030853', 'Heterotaxy', 'XPO:0141788', 'abnormal hormone biosynthetic process', 0.44, 3.334430194052109, 1.2112593798947144, 'UPHENO:0049587', 'abnormal biological_process'),
(473759, 'HP:0030853', 'Heterotaxy', 'XPO:0131675', 'abnormal spindle microtubule', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(473760, 'HP:0030853', 'Heterotaxy', 'XPO:0100533', 'abnormal melanoblast', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(473761, 'HP:0030853', 'Heterotaxy', 'XPO:0132299', 'abnormal development of epicardial precursor cell', 0.4090909090909091, 3.334430194052109, 1.1679405290445888, 'UPHENO:0049587', 'abnormal biological_process'),
(473762, 'HP:0030853', 'Heterotaxy', 'XPO:0131729', 'abnormal regulation of growth rate', 0.5, 3.334430194052109, 1.2912068374300278, 'UPHENO:0049587', 'abnormal biological_process'),
(473763, 'HP:0030853', 'Heterotaxy', 'XPO:0101498', 'abnormal stage II oocyte', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(473764, 'HP:0030853', 'Heterotaxy', 'XPO:0133163', 'abnormal development of nucleate erythrocyte', 0.4090909090909091, 3.334430194052109, 1.1679405290445888, 'UPHENO:0049587', 'abnormal biological_process'),
(473765, 'HP:0030853', 'Heterotaxy', 'XPO:0132501', 'abnormal development of marginal zone (sensu neural)', 0.42857142857142855, 3.334430194052109, 1.195425243056469, 'UPHENO:0049587', 'abnormal biological_process'),
(473766, 'HP:0030853', 'Heterotaxy', 'XPO:0141778', 'abnormal biosynthetic process', 0.5238095238095238, 3.334430194052109, 1.3215923320459049, 'UPHENO:0049587', 'abnormal biological_process'),
(473767, 'HP:0030853', 'Heterotaxy', 'XPO:0131714', 'abnormal establishment of tissue polarity', 0.45, 3.334430194052109, 1.2249463609984925, 'UPHENO:0049587', 'abnormal biological_process'),
(473768, 'HP:0030853', 'Heterotaxy', 'XPO:0131699', 'abnormal axon extension involved in axon guidance', 0.52, 8.819732420846037, 2.141555709954784, 'HP:0001507', 'Growth abnormality'),
(473769, 'HP:0030853', 'Heterotaxy', 'XPO:0132842', 'abnormal development of cementoblast', 0.4090909090909091, 3.334430194052109, 1.1679405290445888, 'UPHENO:0049587', 'abnormal biological_process'),
(473770, 'HP:0030853', 'Heterotaxy', 'XPO:0133295', 'abnormal development of peripheral vegetal yolk mass', 0.4090909090909091, 3.334430194052109, 1.1679405290445888, 'UPHENO:0049587', 'abnormal biological_process'),
(473771, 'HP:0030853', 'Heterotaxy', 'XPO:0131698', 'abnormal apical constriction involved in gastrulation', 0.42857142857142855, 3.334430194052109, 1.195425243056469, 'UPHENO:0049587', 'abnormal biological_process'),
(473772, 'HP:0030853', 'Heterotaxy', 'XPO:0142057', 'abnormal desmosome', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(473773, 'HP:0030853', 'Heterotaxy', 'XPO:0141777', 'abnormal catabolic process', 0.5238095238095238, 3.334430194052109, 1.3215923320459049, 'UPHENO:0049587', 'abnormal biological_process'),
(473774, 'HP:0030853', 'Heterotaxy', 'XPO:0141754', 'abnormal homeostatic process', 0.5, 3.334430194052109, 1.2912068374300278, 'UPHENO:0049587', 'abnormal biological_process'),
(473775, 'HP:0030853', 'Heterotaxy', 'XPO:0141852', 'abnormal glucose metabolic process', 0.4230769230769231, 3.334430194052109, 1.187737541174124, 'UPHENO:0049587', 'abnormal biological_process'),
(473776, 'HP:0030853', 'Heterotaxy', 'XPO:0141759', 'abnormal lipid homeostasis', 0.4090909090909091, 3.334430194052109, 1.1679405290445888, 'UPHENO:0049587', 'abnormal biological_process'),
(473777, 'HP:0030853', 'Heterotaxy', 'XPO:0131973', 'abnormal development of anterior foregut', 0.4090909090909091, 3.334430194052109, 1.1679405290445888, 'UPHENO:0049587', 'abnormal biological_process'),
(473778, 'HP:0030853', 'Heterotaxy', 'XPO:0131715', 'abnormal fibroblast growth factor receptor signaling pathway', 0.45, 3.334430194052109, 1.2249463609984925, 'UPHENO:0049587', 'abnormal biological_process'),
(473779, 'HP:0030853', 'Heterotaxy', 'XPO:0131402', 'abnormal olfactory behavior', 0.4090909090909091, 3.334430194052109, 1.1679405290445888, 'UPHENO:0049587', 'abnormal biological_process'),
(473780, 'HP:0030853', 'Heterotaxy', 'XPO:00000000', 'Xenopus phenotype', 0.5333333333333333, 1.4755025719078136, 0.8870934026456857, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(473781, 'HP:0030853', 'Heterotaxy', 'XPO:0132194', 'abnormal development of midgut', 0.4090909090909091, 3.334430194052109, 1.1679405290445888, 'UPHENO:0049587', 'abnormal biological_process'),
(473782, 'HP:0030853', 'Heterotaxy', 'XPO:0100202', 'abnormal embryo', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(473783, 'HP:0030853', 'Heterotaxy', 'XPO:0132249', 'abnormal development of whole organism', 0.42857142857142855, 3.334430194052109, 1.195425243056469, 'UPHENO:0049587', 'abnormal biological_process'),
