(411291, 'HP:0034709', 'Uterine adenofibroma', 'XPO:0101752', 'abnormal genital system morphology', 0.4230769230769231, 7.005035523447265, 1.7215309684419309, 'HP:0012243', 'Abnormal reproductive system morphology'),
(411292, 'HP:0034709', 'Uterine adenofibroma', 'XPO:0126964', 'abnormally localised female genitalia', 0.4067796610169492, 7.960567433004586, 1.7994990752707185, 'UPHENO:0005170', 'abnormal female reproductive system'),
(411293, 'HP:0034709', 'Uterine adenofibroma', 'XPO:0100278', 'abnormal follicle cell', 0.45454545454545453, 8.550271745852811, 1.971417550192202, 'UPHENO:0076766', 'abnormal internal female genitalia morphology'),
(411294, 'HP:0034709', 'Uterine adenofibroma', 'XPO:0102260', 'abnormal primary oogonium morphology', 0.40540540540540543, 8.550271745852811, 1.861807289558681, 'UPHENO:0076766', 'abnormal internal female genitalia morphology'),
(411295, 'HP:0034709', 'Uterine adenofibroma', 'XPO:0101262', 'abnormal oviduct', 0.4444444444444444, 7.960567433004586, 1.8809651698594156, 'UPHENO:0005170', 'abnormal female reproductive system'),
(411296, 'HP:0034709', 'Uterine adenofibroma', 'XPO:0127178', 'abnormally localised follicle cell', 0.410958904109589, 8.550271745852811, 1.874516019274003, 'UPHENO:0076766', 'abnormal internal female genitalia morphology'),
(411297, 'HP:0034709', 'Uterine adenofibroma', 'XPO:0102596', 'abnormal follicle layer morphology', 0.43478260869565216, 8.550271745852811, 1.9280844003099589, 'UPHENO:0076766', 'abnormal internal female genitalia morphology'),
(411298, 'HP:0034709', 'Uterine adenofibroma', 'XPO:0100628', 'abnormal primary oogonium', 0.44776119402985076, 8.550271745852811, 1.9566501696017997, 'UPHENO:0076766', 'abnormal internal female genitalia morphology'),
(411299, 'HP:0034709', 'Uterine adenofibroma', 'XPO:0100036', 'abnormal ovary', 0.4838709677419355, 8.550271745852811, 2.0340177639642993, 'UPHENO:0076766', 'abnormal internal female genitalia morphology'),
(411300, 'HP:0034709', 'Uterine adenofibroma', 'XPO:0102864', 'abnormal female genitalia morphology', 0.45454545454545453, 8.209234828017744, 1.9317014200884415, 'UPHENO:0087974', 'abnormal female reproductive system morphology'),
(411301, 'HP:0034709', 'Uterine adenofibroma', 'XPO:0101668', 'abnormal ovary morphology', 0.4166666666666667, 8.550271745852811, 1.8874886032606055, 'UPHENO:0076766', 'abnormal internal female genitalia morphology'),
(411302, 'HP:0034709', 'Uterine adenofibroma', 'XPO:0126166', 'absent follicle layer', 0.40540540540540543, 8.550271745852811, 1.861807289558681, 'UPHENO:0076766', 'abnormal internal female genitalia morphology'),
(411303, 'HP:0005678', 'Anterior atlanto-occipital dislocation', 'XPO:0102216', 'abnormal vertebral column morphology', 0.5208333333333334, 8.05344015541032, 2.048047870764469, 'UPHENO:0002813', 'abnormal vertebral column'),
(411304, 'HP:0005678', 'Anterior atlanto-occipital dislocation', 'XPO:0100693', 'abnormal vertebral centrum', 0.5102040816326531, 8.05344015541032, 2.0270416962841815, 'UPHENO:0002813', 'abnormal vertebral column'),
(411305, 'HP:0005678', 'Anterior atlanto-occipital dislocation', 'XPO:0141713', 'increased size of the posterior notochord', 0.40816326530612246, 4.638757693672553, 1.3759979968056957, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(411306, 'HP:0005678', 'Anterior atlanto-occipital dislocation', 'XPO:0139774', 'abnormally necrotic elastica externa', 0.4444444444444444, 4.638757693672553, 1.4358516936218344, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(411307, 'HP:0005678', 'Anterior atlanto-occipital dislocation', 'XPO:0141703', 'abnormally necrotic posterior notochord', 0.425531914893617, 4.638757693672553, 1.404969552736279, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(411308, 'HP:0005678', 'Anterior atlanto-occipital dislocation', 'XPO:0127548', 'abnormally localised vertebral element', 0.423728813559322, 8.05344015541032, 1.8472884566637167, 'UPHENO:0002813', 'abnormal vertebral column'),
(411309, 'HP:0005678', 'Anterior atlanto-occipital dislocation', 'XPO:0130908', 'increased size of the notochordal sheath', 0.40816326530612246, 4.638757693672553, 1.3759979968056957, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(411310, 'HP:0005678', 'Anterior atlanto-occipital dislocation', 'XPO:0130368', 'increased size of the elastica externa', 0.425531914893617, 4.638757693672553, 1.404969552736279, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(411311, 'HP:0005678', 'Anterior atlanto-occipital dislocation', 'XPO:0101680', 'abnormal skeletal element morphology', 0.40816326530612246, 4.638757693672553, 1.3759979968056957, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(411312, 'HP:0005678', 'Anterior atlanto-occipital dislocation', 'XPO:0140683', 'abnormally necrotic flexural organ', 0.425531914893617, 4.638757693672553, 1.404969552736279, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(411313, 'HP:0005678', 'Anterior atlanto-occipital dislocation', 'XPO:0139771', 'abnormally necrotic skeletal subdivision', 0.4166666666666667, 4.638757693672553, 1.3902574242552699, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(411314, 'HP:0005678', 'Anterior atlanto-occipital dislocation', 'XPO:0101860', 'abnormal skeletal subdivision morphology', 0.46511627906976744, 4.638757693672553, 1.4688640910537754, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(411315, 'HP:0005678', 'Anterior atlanto-occipital dislocation', 'XPO:0102054', 'abnormal notochord morphology', 0.47619047619047616, 4.638757693672553, 1.4862477031377266, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(411316, 'HP:0005678', 'Anterior atlanto-occipital dislocation', 'XPO:0128580', 'decreased size of the postcranial axial skeleton', 0.42592592592592593, 6.272837960958401, 1.6345532468244968, 'UPHENO:0022529', 'abnormal postcranial axial skeleton morphology'),
(411317, 'HP:0005678', 'Anterior atlanto-occipital dislocation', 'XPO:0102164', 'abnormal mandibular mesenchyme morphology', 0.4117647058823529, 6.211345574613551, 1.599253852164941, 'UPHENO:0087089', 'abnormal axial skeleton plus cranial skeleton morphology'),
(411318, 'HP:0005678', 'Anterior atlanto-occipital dislocation', 'XPO:0102325', 'abnormal vertebral centrum morphology', 0.43859649122807015, 8.05344015541032, 1.8794176210938882, 'UPHENO:0002813', 'abnormal vertebral column'),
(411319, 'HP:0005678', 'Anterior atlanto-occipital dislocation', 'XPO:0102461', 'abnormal postcranial axial skeleton morphology', 0.5, 6.272837960958401, 1.770993783297728, 'UPHENO:0022529', 'abnormal postcranial axial skeleton morphology'),
(411320, 'HP:0005678', 'Anterior atlanto-occipital dislocation', 'XPO:0140510', 'abnormally necrotic postcranial axial skeleton', 0.4423076923076923, 6.272837960958401, 1.6656903922192745, 'UPHENO:0022529', 'abnormal postcranial axial skeleton morphology'),
(411321, 'HP:0005678', 'Anterior atlanto-occipital dislocation', 'XPO:0141704', 'decreased size of the anterior notochord', 0.40816326530612246, 4.638757693672553, 1.3759979968056957, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(411322, 'HP:0005678', 'Anterior atlanto-occipital dislocation', 'XPO:0101638', 'abnormal anatomical structure morphology', 0.40625, 2.786899518863159, 1.0640385000262718, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(411323, 'HP:0005678', 'Anterior atlanto-occipital dislocation', 'XPO:0140103', 'abnormally necrotic vertebral column', 0.46296296296296297, 8.05344015541032, 1.9309180501496346, 'UPHENO:0002813', 'abnormal vertebral column'),
(411324, 'HP:0005678', 'Anterior atlanto-occipital dislocation', 'XPO:0102351', 'abnormal sphenoid region morphology', 0.40350877192982454, 6.272837960958401, 1.5909573036826314, 'UPHENO:0022529', 'abnormal postcranial axial skeleton morphology'),
(411325, 'HP:0005678', 'Anterior atlanto-occipital dislocation', 'XPO:0101226', 'abnormal postsacral vertebra', 0.4166666666666667, 8.05344015541032, 1.8318297040812228, 'UPHENO:0002813', 'abnormal vertebral column'),
(411326, 'HP:0005678', 'Anterior atlanto-occipital dislocation', 'XPO:0141708', 'decreased size of the posterior notochord', 0.40816326530612246, 4.638757693672553, 1.3759979968056957, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(411327, 'HP:0005678', 'Anterior atlanto-occipital dislocation', 'XPO:0129786', 'increased size of the articular system', 0.4166666666666667, 4.638757693672553, 1.3902574242552699, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(411328, 'HP:0005678', 'Anterior atlanto-occipital dislocation', 'XPO:0102806', 'abnormal articular system morphology', 0.4878048780487805, 4.638757693672553, 1.5042634845863214, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(411329, 'HP:0005678', 'Anterior atlanto-occipital dislocation', 'XPO:0100927', 'abnormal sacral vertebra', 0.4166666666666667, 8.05344015541032, 1.8318297040812228, 'UPHENO:0002813', 'abnormal vertebral column'),
(411330, 'HP:0005678', 'Anterior atlanto-occipital dislocation', 'XPO:0103218', 'abnormal joint morphology', 0.4166666666666667, 4.638757693672553, 1.3902574242552699, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(411331, 'HP:0005678', 'Anterior atlanto-occipital dislocation', 'XPO:0140432', 'abnormally necrotic skeleton', 0.425531914893617, 4.638757693672553, 1.404969552736279, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(411332, 'HP:0005678', 'Anterior atlanto-occipital dislocation', 'XPO:0140350', 'abnormally necrotic notochordal sheath', 0.425531914893617, 4.638757693672553, 1.404969552736279, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(411333, 'HP:0005678', 'Anterior atlanto-occipital dislocation', 'XPO:0102097', 'abnormal skeletal system morphology', 0.5, 4.638757693672553, 1.5229507040072823, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(411334, 'HP:0005678', 'Anterior atlanto-occipital dislocation', 'XPO:0130188', 'increased size of the flexural organ', 0.40816326530612246, 4.638757693672553, 1.3759979968056957, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(411335, 'HP:0005678', 'Anterior atlanto-occipital dislocation', 'XPO:0102113', 'abnormal anatomical line morphology', 0.40625, 2.786899518863159, 1.0640385000262718, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(411336, 'HP:0005678', 'Anterior atlanto-occipital dislocation', 'XPO:0101982', 'abnormal appendicular skeleton morphology', 0.425531914893617, 4.638757693672553, 1.404969552736279, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(411337, 'HP:0005678', 'Anterior atlanto-occipital dislocation', 'XPO:0102130', 'abnormal endoskeleton morphology', 0.4444444444444444, 4.638757693672553, 1.4358516936218344, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(411338, 'HP:0005678', 'Anterior atlanto-occipital dislocation', 'XPO:0129664', 'increased size of the skeleton', 0.40816326530612246, 4.638757693672553, 1.3759979968056957, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(411339, 'HP:0005678', 'Anterior atlanto-occipital dislocation', 'XPO:0102093', 'abnormal craniofacial skeleton morphology', 0.4375, 6.211345574613551, 1.6484731386629958, 'UPHENO:0087089', 'abnormal axial skeleton plus cranial skeleton morphology'),
(411340, 'HP:0005678', 'Anterior atlanto-occipital dislocation', 'XPO:0102728', 'abnormal tendon morphology', 0.4166666666666667, 4.638757693672553, 1.3902574242552699, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(411341, 'HP:0005678', 'Anterior atlanto-occipital dislocation', 'XPO:0103116', 'abnormal bone marrow morphology', 0.40816326530612246, 4.638757693672553, 1.3759979968056957, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(411342, 'HP:0005678', 'Anterior atlanto-occipital dislocation', 'XPO:0102980', 'abnormal perichordal tissue morphology', 0.43478260869565216, 4.638757693672553, 1.4201588541997616, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(411343, 'HP:0005678', 'Anterior atlanto-occipital dislocation', 'XPO:0103152', 'abnormal otic region morphology', 0.40350877192982454, 6.272837960958401, 1.5909573036826314, 'UPHENO:0022529', 'abnormal postcranial axial skeleton morphology'),
(411344, 'HP:0005678', 'Anterior atlanto-occipital dislocation', 'XPO:0102564', 'abnormal olfactory region morphology', 0.40350877192982454, 6.272837960958401, 1.5909573036826314, 'UPHENO:0022529', 'abnormal postcranial axial skeleton morphology'),
(411345, 'HP:0005678', 'Anterior atlanto-occipital dislocation', 'XPO:0140019', 'abnormally necrotic skeletal system', 0.4444444444444444, 4.638757693672553, 1.4358516936218344, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(411346, 'HP:0005678', 'Anterior atlanto-occipital dislocation', 'XPO:0102567', 'abnormal skeleton morphology', 0.47619047619047616, 4.638757693672553, 1.4862477031377266, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(411347, 'HP:0005678', 'Anterior atlanto-occipital dislocation', 'XPO:0128709', 'decreased size of the flexural organ', 0.40816326530612246, 4.638757693672553, 1.3759979968056957, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(411348, 'HP:0005678', 'Anterior atlanto-occipital dislocation', 'XPO:0139998', 'abnormally necrotic axial skeleton', 0.4117647058823529, 6.211345574613551, 1.599253852164941, 'UPHENO:0087089', 'abnormal axial skeleton plus cranial skeleton morphology'),
(411349, 'HP:0005678', 'Anterior atlanto-occipital dislocation', 'XPO:0140559', 'abnormally necrotic articular system', 0.43478260869565216, 4.638757693672553, 1.4201588541997616, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(411350, 'HP:0005678', 'Anterior atlanto-occipital dislocation', 'XPO:0101446', 'abnormal transverse process', 0.4098360655737705, 8.05344015541032, 1.816752660002781, 'UPHENO:0002813', 'abnormal vertebral column'),
(411351, 'HP:0005678', 'Anterior atlanto-occipital dislocation', 'XPO:0107372', 'abnormal flexural organ morphology', 0.47619047619047616, 4.638757693672553, 1.4862477031377266, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(411352, 'HP:0005678', 'Anterior atlanto-occipital dislocation', 'XPO:0100895', 'abnormal presacral vertebra', 0.4166666666666667, 8.05344015541032, 1.8318297040812228, 'UPHENO:0002813', 'abnormal vertebral column'),
(411353, 'HP:0005678', 'Anterior atlanto-occipital dislocation', 'XPO:0128227', 'decreased size of the vertebral column', 0.44642857142857145, 8.05344015541032, 1.8961238840501222, 'UPHENO:0002813', 'abnormal vertebral column'),
(411354, 'HP:0005678', 'Anterior atlanto-occipital dislocation', 'XPO:0141723', 'abnormal posterior notochord morphology', 0.47619047619047616, 4.638757693672553, 1.4862477031377266, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(411355, 'HP:0005678', 'Anterior atlanto-occipital dislocation', 'XPO:0128184', 'decreased size of the skeleton', 0.40816326530612246, 4.638757693672553, 1.3759979968056957, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(411356, 'HP:0005678', 'Anterior atlanto-occipital dislocation', 'XPO:0141719', 'abnormal anterior notochord morphology', 0.47619047619047616, 4.638757693672553, 1.4862477031377266, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(411357, 'HP:0005678', 'Anterior atlanto-occipital dislocation', 'XPO:0102605', 'abnormal dermal skeleton morphology', 0.4444444444444444, 4.638757693672553, 1.4358516936218344, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(411358, 'HP:0005678', 'Anterior atlanto-occipital dislocation', 'XPO:0128352', 'decreased size of the skeletal system', 0.425531914893617, 4.638757693672553, 1.404969552736279, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(411359, 'HP:0005678', 'Anterior atlanto-occipital dislocation', 'XPO:0128890', 'decreased size of the elastica externa', 0.425531914893617, 4.638757693672553, 1.404969552736279, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(411360, 'HP:0005678', 'Anterior atlanto-occipital dislocation', 'XPO:0102542', 'abnormal vacuolated notochordal tissue morphology', 0.43478260869565216, 4.638757693672553, 1.4201588541997616, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(411361, 'HP:0005678', 'Anterior atlanto-occipital dislocation', 'XPO:0128306', 'decreased size of the articular system', 0.4166666666666667, 4.638757693672553, 1.3902574242552699, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(411362, 'HP:0005678', 'Anterior atlanto-occipital dislocation', 'XPO:0101713', 'abnormal anatomical entity in vitro morphology', 0.40625, 2.786899518863159, 1.0640385000262718, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(411363, 'HP:0005678', 'Anterior atlanto-occipital dislocation', 'XPO:0129707', 'increased size of the vertebral column', 0.44642857142857145, 8.05344015541032, 1.8961238840501222, 'UPHENO:0002813', 'abnormal vertebral column'),
(411364, 'HP:0005678', 'Anterior atlanto-occipital dislocation', 'XPO:0100226', 'abnormal vertebral element', 0.5208333333333334, 8.05344015541032, 2.048047870764469, 'UPHENO:0002813', 'abnormal vertebral column'),
(411365, 'HP:0005678', 'Anterior atlanto-occipital dislocation', 'XPO:0101976', 'abnormal portion of organism substance morphology', 0.40625, 2.786899518863159, 1.0640385000262718, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(411366, 'HP:0005678', 'Anterior atlanto-occipital dislocation', 'XPO:0100253', 'abnormal vertebra', 0.423728813559322, 8.05344015541032, 1.8472884566637167, 'UPHENO:0002813', 'abnormal vertebral column'),
(411367, 'HP:0005678', 'Anterior atlanto-occipital dislocation', 'XPO:0130060', 'increased size of the postcranial axial skeleton', 0.42592592592592593, 6.272837960958401, 1.6345532468244968, 'UPHENO:0022529', 'abnormal postcranial axial skeleton morphology'),
(411368, 'HP:0005678', 'Anterior atlanto-occipital dislocation', 'XPO:0141709', 'increased size of the anterior notochord', 0.40816326530612246, 4.638757693672553, 1.3759979968056957, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(411369, 'HP:0005678', 'Anterior atlanto-occipital dislocation', 'XPO:0100252', 'abnormal caudal vertebra', 0.4032258064516129, 8.05344015541032, 1.8020418700394085, 'UPHENO:0002813', 'abnormal vertebral column'),
(411370, 'HP:0005678', 'Anterior atlanto-occipital dislocation', 'XPO:0126787', 'abnormally localised vertebral centrum', 0.4166666666666667, 8.05344015541032, 1.8318297040812228, 'UPHENO:0002813', 'abnormal vertebral column'),
(411371, 'HP:0005678', 'Anterior atlanto-occipital dislocation', 'XPO:0125260', 'absent vertebral column', 0.46296296296296297, 8.05344015541032, 1.9309180501496346, 'UPHENO:0002813', 'abnormal vertebral column'),
(411372, 'HP:0005678', 'Anterior atlanto-occipital dislocation', 'XPO:0129832', 'increased size of the skeletal system', 0.425531914893617, 4.638757693672553, 1.404969552736279, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(411373, 'HP:0005678', 'Anterior atlanto-occipital dislocation', 'XPO:0141699', 'abnormally necrotic anterior notochord', 0.425531914893617, 4.638757693672553, 1.404969552736279, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(411374, 'HP:0005678', 'Anterior atlanto-occipital dislocation', 'XPO:0102828', 'abnormal occipital region morphology', 0.4107142857142857, 6.272837960958401, 1.6050994245019483, 'UPHENO:0022529', 'abnormal postcranial axial skeleton morphology'),
(411375, 'HP:0005678', 'Anterior atlanto-occipital dislocation', 'XPO:0100584', 'abnormal vertebral column', 0.5952380952380952, 8.05344015541032, 2.1894552697464333, 'UPHENO:0002813', 'abnormal vertebral column'),
(411376, 'HP:0005678', 'Anterior atlanto-occipital dislocation', 'XPO:0102144', 'abnormal cranial skeleton morphology', 0.45652173913043476, 6.211345574613551, 1.6839282300806968, 'UPHENO:0087089', 'abnormal axial skeleton plus cranial skeleton morphology'),
(411377, 'HP:0005678', 'Anterior atlanto-occipital dislocation', 'XPO:0140043', 'abnormally necrotic perichondrium', 0.40816326530612246, 4.638757693672553, 1.3759979968056957, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(411378, 'HP:0005678', 'Anterior atlanto-occipital dislocation', 'XPO:0102514', 'abnormal perichondrial cell morphology', 0.425531914893617, 4.638757693672553, 1.404969552736279, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(411379, 'HP:0005678', 'Anterior atlanto-occipital dislocation', 'XPO:0139889', 'abnormally necrotic cranial skeleton', 0.40384615384615385, 6.211345574613551, 1.5838017617482976, 'UPHENO:0087089', 'abnormal axial skeleton plus cranial skeleton morphology'),
(411380, 'HP:0005678', 'Anterior atlanto-occipital dislocation', 'XPO:0102272', 'abnormal notochordal sheath morphology', 0.47619047619047616, 4.638757693672553, 1.4862477031377266, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(411381, 'HP:0005678', 'Anterior atlanto-occipital dislocation', 'XPO:0102010', 'abnormal perichondrium morphology', 0.46511627906976744, 4.638757693672553, 1.4688640910537754, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(411382, 'HP:0005678', 'Anterior atlanto-occipital dislocation', 'XPO:0101070', 'abnormal rib', 0.4098360655737705, 8.05344015541032, 1.816752660002781, 'UPHENO:0002813', 'abnormal vertebral column'),
(411383, 'HP:0005678', 'Anterior atlanto-occipital dislocation', 'XPO:0101858', 'abnormal vertebral element morphology', 0.44642857142857145, 8.05344015541032, 1.8961238840501222, 'UPHENO:0002813', 'abnormal vertebral column'),
(411384, 'HP:0005678', 'Anterior atlanto-occipital dislocation', 'XPO:0126886', 'abnormally localised vertebral column', 0.49019607843137253, 8.05344015541032, 1.9868982817607654, 'UPHENO:0002813', 'abnormal vertebral column'),
(411385, 'HP:0005678', 'Anterior atlanto-occipital dislocation', 'XPO:0139917', 'abnormally necrotic notochord', 0.4166666666666667, 4.638757693672553, 1.3902574242552699, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(411386, 'HP:0005678', 'Anterior atlanto-occipital dislocation', 'XPO:0102217', 'abnormal elastica externa morphology', 0.5, 4.638757693672553, 1.5229507040072823, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(411387, 'HP:0005678', 'Anterior atlanto-occipital dislocation', 'XPO:0102401', 'abnormal neurocranium morphology', 0.40350877192982454, 6.272837960958401, 1.5909573036826314, 'UPHENO:0022529', 'abnormal postcranial axial skeleton morphology'),
(411388, 'HP:0005678', 'Anterior atlanto-occipital dislocation', 'XPO:0129434', 'decreased size of the notochordal sheath', 0.40816326530612246, 4.638757693672553, 1.3759979968056957, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(411389, 'HP:0005678', 'Anterior atlanto-occipital dislocation', 'XPO:0101957', 'abnormal axial skeleton morphology', 0.4666666666666667, 6.211345574613551, 1.702535736723214, 'UPHENO:0087089', 'abnormal axial skeleton plus cranial skeleton morphology'),
(411390, 'HP:0030732', 'Dysplastic tricuspid valve', 'XPO:0140009', 'abnormally necrotic right atrium', 0.4084507042253521, 11.854497839006713, 2.2004494973937048, 'UPHENO:0019915', 'abnormal right cardiac atrium morphology'),
(411391, 'HP:0030732', 'Dysplastic tricuspid valve', 'XPO:0102510', 'abnormal right atrium morphology', 0.453125, 11.854497839006713, 2.3176646291687493, 'UPHENO:0019915', 'abnormal right cardiac atrium morphology'),
(411392, 'HP:0030732', 'Dysplastic tricuspid valve', 'XPO:0102769', 'abnormal cardiac valve morphology', 0.41935483870967744, 10.21769640676594, 2.06998561073351, 'UPHENO:0015319', 'abnormal cardiac valve morphology in the heart'),
(411393, 'HP:0030732', 'Dysplastic tricuspid valve', 'XPO:0141651', 'neoplastic right atrium', 0.43283582089552236, 11.854497839006713, 2.2651823995984666, 'UPHENO:0019915', 'abnormal right cardiac atrium morphology'),
(411394, 'HP:4000171', 'Anti-voltage-gated potassium channel antibody positivity', 'XPO:0100004', 'abnormal cell', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(411395, 'HP:4000171', 'Anti-voltage-gated potassium channel antibody positivity', 'XPO:0100242', 'abnormal right lymph heart', 0.40625, 5.64885357140806, 1.5148751642906173, 'HP:0002715', 'Abnormality of the immune system'),
(411396, 'HP:4000171', 'Anti-voltage-gated potassium channel antibody positivity', 'XPO:0101029', 'abnormal right spleen primordium', 0.41935483870967744, 5.64885357140806, 1.5391147060347428, 'HP:0002715', 'Abnormality of the immune system'),
(411397, 'HP:4000171', 'Anti-voltage-gated potassium channel antibody positivity', 'XPO:0100540', 'abnormal left lymph heart', 0.40625, 5.64885357140806, 1.5148751642906173, 'HP:0002715', 'Abnormality of the immune system'),
(411398, 'HP:4000171', 'Anti-voltage-gated potassium channel antibody positivity', 'XPO:0100599', 'abnormal adult immune system', 0.4642857142857143, 5.64885357140806, 1.6194696710023933, 'HP:0002715', 'Abnormality of the immune system'),
(411399, 'HP:4000171', 'Anti-voltage-gated potassium channel antibody positivity', 'XPO:0101518', 'abnormal B cell', 0.40625, 5.64885357140806, 1.5148751642906173, 'HP:0002715', 'Abnormality of the immune system'),
(411400, 'HP:4000171', 'Anti-voltage-gated potassium channel antibody positivity', 'XPO:0101451', 'abnormal dorsal lymph space', 0.4482758620689655, 5.64885357140806, 1.5913028324062968, 'HP:0002715', 'Abnormality of the immune system'),
(411401, 'HP:4000171', 'Anti-voltage-gated potassium channel antibody positivity', 'XPO:0100745', 'abnormal anterior lymph sac', 0.43333333333333335, 5.64885357140806, 1.5645563421015427, 'HP:0002715', 'Abnormality of the immune system'),
(411402, 'HP:4000171', 'Anti-voltage-gated potassium channel antibody positivity', 'XPO:0101221', 'abnormal larval immune system', 0.4642857142857143, 5.64885357140806, 1.6194696710023933, 'HP:0002715', 'Abnormality of the immune system'),
(411403, 'HP:4000171', 'Anti-voltage-gated potassium channel antibody positivity', 'XPO:0101083', 'abnormal T cell', 0.40625, 5.64885357140806, 1.5148751642906173, 'HP:0002715', 'Abnormality of the immune system'),
(411404, 'HP:4000171', 'Anti-voltage-gated potassium channel antibody positivity', 'XPO:0141497', 'abnormal lymphoblast', 0.41935483870967744, 5.64885357140806, 1.5391147060347428, 'HP:0002715', 'Abnormality of the immune system'),
(411405, 'HP:4000171', 'Anti-voltage-gated potassium channel antibody positivity', 'XPO:0100581', 'abnormal immune system', 0.48148148148148145, 5.64885357140806, 1.6491871895674883, 'HP:0002715', 'Abnormality of the immune system'),
(411406, 'HP:4000171', 'Anti-voltage-gated potassium channel antibody positivity', 'XPO:0100449', 'abnormal lymphocyte', 0.41935483870967744, 5.64885357140806, 1.5391147060347428, 'HP:0002715', 'Abnormality of the immune system'),
(411407, 'HP:4000171', 'Anti-voltage-gated potassium channel antibody positivity', 'XPO:0100232', 'abnormal lymphatic system', 0.48148148148148145, 5.64885357140806, 1.6491871895674883, 'HP:0002715', 'Abnormality of the immune system'),
(411408, 'HP:0032831', 'Neonatal bilateral asymmetric tonic seizure', 'XPO:0100031', 'abnormal central nervous system', 0.40625, 3.94131651835137, 1.2653694462805098, 'UPHENO:0004523', 'abnormal nervous system'),
(411409, 'HP:0032831', 'Neonatal bilateral asymmetric tonic seizure', 'XPO:0107253', 'abnormal enteric nervous system', 0.40625, 3.94131651835137, 1.2653694462805098, 'UPHENO:0004523', 'abnormal nervous system'),
(411410, 'HP:0032831', 'Neonatal bilateral asymmetric tonic seizure', 'XPO:0100032', 'abnormal nervous system', 0.41935483870967744, 3.94131651835137, 1.2856166430382838, 'UPHENO:0004523', 'abnormal nervous system'),
(411411, 'HP:0032831', 'Neonatal bilateral asymmetric tonic seizure', 'XPO:0100274', 'abnormal sensory system', 0.40625, 3.94131651835137, 1.2653694462805098, 'UPHENO:0004523', 'abnormal nervous system'),
(411412, 'HP:0025007', 'Ectopic fovea', 'XPO:0103184', 'abnormal inner limiting membrane morphology', 0.5, 8.040873045973026, 2.0051026215599324, 'HP:0000479', 'Abnormal retinal morphology'),
(411413, 'HP:0025007', 'Ectopic fovea', 'XPO:0128935', 'decreased size of the central retina', 0.5584415584415584, 8.040873045973026, 2.1190464070010115, 'HP:0000479', 'Abnormal retinal morphology'),
(411414, 'HP:0025007', 'Ectopic fovea', 'XPO:0102851', 'abnormal retinal rod cell morphology', 0.4725274725274725, 8.040873045973026, 1.9492391893577128, 'HP:0000479', 'Abnormal retinal morphology'),
(411415, 'HP:0025007', 'Ectopic fovea', 'XPO:0102963', 'abnormal retinal outer nuclear layer morphology', 0.5, 8.040873045973026, 2.0051026215599324, 'HP:0000479', 'Abnormal retinal morphology'),
(411416, 'HP:0025007', 'Ectopic fovea', 'XPO:0129780', 'increased size of the retina', 0.5443037974683544, 8.040873045973026, 2.0920510830006163, 'HP:0000479', 'Abnormal retinal morphology'),
(411417, 'HP:0025007', 'Ectopic fovea', 'XPO:0129388', 'decreased size of the sclera', 0.43209876543209874, 6.887869297006056, 1.7251781994025936, 'HP:0012372', 'Abnormal eye morphology'),
(411418, 'HP:0025007', 'Ectopic fovea', 'XPO:0130362', 'increased size of the retinal pigmented epithelium', 0.45263157894736844, 8.040873045973026, 1.9077612698957138, 'HP:0000479', 'Abnormal retinal morphology'),
(411419, 'HP:0025007', 'Ectopic fovea', 'XPO:0100710', 'abnormal hyaloid vein', 0.43661971830985913, 6.887869297006056, 1.734179792355427, 'UPHENO:0021474', 'abnormal camera-type eye morphology'),
(411420, 'HP:0025007', 'Ectopic fovea', 'XPO:0128779', 'decreased size of the retinal blood vessel', 0.4387755102040816, 8.040873045973026, 1.8783338822565765, 'HP:0000479', 'Abnormal retinal morphology'),
(411421, 'HP:0025007', 'Ectopic fovea', 'XPO:0128300', 'decreased size of the retina', 0.5443037974683544, 8.040873045973026, 2.0920510830006163, 'HP:0000479', 'Abnormal retinal morphology'),
(411422, 'HP:0025007', 'Ectopic fovea', 'XPO:0102581', 'abnormal outer limiting membrane morphology', 0.5, 8.040873045973026, 2.0051026215599324, 'HP:0000479', 'Abnormal retinal morphology'),
(411423, 'HP:0025007', 'Ectopic fovea', 'XPO:0141014', 'abnormally necrotic retinal outer plexiform layer', 0.46236559139784944, 8.040873045973026, 1.9281657141584967, 'HP:0000479', 'Abnormal retinal morphology'),
(411424, 'HP:0025007', 'Ectopic fovea', 'XPO:0140808', 'abnormally necrotic retinal cone cell', 0.4479166666666667, 8.040873045973026, 1.8977990019604511, 'HP:0000479', 'Abnormal retinal morphology'),
(411425, 'HP:0025007', 'Ectopic fovea', 'XPO:0140620', 'abnormally necrotic horizontal cell', 0.45263157894736844, 8.040873045973026, 1.9077612698957138, 'HP:0000479', 'Abnormal retinal morphology'),
(411426, 'HP:0025007', 'Ectopic fovea', 'XPO:0140473', 'abnormally necrotic lens transitional zone', 0.4166666666666667, 6.887869297006056, 1.6940913612964297, 'UPHENO:0021474', 'abnormal camera-type eye morphology'),
(411427, 'HP:0025007', 'Ectopic fovea', 'XPO:0140820', 'abnormally necrotic globe', 0.4025974025974026, 6.575878401988876, 1.627092979653308, 'UPHENO:0087924', 'abnormal camera-type eye morphology'),
(411428, 'HP:0025007', 'Ectopic fovea', 'XPO:0130506', 'increased size of the Muller cell', 0.46236559139784944, 8.040873045973026, 1.9281657141584967, 'HP:0000479', 'Abnormal retinal morphology'),
(411429, 'HP:0025007', 'Ectopic fovea', 'XPO:0102411', 'abnormal optic choroid vascular plexus morphology', 0.40217391304347827, 7.796308075334707, 1.7707263272312377, 'UPHENO:0021656', 'abnormal ocular fundus morphology'),
(411430, 'HP:0025007', 'Ectopic fovea', 'XPO:0139731', 'abnormally necrotic eye', 0.4375, 6.887869297006056, 1.7359270772241988, 'HP:0012372', 'Abnormal eye morphology'),
(411431, 'HP:0025007', 'Ectopic fovea', 'XPO:0101961', 'abnormal retinal blood vessel morphology', 0.48314606741573035, 8.040873045973026, 1.9710190741722953, 'HP:0000479', 'Abnormal retinal morphology'),
(411432, 'HP:0025007', 'Ectopic fovea', 'XPO:0140671', 'abnormally necrotic retinal ganglion cell', 0.44329896907216493, 8.040873045973026, 1.8879911895239345, 'HP:0000479', 'Abnormal retinal morphology'),
(411433, 'HP:0025007', 'Ectopic fovea', 'XPO:0102450', 'abnormal retinal stem cell morphology', 0.5058823529411764, 8.040873045973026, 2.0168628550791743, 'HP:0000479', 'Abnormal retinal morphology'),
(411434, 'HP:0025007', 'Ectopic fovea', 'XPO:0130326', 'increased size of the retinal cone cell', 0.41346153846153844, 8.040873045973026, 1.8233463028623837, 'HP:0000479', 'Abnormal retinal morphology'),
(411435, 'HP:0025007', 'Ectopic fovea', 'XPO:0102162', 'abnormal ciliary marginal zone morphology', 0.5375, 8.040873045973026, 2.0789346459690603, 'HP:0000479', 'Abnormal retinal morphology'),
(411436, 'HP:0025007', 'Ectopic fovea', 'XPO:0133370', 'olfactory pit fused with brain', 0.4057971014492754, 5.788671267106304, 1.532653261972336, 'UPHENO:0087472', 'abnormal face morphology'),
(411437, 'HP:0025007', 'Ectopic fovea', 'XPO:0129810', 'increased size of the retinal progenitor cell region', 0.5308641975308642, 8.040873045973026, 2.066061861851679, 'HP:0000479', 'Abnormal retinal morphology'),
(411438, 'HP:0025007', 'Ectopic fovea', 'XPO:0101315', 'abnormal hyaloid vascular plexus', 0.43661971830985913, 6.887869297006056, 1.734179792355427, 'HP:0012372', 'Abnormal eye morphology'),
(411439, 'HP:0025007', 'Ectopic fovea', 'XPO:0102805', 'abnormal retinal layer morphology', 0.6142857142857143, 8.040873045973026, 2.2224746213458295, 'HP:0000479', 'Abnormal retinal morphology'),
(411440, 'HP:0025007', 'Ectopic fovea', 'XPO:0102117', 'abnormal retina morphology', 0.5972222222222222, 8.040873045973026, 2.191389529299339, 'HP:0000479', 'Abnormal retinal morphology'),
(411441, 'HP:0025007', 'Ectopic fovea', 'XPO:0141033', 'abnormally necrotic photoreceptor layer', 0.4673913043478261, 8.040873045973026, 1.938616553383523, 'HP:0000479', 'Abnormal retinal morphology'),
(411442, 'HP:0025007', 'Ectopic fovea', 'XPO:0140869', 'abnormally necrotic optic chiasm', 0.45555555555555555, 7.796308075334707, 1.884582568247241, 'UPHENO:0021656', 'abnormal ocular fundus morphology'),
(411443, 'HP:0025007', 'Ectopic fovea', 'XPO:0140799', 'abnormally necrotic ciliary body', 0.40229885057471265, 6.887869297006056, 1.6646266551675757, 'UPHENO:0021474', 'abnormal camera-type eye morphology'),
(411444, 'HP:0025007', 'Ectopic fovea', 'XPO:0128475', 'decreased size of the retinal stem cell region', 0.5308641975308642, 8.040873045973026, 2.066061861851679, 'HP:0000479', 'Abnormal retinal morphology'),
(411445, 'HP:0025007', 'Ectopic fovea', 'XPO:0139887', 'abnormally necrotic Muller cell', 0.5058823529411764, 8.040873045973026, 2.0168628550791743, 'HP:0000479', 'Abnormal retinal morphology'),
(411446, 'HP:0025007', 'Ectopic fovea', 'XPO:0103186', 'abnormal peripheral retina morphology', 0.5733333333333334, 8.040873045973026, 2.147114469784475, 'HP:0000479', 'Abnormal retinal morphology'),
(411447, 'HP:0025007', 'Ectopic fovea', 'XPO:0130257', 'increased size of the retinal blood vessel', 0.4387755102040816, 8.040873045973026, 1.8783338822565765, 'HP:0000479', 'Abnormal retinal morphology'),
(411448, 'HP:0025007', 'Ectopic fovea', 'XPO:0103926', 'decreased pigmentation in the retinal pigmented epithelium', 0.48314606741573035, 8.040873045973026, 1.9710190741722953, 'HP:0000479', 'Abnormal retinal morphology'),
(411449, 'HP:0025007', 'Ectopic fovea', 'XPO:0103376', 'increased size of the eye', 0.4166666666666667, 6.887869297006056, 1.6940913612964297, 'HP:0012372', 'Abnormal eye morphology'),
(411450, 'HP:0025007', 'Ectopic fovea', 'XPO:0140531', 'abnormally necrotic retinal progenitor cell region', 0.5443037974683544, 8.040873045973026, 2.0920510830006163, 'HP:0000479', 'Abnormal retinal morphology'),
(411451, 'HP:0025007', 'Ectopic fovea', 'XPO:0129432', 'decreased size of the retinal stem cell', 0.4387755102040816, 8.040873045973026, 1.8783338822565765, 'HP:0000479', 'Abnormal retinal morphology'),
(411452, 'HP:0025007', 'Ectopic fovea', 'XPO:0102818', 'abnormal optic chiasm morphology', 0.4823529411764706, 7.796308075334707, 1.9392194642318246, 'UPHENO:0021656', 'abnormal ocular fundus morphology'),
(411453, 'HP:0025007', 'Ectopic fovea', 'XPO:0102831', 'abnormal optic disc morphology', 0.44285714285714284, 6.575878401988876, 1.7065095138559256, 'UPHENO:0087924', 'abnormal camera-type eye morphology'),
(411454, 'HP:0025007', 'Ectopic fovea', 'XPO:0103336', 'decreased size of the eye', 0.4166666666666667, 6.887869297006056, 1.6940913612964297, 'UPHENO:0021474', 'abnormal camera-type eye morphology'),
(411455, 'HP:0025007', 'Ectopic fovea', 'XPO:0128295', 'decreased size of the retinal neural layer', 0.4574468085106383, 8.040873045973026, 1.9178820903589395, 'HP:0000479', 'Abnormal retinal morphology'),
(411456, 'HP:0025007', 'Ectopic fovea', 'XPO:0100329', 'abnormal retinal blood vessel', 0.6056338028169014, 8.040873045973026, 2.206767890105474, 'HP:0000479', 'Abnormal retinal morphology'),
(411457, 'HP:0025007', 'Ectopic fovea', 'XPO:0140489', 'abnormally necrotic ciliary marginal zone', 0.48863636363636365, 8.040873045973026, 1.982186410418029, 'HP:0000479', 'Abnormal retinal morphology'),
(411458, 'HP:0025007', 'Ectopic fovea', 'XPO:0129741', 'increased size of the optic fiber layer', 0.4574468085106383, 8.040873045973026, 1.9178820903589395, 'HP:0000479', 'Abnormal retinal morphology'),
(411459, 'HP:0025007', 'Ectopic fovea', 'XPO:0140491', 'abnormally necrotic retinal rod cell', 0.4479166666666667, 8.040873045973026, 1.8977990019604511, 'HP:0000479', 'Abnormal retinal morphology'),
(411460, 'HP:0025007', 'Ectopic fovea', 'XPO:0129947', 'increased size of the lens', 0.4117647058823529, 6.887869297006056, 1.6840966347682629, 'HP:0012372', 'Abnormal eye morphology'),
(411461, 'HP:0025007', 'Ectopic fovea', 'XPO:0125909', 'absent retinal blood vessel', 0.5, 8.040873045973026, 2.0051026215599324, 'HP:0000479', 'Abnormal retinal morphology'),
(411462, 'HP:0025007', 'Ectopic fovea', 'XPO:0129038', 'decreased size of the retinal outer nuclear layer', 0.4574468085106383, 8.040873045973026, 1.9178820903589395, 'HP:0000479', 'Abnormal retinal morphology'),
(411463, 'HP:0025007', 'Ectopic fovea', 'XPO:0101861', 'abnormal photoreceptor layer morphology', 0.5058823529411764, 8.040873045973026, 2.0168628550791743, 'HP:0000479', 'Abnormal retinal morphology'),
(411464, 'HP:0025007', 'Ectopic fovea', 'XPO:0140218', 'abnormally necrotic sclera', 0.4430379746835443, 6.887869297006056, 1.7468794071802813, 'HP:0012372', 'Abnormal eye morphology'),
(411465, 'HP:0025007', 'Ectopic fovea', 'XPO:0102946', 'abnormal retinal inner nuclear layer morphology', 0.5, 8.040873045973026, 2.0051026215599324, 'HP:0000479', 'Abnormal retinal morphology'),
(411466, 'HP:0025007', 'Ectopic fovea', 'XPO:0128643', 'decreased size of the retinal layer', 0.5584415584415584, 8.040873045973026, 2.1190464070010115, 'HP:0000479', 'Abnormal retinal morphology'),
(411467, 'HP:0025007', 'Ectopic fovea', 'XPO:0129029', 'decreased size of the Muller cell', 0.46236559139784944, 8.040873045973026, 1.9281657141584967, 'HP:0000479', 'Abnormal retinal morphology'),
(411468, 'HP:0025007', 'Ectopic fovea', 'XPO:0130148', 'increased size of the ciliary marginal zone', 0.4777777777777778, 8.040873045973026, 1.960038381077836, 'HP:0000479', 'Abnormal retinal morphology'),
(411469, 'HP:0025007', 'Ectopic fovea', 'XPO:0128330', 'decreased size of the retinal progenitor cell region', 0.5308641975308642, 8.040873045973026, 2.066061861851679, 'HP:0000479', 'Abnormal retinal morphology'),
(411470, 'HP:0025007', 'Ectopic fovea', 'XPO:0100371', 'abnormal hyaloid blood vessel', 0.4492753623188406, 6.887869297006056, 1.759133301946505, 'UPHENO:0021474', 'abnormal camera-type eye morphology'),
(411471, 'HP:0025007', 'Ectopic fovea', 'XPO:0103142', 'abnormal optic nerve morphology', 0.41414141414141414, 7.796308075334707, 1.7968789751681224, 'UPHENO:0021656', 'abnormal ocular fundus morphology'),
(411472, 'HP:0025007', 'Ectopic fovea', 'XPO:0141337', 'increased pigmentation in the eye', 0.4605263157894737, 6.887869297006056, 1.7810236020304815, 'HP:0012372', 'Abnormal eye morphology'),
(411473, 'HP:0025007', 'Ectopic fovea', 'XPO:0128200', 'decreased size of the retinal rod cell', 0.41346153846153844, 8.040873045973026, 1.8233463028623837, 'HP:0000479', 'Abnormal retinal morphology'),
(411474, 'HP:0025007', 'Ectopic fovea', 'XPO:0139912', 'abnormally necrotic optic fiber layer', 0.46236559139784944, 8.040873045973026, 1.9281657141584967, 'HP:0000479', 'Abnormal retinal morphology'),
(411475, 'HP:0025007', 'Ectopic fovea', 'XPO:0128431', 'decreased size of the retinal inner nuclear layer', 0.4574468085106383, 8.040873045973026, 1.9178820903589395, 'HP:0000479', 'Abnormal retinal morphology'),
(411476, 'HP:0025007', 'Ectopic fovea', 'XPO:0129285', 'decreased size of the retinal inner plexiform layer', 0.4574468085106383, 8.040873045973026, 1.9178820903589395, 'HP:0000479', 'Abnormal retinal morphology'),
(411477, 'HP:0025007', 'Ectopic fovea', 'XPO:0129138', 'decreased size of the retinal progenitor cell', 0.4387755102040816, 8.040873045973026, 1.8783338822565765, 'HP:0000479', 'Abnormal retinal morphology'),
(411478, 'HP:0025007', 'Ectopic fovea', 'XPO:0129258', 'decreased size of the amacrine cell', 0.40186915887850466, 8.040873045973026, 1.797603651429875, 'HP:0000479', 'Abnormal retinal morphology'),
(411479, 'HP:0025007', 'Ectopic fovea', 'XPO:0130353', 'increased size of the photoreceptor layer', 0.46236559139784944, 8.040873045973026, 1.9281657141584967, 'HP:0000479', 'Abnormal retinal morphology'),
(411480, 'HP:0025007', 'Ectopic fovea', 'XPO:0129083', 'decreased size of the bipolar neuron', 0.40186915887850466, 8.040873045973026, 1.797603651429875, 'HP:0000479', 'Abnormal retinal morphology'),
(411481, 'HP:0025007', 'Ectopic fovea', 'XPO:0128884', 'decreased size of the retinal pigmented epithelium', 0.45263157894736844, 8.040873045973026, 1.9077612698957138, 'HP:0000479', 'Abnormal retinal morphology'),
(411482, 'HP:0025007', 'Ectopic fovea', 'XPO:0128467', 'decreased size of the lens', 0.4117647058823529, 6.887869297006056, 1.6840966347682629, 'HP:0012372', 'Abnormal eye morphology'),
(411483, 'HP:0025007', 'Ectopic fovea', 'XPO:0128710', 'decreased size of the optic chiasm', 0.43617021276595747, 7.796308075334707, 1.844049172882245, 'UPHENO:0021656', 'abnormal ocular fundus morphology'),
(411484, 'HP:0025007', 'Ectopic fovea', 'XPO:0129955', 'increased size of the retinal stem cell region', 0.5308641975308642, 8.040873045973026, 2.066061861851679, 'HP:0000479', 'Abnormal retinal morphology'),
(411485, 'HP:0025007', 'Ectopic fovea', 'XPO:0140391', 'abnormally necrotic central retina', 0.5733333333333334, 8.040873045973026, 2.147114469784475, 'HP:0000479', 'Abnormal retinal morphology'),
(411486, 'HP:0025007', 'Ectopic fovea', 'XPO:0130189', 'increased size of the optic chiasm', 0.43617021276595747, 7.796308075334707, 1.844049172882245, 'UPHENO:0021656', 'abnormal ocular fundus morphology'),
(411487, 'HP:0025007', 'Ectopic fovea', 'XPO:0141138', 'abnormally necrotic retinal inner plexiform layer', 0.46236559139784944, 8.040873045973026, 1.9281657141584967, 'HP:0000479', 'Abnormal retinal morphology'),
(411488, 'HP:0025007', 'Ectopic fovea', 'XPO:0128669', 'decreased size of the ciliary marginal zone', 0.4777777777777778, 8.040873045973026, 1.960038381077836, 'HP:0000479', 'Abnormal retinal morphology'),
(411489, 'HP:0025007', 'Ectopic fovea', 'XPO:0101823', 'abnormal lens epithelium morphology', 0.4069767441860465, 6.887869297006056, 1.6742767456052652, 'HP:0012372', 'Abnormal eye morphology'),
(411490, 'HP:0025007', 'Ectopic fovea', 'XPO:0141333', 'increased pigmentation in the retinal pigmented epithelium', 0.48314606741573035, 8.040873045973026, 1.9710190741722953, 'HP:0000479', 'Abnormal retinal morphology'),
(411491, 'HP:0025007', 'Ectopic fovea', 'XPO:0130285', 'increased size of the lens transitional zone', 0.4069767441860465, 6.887869297006056, 1.6742767456052652, 'HP:0012372', 'Abnormal eye morphology'),
(411492, 'HP:0025007', 'Ectopic fovea', 'XPO:0130863', 'increased size of the sclera', 0.43209876543209874, 6.887869297006056, 1.7251781994025936, 'UPHENO:0021474', 'abnormal camera-type eye morphology'),
(411493, 'HP:0025007', 'Ectopic fovea', 'XPO:0130515', 'increased size of the retinal outer nuclear layer', 0.4574468085106383, 8.040873045973026, 1.9178820903589395, 'HP:0000479', 'Abnormal retinal morphology'),
(411494, 'HP:0025007', 'Ectopic fovea', 'XPO:0128521', 'decreased size of the horizontal cell', 0.4174757281553398, 8.040873045973026, 1.8321761186829812, 'HP:0000479', 'Abnormal retinal morphology'),
(411495, 'HP:0025007', 'Ectopic fovea', 'XPO:0133372', 'eye fused with olfactory epithelium', 0.4605263157894737, 6.887869297006056, 1.7810236020304815, 'HP:0012372', 'Abnormal eye morphology'),
(411496, 'HP:0025007', 'Ectopic fovea', 'XPO:0133371', 'eye fused with olfactory pit', 0.4605263157894737, 6.887869297006056, 1.7810236020304815, 'UPHENO:0021474', 'abnormal camera-type eye morphology'),
(411497, 'HP:0025007', 'Ectopic fovea', 'XPO:0140948', 'abnormally necrotic retinal inner nuclear layer', 0.46236559139784944, 8.040873045973026, 1.9281657141584967, 'HP:0000479', 'Abnormal retinal morphology'),
(411498, 'HP:0025007', 'Ectopic fovea', 'XPO:0129971', 'increased size of the retinal ganglion cell', 0.4095238095238095, 8.040873045973026, 1.8146429295275122, 'HP:0000479', 'Abnormal retinal morphology'),
(411499, 'HP:0025007', 'Ectopic fovea', 'XPO:0128100', 'decreased size of the inner limiting membrane', 0.4574468085106383, 8.040873045973026, 1.9178820903589395, 'HP:0000479', 'Abnormal retinal morphology'),
(411500, 'HP:0025007', 'Ectopic fovea', 'XPO:0133369', 'eye fused with brain', 0.4605263157894737, 6.887869297006056, 1.7810236020304815, 'HP:0012372', 'Abnormal eye morphology'),
(411501, 'HP:0025007', 'Ectopic fovea', 'XPO:0128875', 'decreased size of the photoreceptor layer', 0.46236559139784944, 8.040873045973026, 1.9281657141584967, 'HP:0000479', 'Abnormal retinal morphology'),
(411502, 'HP:0025007', 'Ectopic fovea', 'XPO:0102476', 'abnormal lens transitional zone morphology', 0.4430379746835443, 6.887869297006056, 1.7468794071802813, 'UPHENO:0021474', 'abnormal camera-type eye morphology'),
(411503, 'HP:0025007', 'Ectopic fovea', 'XPO:0102226', 'abnormal Jacobsons organ morphology', 0.4117647058823529, 5.788671267106304, 1.5438816411077807, 'UPHENO:0087472', 'abnormal face morphology'),
(411504, 'HP:0025007', 'Ectopic fovea', 'XPO:0100779', 'abnormal optic choroid vascular plexus', 0.44285714285714284, 6.887869297006056, 1.7465228647932265, 'HP:0012372', 'Abnormal eye morphology'),
(411505, 'HP:0025007', 'Ectopic fovea', 'XPO:0130265', 'increased size of the peripheral retina', 0.5180722891566265, 8.040873045973026, 2.0410177622316423, 'HP:0000479', 'Abnormal retinal morphology'),
(411506, 'HP:0025007', 'Ectopic fovea', 'XPO:0128807', 'decreased size of the lens transitional zone', 0.4069767441860465, 6.887869297006056, 1.6742767456052652, 'HP:0012372', 'Abnormal eye morphology'),
(411507, 'HP:0025007', 'Ectopic fovea', 'XPO:0102505', 'abnormal retinal stem cell region morphology', 0.5657894736842105, 8.040873045973026, 2.1329419421640696, 'HP:0000479', 'Abnormal retinal morphology'),
(411508, 'HP:0025007', 'Ectopic fovea', 'XPO:0102266', 'abnormal horizontal cell morphology', 0.4777777777777778, 8.040873045973026, 1.960038381077836, 'HP:0000479', 'Abnormal retinal morphology'),
(411509, 'HP:0025007', 'Ectopic fovea', 'XPO:0102550', 'abnormal lens morphology', 0.45454545454545453, 6.887869297006056, 1.769420718895678, 'UPHENO:0021474', 'abnormal camera-type eye morphology'),
(411510, 'HP:0025007', 'Ectopic fovea', 'XPO:0130906', 'increased size of the retinal stem cell', 0.4387755102040816, 8.040873045973026, 1.8783338822565765, 'HP:0000479', 'Abnormal retinal morphology'),
(411511, 'HP:0025007', 'Ectopic fovea', 'XPO:0140346', 'abnormally necrotic retinal blood vessel', 0.4479166666666667, 8.040873045973026, 1.8977990019604511, 'HP:0000479', 'Abnormal retinal morphology'),
(411512, 'HP:0025007', 'Ectopic fovea', 'XPO:0140553', 'abnormally necrotic retinal stem cell region', 0.5443037974683544, 8.040873045973026, 2.0920510830006163, 'HP:0000479', 'Abnormal retinal morphology'),
(411513, 'HP:0025007', 'Ectopic fovea', 'XPO:0115417', 'abnormally wholly ventralized eye', 0.4375, 6.887869297006056, 1.7359270772241988, 'UPHENO:0021474', 'abnormal camera-type eye morphology'),
(411514, 'HP:0025007', 'Ectopic fovea', 'XPO:0140081', 'abnormally necrotic amacrine cell', 0.43434343434343436, 8.040873045973026, 1.8688232698432123, 'HP:0000479', 'Abnormal retinal morphology'),
(411515, 'HP:0025007', 'Ectopic fovea', 'XPO:0129911', 'increased size of the retinal inner nuclear layer', 0.4574468085106383, 8.040873045973026, 1.9178820903589395, 'HP:0000479', 'Abnormal retinal morphology'),
(411516, 'HP:0025007', 'Ectopic fovea', 'XPO:0102441', 'abnormal retinal inner plexiform layer morphology', 0.5, 8.040873045973026, 2.0051026215599324, 'HP:0000479', 'Abnormal retinal morphology'),
(411517, 'HP:0025007', 'Ectopic fovea', 'XPO:0103210', 'abnormal pupil morphology', 0.42168674698795183, 6.887869297006056, 1.7042661756699493, 'UPHENO:0021474', 'abnormal camera-type eye morphology'),
(411518, 'HP:0025007', 'Ectopic fovea', 'XPO:0140006', 'abnormally necrotic retinal neural layer', 0.46236559139784944, 8.040873045973026, 1.9281657141584967, 'HP:0000479', 'Abnormal retinal morphology'),
(411519, 'HP:0025007', 'Ectopic fovea', 'XPO:0115423', 'abnormally incomplete structure of eye', 0.47297297297297297, 6.887869297006056, 1.8049310288357878, 'HP:0012372', 'Abnormal eye morphology'),
(411520, 'HP:0025007', 'Ectopic fovea', 'XPO:0140317', 'abnormally necrotic retinal progenitor cell', 0.4777777777777778, 8.040873045973026, 1.960038381077836, 'HP:0000479', 'Abnormal retinal morphology'),
(411521, 'HP:0025007', 'Ectopic fovea', 'XPO:0102196', 'abnormal central retina morphology', 0.5972222222222222, 8.040873045973026, 2.191389529299339, 'HP:0000479', 'Abnormal retinal morphology'),
(411522, 'HP:0025007', 'Ectopic fovea', 'XPO:0102212', 'abnormal globe morphology', 0.4305555555555556, 6.575878401988876, 1.6826410724316994, 'UPHENO:0087924', 'abnormal camera-type eye morphology'),
(411523, 'HP:0025007', 'Ectopic fovea', 'XPO:0102966', 'abnormal olfactory pit morphology', 0.42424242424242425, 5.788671267106304, 1.5670992092077785, 'UPHENO:0087472', 'abnormal face morphology'),
(411524, 'HP:0025007', 'Ectopic fovea', 'XPO:0130048', 'increased size of the optic disc', 0.41333333333333333, 6.575878401988876, 1.6486448190828538, 'UPHENO:0087924', 'abnormal camera-type eye morphology'),
(411525, 'HP:0025007', 'Ectopic fovea', 'XPO:0130413', 'increased size of the central retina', 0.5584415584415584, 8.040873045973026, 2.1190464070010115, 'HP:0000479', 'Abnormal retinal morphology'),
(411526, 'HP:0025007', 'Ectopic fovea', 'XPO:0130001', 'increased size of the horizontal cell', 0.4174757281553398, 8.040873045973026, 1.8321761186829812, 'HP:0000479', 'Abnormal retinal morphology'),
(411527, 'HP:0025007', 'Ectopic fovea', 'XPO:0141141', 'abnormally necrotic cornea', 0.40229885057471265, 6.887869297006056, 1.6646266551675757, 'HP:0012372', 'Abnormal eye morphology'),
(411528, 'HP:0025007', 'Ectopic fovea', 'XPO:0128568', 'decreased size of the optic disc', 0.41333333333333333, 6.575878401988876, 1.6486448190828538, 'UPHENO:0087924', 'abnormal camera-type eye morphology'),
(411529, 'HP:0025007', 'Ectopic fovea', 'XPO:0102784', 'abnormal retinal progenitor cell region morphology', 0.5657894736842105, 8.040873045973026, 2.1329419421640696, 'HP:0000479', 'Abnormal retinal morphology'),
(411530, 'HP:0025007', 'Ectopic fovea', 'XPO:0140271', 'abnormally necrotic peripheral retina', 0.5308641975308642, 8.040873045973026, 2.066061861851679, 'HP:0000479', 'Abnormal retinal morphology'),
(411531, 'HP:0025007', 'Ectopic fovea', 'XPO:0133354', 'fused eyes', 0.4605263157894737, 6.887869297006056, 1.7810236020304815, 'UPHENO:0021474', 'abnormal camera-type eye morphology'),
(411532, 'HP:0025007', 'Ectopic fovea', 'XPO:0129775', 'increased size of the retinal neural layer', 0.4574468085106383, 8.040873045973026, 1.9178820903589395, 'HP:0000479', 'Abnormal retinal morphology'),
(411533, 'HP:0025007', 'Ectopic fovea', 'XPO:0102017', 'abnormal retinal neural layer morphology', 0.5058823529411764, 8.040873045973026, 2.0168628550791743, 'HP:0000479', 'Abnormal retinal morphology'),
(411534, 'HP:0025007', 'Ectopic fovea', 'XPO:0141343', 'decreased pigmentation in the eye', 0.4605263157894737, 6.887869297006056, 1.7810236020304815, 'HP:0012372', 'Abnormal eye morphology'),
(411535, 'HP:0025007', 'Ectopic fovea', 'XPO:0140797', 'abnormally necrotic bipolar neuron', 0.43434343434343436, 8.040873045973026, 1.8688232698432123, 'HP:0000479', 'Abnormal retinal morphology'),
(411536, 'HP:0025007', 'Ectopic fovea', 'XPO:0130560', 'increased size of the bipolar neuron', 0.40186915887850466, 8.040873045973026, 1.797603651429875, 'HP:0000479', 'Abnormal retinal morphology'),
(411537, 'HP:0025007', 'Ectopic fovea', 'XPO:0128491', 'decreased size of the retinal ganglion cell', 0.4095238095238095, 8.040873045973026, 1.8146429295275122, 'HP:0000479', 'Abnormal retinal morphology'),
(411538, 'HP:0025007', 'Ectopic fovea', 'XPO:0102996', 'abnormal optic fiber layer morphology', 0.5, 8.040873045973026, 2.0051026215599324, 'HP:0000479', 'Abnormal retinal morphology'),
(411539, 'HP:0025007', 'Ectopic fovea', 'XPO:0102663', 'abnormal retinal progenitor cell morphology', 0.5058823529411764, 8.040873045973026, 2.0168628550791743, 'HP:0000479', 'Abnormal retinal morphology'),
(411540, 'HP:0025007', 'Ectopic fovea', 'XPO:0102815', 'abnormal retinal ganglion cell morphology', 0.4673913043478261, 8.040873045973026, 1.938616553383523, 'HP:0000479', 'Abnormal retinal morphology'),
(411541, 'HP:0025007', 'Ectopic fovea', 'XPO:0128646', 'decreased size of the outer limiting membrane', 0.4574468085106383, 8.040873045973026, 1.9178820903589395, 'HP:0000479', 'Abnormal retinal morphology'),
(411542, 'HP:0025007', 'Ectopic fovea', 'XPO:0102239', 'abnormal retinal pigmented epithelium morphology', 0.5, 8.040873045973026, 2.0051026215599324, 'HP:0000479', 'Abnormal retinal morphology'),
(411543, 'HP:0025007', 'Ectopic fovea', 'XPO:0129981', 'increased size of the retinal ganglion cell layer', 0.4574468085106383, 8.040873045973026, 1.9178820903589395, 'HP:0000479', 'Abnormal retinal morphology'),
(411544, 'HP:0025007', 'Ectopic fovea', 'XPO:0129580', 'increased size of the inner limiting membrane', 0.4574468085106383, 8.040873045973026, 1.9178820903589395, 'HP:0000479', 'Abnormal retinal morphology'),
(411545, 'HP:0025007', 'Ectopic fovea', 'XPO:0102232', 'abnormal eye photoreceptor cell morphology', 0.48314606741573035, 8.040873045973026, 1.9710190741722953, 'HP:0000479', 'Abnormal retinal morphology'),
(411546, 'HP:0025007', 'Ectopic fovea', 'XPO:0130122', 'increased size of the retinal layer', 0.5584415584415584, 8.040873045973026, 2.1190464070010115, 'HP:0000479', 'Abnormal retinal morphology'),
(411547, 'HP:0025007', 'Ectopic fovea', 'XPO:0130734', 'increased size of the amacrine cell', 0.40186915887850466, 8.040873045973026, 1.797603651429875, 'HP:0000479', 'Abnormal retinal morphology'),
(411548, 'HP:0025007', 'Ectopic fovea', 'XPO:0140538', 'abnormally necrotic optic disc', 0.4246575342465753, 6.575878401988876, 1.6710763919384135, 'UPHENO:0087924', 'abnormal camera-type eye morphology'),
(411549, 'HP:0025007', 'Ectopic fovea', 'XPO:0102939', 'abnormal retinal ganglion cell layer morphology', 0.5, 8.040873045973026, 2.0051026215599324, 'HP:0000479', 'Abnormal retinal morphology'),
(411550, 'HP:0025007', 'Ectopic fovea', 'XPO:0140375', 'abnormally necrotic lens', 0.4268292682926829, 6.887869297006056, 1.714626551799759, 'UPHENO:0021474', 'abnormal camera-type eye morphology'),
(411551, 'HP:0025007', 'Ectopic fovea', 'XPO:0140520', 'abnormally necrotic retinal outer nuclear layer', 0.46236559139784944, 8.040873045973026, 1.9281657141584967, 'HP:0000479', 'Abnormal retinal morphology'),
(411552, 'HP:0025007', 'Ectopic fovea', 'XPO:0128261', 'decreased size of the optic fiber layer', 0.4574468085106383, 8.040873045973026, 1.9178820903589395, 'HP:0000479', 'Abnormal retinal morphology'),
(411553, 'HP:0025007', 'Ectopic fovea', 'XPO:0130761', 'increased size of the retinal inner plexiform layer', 0.4574468085106383, 8.040873045973026, 1.9178820903589395, 'HP:0000479', 'Abnormal retinal morphology'),
(411554, 'HP:0025007', 'Ectopic fovea', 'XPO:0140945', 'abnormally necrotic retinal ganglion cell layer', 0.46236559139784944, 8.040873045973026, 1.9281657141584967, 'HP:0000479', 'Abnormal retinal morphology'),
(411555, 'HP:0025007', 'Ectopic fovea', 'XPO:0128787', 'decreased size of the peripheral retina', 0.5180722891566265, 8.040873045973026, 2.0410177622316423, 'HP:0000479', 'Abnormal retinal morphology'),
(411556, 'HP:0025007', 'Ectopic fovea', 'XPO:0141338', 'decreased pigmentation in the optic nerve', 0.4019607843137255, 7.796308075334707, 1.7702570741880883, 'UPHENO:0021656', 'abnormal ocular fundus morphology'),
(411557, 'HP:0025007', 'Ectopic fovea', 'XPO:0103160', 'abnormal choroid morphology', 0.4189189189189189, 6.575878401988876, 1.6597469298370302, 'UPHENO:0087924', 'abnormal camera-type eye morphology'),
(411558, 'HP:0025007', 'Ectopic fovea', 'XPO:0103814', 'decreased length of axon in retinal ganglion cell', 0.41346153846153844, 8.040873045973026, 1.8233463028623837, 'HP:0000479', 'Abnormal retinal morphology'),
(411559, 'HP:0025007', 'Ectopic fovea', 'XPO:0130845', 'increased size of the retinal outer plexiform layer', 0.4574468085106383, 8.040873045973026, 1.9178820903589395, 'HP:0000479', 'Abnormal retinal morphology'),
(411560, 'HP:0025007', 'Ectopic fovea', 'XPO:0127563', 'abnormally localised retinal blood vessel', 0.5308641975308642, 8.040873045973026, 2.066061861851679, 'HP:0000479', 'Abnormal retinal morphology'),
(411561, 'HP:0025007', 'Ectopic fovea', 'XPO:0103226', 'abnormal retinal outer plexiform layer morphology', 0.5, 8.040873045973026, 2.0051026215599324, 'HP:0000479', 'Abnormal retinal morphology'),
(411562, 'HP:0025007', 'Ectopic fovea', 'XPO:0129680', 'increased size of the retinal rod cell', 0.41346153846153844, 8.040873045973026, 1.8233463028623837, 'HP:0000479', 'Abnormal retinal morphology'),
(411563, 'HP:0025007', 'Ectopic fovea', 'XPO:0140439', 'abnormally necrotic retinal stem cell', 0.4777777777777778, 8.040873045973026, 1.960038381077836, 'HP:0000479', 'Abnormal retinal morphology'),
(411564, 'HP:0025007', 'Ectopic fovea', 'XPO:0128501', 'decreased size of the retinal ganglion cell layer', 0.4574468085106383, 8.040873045973026, 1.9178820903589395, 'HP:0000479', 'Abnormal retinal morphology'),
(411565, 'HP:0025007', 'Ectopic fovea', 'XPO:0141182', 'abnormally necrotic inner limiting membrane', 0.46236559139784944, 8.040873045973026, 1.9281657141584967, 'HP:0000479', 'Abnormal retinal morphology'),
(411566, 'HP:0025007', 'Ectopic fovea', 'XPO:0103155', 'abnormal bipolar neuron morphology', 0.46236559139784944, 8.040873045973026, 1.9281657141584967, 'HP:0000479', 'Abnormal retinal morphology'),
(411567, 'HP:0025007', 'Ectopic fovea', 'XPO:0130125', 'increased size of the outer limiting membrane', 0.4574468085106383, 8.040873045973026, 1.9178820903589395, 'HP:0000479', 'Abnormal retinal morphology'),
(411568, 'HP:0025007', 'Ectopic fovea', 'XPO:0103706', 'increased pigmentation in the optic nerve', 0.4019607843137255, 7.796308075334707, 1.7702570741880883, 'UPHENO:0021656', 'abnormal ocular fundus morphology'),
(411569, 'HP:0025007', 'Ectopic fovea', 'XPO:0129371', 'decreased size of the retinal outer plexiform layer', 0.4574468085106383, 8.040873045973026, 1.9178820903589395, 'HP:0000479', 'Abnormal retinal morphology'),
(411570, 'HP:0025007', 'Ectopic fovea', 'XPO:0129681', 'increased size of the eye photoreceptor cell', 0.42574257425742573, 8.040873045973026, 1.850227550835222, 'HP:0000479', 'Abnormal retinal morphology'),
(411571, 'HP:0025007', 'Ectopic fovea', 'XPO:0102513', 'abnormal sclera morphology', 0.47297297297297297, 6.887869297006056, 1.8049310288357878, 'UPHENO:0021474', 'abnormal camera-type eye morphology'),
(411572, 'HP:0025007', 'Ectopic fovea', 'XPO:0140240', 'abnormally necrotic eye photoreceptor cell', 0.46236559139784944, 8.040873045973026, 1.9281657141584967, 'HP:0000479', 'Abnormal retinal morphology'),
(411573, 'HP:0025007', 'Ectopic fovea', 'XPO:0102756', 'abnormal Muller cell morphology', 0.5375, 8.040873045973026, 2.0789346459690603, 'HP:0000479', 'Abnormal retinal morphology'),
(411574, 'HP:0025007', 'Ectopic fovea', 'XPO:0140487', 'abnormally necrotic retinal layer', 0.5657894736842105, 8.040873045973026, 2.1329419421640696, 'HP:0000479', 'Abnormal retinal morphology'),
(411575, 'HP:0025007', 'Ectopic fovea', 'XPO:0102862', 'abnormal iris morphology', 0.42168674698795183, 6.887869297006056, 1.7042661756699493, 'UPHENO:0021474', 'abnormal camera-type eye morphology'),
(411576, 'HP:0025007', 'Ectopic fovea', 'XPO:0141323', 'edematous eye', 0.4666666666666667, 6.887869297006056, 1.7928577760852904, 'UPHENO:0021474', 'abnormal camera-type eye morphology'),
(411577, 'HP:0025007', 'Ectopic fovea', 'XPO:0102882', 'abnormal retinal cone cell morphology', 0.4725274725274725, 8.040873045973026, 1.9492391893577128, 'HP:0000479', 'Abnormal retinal morphology'),
(411578, 'HP:0025007', 'Ectopic fovea', 'XPO:0103022', 'abnormal ciliary body morphology', 0.43209876543209874, 6.887869297006056, 1.7251781994025936, 'UPHENO:0021474', 'abnormal camera-type eye morphology'),
(411579, 'HP:0025007', 'Ectopic fovea', 'XPO:0103086', 'abnormal amacrine cell morphology', 0.46236559139784944, 8.040873045973026, 1.9281657141584967, 'HP:0000479', 'Abnormal retinal morphology'),
(411580, 'HP:0025007', 'Ectopic fovea', 'XPO:0101817', 'abnormal eye morphology', 0.4794520547945205, 6.887869297006056, 1.81725152018251, 'UPHENO:0021474', 'abnormal camera-type eye morphology'),
(411581, 'HP:0025007', 'Ectopic fovea', 'XPO:0128848', 'decreased size of the retinal cone cell', 0.41346153846153844, 8.040873045973026, 1.8233463028623837, 'HP:0000479', 'Abnormal retinal morphology'),
(411582, 'HP:0025007', 'Ectopic fovea', 'XPO:0141156', 'abnormally necrotic outer limiting membrane', 0.46236559139784944, 8.040873045973026, 1.9281657141584967, 'HP:0000479', 'Abnormal retinal morphology'),
(411583, 'HP:0025007', 'Ectopic fovea', 'XPO:0128201', 'decreased size of the eye photoreceptor cell', 0.42574257425742573, 8.040873045973026, 1.850227550835222, 'HP:0000479', 'Abnormal retinal morphology'),
(411584, 'HP:0025007', 'Ectopic fovea', 'XPO:0141638', 'neoplastic eye', 0.4605263157894737, 6.887869297006056, 1.7810236020304815, 'HP:0012372', 'Abnormal eye morphology'),
(411585, 'HP:0025007', 'Ectopic fovea', 'XPO:0140192', 'abnormally necrotic retina', 0.5584415584415584, 8.040873045973026, 2.1190464070010115, 'HP:0000479', 'Abnormal retinal morphology'),
(411586, 'HP:0025007', 'Ectopic fovea', 'XPO:0101359', 'abnormal hyaloid artery', 0.43209876543209874, 6.887869297006056, 1.7251781994025936, 'UPHENO:0021474', 'abnormal camera-type eye morphology'),
(411587, 'HP:0025007', 'Ectopic fovea', 'XPO:0130614', 'increased size of the retinal progenitor cell', 0.4387755102040816, 8.040873045973026, 1.8783338822565765, 'HP:0000479', 'Abnormal retinal morphology'),
(411588, 'HP:0025007', 'Ectopic fovea', 'XPO:0103048', 'abnormal cornea morphology', 0.43209876543209874, 6.887869297006056, 1.7251781994025936, 'HP:0012372', 'Abnormal eye morphology'),
(411589, 'HP:0025007', 'Ectopic fovea', 'XPO:0140464', 'abnormally necrotic retinal pigmented epithelium', 0.4574468085106383, 8.040873045973026, 1.9178820903589395, 'HP:0000479', 'Abnormal retinal morphology'),
(411590, 'HP:0010524', 'Agnosia', 'XPO:0100358', 'abnormal ganglion', 0.40625, 3.94131651835137, 1.2653694462805098, 'UPHENO:0004523', 'abnormal nervous system'),
(411591, 'HP:0010524', 'Agnosia', 'XPO:0100032', 'abnormal nervous system', 0.5, 3.94131651835137, 1.4038013602984167, 'UPHENO:0004523', 'abnormal nervous system'),
(411592, 'HP:0010524', 'Agnosia', 'XPO:0100864', 'abnormal dorsolateral ascending neuron', 0.41935483870967744, 3.94131651835137, 1.2856166430382838, 'UPHENO:0004523', 'abnormal nervous system'),
(411593, 'HP:0010524', 'Agnosia', 'XPO:0100481', 'abnormal anatomical line', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(411594, 'HP:0010524', 'Agnosia', 'XPO:0100438', 'abnormal spinal cord', 0.40625, 3.94131651835137, 1.2653694462805098, 'UPHENO:0004523', 'abnormal nervous system'),
(411595, 'HP:0010524', 'Agnosia', 'XPO:0100337', 'abnormal zygote', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(411596, 'HP:0010524', 'Agnosia', 'XPO:0100852', 'abnormal interdigital region', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(411597, 'HP:0010524', 'Agnosia', 'XPO:0101297', 'abnormal barrier cell', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(411598, 'HP:0010524', 'Agnosia', 'XPO:0101239', 'abnormal olfactory epithelial support cell', 0.40625, 3.94131651835137, 1.2653694462805098, 'UPHENO:0004523', 'abnormal nervous system'),
(411599, 'HP:0010524', 'Agnosia', 'XPO:0142051', 'abnormal cerebrospinal fluid', 0.4482758620689655, 3.94131651835137, 1.3292091859262085, 'UPHENO:0004523', 'abnormal nervous system'),
(411600, 'HP:0010524', 'Agnosia', 'XPO:0100108', 'abnormal cell part', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(411601, 'HP:0010524', 'Agnosia', 'XPO:0101133', 'abnormal motor neuron', 0.41935483870967744, 3.94131651835137, 1.2856166430382838, 'UPHENO:0004523', 'abnormal nervous system'),
(411602, 'HP:0010524', 'Agnosia', 'XPO:0101448', 'abnormal myelin accumulating cell', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(411603, 'HP:0010524', 'Agnosia', 'XPO:0107253', 'abnormal enteric nervous system', 0.48148148148148145, 3.94131651835137, 1.3775597686645948, 'UPHENO:0004523', 'abnormal nervous system'),
(411604, 'HP:0010524', 'Agnosia', 'XPO:0100802', 'abnormal exocrine cell', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(411605, 'HP:0010524', 'Agnosia', 'XPO:0100026', 'abnormal germ cell', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(411606, 'HP:0010524', 'Agnosia', 'XPO:0100031', 'abnormal central nervous system', 0.48148148148148145, 3.94131651835137, 1.3775597686645948, 'UPHENO:0004523', 'abnormal nervous system'),
(411607, 'HP:0010524', 'Agnosia', 'XPO:0100760', 'abnormal Stirnorgan', 0.41935483870967744, 3.94131651835137, 1.2856166430382838, 'UPHENO:0004523', 'abnormal nervous system'),
(411608, 'HP:0010524', 'Agnosia', 'XPO:0100164', 'abnormal neural nucleus', 0.4482758620689655, 3.94131651835137, 1.3292091859262085, 'UPHENO:0004523', 'abnormal nervous system'),
(411609, 'HP:0010524', 'Agnosia', 'XPO:0100691', 'abnormal keratin accumulating cell', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(411610, 'HP:0010524', 'Agnosia', 'XPO:0101004', 'abnormal acid secreting cell', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(411611, 'HP:0010524', 'Agnosia', 'XPO:0100285', 'abnormal progenitor cell', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(411612, 'HP:0010524', 'Agnosia', 'XPO:0100289', 'abnormal chondroblast', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(411613, 'HP:0010524', 'Agnosia', 'XPO:0126887', 'abnormally localised nervous system', 0.4117647058823529, 3.94131651835137, 1.2739289764222381, 'UPHENO:0004523', 'abnormal nervous system'),
(411614, 'HP:0010524', 'Agnosia', 'XPO:0100081', 'abnormal anatomical entity in vitro', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(411615, 'HP:0010524', 'Agnosia', 'XPO:0100537', 'abnormal medium cavity', 0.43333333333333335, 3.94131651835137, 1.3068679445984308, 'UPHENO:0004523', 'abnormal nervous system'),
(411616, 'HP:0010524', 'Agnosia', 'XPO:0100954', 'abnormal neural progenitor cell', 0.41935483870967744, 3.94131651835137, 1.2856166430382838, 'UPHENO:0004523', 'abnormal nervous system'),
(411617, 'HP:0010524', 'Agnosia', 'XPO:0100754', 'abnormal electrically active cell', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(411618, 'HP:0010524', 'Agnosia', 'XPO:0100004', 'abnormal cell', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(411619, 'HP:0010524', 'Agnosia', 'XPO:0100533', 'abnormal melanoblast', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(411620, 'HP:0010524', 'Agnosia', 'XPO:0100704', 'abnormal Merkel cell', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(411621, 'HP:0010524', 'Agnosia', 'XPO:0100114', 'abnormal peripheral nervous system', 0.4482758620689655, 3.94131651835137, 1.3292091859262085, 'UPHENO:0004523', 'abnormal nervous system'),
(411622, 'HP:0010524', 'Agnosia', 'XPO:0100274', 'abnormal sensory system', 0.48148148148148145, 3.94131651835137, 1.3775597686645948, 'UPHENO:0004523', 'abnormal nervous system'),
(411623, 'HP:0010524', 'Agnosia', 'XPO:0100702', 'abnormal glial cell', 0.43333333333333335, 3.94131651835137, 1.3068679445984308, 'UPHENO:0004523', 'abnormal nervous system'),
(411624, 'HP:0010524', 'Agnosia', 'XPO:0101535', 'abnormal absorptive cell', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(411625, 'HP:0010524', 'Agnosia', 'XPO:0100734', 'abnormal lateral line system', 0.41935483870967744, 3.94131651835137, 1.2856166430382838, 'UPHENO:0004523', 'abnormal nervous system'),
(411626, 'HP:0010524', 'Agnosia', 'XPO:0100344', 'abnormal portion of organism substance', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(411627, 'HP:0010524', 'Agnosia', 'XPO:0101333', 'abnormal barrier epithelial cell', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(411628, 'HP:0010524', 'Agnosia', 'XPO:0100158', 'abnormal neuromere', 0.43333333333333335, 3.94131651835137, 1.3068679445984308, 'UPHENO:0004523', 'abnormal nervous system'),
(411629, 'HP:0010524', 'Agnosia', 'XPO:0100172', 'abnormal stem cell', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(411630, 'HP:0010524', 'Agnosia', 'XPO:0100549', 'abnormal mitotic cell', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(411631, 'HP:0010524', 'Agnosia', 'XPO:0100273', 'abnormal visual system', 0.4642857142857143, 3.94131651835137, 1.3527368387638634, 'UPHENO:0004523', 'abnormal nervous system'),
(411632, 'HP:0010524', 'Agnosia', 'XPO:0100638', 'abnormal polar body', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(411633, 'HP:0010524', 'Agnosia', 'XPO:0101326', 'abnormal cementoblast', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(411634, 'HP:0010524', 'Agnosia', 'XPO:0100715', 'abnormal ciliated cell', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(411635, 'HP:0010524', 'Agnosia', 'XPO:0100477', 'abnormal pericyte', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(411636, 'HP:0010524', 'Agnosia', 'XPO:0101187', 'abnormal dorsolateral commissural neuron', 0.41935483870967744, 3.94131651835137, 1.2856166430382838, 'UPHENO:0004523', 'abnormal nervous system'),
(411637, 'HP:0010524', 'Agnosia', 'XPO:0100642', 'abnormal gustatory system', 0.4642857142857143, 3.94131651835137, 1.3527368387638634, 'UPHENO:0004523', 'abnormal nervous system'),
(411638, 'HP:0010524', 'Agnosia', 'XPO:0101237', 'abnormal mucus secreting cell', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(411639, 'HP:0010524', 'Agnosia', 'XPO:0107286', 'abnormal efferent neuron', 0.40625, 3.94131651835137, 1.2653694462805098, 'UPHENO:0004523', 'abnormal nervous system'),
(411640, 'HP:0010524', 'Agnosia', 'XPO:0100701', 'abnormal microglial cell', 0.41935483870967744, 3.94131651835137, 1.2856166430382838, 'UPHENO:0004523', 'abnormal nervous system'),
(411641, 'HP:0010524', 'Agnosia', 'XPO:0100336', 'abnormal interneuron', 0.40625, 3.94131651835137, 1.2653694462805098, 'UPHENO:0004523', 'abnormal nervous system'),
(411642, 'HP:0010524', 'Agnosia', 'XPO:0100056', 'abnormal olfactory epithelium', 0.40625, 3.94131651835137, 1.2653694462805098, 'UPHENO:0004523', 'abnormal nervous system'),
(411643, 'HP:0010524', 'Agnosia', 'XPO:0101435', 'abnormal paracrine cell', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(411644, 'HP:0010524', 'Agnosia', 'XPO:0100653', 'abnormal myoblast', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(411645, 'HP:0010524', 'Agnosia', 'XPO:0100858', 'abnormal presumptive midbrain-hindbrain boundary', 0.43333333333333335, 3.94131651835137, 1.3068679445984308, 'UPHENO:0004523', 'abnormal nervous system'),
(411646, 'HP:0010524', 'Agnosia', 'XPO:0101241', 'abnormal nucleate erythrocyte', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(411647, 'HP:0010524', 'Agnosia', 'XPO:0100196', 'abnormal neuron', 0.43333333333333335, 3.94131651835137, 1.3068679445984308, 'UPHENO:0004523', 'abnormal nervous system'),
(411648, 'HP:0010524', 'Agnosia', 'XPO:0131654', 'abnormal neuron projection', 0.40625, 3.94131651835137, 1.2653694462805098, 'UPHENO:0004523', 'abnormal nervous system'),
(411649, 'HP:0010524', 'Agnosia', 'XPO:0101373', 'abnormal oxygen accumulating cell', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(411650, 'HP:0010524', 'Agnosia', 'XPO:0107287', 'abnormal afferent neuron', 0.40625, 3.94131651835137, 1.2653694462805098, 'UPHENO:0004523', 'abnormal nervous system'),
(411651, 'HP:0010524', 'Agnosia', 'XPO:0100006', 'abnormal anatomical structure', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(411652, 'HP:0010524', 'Agnosia', 'XPO:0101467', 'abnormal alkali secreting cell', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(411653, 'HP:0010524', 'Agnosia', 'XPO:0100427', 'abnormal olfactory system', 0.4642857142857143, 3.94131651835137, 1.3527368387638634, 'UPHENO:0004523', 'abnormal nervous system'),
(411654, 'HP:0010524', 'Agnosia', 'XPO:0101501', 'abnormal parabrachial area', 0.43333333333333335, 3.94131651835137, 1.3068679445984308, 'UPHENO:0004523', 'abnormal nervous system'),
(411655, 'HP:0010524', 'Agnosia', 'XPO:0100175', 'abnormal migrating neuroblast', 0.43333333333333335, 3.94131651835137, 1.3068679445984308, 'UPHENO:0004523', 'abnormal nervous system'),
(411656, 'HP:0010524', 'Agnosia', 'XPO:0100587', 'abnormal vestibuloauditory system', 0.4642857142857143, 3.94131651835137, 1.3527368387638634, 'UPHENO:0004523', 'abnormal nervous system'),
(411657, 'HP:0010524', 'Agnosia', 'XPO:0100791', 'abnormal multiciliated cell precursor', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(411658, 'HP:0010524', 'Agnosia', 'XPO:0101132', 'abnormal apoptotic cell', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(411659, 'HP:0010524', 'Agnosia', 'XPO:0100916', 'abnormal principal cavity', 0.43333333333333335, 3.94131651835137, 1.3068679445984308, 'UPHENO:0004523', 'abnormal nervous system'),
(411660, 'HP:0034004', 'Parosmia', 'XPO:0126229', 'absent Jacobsons organ', 0.4230769230769231, 9.116652820832241, 1.9639362067537367, 'HP:0000366', 'Abnormality of the nose'),
(411661, 'HP:0034004', 'Parosmia', 'XPO:0131418', 'abnormally increased number of cilium in the olfactory pit', 0.43137254901960786, 9.116652820832241, 1.9830970137260564, 'HP:0000366', 'Abnormality of the nose'),
(411662, 'HP:0034004', 'Parosmia', 'XPO:0102226', 'abnormal Jacobsons organ morphology', 0.4074074074074074, 9.116652820832241, 1.927223881641334, 'HP:0000366', 'Abnormality of the nose'),
(411663, 'HP:0034004', 'Parosmia', 'XPO:0100594', 'abnormal Jacobsons organ', 0.5384615384615384, 9.116652820832241, 2.2156188533962813, 'HP:0000366', 'Abnormality of the nose'),
(411664, 'HP:0034004', 'Parosmia', 'XPO:0100185', 'abnormal eye', 0.40425531914893614, 5.0624614801082695, 1.430568761479281, 'UPHENO:0002910', 'abnormal face'),
(411665, 'HP:0034004', 'Parosmia', 'XPO:0101334', 'abnormal olfactory pit', 0.5526315789473685, 9.116652820832241, 2.244582420650109, 'HP:0000366', 'Abnormality of the nose'),
(411666, 'HP:0034004', 'Parosmia', 'XPO:0100627', 'abnormal pharyngeal region', 0.4166666666666667, 3.868794716113063, 1.2696447528267278, 'UPHENO:0002844', 'abnormal head'),
(411667, 'HP:0034004', 'Parosmia', 'XPO:0127893', 'abnormally localised Jacobsons organ', 0.46808510638297873, 9.116652820832241, 2.0657612169599715, 'HP:0000366', 'Abnormality of the nose'),
(411668, 'HP:0034004', 'Parosmia', 'XPO:0102966', 'abnormal olfactory pit morphology', 0.4230769230769231, 9.116652820832241, 1.9639362067537367, 'HP:0000366', 'Abnormality of the nose'),
(411669, 'HP:0034004', 'Parosmia', 'XPO:0127208', 'abnormally localised olfactory pit', 0.5, 9.116652820832241, 2.13502374937988, 'HP:0000366', 'Abnormality of the nose'),
(411670, 'HP:0034004', 'Parosmia', 'XPO:0100687', 'abnormal periotic region', 0.40540540540540543, 3.868794716113063, 1.2523698696136485, 'UPHENO:0002844', 'abnormal head'),
(411671, 'HP:0034004', 'Parosmia', 'XPO:0101483', 'abnormal nostril', 0.40816326530612246, 9.116652820832241, 1.9290108304551221, 'HP:0000366', 'Abnormality of the nose'),
(411672, 'HP:0034004', 'Parosmia', 'XPO:0103304', 'absent olfactory pit', 0.4489795918367347, 9.116652820832241, 2.023163627197384, 'HP:0000366', 'Abnormality of the nose'),
(411673, 'HP:0034004', 'Parosmia', 'XPO:0100002', 'abnormal head', 0.42857142857142855, 3.868794716113063, 1.2876547978142938, 'UPHENO:0002844', 'abnormal head'),
(411674, 'HP:0034004', 'Parosmia', 'XPO:0131434', 'abnormally decreased number of cilium in the olfactory pit', 0.4230769230769231, 9.116652820832241, 1.9639362067537367, 'HP:0000366', 'Abnormality of the nose'),
(411675, 'HP:0034004', 'Parosmia', 'XPO:0100727', 'abnormal odontogenic papilla', 0.4166666666666667, 3.868794716113063, 1.2696447528267278, 'UPHENO:0002844', 'abnormal head'),
(411676, 'HP:0034004', 'Parosmia', 'XPO:0101173', 'abnormal retinal layer', 0.41304347826086957, 5.0624614801082695, 1.4460348191885248, 'UPHENO:0002910', 'abnormal face'),
(411677, 'HP:0034004', 'Parosmia', 'XPO:0142052', 'abnormal nasal region', 0.42857142857142855, 3.868794716113063, 1.2876547978142938, 'UPHENO:0002844', 'abnormal head'),
(411678, 'HP:0034004', 'Parosmia', 'XPO:0101402', 'abnormal oropharyngeal papilla', 0.40540540540540543, 3.868794716113063, 1.2523698696136485, 'UPHENO:0002844', 'abnormal head'),
(411679, 'HP:0034004', 'Parosmia', 'XPO:0100664', 'abnormal periocular region', 0.40540540540540543, 3.868794716113063, 1.2523698696136485, 'UPHENO:0002844', 'abnormal head'),
(411680, 'HP:0006441', 'Lateral humeral condyle aplasia', 'XPO:0128497', 'decreased size of the digit-joint region', 0.4084507042253521, 5.802924133159483, 1.539548131353899, 'UPHENO:0076727', 'abnormal limb bone morphology'),
(411681, 'HP:0006441', 'Lateral humeral condyle aplasia', 'XPO:0129977', 'increased size of the digit-joint region', 0.4084507042253521, 5.802924133159483, 1.539548131353899, 'UPHENO:0076727', 'abnormal limb bone morphology'),
(411682, 'HP:0006441', 'Lateral humeral condyle aplasia', 'XPO:0141208', 'abnormally necrotic digit-joint region', 0.42028985507246375, 5.802924133159483, 1.561701041467957, 'UPHENO:0076727', 'abnormal limb bone morphology'),
(411683, 'HP:0006441', 'Lateral humeral condyle aplasia', 'XPO:0126603', 'abnormally localised digit', 0.40298507462686567, 5.802924133159483, 1.5292128088841377, 'UPHENO:0076727', 'abnormal limb bone morphology'),
(411684, 'HP:0006441', 'Lateral humeral condyle aplasia', 'XPO:0141568', 'abnormal digit-joint region morphology in the regenerating forelimb', 0.4084507042253521, 5.802924133159483, 1.539548131353899, 'UPHENO:0076727', 'abnormal limb bone morphology'),
(411685, 'HP:0006441', 'Lateral humeral condyle aplasia', 'XPO:0127078', 'abnormally localised digit-joint region', 0.4090909090909091, 5.802924133159483, 1.5407542013636661, 'UPHENO:0076727', 'abnormal limb bone morphology'),
(411686, 'HP:0006441', 'Lateral humeral condyle aplasia', 'XPO:0101248', 'abnormal digit-joint region', 0.4406779661016949, 5.802924133159483, 1.5991312655448777, 'UPHENO:0076727', 'abnormal limb bone morphology'),
(411687, 'HP:0006441', 'Lateral humeral condyle aplasia', 'XPO:0100178', 'abnormal digit', 0.4642857142857143, 5.802924133159483, 1.6414063409496626, 'UPHENO:0076727', 'abnormal limb bone morphology'),
(411688, 'HP:0006441', 'Lateral humeral condyle aplasia', 'XPO:0103632', 'abnormally increased number of digit', 0.40298507462686567, 5.802924133159483, 1.5292128088841377, 'UPHENO:0076727', 'abnormal limb bone morphology'),
(411689, 'HP:0006441', 'Lateral humeral condyle aplasia', 'XPO:0100298', 'abnormal humerus', 0.425, 10.65746099194716, 2.128243623643107, 'HP:0003063', 'Abnormality of the humerus'),
(411690, 'HP:0006441', 'Lateral humeral condyle aplasia', 'XPO:0141569', 'abnormal digit-joint region morphology in the regenerating hindlimb', 0.4084507042253521, 5.802924133159483, 1.539548131353899, 'UPHENO:0076727', 'abnormal limb bone morphology'),
(411691, 'HP:0006441', 'Lateral humeral condyle aplasia', 'XPO:0101810', 'abnormal digit morphology', 0.4461538461538462, 5.802924133159483, 1.6090360222655293, 'UPHENO:0076727', 'abnormal limb bone morphology'),
(411692, 'HP:0006441', 'Lateral humeral condyle aplasia', 'XPO:0139962', 'abnormally necrotic digit', 0.4027777777777778, 5.802924133159483, 1.5288194422386883, 'UPHENO:0076727', 'abnormal limb bone morphology'),
(411693, 'HP:0006441', 'Lateral humeral condyle aplasia', 'XPO:0102880', 'abnormal digit-joint region morphology', 0.4461538461538462, 5.802924133159483, 1.6090360222655293, 'UPHENO:0076727', 'abnormal limb bone morphology'),
(411694, 'HP:0000805', 'Enuresis', 'XPO:0100501', 'abnormal urogenital system', 0.41935483870967744, 5.4478002382576385, 1.5114765596055648, 'HP:0000119', 'Abnormality of the genitourinary system'),
(411695, 'HP:0000805', 'Enuresis', 'XPO:0100069', 'abnormal urinary system', 0.46875, 6.355235291121788, 1.725982775902859, 'HP:0000079', 'Abnormality of the urinary system'),
(411696, 'HP:0000805', 'Enuresis', 'XPO:0101579', 'abnormal urethra', 0.4594594594594595, 10.167655724266345, 2.161394365459782, 'HP:0010936', 'Abnormality of the lower urinary tract'),
(411697, 'HP:0000805', 'Enuresis', 'XPO:0100085', 'abnormal mesonephric sinus', 0.40540540540540543, 6.355235291121788, 1.6051313776896794, 'HP:0000079', 'Abnormality of the urinary system'),
(411698, 'HP:0000805', 'Enuresis', 'XPO:0100831', 'abnormal bladder', 0.4418604651162791, 11.062302724120116, 2.2108808712675576, 'UPHENO:0002827', 'abnormal urinary bladder'),
(411699, 'HP:0000805', 'Enuresis', 'XPO:0141602', 'metaplastic bladder', 0.43478260869565216, 11.062302724120116, 2.1931021035451046, 'HP:0000014', 'Abnormality of the bladder'),
(411700, 'HP:0001249', 'Intellectual disability', 'XPO:0100427', 'abnormal olfactory system', 0.43333333333333335, 3.94131651835137, 1.3068679445984308, 'UPHENO:0004523', 'abnormal nervous system'),
(411701, 'HP:0001249', 'Intellectual disability', 'XPO:0101501', 'abnormal parabrachial area', 0.40625, 3.94131651835137, 1.2653694462805098, 'UPHENO:0004523', 'abnormal nervous system'),
(411702, 'HP:0001249', 'Intellectual disability', 'XPO:0107253', 'abnormal enteric nervous system', 0.4482758620689655, 3.94131651835137, 1.3292091859262085, 'UPHENO:0004523', 'abnormal nervous system'),
(411703, 'HP:0001249', 'Intellectual disability', 'XPO:0100164', 'abnormal neural nucleus', 0.41935483870967744, 3.94131651835137, 1.2856166430382838, 'UPHENO:0004523', 'abnormal nervous system'),
(411704, 'HP:0001249', 'Intellectual disability', 'XPO:0100916', 'abnormal principal cavity', 0.40625, 3.94131651835137, 1.2653694462805098, 'UPHENO:0004523', 'abnormal nervous system'),
(411705, 'HP:0001249', 'Intellectual disability', 'XPO:0100031', 'abnormal central nervous system', 0.4482758620689655, 3.94131651835137, 1.3292091859262085, 'UPHENO:0004523', 'abnormal nervous system'),
(411706, 'HP:0001249', 'Intellectual disability', 'XPO:0100175', 'abnormal migrating neuroblast', 0.40625, 3.94131651835137, 1.2653694462805098, 'UPHENO:0004523', 'abnormal nervous system'),
(411707, 'HP:0001249', 'Intellectual disability', 'XPO:0100642', 'abnormal gustatory system', 0.43333333333333335, 3.94131651835137, 1.3068679445984308, 'UPHENO:0004523', 'abnormal nervous system'),
(411708, 'HP:0001249', 'Intellectual disability', 'XPO:0100032', 'abnormal nervous system', 0.4642857142857143, 3.94131651835137, 1.3527368387638634, 'UPHENO:0004523', 'abnormal nervous system'),
(411709, 'HP:0001249', 'Intellectual disability', 'XPO:0100702', 'abnormal glial cell', 0.40625, 3.94131651835137, 1.2653694462805098, 'UPHENO:0004523', 'abnormal nervous system'),
(411710, 'HP:0001249', 'Intellectual disability', 'XPO:0100587', 'abnormal vestibuloauditory system', 0.43333333333333335, 3.94131651835137, 1.3068679445984308, 'UPHENO:0004523', 'abnormal nervous system'),
(411711, 'HP:0001249', 'Intellectual disability', 'XPO:0100114', 'abnormal peripheral nervous system', 0.41935483870967744, 3.94131651835137, 1.2856166430382838, 'UPHENO:0004523', 'abnormal nervous system'),
(411712, 'HP:0001249', 'Intellectual disability', 'XPO:0100537', 'abnormal medium cavity', 0.40625, 3.94131651835137, 1.2653694462805098, 'UPHENO:0004523', 'abnormal nervous system'),
(411713, 'HP:0001249', 'Intellectual disability', 'XPO:0100858', 'abnormal presumptive midbrain-hindbrain boundary', 0.40625, 3.94131651835137, 1.2653694462805098, 'UPHENO:0004523', 'abnormal nervous system'),
(411714, 'HP:0001249', 'Intellectual disability', 'XPO:0142051', 'abnormal cerebrospinal fluid', 0.41935483870967744, 3.94131651835137, 1.2856166430382838, 'UPHENO:0004523', 'abnormal nervous system'),
(411715, 'HP:0001249', 'Intellectual disability', 'XPO:0100196', 'abnormal neuron', 0.40625, 3.94131651835137, 1.2653694462805098, 'UPHENO:0004523', 'abnormal nervous system'),
(411716, 'HP:0001249', 'Intellectual disability', 'XPO:0100158', 'abnormal neuromere', 0.40625, 3.94131651835137, 1.2653694462805098, 'UPHENO:0004523', 'abnormal nervous system'),
(411717, 'HP:0001249', 'Intellectual disability', 'XPO:0100274', 'abnormal sensory system', 0.4482758620689655, 3.94131651835137, 1.3292091859262085, 'UPHENO:0004523', 'abnormal nervous system'),
(411718, 'HP:0001249', 'Intellectual disability', 'XPO:0100273', 'abnormal visual system', 0.43333333333333335, 3.94131651835137, 1.3068679445984308, 'UPHENO:0004523', 'abnormal nervous system'),
(411719, 'HP:4000068', 'Abnormal interest', 'XPO:0100032', 'abnormal nervous system', 0.40625, 3.94131651835137, 1.2653694462805098, 'UPHENO:0004523', 'abnormal nervous system'),
(411720, 'HP:0011932', 'Abnormal superior cerebellar peduncle morphology', 'XPO:0100541', 'abnormal nucleus reticularis superior', 0.42028985507246375, 8.826187442983336, 1.9260210386322019, 'UPHENO:0076808', 'abnormal brainstem morphology'),
(411721, 'HP:0011932', 'Abnormal superior cerebellar peduncle morphology', 'XPO:0100304', 'abnormal medulla oblongata', 0.4393939393939394, 8.826187442983336, 1.9693078150461316, 'UPHENO:0076808', 'abnormal brainstem morphology'),
(411722, 'HP:0011932', 'Abnormal superior cerebellar peduncle morphology', 'XPO:0101549', 'abnormal dorsal column nucleus', 0.42028985507246375, 8.826187442983336, 1.9260210386322019, 'UPHENO:0076808', 'abnormal brainstem morphology'),
(411723, 'HP:0011932', 'Abnormal superior cerebellar peduncle morphology', 'XPO:0101265', 'abnormal nucleus reticularis medialis', 0.42028985507246375, 8.826187442983336, 1.9260210386322019, 'UPHENO:0076808', 'abnormal brainstem morphology'),
(411724, 'HP:0011932', 'Abnormal superior cerebellar peduncle morphology', 'XPO:0140715', 'abnormally necrotic granule cell layer of the cerebellum', 0.4025974025974026, 9.66901802336956, 1.9729981099524796, 'HP:0001317', 'Abnormal cerebellum morphology'),
(411725, 'HP:0011932', 'Abnormal superior cerebellar peduncle morphology', 'XPO:0140579', 'abnormally necrotic cerebellum', 0.41333333333333333, 9.66901802336956, 1.999131673917308, 'HP:0001317', 'Abnormal cerebellum morphology'),
(411726, 'HP:0011932', 'Abnormal superior cerebellar peduncle morphology', 'XPO:0100436', 'abnormal nucleus of the solitary tract', 0.42028985507246375, 8.826187442983336, 1.9260210386322019, 'UPHENO:0076808', 'abnormal brainstem morphology'),
(411727, 'HP:0011932', 'Abnormal superior cerebellar peduncle morphology', 'XPO:0101134', 'abnormal nucleus reticularis inferior', 0.42028985507246375, 8.826187442983336, 1.9260210386322019, 'UPHENO:0076808', 'abnormal brainstem morphology'),
(411728, 'HP:0011932', 'Abnormal superior cerebellar peduncle morphology', 'XPO:0102555', 'abnormal granule cell layer of the cerebellum morphology', 0.4305555555555556, 9.66901802336956, 2.0403552207222546, 'HP:0001317', 'Abnormal cerebellum morphology'),
(411729, 'HP:0011932', 'Abnormal superior cerebellar peduncle morphology', 'XPO:0102148', 'abnormal cerebellum morphology', 0.44285714285714284, 9.66901802336956, 2.069297875141146, 'HP:0001317', 'Abnormal cerebellum morphology'),
(411730, 'HP:0011932', 'Abnormal superior cerebellar peduncle morphology', 'XPO:0101292', 'abnormal solitary tract', 0.4084507042253521, 8.826187442983336, 1.8987002071710803, 'UPHENO:0076808', 'abnormal brainstem morphology'),
(411731, 'HP:0011932', 'Abnormal superior cerebellar peduncle morphology', 'XPO:0101599', 'abnormal raphe nucleus', 0.43283582089552236, 8.826187442983336, 1.9545562379377688, 'UPHENO:0076808', 'abnormal brainstem morphology'),
(411732, 'HP:0008263', 'Thyroid defect in oxidation and organification of iodide', 'XPO:0100840', 'abnormal thyroid', 0.45454545454545453, 10.665155383737162, 2.201771537126118, 'UPHENO:0002689', 'abnormal thyroid gland'),
(411733, 'HP:0008263', 'Thyroid defect in oxidation and organification of iodide', 'XPO:0100225', 'abnormal endocrine system', 0.4482758620689655, 6.2194654996189955, 1.669741374719419, 'UPHENO:0003116', 'abnormal endocrine system'),
(411734, 'HP:0008263', 'Thyroid defect in oxidation and organification of iodide', 'XPO:0141629', 'metaplastic thyroid', 0.45714285714285713, 10.665155383737162, 2.208053351709177, 'UPHENO:0002689', 'abnormal thyroid gland'),
(411735, 'HP:0008263', 'Thyroid defect in oxidation and organification of iodide', 'XPO:0101023', 'abnormal ultimobranchial body', 0.40625, 6.2194654996189955, 1.5895464319170476, 'UPHENO:0003116', 'abnormal endocrine system'),
(411736, 'HP:0020185', 'Superior cerebellar dysplasia', 'XPO:0103231', 'abnormal raphe nucleus morphology', 0.40298507462686567, 8.435616811180065, 1.8437536902138099, 'HP:0011282', 'Abnormal hindbrain morphology'),
(411737, 'HP:0020185', 'Superior cerebellar dysplasia', 'XPO:0102490', 'abnormal presumptive midbrain-hindbrain boundary morphology', 0.4117647058823529, 5.483278994082134, 1.502604659339613, 'HP:0002011', 'Morphological central nervous system abnormality'),
(411738, 'HP:0020185', 'Superior cerebellar dysplasia', 'XPO:0102633', 'abnormal ventricular zone morphology', 0.4067796610169492, 6.005340694266148, 1.562962076284922, 'UPHENO:0081435', 'abnormal anatomical entity morphology in the brain'),
(411739, 'HP:0020185', 'Superior cerebellar dysplasia', 'XPO:0102148', 'abnormal cerebellum morphology', 0.5, 9.66901802336956, 2.198751693958365, 'HP:0001317', 'Abnormal cerebellum morphology'),
(411740, 'HP:0020185', 'Superior cerebellar dysplasia', 'XPO:0130251', 'increased size of the granule cell layer of the cerebellum', 0.43661971830985913, 9.66901802336956, 2.054673678640131, 'HP:0001317', 'Abnormal cerebellum morphology'),
(411741, 'HP:0020185', 'Superior cerebellar dysplasia', 'XPO:0101793', 'abnormal hindbrain morphology', 0.4426229508196721, 8.435616811180065, 1.932303704118106, 'HP:0011282', 'Abnormal hindbrain morphology'),
(411742, 'HP:0020185', 'Superior cerebellar dysplasia', 'XPO:0101292', 'abnormal solitary tract', 0.4153846153846154, 8.435616811180065, 1.8719042295598425, 'HP:0011282', 'Abnormal hindbrain morphology'),
(411743, 'HP:0020185', 'Superior cerebellar dysplasia', 'XPO:0101664', 'abnormal nervous system morphology', 0.4222222222222222, 4.7814666189787065, 1.4208594094232423, 'HP:0012639', 'Abnormal nervous system morphology'),
(411744, 'HP:0020185', 'Superior cerebellar dysplasia', 'XPO:0101599', 'abnormal raphe nucleus', 0.4426229508196721, 8.435616811180065, 1.932303704118106, 'HP:0011282', 'Abnormal hindbrain morphology'),
(411745, 'HP:0020185', 'Superior cerebellar dysplasia', 'XPO:0130621', 'increased size of the cerebellum', 0.43661971830985913, 9.66901802336956, 2.054673678640131, 'HP:0001317', 'Abnormal cerebellum morphology'),
(411746, 'HP:0020185', 'Superior cerebellar dysplasia', 'XPO:0129145', 'decreased size of the cerebellum', 0.44285714285714284, 9.66901802336956, 2.069297875141146, 'HP:0001317', 'Abnormal cerebellum morphology'),
(411747, 'HP:0020185', 'Superior cerebellar dysplasia', 'XPO:0142037', 'decreased size of the cerebrospinal fluid', 0.4117647058823529, 5.483278994082134, 1.502604659339613, 'HP:0002011', 'Morphological central nervous system abnormality'),
(411748, 'HP:0020185', 'Superior cerebellar dysplasia', 'XPO:0142031', 'abnormally necrotic cerebrospinal fluid', 0.42857142857142855, 5.483278994082134, 1.5329633758669794, 'HP:0002011', 'Morphological central nervous system abnormality'),
(411749, 'HP:0020185', 'Superior cerebellar dysplasia', 'XPO:0101549', 'abnormal dorsal column nucleus', 0.42857142857142855, 8.435616811180065, 1.9013848499576826, 'HP:0011282', 'Abnormal hindbrain morphology'),
(411750, 'HP:0020185', 'Superior cerebellar dysplasia', 'XPO:0101936', 'abnormal medulla oblongata morphology', 0.40298507462686567, 8.435616811180065, 1.8437536902138099, 'HP:0011282', 'Abnormal hindbrain morphology'),
(411751, 'HP:0020185', 'Superior cerebellar dysplasia', 'XPO:0101265', 'abnormal nucleus reticularis medialis', 0.42857142857142855, 8.435616811180065, 1.9013848499576826, 'HP:0011282', 'Abnormal hindbrain morphology'),
(411752, 'HP:0020185', 'Superior cerebellar dysplasia', 'XPO:0131746', 'abnormal neural tube closure', 0.42, 5.483278994082134, 1.5175563177406288, 'HP:0002011', 'Morphological central nervous system abnormality'),
(411753, 'HP:0020185', 'Superior cerebellar dysplasia', 'XPO:0142058', 'abnormal cerebrospinal fluid morphology', 0.45652173913043476, 5.483278994082134, 1.5821618319614958, 'HP:0002011', 'Morphological central nervous system abnormality'),
(411754, 'HP:0020185', 'Superior cerebellar dysplasia', 'XPO:0101663', 'abnormal central nervous system morphology', 0.44680851063829785, 5.483278994082134, 1.5652398285119449, 'HP:0002011', 'Morphological central nervous system abnormality'),
(411755, 'HP:0020185', 'Superior cerebellar dysplasia', 'XPO:0140579', 'abnormally necrotic cerebellum', 0.4626865671641791, 9.66901802336956, 2.115118142582451, 'HP:0001317', 'Abnormal cerebellum morphology'),
(411756, 'HP:0020185', 'Superior cerebellar dysplasia', 'XPO:0101906', 'abnormal sensory system morphology', 0.41304347826086957, 4.7814666189787065, 1.405330425021534, 'HP:0012639', 'Abnormal nervous system morphology'),
(411757, 'HP:0020185', 'Superior cerebellar dysplasia', 'XPO:0140715', 'abnormally necrotic granule cell layer of the cerebellum', 0.4492753623188406, 9.66901802336956, 2.084238848049033, 'HP:0001317', 'Abnormal cerebellum morphology'),
(411758, 'HP:0020185', 'Superior cerebellar dysplasia', 'XPO:0100541', 'abnormal nucleus reticularis superior', 0.42857142857142855, 8.435616811180065, 1.9013848499576826, 'HP:0011282', 'Abnormal hindbrain morphology'),
(411759, 'HP:0020185', 'Superior cerebellar dysplasia', 'XPO:0100304', 'abnormal medulla oblongata', 0.45, 8.435616811180065, 1.9483396944657851, 'HP:0011282', 'Abnormal hindbrain morphology'),
(411760, 'HP:0020185', 'Superior cerebellar dysplasia', 'XPO:0101796', 'abnormal neural nucleus morphology', 0.4375, 5.483278994082134, 1.5488494310006167, 'HP:0002011', 'Morphological central nervous system abnormality'),
(411761, 'HP:0020185', 'Superior cerebellar dysplasia', 'XPO:0101134', 'abnormal nucleus reticularis inferior', 0.42857142857142855, 8.435616811180065, 1.9013848499576826, 'HP:0011282', 'Abnormal hindbrain morphology'),
(411762, 'HP:0020185', 'Superior cerebellar dysplasia', 'XPO:0101790', 'abnormal neuromere morphology', 0.42857142857142855, 5.483278994082134, 1.5329633758669794, 'HP:0002011', 'Morphological central nervous system abnormality'),
(411763, 'HP:0020185', 'Superior cerebellar dysplasia', 'XPO:0103133', 'abnormal parabrachial area morphology', 0.42, 5.483278994082134, 1.5175563177406288, 'HP:0002011', 'Morphological central nervous system abnormality'),
(411764, 'HP:0020185', 'Superior cerebellar dysplasia', 'XPO:0142044', 'increased size of the cerebrospinal fluid', 0.4117647058823529, 5.483278994082134, 1.502604659339613, 'HP:0002011', 'Morphological central nervous system abnormality'),
(411765, 'HP:0020185', 'Superior cerebellar dysplasia', 'XPO:0139854', 'abnormally necrotic hindbrain', 0.4090909090909091, 8.435616811180065, 1.857669009815314, 'HP:0011282', 'Abnormal hindbrain morphology'),
(411766, 'HP:0020185', 'Superior cerebellar dysplasia', 'XPO:0128773', 'decreased size of the granule cell layer of the cerebellum', 0.43661971830985913, 9.66901802336956, 2.054673678640131, 'HP:0001317', 'Abnormal cerebellum morphology'),
(411767, 'HP:0020185', 'Superior cerebellar dysplasia', 'XPO:0102555', 'abnormal granule cell layer of the cerebellum morphology', 0.484375, 9.66901802336956, 2.164123518903122, 'HP:0001317', 'Abnormal cerebellum morphology'),
(411768, 'HP:0020185', 'Superior cerebellar dysplasia', 'XPO:0100436', 'abnormal nucleus of the solitary tract', 0.42857142857142855, 8.435616811180065, 1.9013848499576826, 'HP:0011282', 'Abnormal hindbrain morphology'),
(411769, 'HP:0020185', 'Superior cerebellar dysplasia', 'XPO:0107340', 'abnormal enteric nervous system morphology', 0.40425531914893614, 4.7814666189787065, 1.3902997209433732, 'HP:0012639', 'Abnormal nervous system morphology'),
(411770, 'HP:0030693', 'Supratentorial neoplasm', 'XPO:0100032', 'abnormal nervous system', 0.40625, 3.94131651835137, 1.2653694462805098, 'UPHENO:0004523', 'abnormal nervous system'),
(411771, 'HP:0030693', 'Supratentorial neoplasm', 'XPO:0142031', 'abnormally necrotic cerebrospinal fluid', 0.4186046511627907, 5.483278994082134, 1.515033362849152, 'HP:0002011', 'Morphological central nervous system abnormality'),
(411772, 'HP:0030693', 'Supratentorial neoplasm', 'XPO:0101664', 'abnormal nervous system morphology', 0.41025641025641024, 4.7814666189787065, 1.4005810690078098, 'HP:0012639', 'Abnormal nervous system morphology'),
(411773, 'HP:0030693', 'Supratentorial neoplasm', 'XPO:0142058', 'abnormal cerebrospinal fluid morphology', 0.45, 5.483278994082134, 1.5708200238528156, 'HP:0002011', 'Morphological central nervous system abnormality'),
(411774, 'HP:0030693', 'Supratentorial neoplasm', 'XPO:0101796', 'abnormal neural nucleus morphology', 0.42857142857142855, 5.483278994082134, 1.5329633758669794, 'HP:0002011', 'Morphological central nervous system abnormality'),
(411775, 'HP:0030693', 'Supratentorial neoplasm', 'XPO:0103133', 'abnormal parabrachial area morphology', 0.4090909090909091, 5.483278994082134, 1.4977181271815287, 'HP:0002011', 'Morphological central nervous system abnormality'),
(411776, 'HP:0030693', 'Supratentorial neoplasm', 'XPO:0101790', 'abnormal neuromere morphology', 0.4186046511627907, 5.483278994082134, 1.515033362849152, 'HP:0002011', 'Morphological central nervous system abnormality'),
(411777, 'HP:0030693', 'Supratentorial neoplasm', 'XPO:0131746', 'abnormal neural tube closure', 0.4090909090909091, 5.483278994082134, 1.4977181271815287, 'HP:0002011', 'Morphological central nervous system abnormality'),
(411778, 'HP:0030693', 'Supratentorial neoplasm', 'XPO:0101663', 'abnormal central nervous system morphology', 0.43902439024390244, 5.483278994082134, 1.5515454285692403, 'HP:0002011', 'Morphological central nervous system abnormality'),
(411779, 'HP:0033127', 'Abnormality of the musculoskeletal system', 'XPO:0100910', 'abnormal vacuolated notochordal tissue', 0.44, 3.9037819259951223, 1.3105968287150147, 'HP:0033127', 'Abnormality of the musculoskeletal system'),
(411780, 'HP:0033127', 'Abnormality of the musculoskeletal system', 'XPO:0141272', 'absent surface breathing', 0.6153846153846154, 1.4755025719078136, 0.9528911704452407, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(411781, 'HP:0033127', 'Abnormality of the musculoskeletal system', 'XPO:0131474', 'absent behavioral response to pain', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(411782, 'HP:0033127', 'Abnormality of the musculoskeletal system', 'XPO:0115391', 'abnormally undifferentiated alimentary system', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(411783, 'HP:0033127', 'Abnormality of the musculoskeletal system', 'XPO:0100888', 'abnormal microtubule', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(411784, 'HP:0033127', 'Abnormality of the musculoskeletal system', 'XPO:0141894', 'abnormal dicarboxylic acid transport', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(411785, 'HP:0033127', 'Abnormality of the musculoskeletal system', 'XPO:0100123', 'abnormal pelvic girdle', 0.4230769230769231, 3.9037819259951223, 1.2851459238597462, 'HP:0033127', 'Abnormality of the musculoskeletal system'),
(411786, 'HP:0033127', 'Abnormality of the musculoskeletal system', 'XPO:0100205', 'abnormal limb segment', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(411787, 'HP:0033127', 'Abnormality of the musculoskeletal system', 'XPO:0100754', 'abnormal electrically active cell', 0.5263157894736842, 1.8210412618256888, 0.9790009036675816, 'HP:0000118', 'Phenotypic abnormality'),
(411788, 'HP:0033127', 'Abnormality of the musculoskeletal system', 'XPO:0100383', 'abnormal amputated fin', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(411789, 'HP:0033127', 'Abnormality of the musculoskeletal system', 'XPO:0101577', 'abnormal notochordal epithelium', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(411790, 'HP:0033127', 'Abnormality of the musculoskeletal system', 'XPO:0100261', 'abnormal multilaminar epithelium', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(411791, 'HP:0033127', 'Abnormality of the musculoskeletal system', 'XPO:0101484', 'abnormal bone marrow', 0.4074074074074074, 3.9037819259951223, 1.2611223864294727, 'HP:0033127', 'Abnormality of the musculoskeletal system'),
(411792, 'HP:0033127', 'Abnormality of the musculoskeletal system', 'XPO:0131739', 'abnormal wound healing', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(411793, 'HP:0033127', 'Abnormality of the musculoskeletal system', 'XPO:0131703', 'abnormal cell division', 0.47058823529411764, 1.4755025719078136, 0.8332791557971614, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(411794, 'HP:0033127', 'Abnormality of the musculoskeletal system', 'XPO:0100890', 'abnormal pharyngeal cavity', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(411795, 'HP:0033127', 'Abnormality of the musculoskeletal system', 'XPO:0100746', 'abnormal smooth muscle', 0.44, 3.9037819259951223, 1.3105968287150147, 'HP:0033127', 'Abnormality of the musculoskeletal system'),
(411796, 'HP:0033127', 'Abnormality of the musculoskeletal system', 'XPO:0100249', 'abnormal avascular GAG-rich matrix', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(411797, 'HP:0033127', 'Abnormality of the musculoskeletal system', 'XPO:0101575', 'abnormal vitelline membrane', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(411798, 'HP:0033127', 'Abnormality of the musculoskeletal system', 'XPO:0101347', 'abnormal hindlimb region', 0.47058823529411764, 1.4755025719078136, 0.8332791557971614, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(411799, 'HP:0033127', 'Abnormality of the musculoskeletal system', 'XPO:0101503', 'abnormal organ cortex', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(411800, 'HP:0033127', 'Abnormality of the musculoskeletal system', 'XPO:0100232', 'abnormal lymphatic system', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(411801, 'HP:0033127', 'Abnormality of the musculoskeletal system', 'XPO:0101149', 'abnormal amputated limb', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(411802, 'HP:0033127', 'Abnormality of the musculoskeletal system', 'XPO:0101107', 'abnormal erythroid cell', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(411803, 'HP:0033127', 'Abnormality of the musculoskeletal system', 'XPO:0100449', 'abnormal lymphocyte', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(411804, 'HP:0033127', 'Abnormality of the musculoskeletal system', 'XPO:0132410', 'abnormal development of anterior region', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(411805, 'HP:0033127', 'Abnormality of the musculoskeletal system', 'XPO:0100207', 'abnormal blastema', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(411806, 'HP:0033127', 'Abnormality of the musculoskeletal system', 'XPO:0100791', 'abnormal multiciliated cell precursor', 0.5263157894736842, 1.8210412618256888, 0.9790009036675816, 'HP:0000118', 'Phenotypic abnormality'),
(411807, 'HP:0033127', 'Abnormality of the musculoskeletal system', 'XPO:00000000', 'Xenopus phenotype', 0.6666666666666666, 1.4755025719078136, 0.9918005753536725, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(411808, 'HP:0033127', 'Abnormality of the musculoskeletal system', 'XPO:0141962', 'absent cilium motility in pronephric kidney', 0.47058823529411764, 1.4755025719078136, 0.8332791557971614, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(411809, 'HP:0033127', 'Abnormality of the musculoskeletal system', 'XPO:0100533', 'abnormal melanoblast', 0.5263157894736842, 1.8210412618256888, 0.9790009036675816, 'HP:0000118', 'Phenotypic abnormality'),
(411810, 'HP:0033127', 'Abnormality of the musculoskeletal system', 'XPO:0100482', 'abnormal Mullerian duct', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(411811, 'HP:0033127', 'Abnormality of the musculoskeletal system', 'XPO:0141970', 'absent cilium motility in multiciliated cell', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(411812, 'HP:0033127', 'Abnormality of the musculoskeletal system', 'XPO:0133325', 'abnormal development of postero-dorsal region', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(411813, 'HP:0033127', 'Abnormality of the musculoskeletal system', 'XPO:0100537', 'abnormal medium cavity', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(411814, 'HP:0033127', 'Abnormality of the musculoskeletal system', 'XPO:0100581', 'abnormal immune system', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(411815, 'HP:0033127', 'Abnormality of the musculoskeletal system', 'XPO:0101602', 'abnormal intersomitic tendon', 0.44, 3.9037819259951223, 1.3105968287150147, 'HP:0033127', 'Abnormality of the musculoskeletal system'),
(411816, 'HP:0033127', 'Abnormality of the musculoskeletal system', 'XPO:0100114', 'abnormal peripheral nervous system', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(411817, 'HP:0033127', 'Abnormality of the musculoskeletal system', 'XPO:0131741', 'abnormal convergent extension', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(411818, 'HP:0033127', 'Abnormality of the musculoskeletal system', 'XPO:0100014', 'abnormal tissue', 0.47058823529411764, 1.4755025719078136, 0.8332791557971614, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(411819, 'HP:0033127', 'Abnormality of the musculoskeletal system', 'XPO:0133402', 'absent determination of left/right symmetry in alimentary system', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(411820, 'HP:0033127', 'Abnormality of the musculoskeletal system', 'XPO:0141265', 'abnormal escape behavior', 0.6153846153846154, 1.4755025719078136, 0.9528911704452407, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(411821, 'HP:0033127', 'Abnormality of the musculoskeletal system', 'XPO:0100887', 'abnormal right-dorsal blastomere', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(411822, 'HP:0033127', 'Abnormality of the musculoskeletal system', 'XPO:0131482', 'absent locomotory behavior', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(411823, 'HP:0033127', 'Abnormality of the musculoskeletal system', 'XPO:0115505', 'dead whole organism', 0.5, 1.4755025719078136, 0.8589244937443028, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(411824, 'HP:0033127', 'Abnormality of the musculoskeletal system', 'XPO:0100258', 'abnormal organ part', 0.5333333333333333, 1.4755025719078136, 0.8870934026456857, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(411825, 'HP:0033127', 'Abnormality of the musculoskeletal system', 'XPO:0141745', 'abnormal creatinine homeostasis', 0.6153846153846154, 1.4755025719078136, 0.9528911704452407, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(411826, 'HP:0033127', 'Abnormality of the musculoskeletal system', 'XPO:0101333', 'abnormal barrier epithelial cell', 0.5263157894736842, 1.8210412618256888, 0.9790009036675816, 'HP:0000118', 'Phenotypic abnormality'),
(411827, 'HP:0033127', 'Abnormality of the musculoskeletal system', 'XPO:0133260', 'abnormal development of posterior region', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(411828, 'HP:0033127', 'Abnormality of the musculoskeletal system', 'XPO:0101162', 'abnormal stromal cell', 0.4583333333333333, 3.9037819259951223, 1.3376222870256627, 'HP:0033127', 'Abnormality of the musculoskeletal system'),
(411829, 'HP:0033127', 'Abnormality of the musculoskeletal system', 'XPO:0131401', 'abnormal behavioral response to pain', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(411830, 'HP:0033127', 'Abnormality of the musculoskeletal system', 'XPO:0103624', 'absent anterior/posterior pattern specification in midgut', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(411831, 'HP:0033127', 'Abnormality of the musculoskeletal system', 'XPO:0101061', 'abnormal plasma membrane', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(411832, 'HP:0033127', 'Abnormality of the musculoskeletal system', 'XPO:0100363', 'abnormal cardiovascular system', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(411833, 'HP:0033127', 'Abnormality of the musculoskeletal system', 'XPO:0100642', 'abnormal gustatory system', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(411834, 'HP:0033127', 'Abnormality of the musculoskeletal system', 'XPO:0101976', 'abnormal portion of organism substance morphology', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(411835, 'HP:0033127', 'Abnormality of the musculoskeletal system', 'XPO:0100868', 'abnormal transporting epithelium', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(411836, 'HP:0033127', 'Abnormality of the musculoskeletal system', 'XPO:0100402', 'abnormal zeugopod', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(411837, 'HP:0033127', 'Abnormality of the musculoskeletal system', 'XPO:0101311', 'abnormal bottle cell', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(411838, 'HP:0033127', 'Abnormality of the musculoskeletal system', 'XPO:0100640', 'abnormal notochordal sheath', 0.5, 3.9037819259951223, 1.3971009136771622, 'HP:0033127', 'Abnormality of the musculoskeletal system'),
(411839, 'HP:0033127', 'Abnormality of the musculoskeletal system', 'XPO:0100031', 'abnormal central nervous system', 0.47619047619047616, 1.8210412618256888, 0.9312156064152277, 'HP:0000118', 'Phenotypic abnormality'),
(411840, 'HP:0033127', 'Abnormality of the musculoskeletal system', 'XPO:0101072', 'abnormal mitochondrial cloud', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(411841, 'HP:0033127', 'Abnormality of the musculoskeletal system', 'XPO:0100028', 'abnormal anatomical cluster', 0.47058823529411764, 1.4755025719078136, 0.8332791557971614, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(411842, 'HP:0033127', 'Abnormality of the musculoskeletal system', 'XPO:0101501', 'abnormal parabrachial area', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(411843, 'HP:0033127', 'Abnormality of the musculoskeletal system', 'XPO:0100503', 'abnormal blastomere D2', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(411844, 'HP:0033127', 'Abnormality of the musculoskeletal system', 'XPO:0100009', 'abnormal multi-tissue structure', 0.47058823529411764, 1.4755025719078136, 0.8332791557971614, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(411845, 'HP:0033127', 'Abnormality of the musculoskeletal system', 'XPO:0132054', 'abnormal development of portion of organism substance', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(411846, 'HP:0033127', 'Abnormality of the musculoskeletal system', 'XPO:0100285', 'abnormal progenitor cell', 0.5263157894736842, 1.8210412618256888, 0.9790009036675816, 'HP:0000118', 'Phenotypic abnormality'),
(411847, 'HP:0033127', 'Abnormality of the musculoskeletal system', 'XPO:0141794', 'abnormal prosthetic group metabolic process', 0.5263157894736842, 1.8210412618256888, 0.9790009036675816, 'HP:0000118', 'Phenotypic abnormality'),
(411848, 'HP:0033127', 'Abnormality of the musculoskeletal system', 'XPO:0101362', 'abnormal vegetal cortex', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(411849, 'HP:0033127', 'Abnormality of the musculoskeletal system', 'XPO:0132787', 'abnormal development of apical region', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(411850, 'HP:0033127', 'Abnormality of the musculoskeletal system', 'XPO:0133164', 'abnormal development of archenteron roof midline', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(411851, 'HP:0033127', 'Abnormality of the musculoskeletal system', 'XPO:0107264', 'abnormal anterior side', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(411852, 'HP:0033127', 'Abnormality of the musculoskeletal system', 'XPO:0100176', 'abnormal stage VI oocyte', 0.47619047619047616, 1.8210412618256888, 0.9312156064152277, 'HP:0000118', 'Phenotypic abnormality'),
(411853, 'HP:0033127', 'Abnormality of the musculoskeletal system', 'XPO:0131867', 'abnormal development of antero-dorsal region', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(411854, 'HP:0033127', 'Abnormality of the musculoskeletal system', 'XPO:0116494', 'absent biological process', 0.5714285714285714, 1.4755025719078136, 0.918228907628411, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(411855, 'HP:0033127', 'Abnormality of the musculoskeletal system', 'XPO:0131705', 'abnormal chemotaxis', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(411856, 'HP:0033127', 'Abnormality of the musculoskeletal system', 'XPO:0131700', 'abnormal BMP signaling pathway', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(411857, 'HP:0033127', 'Abnormality of the musculoskeletal system', 'XPO:0101373', 'abnormal oxygen accumulating cell', 0.5263157894736842, 1.8210412618256888, 0.9790009036675816, 'HP:0000118', 'Phenotypic abnormality'),
(411858, 'HP:0033127', 'Abnormality of the musculoskeletal system', 'XPO:0131408', 'abnormal feeding behavior', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(411859, 'HP:0033127', 'Abnormality of the musculoskeletal system', 'XPO:0132733', 'abnormal development of filter chamber', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(411860, 'HP:0033127', 'Abnormality of the musculoskeletal system', 'XPO:0101586', 'abnormal joint', 0.4230769230769231, 3.9037819259951223, 1.2851459238597462, 'HP:0033127', 'Abnormality of the musculoskeletal system'),
(411861, 'HP:0033127', 'Abnormality of the musculoskeletal system', 'XPO:0100786', 'abnormal presumptive axial mesoderm', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(411862, 'HP:0033127', 'Abnormality of the musculoskeletal system', 'XPO:0100549', 'abnormal mitotic cell', 0.5263157894736842, 1.8210412618256888, 0.9790009036675816, 'HP:0000118', 'Phenotypic abnormality'),
(411863, 'HP:0033127', 'Abnormality of the musculoskeletal system', 'XPO:0100546', 'abnormal whole organism', 0.5333333333333333, 1.4755025719078136, 0.8870934026456857, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(411864, 'HP:0033127', 'Abnormality of the musculoskeletal system', 'XPO:0141783', 'abnormal collagen metabolic process', 0.5263157894736842, 1.8210412618256888, 0.9790009036675816, 'HP:0000118', 'Phenotypic abnormality'),
(411865, 'HP:0033127', 'Abnormality of the musculoskeletal system', 'XPO:0100551', 'abnormal oocyte cortex', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(411866, 'HP:0033127', 'Abnormality of the musculoskeletal system', 'XPO:0101220', 'abnormal centriole', 0.47619047619047616, 1.8210412618256888, 0.9312156064152277, 'HP:0000118', 'Phenotypic abnormality'),
(411867, 'HP:0033127', 'Abnormality of the musculoskeletal system', 'XPO:0131744', 'abnormal apical constriction', 0.47058823529411764, 1.4755025719078136, 0.8332791557971614, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(411868, 'HP:0033127', 'Abnormality of the musculoskeletal system', 'XPO:0100309', 'abnormal vegetal hemisphere', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(411869, 'HP:0033127', 'Abnormality of the musculoskeletal system', 'XPO:0100416', 'abnormal ligament', 0.5, 3.9037819259951223, 1.3971009136771622, 'HP:0033127', 'Abnormality of the musculoskeletal system'),
(411870, 'HP:0033127', 'Abnormality of the musculoskeletal system', 'XPO:0101099', 'abnormal ventro-lateral marginal zone', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(411871, 'HP:0033127', 'Abnormality of the musculoskeletal system', 'XPO:0141778', 'abnormal biosynthetic process', 0.5263157894736842, 1.8210412618256888, 0.9790009036675816, 'HP:0000118', 'Phenotypic abnormality'),
(411872, 'HP:0033127', 'Abnormality of the musculoskeletal system', 'XPO:0141958', 'absent cilium motility in left-right organizer', 0.47058823529411764, 1.4755025719078136, 0.8332791557971614, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(411873, 'HP:0033127', 'Abnormality of the musculoskeletal system', 'XPO:0100308', 'abnormal early embryonic cell', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(411874, 'HP:0033127', 'Abnormality of the musculoskeletal system', 'XPO:0131470', 'abnormal heart contraction', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(411875, 'HP:0033127', 'Abnormality of the musculoskeletal system', 'XPO:0107253', 'abnormal enteric nervous system', 0.47619047619047616, 1.8210412618256888, 0.9312156064152277, 'HP:0000118', 'Phenotypic abnormality'),
(411876, 'HP:0033127', 'Abnormality of the musculoskeletal system', 'XPO:0100665', 'abnormal egg jelly', 0.47058823529411764, 1.4755025719078136, 0.8332791557971614, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(411877, 'HP:0033127', 'Abnormality of the musculoskeletal system', 'XPO:0100162', 'abnormal presumptive rhombomere', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(411878, 'HP:0033127', 'Abnormality of the musculoskeletal system', 'XPO:0100969', 'abnormal disaggregated/reaggregated ectoderm treated with activin', 0.5333333333333333, 1.4755025719078136, 0.8870934026456857, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(411879, 'HP:0033127', 'Abnormality of the musculoskeletal system', 'XPO:0100265', 'abnormal sensory epithelial cell', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(411880, 'HP:0033127', 'Abnormality of the musculoskeletal system', 'XPO:0141788', 'abnormal hormone biosynthetic process', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(411881, 'HP:0033127', 'Abnormality of the musculoskeletal system', 'XPO:0100916', 'abnormal principal cavity', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(411882, 'HP:0033127', 'Abnormality of the musculoskeletal system', 'XPO:0100273', 'abnormal visual system', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(411883, 'HP:0033127', 'Abnormality of the musculoskeletal system', 'XPO:0100062', 'abnormal anatomical space', 0.5, 1.4755025719078136, 0.8589244937443028, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(411884, 'HP:0033127', 'Abnormality of the musculoskeletal system', 'XPO:0132889', 'abnormal development of dorsal lymph space', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(411885, 'HP:0033127', 'Abnormality of the musculoskeletal system', 'XPO:0100392', 'abnormal cilium', 0.47619047619047616, 1.8210412618256888, 0.9312156064152277, 'HP:0000118', 'Phenotypic abnormality'),
(411886, 'HP:0033127', 'Abnormality of the musculoskeletal system', 'XPO:0133049', 'abnormal development of anterior entopeduncular region', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(411887, 'HP:0033127', 'Abnormality of the musculoskeletal system', 'XPO:0100317', 'abnormal respiratory system', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(411888, 'HP:0033127', 'Abnormality of the musculoskeletal system', 'XPO:0100707', 'abnormal central vegetal yolk mass', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(411889, 'HP:0033127', 'Abnormality of the musculoskeletal system', 'XPO:0100060', 'abnormal regenerating tissue', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(411890, 'HP:0033127', 'Abnormality of the musculoskeletal system', 'XPO:0100307', 'abnormal blastomere', 0.47619047619047616, 1.8210412618256888, 0.9312156064152277, 'HP:0000118', 'Phenotypic abnormality'),
(411891, 'HP:0033127', 'Abnormality of the musculoskeletal system', 'XPO:0131833', 'abnormal development of cell part', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(411892, 'HP:0033127', 'Abnormality of the musculoskeletal system', 'XPO:0101297', 'abnormal barrier cell', 0.5263157894736842, 1.8210412618256888, 0.9790009036675816, 'HP:0000118', 'Phenotypic abnormality'),
(411893, 'HP:0033127', 'Abnormality of the musculoskeletal system', 'XPO:0141799', 'decreased catalytic activity', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(411894, 'HP:0033127', 'Abnormality of the musculoskeletal system', 'XPO:0131725', 'abnormal phosphorylation of RNA polymerase II C-terminal domain', 0.6153846153846154, 1.4755025719078136, 0.9528911704452407, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(411895, 'HP:0033127', 'Abnormality of the musculoskeletal system', 'XPO:0101010', 'abnormal dorsal marginal zone', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(411896, 'HP:0033127', 'Abnormality of the musculoskeletal system', 'XPO:0141770', 'abnormal urate homeostasis', 0.6153846153846154, 1.4755025719078136, 0.9528911704452407, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(411897, 'HP:0033127', 'Abnormality of the musculoskeletal system', 'XPO:0100386', 'abnormal limb', 0.47619047619047616, 1.8210412618256888, 0.9312156064152277, 'HP:0000118', 'Phenotypic abnormality'),
(411898, 'HP:0033127', 'Abnormality of the musculoskeletal system', 'XPO:0141967', 'absent cilium motility in esophagus', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(411899, 'HP:0033127', 'Abnormality of the musculoskeletal system', 'XPO:0131691', 'abnormal molecular function', 0.5714285714285714, 1.4755025719078136, 0.918228907628411, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(411900, 'HP:0033127', 'Abnormality of the musculoskeletal system', 'XPO:0100004', 'abnormal cell', 0.5555555555555556, 1.8210412618256888, 1.005827813247954, 'HP:0000118', 'Phenotypic abnormality'),
(411901, 'HP:0033127', 'Abnormality of the musculoskeletal system', 'XPO:0133037', 'abnormal development of dorsal region', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(411902, 'HP:0033127', 'Abnormality of the musculoskeletal system', 'XPO:0100465', 'abnormal skeletal system', 0.5238095238095238, 3.9037819259951223, 1.429978374560864, 'HP:0033127', 'Abnormality of the musculoskeletal system'),
(411903, 'HP:0033127', 'Abnormality of the musculoskeletal system', 'XPO:0102113', 'abnormal anatomical line morphology', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(411904, 'HP:0033127', 'Abnormality of the musculoskeletal system', 'XPO:0133213', 'abnormal development of fenestra basicranialis', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(411905, 'HP:0033127', 'Abnormality of the musculoskeletal system', 'XPO:0100515', 'abnormal somatic stem cell', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(411906, 'HP:0033127', 'Abnormality of the musculoskeletal system', 'XPO:0100429', 'abnormal spermatid', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(411907, 'HP:0033127', 'Abnormality of the musculoskeletal system', 'XPO:0100006', 'abnormal anatomical structure', 0.5714285714285714, 1.4755025719078136, 0.918228907628411, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(411908, 'HP:0033127', 'Abnormality of the musculoskeletal system', 'XPO:0100437', 'abnormal proepicardium', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(411909, 'HP:0033127', 'Abnormality of the musculoskeletal system', 'XPO:0101283', 'abnormal left-ventral blastomere', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(411910, 'HP:0033127', 'Abnormality of the musculoskeletal system', 'XPO:0141810', 'abnormal cyclase activity', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(411911, 'HP:0033127', 'Abnormality of the musculoskeletal system', 'XPO:0131721', 'abnormal nodal signaling pathway', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(411912, 'HP:0033127', 'Abnormality of the musculoskeletal system', 'XPO:0141965', 'absent cilium motility in alimentary system', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(411913, 'HP:0033127', 'Abnormality of the musculoskeletal system', 'XPO:0141900', 'abnormal mannose metabolic process', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(411914, 'HP:0033127', 'Abnormality of the musculoskeletal system', 'XPO:0101587', 'abnormal hemangioblast', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(411915, 'HP:0033127', 'Abnormality of the musculoskeletal system', 'XPO:0141743', 'abnormal chemical homeostasis within a tissue', 0.6153846153846154, 1.4755025719078136, 0.9528911704452407, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(411916, 'HP:0033127', 'Abnormality of the musculoskeletal system', 'XPO:0132807', 'abnormal development of anterior endomesoderm', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(411917, 'HP:0033127', 'Abnormality of the musculoskeletal system', 'XPO:0100231', 'abnormal compound organ', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(411918, 'HP:0033127', 'Abnormality of the musculoskeletal system', 'XPO:0100854', 'abnormal spiracle', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(411919, 'HP:0033127', 'Abnormality of the musculoskeletal system', 'XPO:0132611', 'abnormal development of intercanthal region', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(411920, 'HP:0033127', 'Abnormality of the musculoskeletal system', 'XPO:0100727', 'abnormal odontogenic papilla', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(411921, 'HP:0033127', 'Abnormality of the musculoskeletal system', 'XPO:0101461', 'abnormal sperm entry point', 0.47619047619047616, 1.8210412618256888, 0.9312156064152277, 'HP:0000118', 'Phenotypic abnormality'),
(411922, 'HP:0033127', 'Abnormality of the musculoskeletal system', 'XPO:0100935', 'abnormal skeleton', 0.4782608695652174, 3.9037819259951223, 1.3663916490228585, 'HP:0033127', 'Abnormality of the musculoskeletal system'),
(411923, 'HP:0033127', 'Abnormality of the musculoskeletal system', 'XPO:0131475', 'absent olfactory behavior', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(411924, 'HP:0033127', 'Abnormality of the musculoskeletal system', 'XPO:0100900', 'abnormal angioblast', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(411925, 'HP:0033127', 'Abnormality of the musculoskeletal system', 'XPO:0100781', 'abnormal presumptive ectoderm', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(411926, 'HP:0033127', 'Abnormality of the musculoskeletal system', 'XPO:0141600', 'absent metamorphosis', 0.5, 1.4755025719078136, 0.8589244937443028, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(411927, 'HP:0033127', 'Abnormality of the musculoskeletal system', 'XPO:0101200', 'abnormal joint region', 0.47058823529411764, 1.4755025719078136, 0.8332791557971614, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(411928, 'HP:0033127', 'Abnormality of the musculoskeletal system', 'XPO:0100458', 'abnormal autopod', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(411929, 'HP:0033127', 'Abnormality of the musculoskeletal system', 'XPO:0141841', 'abnormality of whole organism mass', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(411930, 'HP:0033127', 'Abnormality of the musculoskeletal system', 'XPO:0132668', 'abnormal development of anterior endoderm', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(411931, 'HP:0033127', 'Abnormality of the musculoskeletal system', 'XPO:0141781', 'abnormal secondary metabolic process', 0.5263157894736842, 1.8210412618256888, 0.9790009036675816, 'HP:0000118', 'Phenotypic abnormality'),
(411932, 'HP:0033127', 'Abnormality of the musculoskeletal system', 'XPO:0132501', 'abnormal development of marginal zone (sensu neural)', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(411933, 'HP:0033127', 'Abnormality of the musculoskeletal system', 'XPO:0100498', 'abnormal endoskeleton', 0.44, 3.9037819259951223, 1.3105968287150147, 'HP:0033127', 'Abnormality of the musculoskeletal system'),
(411934, 'HP:0033127', 'Abnormality of the musculoskeletal system', 'XPO:0141811', 'abnormal oxidoreductase activity', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(411935, 'HP:0033127', 'Abnormality of the musculoskeletal system', 'XPO:0132249', 'abnormal development of whole organism', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(411936, 'HP:0033127', 'Abnormality of the musculoskeletal system', 'XPO:0101023', 'abnormal ultimobranchial body', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(411937, 'HP:0033127', 'Abnormality of the musculoskeletal system', 'XPO:0141786', 'abnormal pigment metabolic process', 0.5263157894736842, 1.8210412618256888, 0.9790009036675816, 'HP:0000118', 'Phenotypic abnormality'),
(411938, 'HP:0033127', 'Abnormality of the musculoskeletal system', 'XPO:0101560', 'abnormal compound organ component', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(411939, 'HP:0033127', 'Abnormality of the musculoskeletal system', 'XPO:0131472', 'absent vocalization behavior', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(411940, 'HP:0033127', 'Abnormality of the musculoskeletal system', 'XPO:0107272', 'abnormal axial region', 0.47058823529411764, 1.4755025719078136, 0.8332791557971614, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(411941, 'HP:0033127', 'Abnormality of the musculoskeletal system', 'XPO:0131711', 'abnormal establishment of cell polarity', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(411942, 'HP:0033127', 'Abnormality of the musculoskeletal system', 'XPO:0100715', 'abnormal ciliated cell', 0.5263157894736842, 1.8210412618256888, 0.9790009036675816, 'HP:0000118', 'Phenotypic abnormality'),
(411943, 'HP:0033127', 'Abnormality of the musculoskeletal system', 'XPO:0100325', 'abnormal axial skeleton', 0.44, 3.9037819259951223, 1.3105968287150147, 'HP:0033127', 'Abnormality of the musculoskeletal system'),
(411944, 'HP:0033127', 'Abnormality of the musculoskeletal system', 'XPO:0141499', 'abnormal tadpole', 0.5, 1.4755025719078136, 0.8589244937443028, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(411945, 'HP:0033127', 'Abnormality of the musculoskeletal system', 'XPO:0100627', 'abnormal pharyngeal region', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(411946, 'HP:0033127', 'Abnormality of the musculoskeletal system', 'XPO:0100605', 'abnormal prechordal plate', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(411947, 'HP:0033127', 'Abnormality of the musculoskeletal system', 'XPO:0100842', 'abnormal left-dorsal blastomere', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(411948, 'HP:0033127', 'Abnormality of the musculoskeletal system', 'XPO:0103444', 'abnormal gastrulation', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(411949, 'HP:0033127', 'Abnormality of the musculoskeletal system', 'XPO:0141968', 'absent cilium motility in ciliated cell', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(411950, 'HP:0033127', 'Abnormality of the musculoskeletal system', 'XPO:0100610', 'abnormal appendage', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(411951, 'HP:0033127', 'Abnormality of the musculoskeletal system', 'XPO:0100202', 'abnormal embryo', 0.5, 1.4755025719078136, 0.8589244937443028, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(411952, 'HP:0033127', 'Abnormality of the musculoskeletal system', 'XPO:0133328', 'abnormal development of animal pole', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(411953, 'HP:0033127', 'Abnormality of the musculoskeletal system', 'XPO:0101713', 'abnormal anatomical entity in vitro morphology', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(411954, 'HP:0033127', 'Abnormality of the musculoskeletal system', 'XPO:0100587', 'abnormal vestibuloauditory system', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(411955, 'HP:0033127', 'Abnormality of the musculoskeletal system', 'XPO:0101435', 'abnormal paracrine cell', 0.5263157894736842, 1.8210412618256888, 0.9790009036675816, 'HP:0000118', 'Phenotypic abnormality'),
(411956, 'HP:0033127', 'Abnormality of the musculoskeletal system', 'XPO:0131757', 'abnormal development of multicellular anatomical structure', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(411957, 'HP:0033127', 'Abnormality of the musculoskeletal system', 'XPO:0107270', 'abnormal proximal-distal axis', 0.5, 1.4755025719078136, 0.8589244937443028, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(411958, 'HP:0033127', 'Abnormality of the musculoskeletal system', 'XPO:0100547', 'abnormal blastomere V2', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(411959, 'HP:0033127', 'Abnormality of the musculoskeletal system', 'XPO:0100742', 'abnormal musculoskeletal system', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(411960, 'HP:0033127', 'Abnormality of the musculoskeletal system', 'XPO:0101224', 'abnormal dorsal involuting marginal zone', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(411961, 'HP:0033127', 'Abnormality of the musculoskeletal system', 'XPO:0141777', 'abnormal catabolic process', 0.5263157894736842, 1.8210412618256888, 0.9790009036675816, 'HP:0000118', 'Phenotypic abnormality'),
(411962, 'HP:0033127', 'Abnormality of the musculoskeletal system', 'XPO:0101389', 'abnormal wedge region', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(411963, 'HP:0033127', 'Abnormality of the musculoskeletal system', 'XPO:0100823', 'abnormal blood', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(411964, 'HP:0033127', 'Abnormality of the musculoskeletal system', 'XPO:0141796', 'abnormal demethylation', 0.5263157894736842, 1.8210412618256888, 0.9790009036675816, 'HP:0000118', 'Phenotypic abnormality'),
(411965, 'HP:0033127', 'Abnormality of the musculoskeletal system', 'XPO:0133335', 'abnormal development of postero-ventral region', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(411966, 'HP:0033127', 'Abnormality of the musculoskeletal system', 'XPO:0101109', 'abnormal egg cell-free extract', 0.5, 1.4755025719078136, 0.8589244937443028, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(411967, 'HP:0033127', 'Abnormality of the musculoskeletal system', 'XPO:0100415', 'abnormal secretory epithelial cell', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(411968, 'HP:0033127', 'Abnormality of the musculoskeletal system', 'XPO:0100108', 'abnormal cell part', 0.5263157894736842, 1.8210412618256888, 0.9790009036675816, 'HP:0000118', 'Phenotypic abnormality'),
(411969, 'HP:0033127', 'Abnormality of the musculoskeletal system', 'XPO:0142010', 'abnormal development of cerebrospinal fluid', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(411970, 'HP:0033127', 'Abnormality of the musculoskeletal system', 'XPO:0103445', 'abnormal left/right axis specification', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(411971, 'HP:0033127', 'Abnormality of the musculoskeletal system', 'XPO:0103446', 'abnormal proximal/distal axis specification', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(411972, 'HP:0033127', 'Abnormality of the musculoskeletal system', 'XPO:0132098', 'abnormal development of organ part', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(411973, 'HP:0033127', 'Abnormality of the musculoskeletal system', 'XPO:0100852', 'abnormal interdigital region', 0.5263157894736842, 1.8210412618256888, 0.9790009036675816, 'HP:0000118', 'Phenotypic abnormality'),
(411974, 'HP:0033127', 'Abnormality of the musculoskeletal system', 'XPO:0131409', 'abnormal locomotory behavior', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(411975, 'HP:0033127', 'Abnormality of the musculoskeletal system', 'XPO:0141960', 'absent cilium motility in brain', 0.47058823529411764, 1.4755025719078136, 0.8332791557971614, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(411976, 'HP:0033127', 'Abnormality of the musculoskeletal system', 'XPO:0107261', 'abnormal dorsal-ventral axis', 0.5, 1.4755025719078136, 0.8589244937443028, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(411977, 'HP:0033127', 'Abnormality of the musculoskeletal system', 'XPO:0101040', 'abnormal axial mesoderm', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(411978, 'HP:0033127', 'Abnormality of the musculoskeletal system', 'XPO:0100653', 'abnormal myoblast', 0.5263157894736842, 1.8210412618256888, 0.9790009036675816, 'HP:0000118', 'Phenotypic abnormality'),
(411979, 'HP:0033127', 'Abnormality of the musculoskeletal system', 'XPO:0107273', 'abnormal basal region', 0.47058823529411764, 1.4755025719078136, 0.8332791557971614, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(411980, 'HP:0033127', 'Abnormality of the musculoskeletal system', 'XPO:0131403', 'abnormal mechanosensory behavior', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(411981, 'HP:0033127', 'Abnormality of the musculoskeletal system', 'XPO:0101547', 'abnormal lampbrush chromosome', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(411982, 'HP:0033127', 'Abnormality of the musculoskeletal system', 'XPO:0133026', 'abnormal development of forebrain-midbrain boundary', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(411983, 'HP:0033127', 'Abnormality of the musculoskeletal system', 'XPO:0141714', 'abnormal anterior notochord', 0.5, 3.9037819259951223, 1.3971009136771622, 'HP:0033127', 'Abnormality of the musculoskeletal system'),
(411984, 'HP:0033127', 'Abnormality of the musculoskeletal system', 'XPO:0100394', 'abnormal marginal zone', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(411985, 'HP:0033127', 'Abnormality of the musculoskeletal system', 'XPO:0132400', 'abnormal development of oval window', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(411986, 'HP:0033127', 'Abnormality of the musculoskeletal system', 'XPO:0100251', 'abnormal proteinaceous extracellular matrix', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(411987, 'HP:0033127', 'Abnormality of the musculoskeletal system', 'XPO:0141267', 'abnormal resting posture', 0.6153846153846154, 1.4755025719078136, 0.9528911704452407, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(411988, 'HP:0033127', 'Abnormality of the musculoskeletal system', 'XPO:0101074', 'abnormal germinal vesicle', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(411989, 'HP:0033127', 'Abnormality of the musculoskeletal system', 'XPO:0101638', 'abnormal anatomical structure morphology', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(411990, 'HP:0033127', 'Abnormality of the musculoskeletal system', 'XPO:0103625', 'absent mitotic cytokinesis in primary spermatogonium', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(411991, 'HP:0033127', 'Abnormality of the musculoskeletal system', 'XPO:0100912', 'abnormal trabecula', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(411992, 'HP:0033127', 'Abnormality of the musculoskeletal system', 'XPO:0100172', 'abnormal stem cell', 0.5263157894736842, 1.8210412618256888, 0.9790009036675816, 'HP:0000118', 'Phenotypic abnormality'),
(411993, 'HP:0033127', 'Abnormality of the musculoskeletal system', 'XPO:0132991', 'abnormal development of antero-ventral region', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(411994, 'HP:0033127', 'Abnormality of the musculoskeletal system', 'XPO:0100745', 'abnormal anterior lymph sac', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(411995, 'HP:0033127', 'Abnormality of the musculoskeletal system', 'XPO:0131669', 'abnormal Roux spot', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(411996, 'HP:0033127', 'Abnormality of the musculoskeletal system', 'XPO:0100032', 'abnormal nervous system', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(411997, 'HP:0033127', 'Abnormality of the musculoskeletal system', 'XPO:0100899', 'abnormal secondary spermatogonium', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(411998, 'HP:0033127', 'Abnormality of the musculoskeletal system', 'XPO:0100493', 'abnormal liver and biliary system', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(411999, 'HP:0033127', 'Abnormality of the musculoskeletal system', 'XPO:0141787', 'abnormal hormone metabolic process', 0.5263157894736842, 1.8210412618256888, 0.9790009036675816, 'HP:0000118', 'Phenotypic abnormality'),
(412000, 'HP:0033127', 'Abnormality of the musculoskeletal system', 'XPO:0100026', 'abnormal germ cell', 0.5263157894736842, 1.8210412618256888, 0.9790009036675816, 'HP:0000118', 'Phenotypic abnormality'),
(412001, 'HP:0033127', 'Abnormality of the musculoskeletal system', 'XPO:0101463', 'abnormal right-ventral blastomere', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(412002, 'HP:0033127', 'Abnormality of the musculoskeletal system', 'XPO:0101411', 'abnormal marginal zone (sensu neural)', 0.47058823529411764, 1.4755025719078136, 0.8332791557971614, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(412003, 'HP:0033127', 'Abnormality of the musculoskeletal system', 'XPO:0101240', 'abnormal ciliated non-epidermal cell', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(412004, 'HP:0033127', 'Abnormality of the musculoskeletal system', 'XPO:0101098', 'abnormal mineralized extracellular matrix', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(412005, 'HP:0033127', 'Abnormality of the musculoskeletal system', 'XPO:0100894', 'abnormal nucleus', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(412006, 'HP:0033127', 'Abnormality of the musculoskeletal system', 'XPO:0131480', 'absent mating behavior', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(412007, 'HP:0033127', 'Abnormality of the musculoskeletal system', 'XPO:0100557', 'abnormal prime meridian', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(412008, 'HP:0033127', 'Abnormality of the musculoskeletal system', 'XPO:0101212', 'abnormal glomeral mesenchyme', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(412009, 'HP:0033127', 'Abnormality of the musculoskeletal system', 'XPO:0141892', 'abnormal inositol metabolic process', 0.47619047619047616, 1.8210412618256888, 0.9312156064152277, 'HP:0000118', 'Phenotypic abnormality'),
(412010, 'HP:0033127', 'Abnormality of the musculoskeletal system', 'XPO:0100674', 'abnormal secondary oogonium', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(412011, 'HP:0033127', 'Abnormality of the musculoskeletal system', 'XPO:0100277', 'abnormal blastocoel', 0.47058823529411764, 1.4755025719078136, 0.8332791557971614, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(412012, 'HP:0033127', 'Abnormality of the musculoskeletal system', 'XPO:0100829', 'abnormal postcranial axial skeleton', 0.4230769230769231, 3.9037819259951223, 1.2851459238597462, 'HP:0033127', 'Abnormality of the musculoskeletal system'),
(412013, 'HP:0033127', 'Abnormality of the musculoskeletal system', 'XPO:0131818', 'abnormal development of mesonephric sinus', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(412014, 'HP:0033127', 'Abnormality of the musculoskeletal system', 'XPO:0100484', 'abnormal cement gland primordium', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(412015, 'HP:0033127', 'Abnormality of the musculoskeletal system', 'XPO:0141816', 'abnormal ligase activity', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(412016, 'HP:0033127', 'Abnormality of the musculoskeletal system', 'XPO:0100339', 'abnormal circumblastoporal collar', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(412017, 'HP:0033127', 'Abnormality of the musculoskeletal system', 'XPO:0101096', 'abnormal tendon', 0.5, 3.9037819259951223, 1.3971009136771622, 'HP:0033127', 'Abnormality of the musculoskeletal system'),
(412018, 'HP:0033127', 'Abnormality of the musculoskeletal system', 'XPO:0100816', 'abnormal blastocoel anlage', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(412019, 'HP:0033127', 'Abnormality of the musculoskeletal system', 'XPO:0100274', 'abnormal sensory system', 0.47619047619047616, 1.8210412618256888, 0.9312156064152277, 'HP:0000118', 'Phenotypic abnormality'),
(412020, 'HP:0033127', 'Abnormality of the musculoskeletal system', 'XPO:0107276', 'abnormal dorsal region', 0.47058823529411764, 1.4755025719078136, 0.8332791557971614, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(412021, 'HP:0033127', 'Abnormality of the musculoskeletal system', 'XPO:0132695', 'abnormal development of posterior endomesoderm', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(412022, 'HP:0033127', 'Abnormality of the musculoskeletal system', 'XPO:0141908', 'abnormal pyridine metabolic process', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(412023, 'HP:0033127', 'Abnormality of the musculoskeletal system', 'XPO:0101468', 'abnormal stage I oocyte', 0.47619047619047616, 1.8210412618256888, 0.9312156064152277, 'HP:0000118', 'Phenotypic abnormality'),
(412024, 'HP:0033127', 'Abnormality of the musculoskeletal system', 'XPO:0131719', 'abnormal activation of meiosis', 0.47058823529411764, 1.4755025719078136, 0.8332791557971614, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(412025, 'HP:0033127', 'Abnormality of the musculoskeletal system', 'XPO:0107268', 'abnormal left side', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(412026, 'HP:0033127', 'Abnormality of the musculoskeletal system', 'XPO:0100225', 'abnormal endocrine system', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(412027, 'HP:0033127', 'Abnormality of the musculoskeletal system', 'XPO:0141597', 'abnormal metamorphosis', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(412028, 'HP:0033127', 'Abnormality of the musculoskeletal system', 'XPO:0131760', 'abnormal development of anatomical structure', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(412029, 'HP:0033127', 'Abnormality of the musculoskeletal system', 'XPO:0107285', 'abnormal flexural organ', 0.5, 3.9037819259951223, 1.3971009136771622, 'HP:0033127', 'Abnormality of the musculoskeletal system'),
(412030, 'HP:0033127', 'Abnormality of the musculoskeletal system', 'XPO:0101535', 'abnormal absorptive cell', 0.5263157894736842, 1.8210412618256888, 0.9790009036675816, 'HP:0000118', 'Phenotypic abnormality'),
(412031, 'HP:0033127', 'Abnormality of the musculoskeletal system', 'XPO:0100991', 'abnormal iliac process primordium', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(412032, 'HP:0033127', 'Abnormality of the musculoskeletal system', 'XPO:0100201', 'abnormal cavitated compound organ', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(412033, 'HP:0033127', 'Abnormality of the musculoskeletal system', 'XPO:0131687', 'abnormal astral microtubule', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(412034, 'HP:0033127', 'Abnormality of the musculoskeletal system', 'XPO:0131745', 'abnormal axis elongation', 0.47619047619047616, 1.8210412618256888, 0.9312156064152277, 'HP:0000118', 'Phenotypic abnormality'),
(412035, 'HP:0033127', 'Abnormality of the musculoskeletal system', 'XPO:0131723', 'abnormal pathway-restricted SMAD protein phosphorylation', 0.6153846153846154, 1.4755025719078136, 0.9528911704452407, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(412036, 'HP:0033127', 'Abnormality of the musculoskeletal system', 'XPO:0141854', 'abnormal glutathione metabolic process', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(412037, 'HP:0033127', 'Abnormality of the musculoskeletal system', 'XPO:0101326', 'abnormal cementoblast', 0.5263157894736842, 1.8210412618256888, 0.9790009036675816, 'HP:0000118', 'Phenotypic abnormality'),
(412038, 'HP:0033127', 'Abnormality of the musculoskeletal system', 'XPO:0100337', 'abnormal zygote', 0.5263157894736842, 1.8210412618256888, 0.9790009036675816, 'HP:0000118', 'Phenotypic abnormality'),
(412039, 'HP:0033127', 'Abnormality of the musculoskeletal system', 'XPO:0142052', 'abnormal nasal region', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(412040, 'HP:0033127', 'Abnormality of the musculoskeletal system', 'XPO:0107260', 'abnormal anterior-posterior axis', 0.5, 1.4755025719078136, 0.8589244937443028, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(412041, 'HP:0033127', 'Abnormality of the musculoskeletal system', 'XPO:0141871', 'abnormal cadaverine transport', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(412042, 'HP:0033127', 'Abnormality of the musculoskeletal system', 'XPO:0101570', 'abnormal forelimb region', 0.47058823529411764, 1.4755025719078136, 0.8332791557971614, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(412043, 'HP:0033127', 'Abnormality of the musculoskeletal system', 'XPO:0103443', 'abnormal dorsal/ventral axis specification', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(412044, 'HP:0033127', 'Abnormality of the musculoskeletal system', 'XPO:0101424', 'abnormal coelomic epithelium', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(412045, 'HP:0033127', 'Abnormality of the musculoskeletal system', 'XPO:0141784', 'abnormal cellular hormone metabolic process', 0.6153846153846154, 1.4755025719078136, 0.9528911704452407, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(412046, 'HP:0033127', 'Abnormality of the musculoskeletal system', 'XPO:0107263', 'abnormal anatomical side', 0.47058823529411764, 1.4755025719078136, 0.8332791557971614, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(412047, 'HP:0033127', 'Abnormality of the musculoskeletal system', 'XPO:0100481', 'abnormal anatomical line', 0.5714285714285714, 1.4755025719078136, 0.918228907628411, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(412048, 'HP:0033127', 'Abnormality of the musculoskeletal system', 'XPO:0100203', 'abnormal endocrine cell', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(412049, 'HP:0033127', 'Abnormality of the musculoskeletal system', 'XPO:0101448', 'abnormal myelin accumulating cell', 0.5263157894736842, 1.8210412618256888, 0.9790009036675816, 'HP:0000118', 'Phenotypic abnormality'),
(412050, 'HP:0033127', 'Abnormality of the musculoskeletal system', 'XPO:0132006', 'abnormal development of extraembryonic structure', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(412051, 'HP:0033127', 'Abnormality of the musculoskeletal system', 'XPO:0141815', 'abnormal isomerase activity', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(412052, 'HP:0033127', 'Abnormality of the musculoskeletal system', 'XPO:0133261', 'abnormal development of pronephric sinus', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(412053, 'HP:0033127', 'Abnormality of the musculoskeletal system', 'XPO:0132906', 'abnormal development of optic disc', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(412054, 'HP:0033127', 'Abnormality of the musculoskeletal system', 'XPO:0132053', 'abnormal development of blood', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(412055, 'HP:0033127', 'Abnormality of the musculoskeletal system', 'XPO:0141798', 'abnormal lipid metabolic process', 0.47619047619047616, 1.8210412618256888, 0.9312156064152277, 'HP:0000118', 'Phenotypic abnormality'),
(412056, 'HP:0033127', 'Abnormality of the musculoskeletal system', 'XPO:0141903', 'abnormal inositol phosphate metabolic process', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(412057, 'HP:0033127', 'Abnormality of the musculoskeletal system', 'XPO:0107278', 'abnormal medial region', 0.47058823529411764, 1.4755025719078136, 0.8332791557971614, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(412058, 'HP:0033127', 'Abnormality of the musculoskeletal system', 'XPO:0131701', 'abnormal calcium ion transport', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(412059, 'HP:0033127', 'Abnormality of the musculoskeletal system', 'XPO:0100135', 'abnormal surface structure', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(412060, 'HP:0033127', 'Abnormality of the musculoskeletal system', 'XPO:0132953', 'abnormal development of thoracic region', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(412061, 'HP:0033127', 'Abnormality of the musculoskeletal system', 'XPO:0100512', 'abnormal cranial skeleton', 0.4230769230769231, 3.9037819259951223, 1.2851459238597462, 'HP:0033127', 'Abnormality of the musculoskeletal system'),
(412062, 'HP:0033127', 'Abnormality of the musculoskeletal system', 'XPO:0100531', 'abnormal proliferative region', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(412063, 'HP:0033127', 'Abnormality of the musculoskeletal system', 'XPO:0132403', 'abnormal development of cell condensation', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(412064, 'HP:0033127', 'Abnormality of the musculoskeletal system', 'XPO:0132678', 'abnormal development of proximal tubule branch', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(412065, 'HP:0033127', 'Abnormality of the musculoskeletal system', 'XPO:0141767', 'abnormal temperature homeostasis', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(412066, 'HP:0033127', 'Abnormality of the musculoskeletal system', 'XPO:0100702', 'abnormal glial cell', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(412067, 'HP:0033127', 'Abnormality of the musculoskeletal system', 'XPO:0116429', 'abnormal behavior', 0.47058823529411764, 1.4755025719078136, 0.8332791557971614, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(412068, 'HP:0033127', 'Abnormality of the musculoskeletal system', 'XPO:0132585', 'abnormal development of pharyngeal cavity', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(412069, 'HP:0033127', 'Abnormality of the musculoskeletal system', 'XPO:0101409', 'abnormal perivitelline space', 0.47619047619047616, 1.8210412618256888, 0.9312156064152277, 'HP:0000118', 'Phenotypic abnormality'),
(412070, 'HP:0033127', 'Abnormality of the musculoskeletal system', 'XPO:0107288', 'abnormal larval alimentary system', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(412071, 'HP:0033127', 'Abnormality of the musculoskeletal system', 'XPO:0100378', 'abnormal perichondrium', 0.4782608695652174, 3.9037819259951223, 1.3663916490228585, 'HP:0033127', 'Abnormality of the musculoskeletal system'),
(412072, 'HP:0033127', 'Abnormality of the musculoskeletal system', 'XPO:0141760', 'abnormal multicellular organismal homeostasis', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(412073, 'HP:0033127', 'Abnormality of the musculoskeletal system', 'XPO:0100704', 'abnormal Merkel cell', 0.5263157894736842, 1.8210412618256888, 0.9790009036675816, 'HP:0000118', 'Phenotypic abnormality'),
(412074, 'HP:0033127', 'Abnormality of the musculoskeletal system', 'XPO:0100553', 'abnormal laryngeal muscle primordium', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(412075, 'HP:0033127', 'Abnormality of the musculoskeletal system', 'XPO:0100192', 'abnormal epithelium', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(412076, 'HP:0033127', 'Abnormality of the musculoskeletal system', 'XPO:0131864', 'abnormal development of coelom', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(412077, 'HP:0033127', 'Abnormality of the musculoskeletal system', 'XPO:0141271', 'increased surface breathing', 0.5714285714285714, 1.4755025719078136, 0.918228907628411, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(412078, 'HP:0033127', 'Abnormality of the musculoskeletal system', 'XPO:0101480', 'abnormal stage V oocyte', 0.47619047619047616, 1.8210412618256888, 0.9312156064152277, 'HP:0000118', 'Phenotypic abnormality'),
(412079, 'HP:0033127', 'Abnormality of the musculoskeletal system', 'XPO:0101078', 'abnormal mucous gland', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(412080, 'HP:0033127', 'Abnormality of the musculoskeletal system', 'XPO:0107259', 'abnormal animal-vegetal axis', 0.5, 1.4755025719078136, 0.8589244937443028, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(412081, 'HP:0033127', 'Abnormality of the musculoskeletal system', 'XPO:0100186', 'abnormal uveal tract', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(412082, 'HP:0033127', 'Abnormality of the musculoskeletal system', 'XPO:0100104', 'abnormal embryonic structure', 0.47058823529411764, 1.4755025719078136, 0.8332791557971614, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(412083, 'HP:0033127', 'Abnormality of the musculoskeletal system', 'XPO:0100722', 'abnormal barbel', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(412084, 'HP:0033127', 'Abnormality of the musculoskeletal system', 'XPO:0100626', 'abnormal primordial germ cell', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(412085, 'HP:0033127', 'Abnormality of the musculoskeletal system', 'XPO:0141791', 'abnormal primary metabolic process', 0.5263157894736842, 1.8210412618256888, 0.9790009036675816, 'HP:0000118', 'Phenotypic abnormality'),
(412086, 'HP:0033127', 'Abnormality of the musculoskeletal system', 'XPO:0101472', 'abnormal zygote cortex', 0.47619047619047616, 1.8210412618256888, 0.9312156064152277, 'HP:0000118', 'Phenotypic abnormality'),
(412087, 'HP:0033127', 'Abnormality of the musculoskeletal system', 'XPO:0100228', 'abnormal skeletal subdivision', 0.4583333333333333, 3.9037819259951223, 1.3376222870256627, 'HP:0033127', 'Abnormality of the musculoskeletal system'),
(412088, 'HP:0033127', 'Abnormality of the musculoskeletal system', 'XPO:0141964', 'absent cilium motility in olfactory pit', 0.47058823529411764, 1.4755025719078136, 0.8332791557971614, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(412089, 'HP:0033127', 'Abnormality of the musculoskeletal system', 'XPO:0100084', 'abnormal anatomical group', 0.5, 1.4755025719078136, 0.8589244937443028, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(412090, 'HP:0033127', 'Abnormality of the musculoskeletal system', 'XPO:0116434', 'abnormal biological process', 0.5714285714285714, 1.4755025719078136, 0.918228907628411, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(412091, 'HP:0033127', 'Abnormality of the musculoskeletal system', 'XPO:0131765', 'abnormal development of anatomical region', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(412092, 'HP:0033127', 'Abnormality of the musculoskeletal system', 'XPO:0103447', 'abnormal anterior/posterior axis specification', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(412093, 'HP:0033127', 'Abnormality of the musculoskeletal system', 'XPO:0107339', 'abnormal yolk platelet', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(412094, 'HP:0033127', 'Abnormality of the musculoskeletal system', 'XPO:0107266', 'abnormal dorsal side', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(412095, 'HP:0033127', 'Abnormality of the musculoskeletal system', 'XPO:0100843', 'abnormal fasciculated network of fibrils', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(412096, 'HP:0033127', 'Abnormality of the musculoskeletal system', 'XPO:0100588', 'abnormal unicellular gland', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(412097, 'HP:0033127', 'Abnormality of the musculoskeletal system', 'XPO:0141797', 'abnormal hydrogen metabolic process', 0.5263157894736842, 1.8210412618256888, 0.9790009036675816, 'HP:0000118', 'Phenotypic abnormality'),
(412098, 'HP:0033127', 'Abnormality of the musculoskeletal system', 'XPO:0101241', 'abnormal nucleate erythrocyte', 0.5263157894736842, 1.8210412618256888, 0.9790009036675816, 'HP:0000118', 'Phenotypic abnormality'),
(412099, 'HP:0033127', 'Abnormality of the musculoskeletal system', 'XPO:0141715', 'abnormal septum', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(412100, 'HP:0033127', 'Abnormality of the musculoskeletal system', 'XPO:0100667', 'abnormal vegetal yolk mass', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(412101, 'HP:0033127', 'Abnormality of the musculoskeletal system', 'XPO:0107312', 'abnormal filopodium', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(412102, 'HP:0033127', 'Abnormality of the musculoskeletal system', 'XPO:0141910', 'abnormal D-ribose metabolic process', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(412103, 'HP:0033127', 'Abnormality of the musculoskeletal system', 'XPO:0101543', 'abnormal external gill', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(412104, 'HP:0033127', 'Abnormality of the musculoskeletal system', 'XPO:0133148', 'abnormal development of hindlimb region', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(412105, 'HP:0033127', 'Abnormality of the musculoskeletal system', 'XPO:0100372', 'abnormal hematological system', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(412106, 'HP:0033127', 'Abnormality of the musculoskeletal system', 'XPO:0100856', 'abnormal simple organ', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(412107, 'HP:0033127', 'Abnormality of the musculoskeletal system', 'XPO:0132986', 'abnormal development of vegetal pole', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(412108, 'HP:0033127', 'Abnormality of the musculoskeletal system', 'XPO:0100152', 'abnormal alimentary system', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(412109, 'HP:0033127', 'Abnormality of the musculoskeletal system', 'XPO:0107271', 'abnormal apical region', 0.47058823529411764, 1.4755025719078136, 0.8332791557971614, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(412110, 'HP:0033127', 'Abnormality of the musculoskeletal system', 'XPO:0100599', 'abnormal adult immune system', 0.47619047619047616, 1.8210412618256888, 0.9312156064152277, 'HP:0000118', 'Phenotypic abnormality'),
(412111, 'HP:0033127', 'Abnormality of the musculoskeletal system', 'XPO:0132854', 'abnormal development of oral cavity', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(412112, 'HP:0033127', 'Abnormality of the musculoskeletal system', 'XPO:0107258', 'abnormal anatomical axis', 0.5333333333333333, 1.4755025719078136, 0.8870934026456857, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(412113, 'HP:0033127', 'Abnormality of the musculoskeletal system', 'XPO:0100643', 'abnormal thoracic region', 0.47058823529411764, 1.4755025719078136, 0.8332791557971614, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(412114, 'HP:0033127', 'Abnormality of the musculoskeletal system', 'XPO:0131730', 'abnormal regulation of protein folding', 0.5, 1.4755025719078136, 0.8589244937443028, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(412115, 'HP:0033127', 'Abnormality of the musculoskeletal system', 'XPO:0107267', 'abnormal ventral side', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(412116, 'HP:0033127', 'Abnormality of the musculoskeletal system', 'XPO:0141959', 'absent cilium motility in floor plate', 0.47058823529411764, 1.4755025719078136, 0.8332791557971614, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(412117, 'HP:0033127', 'Abnormality of the musculoskeletal system', 'XPO:0132162', 'abnormal development of principal cavity', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(412118, 'HP:0033127', 'Abnormality of the musculoskeletal system', 'XPO:0100268', 'abnormal circulatory system', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(412119, 'HP:0033127', 'Abnormality of the musculoskeletal system', 'XPO:0131729', 'abnormal regulation of growth rate', 0.5, 1.4755025719078136, 0.8589244937443028, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(412120, 'HP:0033127', 'Abnormality of the musculoskeletal system', 'XPO:0141315', 'abnormal anatomical region', 0.5, 1.4755025719078136, 0.8589244937443028, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(412121, 'HP:0033127', 'Abnormality of the musculoskeletal system', 'XPO:0141809', 'abnormal catalytic activity', 0.5, 1.4755025719078136, 0.8589244937443028, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(412122, 'HP:0033127', 'Abnormality of the musculoskeletal system', 'XPO:0141963', 'absent cilium motility in pronephric nephrostome', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(412123, 'HP:0033127', 'Abnormality of the musculoskeletal system', 'XPO:0141795', 'abnormal glycosylation', 0.47619047619047616, 1.8210412618256888, 0.9312156064152277, 'HP:0000118', 'Phenotypic abnormality'),
(412124, 'HP:0033127', 'Abnormality of the musculoskeletal system', 'XPO:0141744', 'abnormal chemical homeostasis', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(412125, 'HP:0033127', 'Abnormality of the musculoskeletal system', 'XPO:0131714', 'abnormal establishment of tissue polarity', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(412126, 'HP:0033127', 'Abnormality of the musculoskeletal system', 'XPO:0107311', 'abnormal apical junction complex', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(412127, 'HP:0033127', 'Abnormality of the musculoskeletal system', 'XPO:0101553', 'abnormal dental epithelium', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(412128, 'HP:0033127', 'Abnormality of the musculoskeletal system', 'XPO:0132996', 'abnormal development of ventricular zone', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(412129, 'HP:0033127', 'Abnormality of the musculoskeletal system', 'XPO:0141883', 'abnormal glycerol metabolic process', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(412130, 'HP:0033127', 'Abnormality of the musculoskeletal system', 'XPO:0132117', 'abnormal development of process', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(412131, 'HP:0033127', 'Abnormality of the musculoskeletal system', 'XPO:0101467', 'abnormal alkali secreting cell', 0.5263157894736842, 1.8210412618256888, 0.9790009036675816, 'HP:0000118', 'Phenotypic abnormality'),
(412132, 'HP:0033127', 'Abnormality of the musculoskeletal system', 'XPO:0133135', 'abnormal development of medial region', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(412133, 'HP:0033127', 'Abnormality of the musculoskeletal system', 'XPO:0100444', 'abnormal cement gland', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(412134, 'HP:0033127', 'Abnormality of the musculoskeletal system', 'XPO:0101573', 'abnormal peripheral vegetal yolk mass', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(412135, 'HP:0033127', 'Abnormality of the musculoskeletal system', 'XPO:0100070', 'abnormal anatomical system', 0.47058823529411764, 1.4755025719078136, 0.8332791557971614, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(412136, 'HP:0033127', 'Abnormality of the musculoskeletal system', 'XPO:0100158', 'abnormal neuromere', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(412137, 'HP:0033127', 'Abnormality of the musculoskeletal system', 'XPO:0131677', 'abnormal actin filament', 0.47619047619047616, 1.8210412618256888, 0.9312156064152277, 'HP:0000118', 'Phenotypic abnormality'),
(412138, 'HP:0033127', 'Abnormality of the musculoskeletal system', 'XPO:0141813', 'abnormal hydrolase activity', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(412139, 'HP:0033127', 'Abnormality of the musculoskeletal system', 'XPO:0100509', 'abnormal germ plasm', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(412140, 'HP:0033127', 'Abnormality of the musculoskeletal system', 'XPO:0100295', 'abnormal extracellular matrix', 0.47058823529411764, 1.4755025719078136, 0.8332791557971614, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(412141, 'HP:0033127', 'Abnormality of the musculoskeletal system', 'XPO:0131481', 'absent feeding behavior', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(412142, 'HP:0033127', 'Abnormality of the musculoskeletal system', 'XPO:0131805', 'abnormal development of embryonic structure', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(412143, 'HP:0033127', 'Abnormality of the musculoskeletal system', 'XPO:0101141', 'abnormal Keller explant', 0.5333333333333333, 1.4755025719078136, 0.8870934026456857, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(412144, 'HP:0033127', 'Abnormality of the musculoskeletal system', 'XPO:0131975', 'abnormal development of anatomical line', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(412145, 'HP:0033127', 'Abnormality of the musculoskeletal system', 'XPO:0133246', 'abnormal development of myocoelic slit', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(412146, 'HP:0033127', 'Abnormality of the musculoskeletal system', 'XPO:0100907', 'abnormal cytoplasm', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(412147, 'HP:0033127', 'Abnormality of the musculoskeletal system', 'XPO:0141969', 'absent cilium motility in monociliated cell', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(412148, 'HP:0033127', 'Abnormality of the musculoskeletal system', 'XPO:0100023', 'abnormal mesenchyme', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(412149, 'HP:0033127', 'Abnormality of the musculoskeletal system', 'XPO:0133090', 'abnormal development of fenestra subocularis', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(412150, 'HP:0033127', 'Abnormality of the musculoskeletal system', 'XPO:0100010', 'abnormal multicellular anatomical structure', 0.5, 1.4755025719078136, 0.8589244937443028, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(412151, 'HP:0033127', 'Abnormality of the musculoskeletal system', 'XPO:0131667', 'abnormal actin cytoskeleton', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(412152, 'HP:0033127', 'Abnormality of the musculoskeletal system', 'XPO:0101029', 'abnormal right spleen primordium', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(412153, 'HP:0033127', 'Abnormality of the musculoskeletal system', 'XPO:0100422', 'abnormal notochord', 0.5238095238095238, 3.9037819259951223, 1.429978374560864, 'HP:0033127', 'Abnormality of the musculoskeletal system'),
(412154, 'HP:0033127', 'Abnormality of the musculoskeletal system', 'XPO:0132114', 'abnormal development of ventral endomesoderm', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(412155, 'HP:0033127', 'Abnormality of the musculoskeletal system', 'XPO:0131875', 'abnormal development of dorsal endomesoderm', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(412156, 'HP:0033127', 'Abnormality of the musculoskeletal system', 'XPO:0100796', 'abnormal pseudoblastema', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(412157, 'HP:0033127', 'Abnormality of the musculoskeletal system', 'XPO:0107284', 'abnormal migrating myoblast', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(412158, 'HP:0033127', 'Abnormality of the musculoskeletal system', 'XPO:0100239', 'abnormal acellular anatomical structure', 0.5, 1.4755025719078136, 0.8589244937443028, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(412159, 'HP:0033127', 'Abnormality of the musculoskeletal system', 'XPO:0100721', 'abnormal centromere', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(412160, 'HP:0033127', 'Abnormality of the musculoskeletal system', 'XPO:0101168', 'abnormal circulating cell', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(412161, 'HP:0033127', 'Abnormality of the musculoskeletal system', 'XPO:0101228', 'abnormal mesenchymal stem cell', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(412162, 'HP:0033127', 'Abnormality of the musculoskeletal system', 'XPO:0133397', 'abnormal insulin receptor signaling pathway', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(412163, 'HP:0033127', 'Abnormality of the musculoskeletal system', 'XPO:0142051', 'abnormal cerebrospinal fluid', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(412164, 'HP:0033127', 'Abnormality of the musculoskeletal system', 'XPO:0101493', 'abnormal fat body', 0.4230769230769231, 3.9037819259951223, 1.2851459238597462, 'HP:0033127', 'Abnormality of the musculoskeletal system'),
(412165, 'HP:0033127', 'Abnormality of the musculoskeletal system', 'XPO:0100858', 'abnormal presumptive midbrain-hindbrain boundary', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(412166, 'HP:0033127', 'Abnormality of the musculoskeletal system', 'XPO:0100807', 'abnormal matrix-based tissue', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(412167, 'HP:0033127', 'Abnormality of the musculoskeletal system', 'XPO:0141776', 'abnormal metabolic process', 0.5882352941176471, 1.8210412618256888, 1.034988281214046, 'HP:0000118', 'Phenotypic abnormality'),
(412168, 'HP:0033127', 'Abnormality of the musculoskeletal system', 'XPO:0141911', 'abnormal ribose phosphate metabolic process', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(412169, 'HP:0033127', 'Abnormality of the musculoskeletal system', 'XPO:0101302', 'abnormal subcortical cytoplasm', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(412170, 'HP:0033127', 'Abnormality of the musculoskeletal system', 'XPO:0131479', 'absent social behavior', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(412171, 'HP:0033127', 'Abnormality of the musculoskeletal system', 'XPO:0101110', 'abnormal cell-free extract', 0.5333333333333333, 1.4755025719078136, 0.8870934026456857, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(412172, 'HP:0033127', 'Abnormality of the musculoskeletal system', 'XPO:0141792', 'abnormal small molecule metabolic process', 0.5263157894736842, 1.8210412618256888, 0.9790009036675816, 'HP:0000118', 'Phenotypic abnormality'),
(412173, 'HP:0033127', 'Abnormality of the musculoskeletal system', 'XPO:0100573', 'abnormal extraembryonic structure', 0.5, 1.4755025719078136, 0.8589244937443028, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(412174, 'HP:0033127', 'Abnormality of the musculoskeletal system', 'XPO:0115509', 'abnormally semi-viable whole organism', 0.5, 1.4755025719078136, 0.8589244937443028, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(412175, 'HP:0033127', 'Abnormality of the musculoskeletal system', 'XPO:0100081', 'abnormal anatomical entity in vitro', 0.5714285714285714, 1.4755025719078136, 0.918228907628411, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(412176, 'HP:0033127', 'Abnormality of the musculoskeletal system', 'XPO:0132567', 'abnormal development of retinal stem cell region', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(412177, 'HP:0033127', 'Abnormality of the musculoskeletal system', 'XPO:0100800', 'abnormal ventral marginal zone', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(412178, 'HP:0033127', 'Abnormality of the musculoskeletal system', 'XPO:0133403', 'abnormal developmental process', 0.5, 1.4755025719078136, 0.8589244937443028, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(412179, 'HP:0033127', 'Abnormality of the musculoskeletal system', 'XPO:0100003', 'abnormal organism subdivision', 0.47058823529411764, 1.4755025719078136, 0.8332791557971614, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(412180, 'HP:0033127', 'Abnormality of the musculoskeletal system', 'XPO:0107269', 'abnormal right side', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(412181, 'HP:0033127', 'Abnormality of the musculoskeletal system', 'XPO:0133137', 'abnormal development of posterior endoderm', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(412182, 'HP:0033127', 'Abnormality of the musculoskeletal system', 'XPO:0141497', 'abnormal lymphoblast', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(412183, 'HP:0033127', 'Abnormality of the musculoskeletal system', 'XPO:0100196', 'abnormal neuron', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(412184, 'HP:0033127', 'Abnormality of the musculoskeletal system', 'XPO:0100827', 'abnormal atypical epithelium', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(412185, 'HP:0033127', 'Abnormality of the musculoskeletal system', 'XPO:0100993', 'abnormal ligament cell', 0.4230769230769231, 3.9037819259951223, 1.2851459238597462, 'HP:0033127', 'Abnormality of the musculoskeletal system'),
(412186, 'HP:0033127', 'Abnormality of the musculoskeletal system', 'XPO:0101132', 'abnormal apoptotic cell', 0.5263157894736842, 1.8210412618256888, 0.9790009036675816, 'HP:0000118', 'Phenotypic abnormality'),
(412187, 'HP:0033127', 'Abnormality of the musculoskeletal system', 'XPO:0142057', 'abnormal desmosome', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(412188, 'HP:0033127', 'Abnormality of the musculoskeletal system', 'XPO:0128000', 'absent behavior', 0.5, 1.4755025719078136, 0.8589244937443028, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(412189, 'HP:0033127', 'Abnormality of the musculoskeletal system', 'XPO:0141972', 'absent cilium motility in ciliated non-epidermal cell', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(412190, 'HP:0033127', 'Abnormality of the musculoskeletal system', 'XPO:0141881', 'abnormal fructose metabolic process', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(412191, 'HP:0033127', 'Abnormality of the musculoskeletal system', 'XPO:0101497', 'abnormal ciliary axoneme', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(412192, 'HP:0033127', 'Abnormality of the musculoskeletal system', 'XPO:0141864', 'abnormal 5-methylcytosine metabolic process', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(412193, 'HP:0033127', 'Abnormality of the musculoskeletal system', 'XPO:0131476', 'absent mechanosensory behavior', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(412194, 'HP:0033127', 'Abnormality of the musculoskeletal system', 'XPO:0141775', 'abnormal nitrogen compound metabolic process', 0.5263157894736842, 1.8210412618256888, 0.9790009036675816, 'HP:0000118', 'Phenotypic abnormality'),
(412195, 'HP:0033127', 'Abnormality of the musculoskeletal system', 'XPO:0141966', 'absent cilium motility in stomach', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(412196, 'HP:0033127', 'Abnormality of the musculoskeletal system', 'XPO:0100218', 'abnormal epithelial cell', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(412197, 'HP:0033127', 'Abnormality of the musculoskeletal system', 'XPO:0141961', 'absent cilium motility in mucociliary epithelium', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(412198, 'HP:0033127', 'Abnormality of the musculoskeletal system', 'XPO:0100501', 'abnormal urogenital system', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(412199, 'HP:0033127', 'Abnormality of the musculoskeletal system', 'XPO:0132496', 'abnormal development of left-right organizer', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(412200, 'HP:0033127', 'Abnormality of the musculoskeletal system', 'XPO:0100638', 'abnormal polar body', 0.5263157894736842, 1.8210412618256888, 0.9790009036675816, 'HP:0000118', 'Phenotypic abnormality'),
(412201, 'HP:0033127', 'Abnormality of the musculoskeletal system', 'XPO:0100691', 'abnormal keratin accumulating cell', 0.5263157894736842, 1.8210412618256888, 0.9790009036675816, 'HP:0000118', 'Phenotypic abnormality'),
(412202, 'HP:0033127', 'Abnormality of the musculoskeletal system', 'XPO:0100069', 'abnormal urinary system', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(412203, 'HP:0033127', 'Abnormality of the musculoskeletal system', 'XPO:0101349', 'abnormal trunk region', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(412204, 'HP:0033127', 'Abnormality of the musculoskeletal system', 'XPO:0133400', 'absent determination of left/right symmetry in intestine', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(412205, 'HP:0033127', 'Abnormality of the musculoskeletal system', 'XPO:0100423', 'abnormal process', 0.5, 1.4755025719078136, 0.8589244937443028, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(412206, 'HP:0033127', 'Abnormality of the musculoskeletal system', 'XPO:0100973', 'abnormal dermal skeleton', 0.44, 3.9037819259951223, 1.3105968287150147, 'HP:0033127', 'Abnormality of the musculoskeletal system'),
(412207, 'HP:0033127', 'Abnormality of the musculoskeletal system', 'XPO:0100350', 'abnormal appendicular skeleton', 0.44, 3.9037819259951223, 1.3105968287150147, 'HP:0033127', 'Abnormality of the musculoskeletal system'),
(412208, 'HP:0033127', 'Abnormality of the musculoskeletal system', 'XPO:0100282', 'abnormal pelvic girdle primordium', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(412209, 'HP:0033127', 'Abnormality of the musculoskeletal system', 'XPO:0100164', 'abnormal neural nucleus', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(412210, 'HP:0033127', 'Abnormality of the musculoskeletal system', 'XPO:0101450', 'abnormal myeloid cell', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(412211, 'HP:0033127', 'Abnormality of the musculoskeletal system', 'XPO:0101071', 'abnormal endoplasmic reticulum', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(412212, 'HP:0033127', 'Abnormality of the musculoskeletal system', 'XPO:0141880', 'abnormal ethanolamine metabolic process', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(412213, 'HP:0033127', 'Abnormality of the musculoskeletal system', 'XPO:0141877', 'abnormal 2-deoxyribose 1-phosphate metabolic process', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(412214, 'HP:0033127', 'Abnormality of the musculoskeletal system', 'XPO:0100762', 'abnormal intersomitic region', 0.47058823529411764, 1.4755025719078136, 0.8332791557971614, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(412215, 'HP:0033127', 'Abnormality of the musculoskeletal system', 'XPO:0103783', 'absent hatching behavior', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(412216, 'HP:0033127', 'Abnormality of the musculoskeletal system', 'XPO:0101221', 'abnormal larval immune system', 0.47619047619047616, 1.8210412618256888, 0.9312156064152277, 'HP:0000118', 'Phenotypic abnormality'),
(412217, 'HP:0033127', 'Abnormality of the musculoskeletal system', 'XPO:0100296', 'abnormal tail region', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(412218, 'HP:0033127', 'Abnormality of the musculoskeletal system', 'XPO:0101113', 'abnormal stage IV oocyte', 0.47619047619047616, 1.8210412618256888, 0.9312156064152277, 'HP:0000118', 'Phenotypic abnormality'),
(412219, 'HP:0033127', 'Abnormality of the musculoskeletal system', 'XPO:0101513', 'abnormal basal body', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(412220, 'HP:0033127', 'Abnormality of the musculoskeletal system', 'XPO:0141898', 'abnormal maltose metabolic process', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(412221, 'HP:0033127', 'Abnormality of the musculoskeletal system', 'XPO:0131759', 'abnormal development of cell', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(412222, 'HP:0033127', 'Abnormality of the musculoskeletal system', 'XPO:0132658', 'abnormal development of ventral endoderm', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(412223, 'HP:0033127', 'Abnormality of the musculoskeletal system', 'XPO:0142054', 'abnormal digestive tract', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(412224, 'HP:0033127', 'Abnormality of the musculoskeletal system', 'XPO:0100289', 'abnormal chondroblast', 0.5263157894736842, 1.8210412618256888, 0.9790009036675816, 'HP:0000118', 'Phenotypic abnormality'),
(412225, 'HP:0033127', 'Abnormality of the musculoskeletal system', 'XPO:0101136', 'abnormal ooplasm', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(412226, 'HP:0033127', 'Abnormality of the musculoskeletal system', 'XPO:0100585', 'abnormal elastica externa', 0.55, 3.9037819259951223, 1.4652918000512107, 'HP:0033127', 'Abnormality of the musculoskeletal system'),
(412227, 'HP:0033127', 'Abnormality of the musculoskeletal system', 'XPO:0141724', 'abnormal prevention of polyspermy', 0.47058823529411764, 1.4755025719078136, 0.8332791557971614, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(412228, 'HP:0033127', 'Abnormality of the musculoskeletal system', 'XPO:0141812', 'abnormal transferase activity', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(412229, 'HP:0033127', 'Abnormality of the musculoskeletal system', 'XPO:0101157', 'abnormal female organism', 0.5, 1.4755025719078136, 0.8589244937443028, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(412230, 'HP:0033127', 'Abnormality of the musculoskeletal system', 'XPO:0100175', 'abnormal migrating neuroblast', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(412231, 'HP:0033127', 'Abnormality of the musculoskeletal system', 'XPO:0101498', 'abnormal stage II oocyte', 0.47619047619047616, 1.8210412618256888, 0.9312156064152277, 'HP:0000118', 'Phenotypic abnormality'),
(412232, 'HP:0033127', 'Abnormality of the musculoskeletal system', 'XPO:0133203', 'abnormal development of ventral region', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(412233, 'HP:0033127', 'Abnormality of the musculoskeletal system', 'XPO:0141860', 'abnormal malate-aspartate shuttle', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(412234, 'HP:0033127', 'Abnormality of the musculoskeletal system', 'XPO:0141772', 'abnormal water homeostasis', 0.6153846153846154, 1.4755025719078136, 0.9528911704452407, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(412235, 'HP:0033127', 'Abnormality of the musculoskeletal system', 'XPO:0141904', 'abnormal glucosamine metabolic process', 0.5263157894736842, 1.8210412618256888, 0.9790009036675816, 'HP:0000118', 'Phenotypic abnormality'),
(412236, 'HP:0033127', 'Abnormality of the musculoskeletal system', 'XPO:0101569', 'abnormal activin-induced ectoderm', 0.5333333333333333, 1.4755025719078136, 0.8870934026456857, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(412237, 'HP:0033127', 'Abnormality of the musculoskeletal system', 'XPO:0141790', 'abnormal cellular metabolic process', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(412238, 'HP:0033127', 'Abnormality of the musculoskeletal system', 'XPO:0100468', 'abnormal muscular system', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(412239, 'HP:0033127', 'Abnormality of the musculoskeletal system', 'XPO:0100688', 'abnormal adipose tissue', 0.5238095238095238, 3.9037819259951223, 1.429978374560864, 'HP:0033127', 'Abnormality of the musculoskeletal system'),
(412240, 'HP:0033127', 'Abnormality of the musculoskeletal system', 'XPO:0131862', 'abnormal development of pharyngeal region', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(412241, 'HP:0033127', 'Abnormality of the musculoskeletal system', 'XPO:0141718', 'abnormal posterior notochord', 0.5, 3.9037819259951223, 1.3971009136771622, 'HP:0033127', 'Abnormality of the musculoskeletal system'),
(412242, 'HP:0033127', 'Abnormality of the musculoskeletal system', 'XPO:0141738', 'abnormal carbon dioxide homeostasis', 0.6153846153846154, 1.4755025719078136, 0.9528911704452407, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(412243, 'HP:0033127', 'Abnormality of the musculoskeletal system', 'XPO:0100275', 'abnormal skeletal muscle', 0.44, 3.9037819259951223, 1.3105968287150147, 'HP:0033127', 'Abnormality of the musculoskeletal system'),
(412244, 'HP:0033127', 'Abnormality of the musculoskeletal system', 'XPO:0101004', 'abnormal acid secreting cell', 0.5263157894736842, 1.8210412618256888, 0.9790009036675816, 'HP:0000118', 'Phenotypic abnormality'),
(412245, 'HP:0033127', 'Abnormality of the musculoskeletal system', 'XPO:0133129', 'abnormal development of neurocoel', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(412246, 'HP:0033127', 'Abnormality of the musculoskeletal system', 'XPO:0101264', 'abnormal mitotic spindle', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(412247, 'HP:0033127', 'Abnormality of the musculoskeletal system', 'XPO:0100545', 'abnormal male organism', 0.5, 1.4755025719078136, 0.8589244937443028, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(412248, 'HP:0033127', 'Abnormality of the musculoskeletal system', 'XPO:0141884', 'abnormal phosphagen metabolic process', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(412249, 'HP:0033127', 'Abnormality of the musculoskeletal system', 'XPO:0101405', 'abnormal ring structure', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(412250, 'HP:0033127', 'Abnormality of the musculoskeletal system', 'XPO:0132927', 'abnormal development of central retina', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(412251, 'HP:0033127', 'Abnormality of the musculoskeletal system', 'XPO:0141782', 'abnormal methylation', 0.5263157894736842, 1.8210412618256888, 0.9790009036675816, 'HP:0000118', 'Phenotypic abnormality'),
(412252, 'HP:0033127', 'Abnormality of the musculoskeletal system', 'XPO:0132559', 'abnormal development of anatomical axis', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(412253, 'HP:0033127', 'Abnormality of the musculoskeletal system', 'XPO:0100915', 'abnormal dermal system', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(412254, 'HP:0033127', 'Abnormality of the musculoskeletal system', 'XPO:0131704', 'abnormal cell migration', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(412255, 'HP:0033127', 'Abnormality of the musculoskeletal system', 'XPO:0131764', 'abnormal development of retinal progenitor cell region', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(412256, 'HP:0033127', 'Abnormality of the musculoskeletal system', 'XPO:0115508', 'abnormally peramorphic growth of whole organism', 0.5, 1.4755025719078136, 0.8589244937443028, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(412257, 'HP:0033127', 'Abnormality of the musculoskeletal system', 'XPO:0101237', 'abnormal mucus secreting cell', 0.5263157894736842, 1.8210412618256888, 0.9790009036675816, 'HP:0000118', 'Phenotypic abnormality'),
(412258, 'HP:0033127', 'Abnormality of the musculoskeletal system', 'XPO:0132762', 'abnormal development of blastocoel', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(412259, 'HP:0033127', 'Abnormality of the musculoskeletal system', 'XPO:0100728', 'abnormal cell condensation', 0.5, 1.4755025719078136, 0.8589244937443028, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(412260, 'HP:0033127', 'Abnormality of the musculoskeletal system', 'XPO:0101092', 'abnormal dorso-lateral marginal zone', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(412261, 'HP:0033127', 'Abnormality of the musculoskeletal system', 'XPO:0101451', 'abnormal dorsal lymph space', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(412262, 'HP:0033127', 'Abnormality of the musculoskeletal system', 'XPO:0100902', 'abnormal spermatocyte', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(412263, 'HP:0033127', 'Abnormality of the musculoskeletal system', 'XPO:0101174', 'abnormal articular system', 0.5, 3.9037819259951223, 1.3971009136771622, 'HP:0033127', 'Abnormality of the musculoskeletal system'),
(412264, 'HP:0033127', 'Abnormality of the musculoskeletal system', 'XPO:0133131', 'abnormal development of axial region', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(412265, 'HP:0033127', 'Abnormality of the musculoskeletal system', 'XPO:0132456', 'abnormal development of prime meridian', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(412266, 'HP:0033127', 'Abnormality of the musculoskeletal system', 'XPO:0141859', 'abnormal lactose catabolic process', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(412267, 'HP:0033127', 'Abnormality of the musculoskeletal system', 'XPO:0100067', 'abnormal animal hemisphere', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(412268, 'HP:0033127', 'Abnormality of the musculoskeletal system', 'XPO:0131715', 'abnormal fibroblast growth factor receptor signaling pathway', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(412269, 'HP:0033127', 'Abnormality of the musculoskeletal system', 'XPO:0101378', 'abnormal blastomere D1', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(412270, 'HP:0033127', 'Abnormality of the musculoskeletal system', 'XPO:0131738', 'abnormal Wnt signaling pathway', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(412271, 'HP:0033127', 'Abnormality of the musculoskeletal system', 'XPO:0100574', 'abnormal gastrula cell', 0.47619047619047616, 1.8210412618256888, 0.9312156064152277, 'HP:0000118', 'Phenotypic abnormality'),
(412272, 'HP:0033127', 'Abnormality of the musculoskeletal system', 'XPO:0100999', 'abnormal serous membrane', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(412273, 'HP:0033127', 'Abnormality of the musculoskeletal system', 'XPO:0131728', 'abnormal regulation of cell size', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(412274, 'HP:0033127', 'Abnormality of the musculoskeletal system', 'XPO:0101348', 'abnormal perichordal tissue', 0.44, 3.9037819259951223, 1.3105968287150147, 'HP:0033127', 'Abnormality of the musculoskeletal system'),
(412275, 'HP:0033127', 'Abnormality of the musculoskeletal system', 'XPO:0131477', 'absent visual behavior', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(412276, 'HP:0033127', 'Abnormality of the musculoskeletal system', 'XPO:0100802', 'abnormal exocrine cell', 0.5263157894736842, 1.8210412618256888, 0.9790009036675816, 'HP:0000118', 'Phenotypic abnormality'),
(412277, 'HP:0033127', 'Abnormality of the musculoskeletal system', 'XPO:0100956', 'abnormal centrosome', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(412278, 'HP:0033127', 'Abnormality of the musculoskeletal system', 'XPO:0131685', 'abnormal cortical actin cytoskeleton', 0.47619047619047616, 1.8210412618256888, 0.9312156064152277, 'HP:0000118', 'Phenotypic abnormality'),
(412279, 'HP:0033127', 'Abnormality of the musculoskeletal system', 'XPO:0100120', 'abnormal genital system', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(412280, 'HP:0033127', 'Abnormality of the musculoskeletal system', 'XPO:0132823', 'abnormal development of basal region', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(412281, 'HP:0033127', 'Abnormality of the musculoskeletal system', 'XPO:0141814', 'abnormal lyase activity', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(412282, 'HP:0033127', 'Abnormality of the musculoskeletal system', 'XPO:0131675', 'abnormal spindle microtubule', 0.47619047619047616, 1.8210412618256888, 0.9312156064152277, 'HP:0000118', 'Phenotypic abnormality'),
(412283, 'HP:0033127', 'Abnormality of the musculoskeletal system', 'XPO:0133068', 'abnormal development of joint region', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(412284, 'HP:0033127', 'Abnormality of the musculoskeletal system', 'XPO:0141852', 'abnormal glucose metabolic process', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(412285, 'HP:0033127', 'Abnormality of the musculoskeletal system', 'XPO:0133401', 'absent determination of left/right symmetry in lateral plate mesoderm', 0.47058823529411764, 1.4755025719078136, 0.8332791557971614, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(412286, 'HP:0033127', 'Abnormality of the musculoskeletal system', 'XPO:0100025', 'abnormal oocyte', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(412287, 'HP:0033127', 'Abnormality of the musculoskeletal system', 'XPO:0141263', 'abnormal visually guided collision avoidance behavior', 0.6153846153846154, 1.4755025719078136, 0.9528911704452407, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(412288, 'HP:0033127', 'Abnormality of the musculoskeletal system', 'XPO:0100882', 'abnormal perichondrial cell', 0.4074074074074074, 3.9037819259951223, 1.2611223864294727, 'HP:0033127', 'Abnormality of the musculoskeletal system'),
(412289, 'HP:0033127', 'Abnormality of the musculoskeletal system', 'XPO:0100002', 'abnormal head', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(412290, 'HP:0033127', 'Abnormality of the musculoskeletal system', 'XPO:0100293', 'abnormal duct', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(412291, 'HP:0033127', 'Abnormality of the musculoskeletal system', 'XPO:0100417', 'abnormal dense regular connective tissue', 0.5238095238095238, 3.9037819259951223, 1.429978374560864, 'HP:0033127', 'Abnormality of the musculoskeletal system'),
(412292, 'HP:0033127', 'Abnormality of the musculoskeletal system', 'XPO:0100862', 'abnormal blastomere V1', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(412293, 'HP:0033127', 'Abnormality of the musculoskeletal system', 'XPO:0141748', 'abnormal gas homeostasis', 0.6153846153846154, 1.4755025719078136, 0.9528911704452407, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(412294, 'HP:0033127', 'Abnormality of the musculoskeletal system', 'XPO:0131469', 'abnormal heart process', 0.5, 1.4755025719078136, 0.8589244937443028, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(412295, 'HP:0033127', 'Abnormality of the musculoskeletal system', 'XPO:0132808', 'abnormal development of medium cavity', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(412296, 'HP:0033127', 'Abnormality of the musculoskeletal system', 'XPO:0131940', 'abnormal development of acellular anatomical structure', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(412297, 'HP:0033127', 'Abnormality of the musculoskeletal system', 'XPO:0100511', 'abnormal stylopod', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(412298, 'HP:0033127', 'Abnormality of the musculoskeletal system', 'XPO:0131807', 'abnormal development of anatomical group', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(412299, 'HP:0033127', 'Abnormality of the musculoskeletal system', 'XPO:0100427', 'abnormal olfactory system', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(412300, 'HP:0033127', 'Abnormality of the musculoskeletal system', 'XPO:0116433', 'abnormal axis specification', 0.47058823529411764, 1.4755025719078136, 0.8332791557971614, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(412301, 'HP:0033127', 'Abnormality of the musculoskeletal system', 'XPO:0100344', 'abnormal portion of organism substance', 0.5714285714285714, 1.4755025719078136, 0.918228907628411, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(412302, 'HP:0033127', 'Abnormality of the musculoskeletal system', 'XPO:0131406', 'abnormal social behavior', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(412303, 'HP:0033127', 'Abnormality of the musculoskeletal system', 'XPO:0131722', 'abnormal determination of left/right symmetry', 0.47058823529411764, 1.4755025719078136, 0.8332791557971614, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(412304, 'HP:0033127', 'Abnormality of the musculoskeletal system', 'XPO:0133388', 'absent insulin receptor signaling pathway', 0.5, 1.4755025719078136, 0.8589244937443028, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(412305, 'HP:0033127', 'Abnormality of the musculoskeletal system', 'XPO:0100151', 'abnormal primordium', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(412306, 'HP:0033127', 'Abnormality of the musculoskeletal system', 'XPO:0141266', 'abnormal surface breathing', 0.6153846153846154, 1.4755025719078136, 0.9528911704452407, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(412307, 'HP:0033127', 'Abnormality of the musculoskeletal system', 'XPO:0100100', 'abnormal muscle', 0.4583333333333333, 3.9037819259951223, 1.3376222870256627, 'HP:0033127', 'Abnormality of the musculoskeletal system'),
(412308, 'HP:0033127', 'Abnormality of the musculoskeletal system', 'XPO:0141754', 'abnormal homeostatic process', 0.5, 1.4755025719078136, 0.8589244937443028, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(412309, 'HP:0033127', 'Abnormality of the musculoskeletal system', 'XPO:0141789', 'abnormal hormone catabolic process', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(412310, 'HP:0033127', 'Abnormality of the musculoskeletal system', 'XPO:0100917', 'abnormal stage III oocyte', 0.47619047619047616, 1.8210412618256888, 0.9312156064152277, 'HP:0000118', 'Phenotypic abnormality'),
(412311, 'HP:0033127', 'Abnormality of the musculoskeletal system', 'XPO:0100384', 'abnormal amputated tissue', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(412312, 'HP:0033127', 'Abnormality of the musculoskeletal system', 'XPO:0100377', 'abnormal connective tissue', 0.55, 3.9037819259951223, 1.4652918000512107, 'HP:0033127', 'Abnormality of the musculoskeletal system'),
(412313, 'HP:0033127', 'Abnormality of the musculoskeletal system', 'XPO:0100403', 'abnormal forelimb', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(412314, 'HP:0033127', 'Abnormality of the musculoskeletal system', 'XPO:0141850', 'abnormal galactose metabolic process', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(412315, 'HP:0033127', 'Abnormality of the musculoskeletal system', 'XPO:0100477', 'abnormal pericyte', 0.5263157894736842, 1.8210412618256888, 0.9790009036675816, 'HP:0000118', 'Phenotypic abnormality'),
(412316, 'HP:0033127', 'Abnormality of the musculoskeletal system', 'XPO:0141725', 'increased catalytic activity', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(412317, 'HP:0033127', 'Abnormality of the musculoskeletal system', 'XPO:0142056', 'abnormal main body axis', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(412318, 'HP:0033127', 'Abnormality of the musculoskeletal system', 'XPO:0101406', 'abnormal cleavage furrow', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(412319, 'HP:0033127', 'Abnormality of the musculoskeletal system', 'XPO:0100103', 'abnormal trunk', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(412320, 'HP:0033127', 'Abnormality of the musculoskeletal system', 'XPO:0101176', 'abnormal non-ciliated epithelial cell', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(412321, 'HP:0033127', 'Abnormality of the musculoskeletal system', 'XPO:0131698', 'abnormal apical constriction involved in gastrulation', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(412322, 'HP:0033127', 'Abnormality of the musculoskeletal system', 'XPO:0141817', 'abnormal demethylase activity', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(412323, 'HP:0033127', 'Abnormality of the musculoskeletal system', 'XPO:0100461', 'abnormal craniofacial skeleton', 0.4074074074074074, 3.9037819259951223, 1.2611223864294727, 'HP:0033127', 'Abnormality of the musculoskeletal system'),
(412324, 'HP:0033127', 'Abnormality of the musculoskeletal system', 'XPO:0133184', 'abnormal development of ventro-lateral region', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(412325, 'HP:0033127', 'Abnormality of the musculoskeletal system', 'XPO:0132141', 'abnormal development of olfactory pit', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(412326, 'HP:0033127', 'Abnormality of the musculoskeletal system', 'XPO:0141264', 'abnormal schooling behavior', 0.6153846153846154, 1.4755025719078136, 0.9528911704452407, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(412327, 'HP:0033127', 'Abnormality of the musculoskeletal system', 'XPO:0100612', 'abnormal unilaminar epithelium', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(412328, 'HP:0033127', 'Abnormality of the musculoskeletal system', 'XPO:0100976', 'abnormal multiciliated cell', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(412329, 'HP:0033127', 'Abnormality of the musculoskeletal system', 'XPO:0100989', 'abnormal right blastomere', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(412330, 'HP:0033127', 'Abnormality of the musculoskeletal system', 'XPO:0100784', 'abnormal left blastomere', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(412331, 'HP:0033127', 'Abnormality of the musculoskeletal system', 'XPO:0131666', 'abnormal adherens junction', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(412332, 'HP:0033127', 'Abnormality of the musculoskeletal system', 'XPO:0131936', 'abnormal development of brain ventricle', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(412333, 'HP:0033127', 'Abnormality of the musculoskeletal system', 'XPO:0133276', 'abnormal development of forelimb region', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(412334, 'HP:0033127', 'Abnormality of the musculoskeletal system', 'XPO:0131798', 'abnormal development of anatomical space', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(412335, 'HP:0033127', 'Abnormality of the musculoskeletal system', 'XPO:0115758', 'abnormally decreased mobility of melanoblast', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(412336, 'HP:0033127', 'Abnormality of the musculoskeletal system', 'XPO:0100724', 'abnormal kinetochore', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(412337, 'HP:0033127', 'Abnormality of the musculoskeletal system', 'XPO:0107262', 'abnormal left-right axis', 0.5, 1.4755025719078136, 0.8589244937443028, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(412338, 'HP:0033127', 'Abnormality of the musculoskeletal system', 'XPO:0131694', 'abnormal RNA polymerase II activity', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(412339, 'HP:0033127', 'Abnormality of the musculoskeletal system', 'XPO:0101519', 'abnormal hypobranchial placode', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(412340, 'HP:0033127', 'Abnormality of the musculoskeletal system', 'XPO:0141907', 'abnormal putrescine metabolic process', 0.47619047619047616, 1.8210412618256888, 0.9312156064152277, 'HP:0000118', 'Phenotypic abnormality'),
(412341, 'HP:0033127', 'Abnormality of the musculoskeletal system', 'XPO:0107265', 'abnormal posterior side', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(412342, 'HP:0033127', 'Abnormality of the musculoskeletal system', 'XPO:0100913', 'abnormal Brachets cleft', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(412343, 'HP:0033127', 'Abnormality of the musculoskeletal system', 'XPO:0100133', 'abnormal solid compound organ', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(412344, 'HP:0033127', 'Abnormality of the musculoskeletal system', 'XPO:0100846', 'abnormal hindlimb', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(412345, 'HP:0033127', 'Abnormality of the musculoskeletal system', 'XPO:0133340', 'abnormal cell adhesion', 0.47058823529411764, 1.4755025719078136, 0.8332791557971614, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(412346, 'HP:0033127', 'Abnormality of the musculoskeletal system', 'XPO:0141818', 'abnormal peptidoglycan muralytic activity', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(412347, 'HP:0033127', 'Abnormality of the musculoskeletal system', 'XPO:0115512', 'abnormally semi-erect whole organism', 0.5, 1.4755025719078136, 0.8589244937443028, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(412348, 'HP:0033127', 'Abnormality of the musculoskeletal system', 'XPO:0133028', 'abnormal development of dorso-lateral region', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(412349, 'HP:0033127', 'Abnormality of the musculoskeletal system', 'XPO:0141771', 'abnormal urea homeostasis', 0.6153846153846154, 1.4755025719078136, 0.9528911704452407, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(412350, 'HP:0033127', 'Abnormality of the musculoskeletal system', 'XPO:0141276', 'decreased surface breathing', 0.5714285714285714, 1.4755025719078136, 0.918228907628411, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(412351, 'HP:0033127', 'Abnormality of the musculoskeletal system', 'XPO:0141975', 'abnormal cilium motility', 0.47058823529411764, 1.4755025719078136, 0.8332791557971614, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(412352, 'HP:0033127', 'Abnormality of the musculoskeletal system', 'XPO:0100393', 'abnormal involuting marginal zone', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(412353, 'HP:0033127', 'Abnormality of the musculoskeletal system', 'XPO:0131740', 'abnormal detection of nodal flow', 0.47058823529411764, 1.4755025719078136, 0.8332791557971614, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(412354, 'HP:0033127', 'Abnormality of the musculoskeletal system', 'XPO:0131399', 'abnormal vocalization behavior', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(412355, 'HP:0033127', 'Abnormality of the musculoskeletal system', 'XPO:0100256', 'abnormal paired appendage', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(412356, 'HP:0033127', 'Abnormality of the musculoskeletal system', 'XPO:0101366', 'abnormal morula cell', 0.47619047619047616, 1.8210412618256888, 0.9312156064152277, 'HP:0000118', 'Phenotypic abnormality'),
(412357, 'HP:0033127', 'Abnormality of the musculoskeletal system', 'XPO:0132435', 'abnormal development of pupil', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(412358, 'HP:0100293', 'Hypertrophied muscle fibers', 'XPO:0100691', 'abnormal keratin accumulating cell', 0.4642857142857143, 3.6715585125471644, 1.305623286610558, 'UPHENO:0086172', 'abnormal cell'),
(412359, 'HP:0100293', 'Hypertrophied muscle fibers', 'XPO:0101168', 'abnormal circulating cell', 0.40625, 3.6715585125471644, 1.221298753672616, 'UPHENO:0086172', 'abnormal cell'),
(412360, 'HP:0100293', 'Hypertrophied muscle fibers', 'XPO:0131669', 'abnormal Roux spot', 0.41935483870967744, 3.6715585125471644, 1.240840774572773, 'UPHENO:0086172', 'abnormal cell'),
(412361, 'HP:0100293', 'Hypertrophied muscle fibers', 'XPO:0131677', 'abnormal actin filament', 0.43333333333333335, 3.6715585125471644, 1.2613519289914445, 'UPHENO:0086172', 'abnormal cell'),
(412362, 'HP:0100293', 'Hypertrophied muscle fibers', 'XPO:0100907', 'abnormal cytoplasm', 0.4482758620689655, 3.6715585125471644, 1.2829150624062098, 'UPHENO:0086172', 'abnormal cell'),
(412363, 'HP:0100293', 'Hypertrophied muscle fibers', 'XPO:0102276', 'abnormal smooth muscle myocyte morphology', 0.40425531914893614, 6.895202660022325, 1.6695575317801774, 'HP:0011805', 'Abnormal skeletal muscle morphology'),
(412364, 'HP:0100293', 'Hypertrophied muscle fibers', 'XPO:0100100', 'abnormal muscle', 0.42424242424242425, 5.968280811662945, 1.591225288920281, 'UPHENO:0002816', 'abnormal musculature'),
(412365, 'HP:0100293', 'Hypertrophied muscle fibers', 'XPO:0100533', 'abnormal melanoblast', 0.4642857142857143, 3.6715585125471644, 1.305623286610558, 'UPHENO:0086172', 'abnormal cell'),
(412366, 'HP:0100293', 'Hypertrophied muscle fibers', 'XPO:0100888', 'abnormal microtubule', 0.4482758620689655, 3.6715585125471644, 1.2829150624062098, 'UPHENO:0086172', 'abnormal cell'),
(412367, 'HP:0100293', 'Hypertrophied muscle fibers', 'XPO:0100976', 'abnormal multiciliated cell', 0.4482758620689655, 3.6715585125471644, 1.2829150624062098, 'UPHENO:0086172', 'abnormal cell'),
(412368, 'HP:0100293', 'Hypertrophied muscle fibers', 'XPO:0100549', 'abnormal mitotic cell', 0.4642857142857143, 3.6715585125471644, 1.305623286610558, 'UPHENO:0086172', 'abnormal cell'),
(412369, 'HP:0100293', 'Hypertrophied muscle fibers', 'XPO:0100956', 'abnormal centrosome', 0.4482758620689655, 3.6715585125471644, 1.2829150624062098, 'UPHENO:0086172', 'abnormal cell'),
(412370, 'HP:0100293', 'Hypertrophied muscle fibers', 'XPO:0131655', 'abnormal myofibril', 0.43243243243243246, 5.968280811662945, 1.6065111854037055, 'UPHENO:0002816', 'abnormal musculature'),
(412371, 'HP:0100293', 'Hypertrophied muscle fibers', 'XPO:0100503', 'abnormal blastomere D2', 0.41935483870967744, 3.6715585125471644, 1.240840774572773, 'UPHENO:0086172', 'abnormal cell'),
(412372, 'HP:0100293', 'Hypertrophied muscle fibers', 'XPO:0100218', 'abnormal epithelial cell', 0.41935483870967744, 3.6715585125471644, 1.240840774572773, 'UPHENO:0086172', 'abnormal cell'),
(412373, 'HP:0100293', 'Hypertrophied muscle fibers', 'XPO:0101472', 'abnormal zygote cortex', 0.43333333333333335, 3.6715585125471644, 1.2613519289914445, 'UPHENO:0086172', 'abnormal cell'),
(412374, 'HP:0100293', 'Hypertrophied muscle fibers', 'XPO:0101241', 'abnormal nucleate erythrocyte', 0.4642857142857143, 3.6715585125471644, 1.305623286610558, 'UPHENO:0086172', 'abnormal cell'),
(412375, 'HP:0100293', 'Hypertrophied muscle fibers', 'XPO:0100574', 'abnormal gastrula cell', 0.43333333333333335, 3.6715585125471644, 1.2613519289914445, 'UPHENO:0086172', 'abnormal cell'),
(412376, 'HP:0100293', 'Hypertrophied muscle fibers', 'XPO:0100802', 'abnormal exocrine cell', 0.4642857142857143, 3.6715585125471644, 1.305623286610558, 'UPHENO:0086172', 'abnormal cell'),
(412377, 'HP:0100293', 'Hypertrophied muscle fibers', 'XPO:0101074', 'abnormal germinal vesicle', 0.40625, 3.6715585125471644, 1.221298753672616, 'UPHENO:0086172', 'abnormal cell'),
(412378, 'HP:0100293', 'Hypertrophied muscle fibers', 'XPO:0131666', 'abnormal adherens junction', 0.4482758620689655, 3.6715585125471644, 1.2829150624062098, 'UPHENO:0086172', 'abnormal cell'),
(412379, 'HP:0100293', 'Hypertrophied muscle fibers', 'XPO:0141307', 'abnormal M band morphology', 0.4222222222222222, 6.895202660022325, 1.7062554878409049, 'HP:0011805', 'Abnormal skeletal muscle morphology'),
(412380, 'HP:0100293', 'Hypertrophied muscle fibers', 'XPO:0101132', 'abnormal apoptotic cell', 0.4642857142857143, 3.6715585125471644, 1.305623286610558, 'UPHENO:0086172', 'abnormal cell'),
(412381, 'HP:0100293', 'Hypertrophied muscle fibers', 'XPO:0100902', 'abnormal spermatocyte', 0.4482758620689655, 3.6715585125471644, 1.2829150624062098, 'UPHENO:0086172', 'abnormal cell'),
(412382, 'HP:0100293', 'Hypertrophied muscle fibers', 'XPO:0102471', 'abnormal skeletal myocyte morphology', 0.41304347826086957, 6.895202660022325, 1.687607326960043, 'HP:0011805', 'Abnormal skeletal muscle morphology'),
(412383, 'HP:0100293', 'Hypertrophied muscle fibers', 'XPO:0101072', 'abnormal mitochondrial cloud', 0.41935483870967744, 3.6715585125471644, 1.240840774572773, 'UPHENO:0086172', 'abnormal cell'),
(412384, 'HP:0100293', 'Hypertrophied muscle fibers', 'XPO:0100285', 'abnormal progenitor cell', 0.4642857142857143, 3.6715585125471644, 1.305623286610558, 'UPHENO:0086172', 'abnormal cell'),
(412385, 'HP:0100293', 'Hypertrophied muscle fibers', 'XPO:0101740', 'abnormal cell part morphology', 0.42424242424242425, 3.6715585125471644, 1.2480508339450433, 'UPHENO:0086172', 'abnormal cell'),
(412386, 'HP:0100293', 'Hypertrophied muscle fibers', 'XPO:0101326', 'abnormal cementoblast', 0.4642857142857143, 3.6715585125471644, 1.305623286610558, 'UPHENO:0086172', 'abnormal cell'),
(412387, 'HP:0100293', 'Hypertrophied muscle fibers', 'XPO:0101311', 'abnormal bottle cell', 0.41935483870967744, 3.6715585125471644, 1.240840774572773, 'UPHENO:0086172', 'abnormal cell'),
(412388, 'HP:0100293', 'Hypertrophied muscle fibers', 'XPO:0101513', 'abnormal basal body', 0.4482758620689655, 3.6715585125471644, 1.2829150624062098, 'UPHENO:0086172', 'abnormal cell'),
(412389, 'HP:0100293', 'Hypertrophied muscle fibers', 'XPO:0101467', 'abnormal alkali secreting cell', 0.4642857142857143, 3.6715585125471644, 1.305623286610558, 'UPHENO:0086172', 'abnormal cell'),
(412390, 'HP:0100293', 'Hypertrophied muscle fibers', 'XPO:0101463', 'abnormal right-ventral blastomere', 0.41935483870967744, 3.6715585125471644, 1.240840774572773, 'UPHENO:0086172', 'abnormal cell'),
(412391, 'HP:0100293', 'Hypertrophied muscle fibers', 'XPO:0101297', 'abnormal barrier cell', 0.4642857142857143, 3.6715585125471644, 1.305623286610558, 'UPHENO:0086172', 'abnormal cell'),
(412392, 'HP:0100293', 'Hypertrophied muscle fibers', 'XPO:0101366', 'abnormal morula cell', 0.43333333333333335, 3.6715585125471644, 1.2613519289914445, 'UPHENO:0086172', 'abnormal cell'),
(412393, 'HP:0100293', 'Hypertrophied muscle fibers', 'XPO:0101004', 'abnormal acid secreting cell', 0.4642857142857143, 3.6715585125471644, 1.305623286610558, 'UPHENO:0086172', 'abnormal cell'),
(412394, 'HP:0100293', 'Hypertrophied muscle fibers', 'XPO:0100674', 'abnormal secondary oogonium', 0.4482758620689655, 3.6715585125471644, 1.2829150624062098, 'UPHENO:0086172', 'abnormal cell'),
(412395, 'HP:0100293', 'Hypertrophied muscle fibers', 'XPO:0100791', 'abnormal multiciliated cell precursor', 0.4642857142857143, 3.6715585125471644, 1.305623286610558, 'UPHENO:0086172', 'abnormal cell'),
(412396, 'HP:0100293', 'Hypertrophied muscle fibers', 'XPO:0100917', 'abnormal stage III oocyte', 0.43333333333333335, 3.6715585125471644, 1.2613519289914445, 'UPHENO:0086172', 'abnormal cell'),
(412397, 'HP:0100293', 'Hypertrophied muscle fibers', 'XPO:0101176', 'abnormal non-ciliated epithelial cell', 0.40625, 3.6715585125471644, 1.221298753672616, 'UPHENO:0086172', 'abnormal cell'),
(412398, 'HP:0100293', 'Hypertrophied muscle fibers', 'XPO:0100337', 'abnormal zygote', 0.4642857142857143, 3.6715585125471644, 1.305623286610558, 'UPHENO:0086172', 'abnormal cell'),
(412399, 'HP:0100293', 'Hypertrophied muscle fibers', 'XPO:0101389', 'abnormal wedge region', 0.41935483870967744, 3.6715585125471644, 1.240840774572773, 'UPHENO:0086172', 'abnormal cell'),
(412400, 'HP:0100293', 'Hypertrophied muscle fibers', 'XPO:0100839', 'abnormal skeletal myocyte', 0.43243243243243246, 5.968280811662945, 1.6065111854037055, 'UPHENO:0002816', 'abnormal musculature'),
(412401, 'HP:0100293', 'Hypertrophied muscle fibers', 'XPO:0101547', 'abnormal lampbrush chromosome', 0.4482758620689655, 3.6715585125471644, 1.2829150624062098, 'UPHENO:0086172', 'abnormal cell'),
(412402, 'HP:0100293', 'Hypertrophied muscle fibers', 'XPO:0101405', 'abnormal ring structure', 0.41935483870967744, 3.6715585125471644, 1.240840774572773, 'UPHENO:0086172', 'abnormal cell'),
(412403, 'HP:0100293', 'Hypertrophied muscle fibers', 'XPO:0100415', 'abnormal secretory epithelial cell', 0.40625, 3.6715585125471644, 1.221298753672616, 'UPHENO:0086172', 'abnormal cell'),
(412404, 'HP:0100293', 'Hypertrophied muscle fibers', 'XPO:0101480', 'abnormal stage V oocyte', 0.43333333333333335, 3.6715585125471644, 1.2613519289914445, 'UPHENO:0086172', 'abnormal cell'),
(412405, 'HP:0100293', 'Hypertrophied muscle fibers', 'XPO:0101237', 'abnormal mucus secreting cell', 0.4642857142857143, 3.6715585125471644, 1.305623286610558, 'UPHENO:0086172', 'abnormal cell'),
(412406, 'HP:0100293', 'Hypertrophied muscle fibers', 'XPO:0100989', 'abnormal right blastomere', 0.41935483870967744, 3.6715585125471644, 1.240840774572773, 'UPHENO:0086172', 'abnormal cell'),
(412407, 'HP:0100293', 'Hypertrophied muscle fibers', 'XPO:0100715', 'abnormal ciliated cell', 0.4642857142857143, 3.6715585125471644, 1.305623286610558, 'UPHENO:0086172', 'abnormal cell'),
(412408, 'HP:0100293', 'Hypertrophied muscle fibers', 'XPO:0141284', 'abnormal myofibril morphology', 0.4418604651162791, 6.895202660022325, 1.7454848765968924, 'HP:0011805', 'Abnormal skeletal muscle morphology'),
(412409, 'HP:0100293', 'Hypertrophied muscle fibers', 'XPO:0101333', 'abnormal barrier epithelial cell', 0.4642857142857143, 3.6715585125471644, 1.305623286610558, 'UPHENO:0086172', 'abnormal cell'),
(412410, 'HP:0100293', 'Hypertrophied muscle fibers', 'XPO:0100899', 'abnormal secondary spermatogonium', 0.4482758620689655, 3.6715585125471644, 1.2829150624062098, 'UPHENO:0086172', 'abnormal cell'),
(412411, 'HP:0100293', 'Hypertrophied muscle fibers', 'XPO:0101264', 'abnormal mitotic spindle', 0.4482758620689655, 3.6715585125471644, 1.2829150624062098, 'UPHENO:0086172', 'abnormal cell'),
(412412, 'HP:0100293', 'Hypertrophied muscle fibers', 'XPO:0100900', 'abnormal angioblast', 0.40625, 3.6715585125471644, 1.221298753672616, 'UPHENO:0086172', 'abnormal cell'),
(412413, 'HP:0100293', 'Hypertrophied muscle fibers', 'XPO:0107312', 'abnormal filopodium', 0.4482758620689655, 3.6715585125471644, 1.2829150624062098, 'UPHENO:0086172', 'abnormal cell'),
(412414, 'HP:0100293', 'Hypertrophied muscle fibers', 'XPO:0100842', 'abnormal left-dorsal blastomere', 0.41935483870967744, 3.6715585125471644, 1.240840774572773, 'UPHENO:0086172', 'abnormal cell'),
(412415, 'HP:0100293', 'Hypertrophied muscle fibers', 'XPO:0100515', 'abnormal somatic stem cell', 0.4482758620689655, 3.6715585125471644, 1.2829150624062098, 'UPHENO:0086172', 'abnormal cell'),
(412416, 'HP:0100293', 'Hypertrophied muscle fibers', 'XPO:0131660', 'abnormal sarcomere', 0.42105263157894735, 5.968280811662945, 1.5852319520350384, 'UPHENO:0002816', 'abnormal musculature'),
(412417, 'HP:0100293', 'Hypertrophied muscle fibers', 'XPO:0100721', 'abnormal centromere', 0.4482758620689655, 3.6715585125471644, 1.2829150624062098, 'UPHENO:0086172', 'abnormal cell'),
(412418, 'HP:0100293', 'Hypertrophied muscle fibers', 'XPO:0100289', 'abnormal chondroblast', 0.4642857142857143, 3.6715585125471644, 1.305623286610558, 'UPHENO:0086172', 'abnormal cell'),
(412419, 'HP:0100293', 'Hypertrophied muscle fibers', 'XPO:0100596', 'abnormal myocyte', 0.45714285714285713, 5.968280811662945, 1.651773877525156, 'UPHENO:0002816', 'abnormal musculature'),
(412420, 'HP:0100293', 'Hypertrophied muscle fibers', 'XPO:0101468', 'abnormal stage I oocyte', 0.43333333333333335, 3.6715585125471644, 1.2613519289914445, 'UPHENO:0086172', 'abnormal cell'),
(412421, 'HP:0100293', 'Hypertrophied muscle fibers', 'XPO:0103098', 'abnormal secondary myofiber morphology', 0.4418604651162791, 6.895202660022325, 1.7454848765968924, 'HP:0011805', 'Abnormal skeletal muscle morphology'),
(412422, 'HP:0100293', 'Hypertrophied muscle fibers', 'XPO:0100025', 'abnormal oocyte', 0.4482758620689655, 3.6715585125471644, 1.2829150624062098, 'UPHENO:0086172', 'abnormal cell'),
(412423, 'HP:0100293', 'Hypertrophied muscle fibers', 'XPO:0131667', 'abnormal actin cytoskeleton', 0.4482758620689655, 3.6715585125471644, 1.2829150624062098, 'UPHENO:0086172', 'abnormal cell'),
(412424, 'HP:0100293', 'Hypertrophied muscle fibers', 'XPO:0100392', 'abnormal cilium', 0.43333333333333335, 3.6715585125471644, 1.2613519289914445, 'UPHENO:0086172', 'abnormal cell'),
(412425, 'HP:0100293', 'Hypertrophied muscle fibers', 'XPO:0100746', 'abnormal smooth muscle', 0.4117647058823529, 5.968280811662945, 1.5676502776568768, 'UPHENO:0002816', 'abnormal musculature'),
(412426, 'HP:0100293', 'Hypertrophied muscle fibers', 'XPO:0101435', 'abnormal paracrine cell', 0.4642857142857143, 3.6715585125471644, 1.305623286610558, 'UPHENO:0086172', 'abnormal cell'),
(412427, 'HP:0100293', 'Hypertrophied muscle fibers', 'XPO:0101362', 'abnormal vegetal cortex', 0.40625, 3.6715585125471644, 1.221298753672616, 'UPHENO:0086172', 'abnormal cell'),
(412428, 'HP:0100293', 'Hypertrophied muscle fibers', 'XPO:0107339', 'abnormal yolk platelet', 0.41935483870967744, 3.6715585125471644, 1.240840774572773, 'UPHENO:0086172', 'abnormal cell'),
(412429, 'HP:0100293', 'Hypertrophied muscle fibers', 'XPO:0103113', 'abnormal skeletal muscle satellite cell morphology', 0.4318181818181818, 6.895202660022325, 1.725535822844235, 'HP:0011805', 'Abnormal skeletal muscle morphology'),
(412430, 'HP:0100293', 'Hypertrophied muscle fibers', 'XPO:0100754', 'abnormal electrically active cell', 0.4642857142857143, 3.6715585125471644, 1.305623286610558, 'UPHENO:0086172', 'abnormal cell'),
(412431, 'HP:0100293', 'Hypertrophied muscle fibers', 'XPO:0101575', 'abnormal vitelline membrane', 0.41935483870967744, 3.6715585125471644, 1.240840774572773, 'UPHENO:0086172', 'abnormal cell'),
(412432, 'HP:0100293', 'Hypertrophied muscle fibers', 'XPO:0100477', 'abnormal pericyte', 0.4642857142857143, 3.6715585125471644, 1.305623286610558, 'UPHENO:0086172', 'abnormal cell'),
(412433, 'HP:0100293', 'Hypertrophied muscle fibers', 'XPO:0101498', 'abnormal stage II oocyte', 0.43333333333333335, 3.6715585125471644, 1.2613519289914445, 'UPHENO:0086172', 'abnormal cell'),
(412434, 'HP:0100293', 'Hypertrophied muscle fibers', 'XPO:0100547', 'abnormal blastomere V2', 0.41935483870967744, 3.6715585125471644, 1.240840774572773, 'UPHENO:0086172', 'abnormal cell'),
(412435, 'HP:0100293', 'Hypertrophied muscle fibers', 'XPO:0100704', 'abnormal Merkel cell', 0.4642857142857143, 3.6715585125471644, 1.305623286610558, 'UPHENO:0086172', 'abnormal cell'),
(412436, 'HP:0100293', 'Hypertrophied muscle fibers', 'XPO:0100026', 'abnormal germ cell', 0.4642857142857143, 3.6715585125471644, 1.305623286610558, 'UPHENO:0086172', 'abnormal cell'),
(412437, 'HP:0100293', 'Hypertrophied muscle fibers', 'XPO:0101162', 'abnormal stromal cell', 0.42424242424242425, 3.9037819259951223, 1.286914879857223, 'HP:0033127', 'Abnormality of the musculoskeletal system'),
(412438, 'HP:0100293', 'Hypertrophied muscle fibers', 'XPO:0101448', 'abnormal myelin accumulating cell', 0.4642857142857143, 3.6715585125471644, 1.305623286610558, 'UPHENO:0086172', 'abnormal cell'),
(412439, 'HP:0100293', 'Hypertrophied muscle fibers', 'XPO:0100862', 'abnormal blastomere V1', 0.41935483870967744, 3.6715585125471644, 1.240840774572773, 'UPHENO:0086172', 'abnormal cell'),
(412440, 'HP:0100293', 'Hypertrophied muscle fibers', 'XPO:0115758', 'abnormally decreased mobility of melanoblast', 0.40625, 3.6715585125471644, 1.221298753672616, 'UPHENO:0086172', 'abnormal cell'),
(412441, 'HP:0100293', 'Hypertrophied muscle fibers', 'XPO:0101113', 'abnormal stage IV oocyte', 0.43333333333333335, 3.6715585125471644, 1.2613519289914445, 'UPHENO:0086172', 'abnormal cell'),
(412442, 'HP:0100293', 'Hypertrophied muscle fibers', 'XPO:0141294', 'abnormal sarcomere morphology', 0.4318181818181818, 6.895202660022325, 1.725535822844235, 'HP:0011805', 'Abnormal skeletal muscle morphology'),
(412443, 'HP:0100293', 'Hypertrophied muscle fibers', 'XPO:0100265', 'abnormal sensory epithelial cell', 0.40625, 3.6715585125471644, 1.221298753672616, 'UPHENO:0086172', 'abnormal cell'),
(412444, 'HP:0100293', 'Hypertrophied muscle fibers', 'XPO:0141076', 'abnormally necrotic secondary myofiber', 0.40425531914893614, 6.895202660022325, 1.6695575317801774, 'HP:0011805', 'Abnormal skeletal muscle morphology'),
(412445, 'HP:0100293', 'Hypertrophied muscle fibers', 'XPO:0101378', 'abnormal blastomere D1', 0.41935483870967744, 3.6715585125471644, 1.240840774572773, 'UPHENO:0086172', 'abnormal cell'),
(412446, 'HP:0100293', 'Hypertrophied muscle fibers', 'XPO:0131686', 'abnormal M band', 0.41025641025641024, 5.968280811662945, 1.5647764892134128, 'UPHENO:0002816', 'abnormal musculature'),
(412447, 'HP:0100293', 'Hypertrophied muscle fibers', 'XPO:0101409', 'abnormal perivitelline space', 0.43333333333333335, 3.6715585125471644, 1.2613519289914445, 'UPHENO:0086172', 'abnormal cell'),
(412448, 'HP:0100293', 'Hypertrophied muscle fibers', 'XPO:0101481', 'abnormal skeletal muscle satellite cell', 0.4444444444444444, 5.968280811662945, 1.6286710071797728, 'UPHENO:0002816', 'abnormal musculature'),
(412449, 'HP:0100293', 'Hypertrophied muscle fibers', 'XPO:0100653', 'abnormal myoblast', 0.4642857142857143, 3.6715585125471644, 1.305623286610558, 'UPHENO:0086172', 'abnormal cell'),
(412450, 'HP:0100293', 'Hypertrophied muscle fibers', 'XPO:0100724', 'abnormal kinetochore', 0.4482758620689655, 3.6715585125471644, 1.2829150624062098, 'UPHENO:0086172', 'abnormal cell'),
(412451, 'HP:0100293', 'Hypertrophied muscle fibers', 'XPO:0101061', 'abnormal plasma membrane', 0.4482758620689655, 3.6715585125471644, 1.2829150624062098, 'UPHENO:0086172', 'abnormal cell'),
(412452, 'HP:0100293', 'Hypertrophied muscle fibers', 'XPO:0100644', 'abnormal smooth muscle myocyte', 0.43243243243243246, 5.968280811662945, 1.6065111854037055, 'UPHENO:0002816', 'abnormal musculature'),
(412453, 'HP:0100293', 'Hypertrophied muscle fibers', 'XPO:0131685', 'abnormal cortical actin cytoskeleton', 0.43333333333333335, 3.6715585125471644, 1.2613519289914445, 'UPHENO:0086172', 'abnormal cell'),
(412454, 'HP:0100293', 'Hypertrophied muscle fibers', 'XPO:0101302', 'abnormal subcortical cytoplasm', 0.41935483870967744, 3.6715585125471644, 1.240840774572773, 'UPHENO:0086172', 'abnormal cell'),
(412455, 'HP:0100293', 'Hypertrophied muscle fibers', 'XPO:0100004', 'abnormal cell', 0.48148148148148145, 3.6715585125471644, 1.3295816755533123, 'UPHENO:0086172', 'abnormal cell'),
(412456, 'HP:0100293', 'Hypertrophied muscle fibers', 'XPO:0101907', 'abnormal skeletal muscle morphology', 0.40476190476190477, 6.895202660022325, 1.6706032929423995, 'HP:0011805', 'Abnormal skeletal muscle morphology'),
(412457, 'HP:0100293', 'Hypertrophied muscle fibers', 'XPO:0101732', 'abnormal muscle morphology', 0.425, 6.895202660022325, 1.7118589692230748, 'HP:0011805', 'Abnormal skeletal muscle morphology'),
(412458, 'HP:0100293', 'Hypertrophied muscle fibers', 'XPO:0101497', 'abnormal ciliary axoneme', 0.41935483870967744, 3.6715585125471644, 1.240840774572773, 'UPHENO:0086172', 'abnormal cell'),
(412459, 'HP:0100293', 'Hypertrophied muscle fibers', 'XPO:0100894', 'abnormal nucleus', 0.4482758620689655, 3.6715585125471644, 1.2829150624062098, 'UPHENO:0086172', 'abnormal cell'),
(412460, 'HP:0100293', 'Hypertrophied muscle fibers', 'XPO:0100638', 'abnormal polar body', 0.4642857142857143, 3.6715585125471644, 1.305623286610558, 'UPHENO:0086172', 'abnormal cell'),
(412461, 'HP:0100293', 'Hypertrophied muscle fibers', 'XPO:0100275', 'abnormal skeletal muscle', 0.4117647058823529, 5.968280811662945, 1.5676502776568768, 'UPHENO:0002816', 'abnormal musculature'),
(412462, 'HP:0100293', 'Hypertrophied muscle fibers', 'XPO:0100172', 'abnormal stem cell', 0.4642857142857143, 3.6715585125471644, 1.305623286610558, 'UPHENO:0086172', 'abnormal cell'),
(412463, 'HP:0100293', 'Hypertrophied muscle fibers', 'XPO:0131675', 'abnormal spindle microtubule', 0.43333333333333335, 3.6715585125471644, 1.2613519289914445, 'UPHENO:0086172', 'abnormal cell'),
(412464, 'HP:0100293', 'Hypertrophied muscle fibers', 'XPO:0100176', 'abnormal stage VI oocyte', 0.43333333333333335, 3.6715585125471644, 1.2613519289914445, 'UPHENO:0086172', 'abnormal cell'),
(412465, 'HP:0100293', 'Hypertrophied muscle fibers', 'XPO:0100307', 'abnormal blastomere', 0.43333333333333335, 3.6715585125471644, 1.2613519289914445, 'UPHENO:0086172', 'abnormal cell'),
(412466, 'HP:0100293', 'Hypertrophied muscle fibers', 'XPO:0139891', 'abnormally necrotic myocyte', 0.40425531914893614, 6.895202660022325, 1.6695575317801774, 'HP:0011805', 'Abnormal skeletal muscle morphology'),
(412467, 'HP:0100293', 'Hypertrophied muscle fibers', 'XPO:0100108', 'abnormal cell part', 0.4642857142857143, 3.6715585125471644, 1.305623286610558, 'UPHENO:0086172', 'abnormal cell'),
(412468, 'HP:0100293', 'Hypertrophied muscle fibers', 'XPO:0101636', 'abnormal cell morphology', 0.4117647058823529, 3.6715585125471644, 1.229560169755361, 'UPHENO:0086172', 'abnormal cell'),
(412469, 'HP:0100293', 'Hypertrophied muscle fibers', 'XPO:0101535', 'abnormal absorptive cell', 0.4642857142857143, 3.6715585125471644, 1.305623286610558, 'UPHENO:0086172', 'abnormal cell'),
(412470, 'HP:0100293', 'Hypertrophied muscle fibers', 'XPO:0101136', 'abnormal ooplasm', 0.41935483870967744, 3.6715585125471644, 1.240840774572773, 'UPHENO:0086172', 'abnormal cell'),
(412471, 'HP:0100293', 'Hypertrophied muscle fibers', 'XPO:0101220', 'abnormal centriole', 0.43333333333333335, 3.6715585125471644, 1.2613519289914445, 'UPHENO:0086172', 'abnormal cell'),
(412472, 'HP:0100293', 'Hypertrophied muscle fibers', 'XPO:0101071', 'abnormal endoplasmic reticulum', 0.4482758620689655, 3.6715585125471644, 1.2829150624062098, 'UPHENO:0086172', 'abnormal cell'),
(412473, 'HP:0100293', 'Hypertrophied muscle fibers', 'XPO:0101373', 'abnormal oxygen accumulating cell', 0.4642857142857143, 3.6715585125471644, 1.305623286610558, 'UPHENO:0086172', 'abnormal cell'),
(412474, 'HP:0100293', 'Hypertrophied muscle fibers', 'XPO:0100626', 'abnormal primordial germ cell', 0.4482758620689655, 3.6715585125471644, 1.2829150624062098, 'UPHENO:0086172', 'abnormal cell'),
(412475, 'HP:0100293', 'Hypertrophied muscle fibers', 'XPO:0100784', 'abnormal left blastomere', 0.41935483870967744, 3.6715585125471644, 1.240840774572773, 'UPHENO:0086172', 'abnormal cell'),
(412476, 'HP:0100293', 'Hypertrophied muscle fibers', 'XPO:0102228', 'abnormal myocyte morphology', 0.4418604651162791, 6.895202660022325, 1.7454848765968924, 'HP:0011805', 'Abnormal skeletal muscle morphology'),
(412477, 'HP:0100293', 'Hypertrophied muscle fibers', 'XPO:0101466', 'abnormal secondary myofiber', 0.45714285714285713, 5.968280811662945, 1.651773877525156, 'UPHENO:0002816', 'abnormal musculature'),
(412478, 'HP:0100293', 'Hypertrophied muscle fibers', 'XPO:0131687', 'abnormal astral microtubule', 0.41935483870967744, 3.6715585125471644, 1.240840774572773, 'UPHENO:0086172', 'abnormal cell'),
(412479, 'HP:0100293', 'Hypertrophied muscle fibers', 'XPO:0100887', 'abnormal right-dorsal blastomere', 0.41935483870967744, 3.6715585125471644, 1.240840774572773, 'UPHENO:0086172', 'abnormal cell'),
(412480, 'HP:0100293', 'Hypertrophied muscle fibers', 'XPO:0100437', 'abnormal proepicardium', 0.4482758620689655, 3.6715585125471644, 1.2829150624062098, 'UPHENO:0086172', 'abnormal cell'),
(412481, 'HP:0100293', 'Hypertrophied muscle fibers', 'XPO:0101283', 'abnormal left-ventral blastomere', 0.41935483870967744, 3.6715585125471644, 1.240840774572773, 'UPHENO:0086172', 'abnormal cell'),
(412482, 'HP:0100293', 'Hypertrophied muscle fibers', 'XPO:0101240', 'abnormal ciliated non-epidermal cell', 0.4482758620689655, 3.6715585125471644, 1.2829150624062098, 'UPHENO:0086172', 'abnormal cell'),
(412483, 'HP:0100293', 'Hypertrophied muscle fibers', 'XPO:0100429', 'abnormal spermatid', 0.4482758620689655, 3.6715585125471644, 1.2829150624062098, 'UPHENO:0086172', 'abnormal cell'),
(412484, 'HP:0100293', 'Hypertrophied muscle fibers', 'XPO:0107284', 'abnormal migrating myoblast', 0.4482758620689655, 3.6715585125471644, 1.2829150624062098, 'UPHENO:0086172', 'abnormal cell'),
(412485, 'HP:0100293', 'Hypertrophied muscle fibers', 'XPO:0101461', 'abnormal sperm entry point', 0.43333333333333335, 3.6715585125471644, 1.2613519289914445, 'UPHENO:0086172', 'abnormal cell'),
(412486, 'HP:0100293', 'Hypertrophied muscle fibers', 'XPO:0100308', 'abnormal early embryonic cell', 0.4482758620689655, 3.6715585125471644, 1.2829150624062098, 'UPHENO:0086172', 'abnormal cell'),
(412487, 'HP:0100293', 'Hypertrophied muscle fibers', 'XPO:0142057', 'abnormal desmosome', 0.4482758620689655, 3.6715585125471644, 1.2829150624062098, 'UPHENO:0086172', 'abnormal cell'),
(412488, 'HP:0100293', 'Hypertrophied muscle fibers', 'XPO:0100551', 'abnormal oocyte cortex', 0.41935483870967744, 3.6715585125471644, 1.240840774572773, 'UPHENO:0086172', 'abnormal cell'),
(412489, 'HP:0100293', 'Hypertrophied muscle fibers', 'XPO:0101228', 'abnormal mesenchymal stem cell', 0.4482758620689655, 3.6715585125471644, 1.2829150624062098, 'UPHENO:0086172', 'abnormal cell'),
(412490, 'HP:0002910', 'Elevated hepatic transaminase', 'XPO:0131694', 'abnormal RNA polymerase II activity', 0.4583333333333333, 4.758907843651163, 1.4768771428276568, 'HP:0001939', 'Abnormality of metabolism/homeostasis'),
(412491, 'HP:0002910', 'Elevated hepatic transaminase', 'XPO:0100289', 'abnormal chondroblast', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(412492, 'HP:0002910', 'Elevated hepatic transaminase', 'XPO:0141877', 'abnormal 2-deoxyribose 1-phosphate metabolic process', 0.4583333333333333, 4.758907843651163, 1.4768771428276568, 'HP:0001939', 'Abnormality of metabolism/homeostasis'),
(412493, 'HP:0002910', 'Elevated hepatic transaminase', 'XPO:0141850', 'abnormal galactose metabolic process', 0.4230769230769231, 4.758907843651163, 1.418937661667548, 'HP:0001939', 'Abnormality of metabolism/homeostasis'),
(412494, 'HP:0002910', 'Elevated hepatic transaminase', 'XPO:0101472', 'abnormal zygote cortex', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(412495, 'HP:0002910', 'Elevated hepatic transaminase', 'XPO:0100549', 'abnormal mitotic cell', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(412496, 'HP:0002910', 'Elevated hepatic transaminase', 'XPO:0141859', 'abnormal lactose catabolic process', 0.4230769230769231, 4.758907843651163, 1.418937661667548, 'HP:0001939', 'Abnormality of metabolism/homeostasis'),
(412497, 'HP:0002910', 'Elevated hepatic transaminase', 'XPO:0141911', 'abnormal ribose phosphate metabolic process', 0.4583333333333333, 4.758907843651163, 1.4768771428276568, 'HP:0001939', 'Abnormality of metabolism/homeostasis'),
(412498, 'HP:0002910', 'Elevated hepatic transaminase', 'XPO:0141265', 'abnormal escape behavior', 0.5, 1.4755025719078136, 0.8589244937443028, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(412499, 'HP:0002910', 'Elevated hepatic transaminase', 'XPO:0100423', 'abnormal process', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(412500, 'HP:0002910', 'Elevated hepatic transaminase', 'XPO:0100010', 'abnormal multicellular anatomical structure', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(412501, 'HP:0002910', 'Elevated hepatic transaminase', 'XPO:0100574', 'abnormal gastrula cell', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(412502, 'HP:0002910', 'Elevated hepatic transaminase', 'XPO:0141796', 'abnormal demethylation', 0.5238095238095238, 4.758907843651163, 1.5788480773767701, 'HP:0001939', 'Abnormality of metabolism/homeostasis'),
(412503, 'HP:0002910', 'Elevated hepatic transaminase', 'XPO:0131723', 'abnormal pathway-restricted SMAD protein phosphorylation', 0.5, 1.4755025719078136, 0.8589244937443028, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(412504, 'HP:0002910', 'Elevated hepatic transaminase', 'XPO:0101297', 'abnormal barrier cell', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(412505, 'HP:0002910', 'Elevated hepatic transaminase', 'XPO:0100232', 'abnormal lymphatic system', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(412506, 'HP:0002910', 'Elevated hepatic transaminase', 'XPO:0131675', 'abnormal spindle microtubule', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(412507, 'HP:0002910', 'Elevated hepatic transaminase', 'XPO:0101071', 'abnormal endoplasmic reticulum', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(412508, 'HP:0002910', 'Elevated hepatic transaminase', 'XPO:0100599', 'abnormal adult immune system', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(412509, 'HP:0002910', 'Elevated hepatic transaminase', 'XPO:0107261', 'abnormal dorsal-ventral axis', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(412510, 'HP:0002910', 'Elevated hepatic transaminase', 'XPO:0101264', 'abnormal mitotic spindle', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(412511, 'HP:0002910', 'Elevated hepatic transaminase', 'XPO:0141881', 'abnormal fructose metabolic process', 0.4230769230769231, 4.758907843651163, 1.418937661667548, 'HP:0001939', 'Abnormality of metabolism/homeostasis'),
(412512, 'HP:0002910', 'Elevated hepatic transaminase', 'XPO:0100337', 'abnormal zygote', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(412513, 'HP:0002910', 'Elevated hepatic transaminase', 'XPO:0141775', 'abnormal nitrogen compound metabolic process', 0.5238095238095238, 4.758907843651163, 1.5788480773767701, 'HP:0001939', 'Abnormality of metabolism/homeostasis'),
(412514, 'HP:0002910', 'Elevated hepatic transaminase', 'XPO:0100894', 'abnormal nucleus', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(412515, 'HP:0002910', 'Elevated hepatic transaminase', 'XPO:0141809', 'abnormal catalytic activity', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(412516, 'HP:0002910', 'Elevated hepatic transaminase', 'XPO:0141743', 'abnormal chemical homeostasis within a tissue', 0.5, 1.4755025719078136, 0.8589244937443028, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(412517, 'HP:0002910', 'Elevated hepatic transaminase', 'XPO:0131685', 'abnormal cortical actin cytoskeleton', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(412518, 'HP:0002910', 'Elevated hepatic transaminase', 'XPO:0115505', 'dead whole organism', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(412519, 'HP:0002910', 'Elevated hepatic transaminase', 'XPO:0101468', 'abnormal stage I oocyte', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(412520, 'HP:0002910', 'Elevated hepatic transaminase', 'XPO:0141872', 'abnormal cholesterol metabolic process', 0.4074074074074074, 4.758907843651163, 1.392413123563799, 'HP:0001939', 'Abnormality of metabolism/homeostasis'),
(412521, 'HP:0002910', 'Elevated hepatic transaminase', 'XPO:0100546', 'abnormal whole organism', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(412522, 'HP:0002910', 'Elevated hepatic transaminase', 'XPO:0131730', 'abnormal regulation of protein folding', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(412523, 'HP:0002910', 'Elevated hepatic transaminase', 'XPO:0100308', 'abnormal early embryonic cell', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(412524, 'HP:0002910', 'Elevated hepatic transaminase', 'XPO:0101141', 'abnormal Keller explant', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(412525, 'HP:0002910', 'Elevated hepatic transaminase', 'XPO:0100653', 'abnormal myoblast', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(412526, 'HP:0002910', 'Elevated hepatic transaminase', 'XPO:0141854', 'abnormal glutathione metabolic process', 0.4230769230769231, 4.758907843651163, 1.418937661667548, 'HP:0001939', 'Abnormality of metabolism/homeostasis'),
(412527, 'HP:0002910', 'Elevated hepatic transaminase', 'XPO:0141778', 'abnormal biosynthetic process', 0.5238095238095238, 4.758907843651163, 1.5788480773767701, 'HP:0001939', 'Abnormality of metabolism/homeostasis'),
(412528, 'HP:0002910', 'Elevated hepatic transaminase', 'XPO:0141884', 'abnormal phosphagen metabolic process', 0.4230769230769231, 4.758907843651163, 1.418937661667548, 'HP:0001939', 'Abnormality of metabolism/homeostasis'),
(412529, 'HP:0002910', 'Elevated hepatic transaminase', 'XPO:0100392', 'abnormal cilium', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(412530, 'HP:0002910', 'Elevated hepatic transaminase', 'XPO:0101326', 'abnormal cementoblast', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(412531, 'HP:0002910', 'Elevated hepatic transaminase', 'XPO:0133403', 'abnormal developmental process', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(412532, 'HP:0002910', 'Elevated hepatic transaminase', 'XPO:0100084', 'abnormal anatomical group', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(412533, 'HP:0002910', 'Elevated hepatic transaminase', 'XPO:0100917', 'abnormal stage III oocyte', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(412534, 'HP:0002910', 'Elevated hepatic transaminase', 'XPO:0131677', 'abnormal actin filament', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(412535, 'HP:0002910', 'Elevated hepatic transaminase', 'XPO:0128000', 'absent behavior', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(412536, 'HP:0002910', 'Elevated hepatic transaminase', 'XPO:0101547', 'abnormal lampbrush chromosome', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(412537, 'HP:0002910', 'Elevated hepatic transaminase', 'XPO:0101004', 'abnormal acid secreting cell', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(412538, 'HP:0002910', 'Elevated hepatic transaminase', 'XPO:0100031', 'abnormal central nervous system', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(412539, 'HP:0002910', 'Elevated hepatic transaminase', 'XPO:0107259', 'abnormal animal-vegetal axis', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(412540, 'HP:0002910', 'Elevated hepatic transaminase', 'XPO:0101132', 'abnormal apoptotic cell', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(412541, 'HP:0002910', 'Elevated hepatic transaminase', 'XPO:0107260', 'abnormal anterior-posterior axis', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(412542, 'HP:0002910', 'Elevated hepatic transaminase', 'XPO:0141767', 'abnormal temperature homeostasis', 0.44, 4.758907843651163, 1.447038165082909, 'HP:0001939', 'Abnormality of metabolism/homeostasis'),
(412543, 'HP:0002910', 'Elevated hepatic transaminase', 'XPO:0101221', 'abnormal larval immune system', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(412544, 'HP:0002910', 'Elevated hepatic transaminase', 'XPO:0100176', 'abnormal stage VI oocyte', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(412545, 'HP:0002910', 'Elevated hepatic transaminase', 'XPO:0101333', 'abnormal barrier epithelial cell', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(412546, 'HP:0002910', 'Elevated hepatic transaminase', 'XPO:0100899', 'abnormal secondary spermatogonium', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(412547, 'HP:0002910', 'Elevated hepatic transaminase', 'XPO:0100006', 'abnormal anatomical structure', 0.47058823529411764, 1.4755025719078136, 0.8332791557971614, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(412548, 'HP:0002910', 'Elevated hepatic transaminase', 'XPO:0141910', 'abnormal D-ribose metabolic process', 0.4230769230769231, 4.758907843651163, 1.418937661667548, 'HP:0001939', 'Abnormality of metabolism/homeostasis'),
(412549, 'HP:0002910', 'Elevated hepatic transaminase', 'XPO:0141908', 'abnormal pyridine metabolic process', 0.4230769230769231, 4.758907843651163, 1.418937661667548, 'HP:0001939', 'Abnormality of metabolism/homeostasis'),
(412550, 'HP:0002910', 'Elevated hepatic transaminase', 'XPO:0107253', 'abnormal enteric nervous system', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(412551, 'HP:0002910', 'Elevated hepatic transaminase', 'XPO:0100344', 'abnormal portion of organism substance', 0.47058823529411764, 1.4755025719078136, 0.8332791557971614, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(412552, 'HP:0002910', 'Elevated hepatic transaminase', 'XPO:0141263', 'abnormal visually guided collision avoidance behavior', 0.5, 1.4755025719078136, 0.8589244937443028, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(412553, 'HP:0002910', 'Elevated hepatic transaminase', 'XPO:0100626', 'abnormal primordial germ cell', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(412554, 'HP:0002910', 'Elevated hepatic transaminase', 'XPO:0141852', 'abnormal glucose metabolic process', 0.4230769230769231, 4.758907843651163, 1.418937661667548, 'HP:0001939', 'Abnormality of metabolism/homeostasis'),
(412555, 'HP:0002910', 'Elevated hepatic transaminase', 'XPO:0141754', 'abnormal homeostatic process', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(412556, 'HP:0002910', 'Elevated hepatic transaminase', 'XPO:0100585', 'abnormal elastica externa', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(412557, 'HP:0002910', 'Elevated hepatic transaminase', 'XPO:0131691', 'abnormal molecular function', 0.47058823529411764, 1.4755025719078136, 0.8332791557971614, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(412558, 'HP:0002910', 'Elevated hepatic transaminase', 'XPO:0116434', 'abnormal biological process', 0.47058823529411764, 1.4755025719078136, 0.8332791557971614, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(412559, 'HP:0002910', 'Elevated hepatic transaminase', 'XPO:0100285', 'abnormal progenitor cell', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(412560, 'HP:0002910', 'Elevated hepatic transaminase', 'XPO:0141883', 'abnormal glycerol metabolic process', 0.4230769230769231, 4.758907843651163, 1.418937661667548, 'HP:0001939', 'Abnormality of metabolism/homeostasis'),
(412561, 'HP:0002910', 'Elevated hepatic transaminase', 'XPO:0141864', 'abnormal 5-methylcytosine metabolic process', 0.4230769230769231, 4.758907843651163, 1.418937661667548, 'HP:0001939', 'Abnormality of metabolism/homeostasis'),
(412562, 'HP:0002910', 'Elevated hepatic transaminase', 'XPO:0107284', 'abnormal migrating myoblast', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(412563, 'HP:0002910', 'Elevated hepatic transaminase', 'XPO:0101366', 'abnormal morula cell', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(412564, 'HP:0002910', 'Elevated hepatic transaminase', 'XPO:0100715', 'abnormal ciliated cell', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(412565, 'HP:0002910', 'Elevated hepatic transaminase', 'XPO:0141789', 'abnormal hormone catabolic process', 0.44, 4.758907843651163, 1.447038165082909, 'HP:0001939', 'Abnormality of metabolism/homeostasis'),
(412566, 'HP:0002910', 'Elevated hepatic transaminase', 'XPO:0101535', 'abnormal absorptive cell', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(412567, 'HP:0002910', 'Elevated hepatic transaminase', 'XPO:0141787', 'abnormal hormone metabolic process', 0.5238095238095238, 4.758907843651163, 1.5788480773767701, 'HP:0001939', 'Abnormality of metabolism/homeostasis'),
(412568, 'HP:0002910', 'Elevated hepatic transaminase', 'XPO:0115512', 'abnormally semi-erect whole organism', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(412569, 'HP:0002910', 'Elevated hepatic transaminase', 'XPO:0100062', 'abnormal anatomical space', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(412570, 'HP:0002910', 'Elevated hepatic transaminase', 'XPO:0100004', 'abnormal cell', 0.47619047619047616, 1.8210412618256888, 0.9312156064152277, 'HP:0000118', 'Phenotypic abnormality'),
(412571, 'HP:0002910', 'Elevated hepatic transaminase', 'XPO:0100802', 'abnormal exocrine cell', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(412572, 'HP:0002910', 'Elevated hepatic transaminase', 'XPO:0100317', 'abnormal respiratory system', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(412573, 'HP:0002910', 'Elevated hepatic transaminase', 'XPO:0100728', 'abnormal cell condensation', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(412574, 'HP:0002910', 'Elevated hepatic transaminase', 'XPO:0141772', 'abnormal water homeostasis', 0.5, 1.4755025719078136, 0.8589244937443028, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(412575, 'HP:0002910', 'Elevated hepatic transaminase', 'XPO:0141904', 'abnormal glucosamine metabolic process', 0.5238095238095238, 4.758907843651163, 1.5788480773767701, 'HP:0001939', 'Abnormality of metabolism/homeostasis'),
(412576, 'HP:0002910', 'Elevated hepatic transaminase', 'XPO:0100239', 'abnormal acellular anatomical structure', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(412577, 'HP:0002910', 'Elevated hepatic transaminase', 'XPO:0100081', 'abnormal anatomical entity in vitro', 0.47058823529411764, 1.4755025719078136, 0.8332791557971614, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(412578, 'HP:0002910', 'Elevated hepatic transaminase', 'XPO:0101513', 'abnormal basal body', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(412579, 'HP:0002910', 'Elevated hepatic transaminase', 'XPO:00000000', 'Xenopus phenotype', 0.5333333333333333, 1.4755025719078136, 0.8870934026456857, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(412580, 'HP:0002910', 'Elevated hepatic transaminase', 'XPO:0141798', 'abnormal lipid metabolic process', 0.4782608695652174, 4.758907843651163, 1.508641575552437, 'HP:0001939', 'Abnormality of metabolism/homeostasis'),
(412581, 'HP:0002910', 'Elevated hepatic transaminase', 'XPO:0100108', 'abnormal cell part', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(412582, 'HP:0002910', 'Elevated hepatic transaminase', 'XPO:0100545', 'abnormal male organism', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(412583, 'HP:0002910', 'Elevated hepatic transaminase', 'XPO:0100307', 'abnormal blastomere', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(412584, 'HP:0002910', 'Elevated hepatic transaminase', 'XPO:0131667', 'abnormal actin cytoskeleton', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(412585, 'HP:0002910', 'Elevated hepatic transaminase', 'XPO:0100724', 'abnormal kinetochore', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(412586, 'HP:0002910', 'Elevated hepatic transaminase', 'XPO:0100573', 'abnormal extraembryonic structure', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(412587, 'HP:0002910', 'Elevated hepatic transaminase', 'XPO:0100202', 'abnormal embryo', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(412588, 'HP:0002910', 'Elevated hepatic transaminase', 'XPO:0101241', 'abnormal nucleate erythrocyte', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(412589, 'HP:0002910', 'Elevated hepatic transaminase', 'XPO:0141795', 'abnormal glycosylation', 0.4782608695652174, 4.758907843651163, 1.508641575552437, 'HP:0001939', 'Abnormality of metabolism/homeostasis'),
(412590, 'HP:0002910', 'Elevated hepatic transaminase', 'XPO:0115508', 'abnormally peramorphic growth of whole organism', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(412591, 'HP:0002910', 'Elevated hepatic transaminase', 'XPO:0141860', 'abnormal malate-aspartate shuttle', 0.5, 4.758907843651163, 1.5425478669479211, 'HP:0001939', 'Abnormality of metabolism/homeostasis'),
(412592, 'HP:0002910', 'Elevated hepatic transaminase', 'XPO:0101113', 'abnormal stage IV oocyte', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(412593, 'HP:0002910', 'Elevated hepatic transaminase', 'XPO:0100852', 'abnormal interdigital region', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(412594, 'HP:0002910', 'Elevated hepatic transaminase', 'XPO:0101480', 'abnormal stage V oocyte', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(412595, 'HP:0002910', 'Elevated hepatic transaminase', 'XPO:0101373', 'abnormal oxygen accumulating cell', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(412596, 'HP:0002910', 'Elevated hepatic transaminase', 'XPO:0101498', 'abnormal stage II oocyte', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(412597, 'HP:0002910', 'Elevated hepatic transaminase', 'XPO:0100515', 'abnormal somatic stem cell', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(412598, 'HP:0002910', 'Elevated hepatic transaminase', 'XPO:0141264', 'abnormal schooling behavior', 0.5, 1.4755025719078136, 0.8589244937443028, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(412599, 'HP:0002910', 'Elevated hepatic transaminase', 'XPO:0101467', 'abnormal alkali secreting cell', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(412600, 'HP:0002910', 'Elevated hepatic transaminase', 'XPO:0107262', 'abnormal left-right axis', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(412601, 'HP:0002910', 'Elevated hepatic transaminase', 'XPO:0101240', 'abnormal ciliated non-epidermal cell', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(412602, 'HP:0002910', 'Elevated hepatic transaminase', 'XPO:0141786', 'abnormal pigment metabolic process', 0.5238095238095238, 4.758907843651163, 1.5788480773767701, 'HP:0001939', 'Abnormality of metabolism/homeostasis'),
(412603, 'HP:0002910', 'Elevated hepatic transaminase', 'XPO:0141748', 'abnormal gas homeostasis', 0.5, 1.4755025719078136, 0.8589244937443028, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(412604, 'HP:0002910', 'Elevated hepatic transaminase', 'XPO:0141794', 'abnormal prosthetic group metabolic process', 0.5238095238095238, 4.758907843651163, 1.5788480773767701, 'HP:0001939', 'Abnormality of metabolism/homeostasis'),
(412605, 'HP:0002910', 'Elevated hepatic transaminase', 'XPO:0141791', 'abnormal primary metabolic process', 0.5238095238095238, 4.758907843651163, 1.5788480773767701, 'HP:0001939', 'Abnormality of metabolism/homeostasis'),
(412606, 'HP:0002910', 'Elevated hepatic transaminase', 'XPO:0100888', 'abnormal microtubule', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(412607, 'HP:0002910', 'Elevated hepatic transaminase', 'XPO:0141900', 'abnormal mannose metabolic process', 0.4230769230769231, 4.758907843651163, 1.418937661667548, 'HP:0001939', 'Abnormality of metabolism/homeostasis'),
(412608, 'HP:0002910', 'Elevated hepatic transaminase', 'XPO:0100501', 'abnormal urogenital system', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(412609, 'HP:0002910', 'Elevated hepatic transaminase', 'XPO:0133388', 'absent insulin receptor signaling pathway', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(412610, 'HP:0002910', 'Elevated hepatic transaminase', 'XPO:0141797', 'abnormal hydrogen metabolic process', 0.5238095238095238, 4.758907843651163, 1.5788480773767701, 'HP:0001939', 'Abnormality of metabolism/homeostasis'),
(412611, 'HP:0002910', 'Elevated hepatic transaminase', 'XPO:0100674', 'abnormal secondary oogonium', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(412612, 'HP:0002910', 'Elevated hepatic transaminase', 'XPO:0141499', 'abnormal tadpole', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(412613, 'HP:0002910', 'Elevated hepatic transaminase', 'XPO:0141782', 'abnormal methylation', 0.5238095238095238, 4.758907843651163, 1.5788480773767701, 'HP:0001939', 'Abnormality of metabolism/homeostasis'),
(412614, 'HP:0002910', 'Elevated hepatic transaminase', 'XPO:0131666', 'abnormal adherens junction', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(412615, 'HP:0002910', 'Elevated hepatic transaminase', 'XPO:0101220', 'abnormal centriole', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(412616, 'HP:0002910', 'Elevated hepatic transaminase', 'XPO:0107258', 'abnormal anatomical axis', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(412617, 'HP:0002910', 'Elevated hepatic transaminase', 'XPO:0101110', 'abnormal cell-free extract', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(412618, 'HP:0002910', 'Elevated hepatic transaminase', 'XPO:0100032', 'abnormal nervous system', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(412619, 'HP:0002910', 'Elevated hepatic transaminase', 'XPO:0131469', 'abnormal heart process', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(412620, 'HP:0002910', 'Elevated hepatic transaminase', 'XPO:0116494', 'absent biological process', 0.47058823529411764, 1.4755025719078136, 0.8332791557971614, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(412621, 'HP:0002910', 'Elevated hepatic transaminase', 'XPO:0100791', 'abnormal multiciliated cell precursor', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(412622, 'HP:0002910', 'Elevated hepatic transaminase', 'XPO:0141866', 'abnormal dicarboxylic acid metabolic process', 0.4074074074074074, 4.758907843651163, 1.392413123563799, 'HP:0001939', 'Abnormality of metabolism/homeostasis'),
(412623, 'HP:0002910', 'Elevated hepatic transaminase', 'XPO:0107270', 'abnormal proximal-distal axis', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(412624, 'HP:0002910', 'Elevated hepatic transaminase', 'XPO:0100386', 'abnormal limb', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(412625, 'HP:0002910', 'Elevated hepatic transaminase', 'XPO:0141898', 'abnormal maltose metabolic process', 0.4583333333333333, 4.758907843651163, 1.4768771428276568, 'HP:0001939', 'Abnormality of metabolism/homeostasis'),
(412626, 'HP:0002910', 'Elevated hepatic transaminase', 'XPO:0141788', 'abnormal hormone biosynthetic process', 0.44, 4.758907843651163, 1.447038165082909, 'HP:0001939', 'Abnormality of metabolism/homeostasis'),
(412627, 'HP:0002910', 'Elevated hepatic transaminase', 'XPO:0100969', 'abnormal disaggregated/reaggregated ectoderm treated with activin', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(412628, 'HP:0002910', 'Elevated hepatic transaminase', 'XPO:0141266', 'abnormal surface breathing', 0.5, 1.4755025719078136, 0.8589244937443028, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(412629, 'HP:0002910', 'Elevated hepatic transaminase', 'XPO:0141776', 'abnormal metabolic process', 0.5789473684210527, 4.758907843651163, 1.6598666129060333, 'HP:0001939', 'Abnormality of metabolism/homeostasis'),
(412630, 'HP:0002910', 'Elevated hepatic transaminase', 'XPO:0100377', 'abnormal connective tissue', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(412631, 'HP:0002910', 'Elevated hepatic transaminase', 'XPO:0100429', 'abnormal spermatid', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(412632, 'HP:0002910', 'Elevated hepatic transaminase', 'XPO:0101409', 'abnormal perivitelline space', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(412633, 'HP:0002910', 'Elevated hepatic transaminase', 'XPO:0100638', 'abnormal polar body', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(412634, 'HP:0002910', 'Elevated hepatic transaminase', 'XPO:0101109', 'abnormal egg cell-free extract', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(412635, 'HP:0002910', 'Elevated hepatic transaminase', 'XPO:0101237', 'abnormal mucus secreting cell', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(412636, 'HP:0002910', 'Elevated hepatic transaminase', 'XPO:0115509', 'abnormally semi-viable whole organism', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(412637, 'HP:0002910', 'Elevated hepatic transaminase', 'XPO:0100704', 'abnormal Merkel cell', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(412638, 'HP:0002910', 'Elevated hepatic transaminase', 'XPO:0141907', 'abnormal putrescine metabolic process', 0.4782608695652174, 4.758907843651163, 1.508641575552437, 'HP:0001939', 'Abnormality of metabolism/homeostasis'),
(412639, 'HP:0002910', 'Elevated hepatic transaminase', 'XPO:0100754', 'abnormal electrically active cell', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(412640, 'HP:0002910', 'Elevated hepatic transaminase', 'XPO:0100026', 'abnormal germ cell', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(412641, 'HP:0002910', 'Elevated hepatic transaminase', 'XPO:0100437', 'abnormal proepicardium', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(412642, 'HP:0002910', 'Elevated hepatic transaminase', 'XPO:0141271', 'increased surface breathing', 0.47058823529411764, 1.4755025719078136, 0.8332791557971614, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(412643, 'HP:0002910', 'Elevated hepatic transaminase', 'XPO:0141267', 'abnormal resting posture', 0.5, 1.4755025719078136, 0.8589244937443028, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(412644, 'HP:0002910', 'Elevated hepatic transaminase', 'XPO:0141276', 'decreased surface breathing', 0.47058823529411764, 1.4755025719078136, 0.8332791557971614, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(412645, 'HP:0002910', 'Elevated hepatic transaminase', 'XPO:0100976', 'abnormal multiciliated cell', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(412646, 'HP:0002910', 'Elevated hepatic transaminase', 'XPO:0101569', 'abnormal activin-induced ectoderm', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(412647, 'HP:0002910', 'Elevated hepatic transaminase', 'XPO:0101061', 'abnormal plasma membrane', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(412648, 'HP:0002910', 'Elevated hepatic transaminase', 'XPO:0101461', 'abnormal sperm entry point', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(412649, 'HP:0002910', 'Elevated hepatic transaminase', 'XPO:0100477', 'abnormal pericyte', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(412650, 'HP:0002910', 'Elevated hepatic transaminase', 'XPO:0141777', 'abnormal catabolic process', 0.5238095238095238, 4.758907843651163, 1.5788480773767701, 'HP:0001939', 'Abnormality of metabolism/homeostasis'),
(412651, 'HP:0002910', 'Elevated hepatic transaminase', 'XPO:0131745', 'abnormal axis elongation', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(412652, 'HP:0002910', 'Elevated hepatic transaminase', 'XPO:0141781', 'abnormal secondary metabolic process', 0.5238095238095238, 4.758907843651163, 1.5788480773767701, 'HP:0001939', 'Abnormality of metabolism/homeostasis'),
(412653, 'HP:0002910', 'Elevated hepatic transaminase', 'XPO:0100225', 'abnormal endocrine system', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(412654, 'HP:0002910', 'Elevated hepatic transaminase', 'XPO:0141880', 'abnormal ethanolamine metabolic process', 0.44, 4.758907843651163, 1.447038165082909, 'HP:0001939', 'Abnormality of metabolism/homeostasis'),
(412655, 'HP:0002910', 'Elevated hepatic transaminase', 'XPO:0101157', 'abnormal female organism', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(412656, 'HP:0002910', 'Elevated hepatic transaminase', 'XPO:0141892', 'abnormal inositol metabolic process', 0.4782608695652174, 4.758907843651163, 1.508641575552437, 'HP:0001939', 'Abnormality of metabolism/homeostasis'),
(412657, 'HP:0002910', 'Elevated hepatic transaminase', 'XPO:0100372', 'abnormal hematological system', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(412658, 'HP:0002910', 'Elevated hepatic transaminase', 'XPO:0141784', 'abnormal cellular hormone metabolic process', 0.5, 1.4755025719078136, 0.8589244937443028, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(412659, 'HP:0002910', 'Elevated hepatic transaminase', 'XPO:0100581', 'abnormal immune system', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(412660, 'HP:0002910', 'Elevated hepatic transaminase', 'XPO:0131725', 'abnormal phosphorylation of RNA polymerase II C-terminal domain', 0.5, 1.4755025719078136, 0.8589244937443028, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(412661, 'HP:0002910', 'Elevated hepatic transaminase', 'XPO:0100691', 'abnormal keratin accumulating cell', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(412662, 'HP:0002910', 'Elevated hepatic transaminase', 'XPO:0141903', 'abnormal inositol phosphate metabolic process', 0.4230769230769231, 4.758907843651163, 1.418937661667548, 'HP:0001939', 'Abnormality of metabolism/homeostasis'),
(412663, 'HP:0002910', 'Elevated hepatic transaminase', 'XPO:0100025', 'abnormal oocyte', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(412664, 'HP:0002910', 'Elevated hepatic transaminase', 'XPO:0100902', 'abnormal spermatocyte', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(412665, 'HP:0002910', 'Elevated hepatic transaminase', 'XPO:0101435', 'abnormal paracrine cell', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(412666, 'HP:0002910', 'Elevated hepatic transaminase', 'XPO:0141600', 'absent metamorphosis', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(412667, 'HP:0002910', 'Elevated hepatic transaminase', 'XPO:0100956', 'abnormal centrosome', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(412668, 'HP:0002910', 'Elevated hepatic transaminase', 'XPO:0107312', 'abnormal filopodium', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(412669, 'HP:0002910', 'Elevated hepatic transaminase', 'XPO:0141315', 'abnormal anatomical region', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(412670, 'HP:0002910', 'Elevated hepatic transaminase', 'XPO:0101228', 'abnormal mesenchymal stem cell', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(412671, 'HP:0002910', 'Elevated hepatic transaminase', 'XPO:0100481', 'abnormal anatomical line', 0.47058823529411764, 1.4755025719078136, 0.8332791557971614, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(412672, 'HP:0002910', 'Elevated hepatic transaminase', 'XPO:0100172', 'abnormal stem cell', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(412673, 'HP:0002910', 'Elevated hepatic transaminase', 'XPO:0141272', 'absent surface breathing', 0.5, 1.4755025719078136, 0.8589244937443028, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(412674, 'HP:0002910', 'Elevated hepatic transaminase', 'XPO:0100533', 'abnormal melanoblast', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(412675, 'HP:0002910', 'Elevated hepatic transaminase', 'XPO:0141783', 'abnormal collagen metabolic process', 0.5238095238095238, 4.758907843651163, 1.5788480773767701, 'HP:0001939', 'Abnormality of metabolism/homeostasis'),
(412676, 'HP:0002910', 'Elevated hepatic transaminase', 'XPO:0100721', 'abnormal centromere', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(412677, 'HP:0002910', 'Elevated hepatic transaminase', 'XPO:0100258', 'abnormal organ part', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(412678, 'HP:0002910', 'Elevated hepatic transaminase', 'XPO:0141792', 'abnormal small molecule metabolic process', 0.5238095238095238, 4.758907843651163, 1.5788480773767701, 'HP:0001939', 'Abnormality of metabolism/homeostasis'),
(412679, 'HP:0002910', 'Elevated hepatic transaminase', 'XPO:0100274', 'abnormal sensory system', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(412680, 'HP:0002910', 'Elevated hepatic transaminase', 'XPO:0141771', 'abnormal urea homeostasis', 0.5, 1.4755025719078136, 0.8589244937443028, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(412681, 'HP:0002910', 'Elevated hepatic transaminase', 'XPO:0141738', 'abnormal carbon dioxide homeostasis', 0.5, 1.4755025719078136, 0.8589244937443028, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(412682, 'HP:0002910', 'Elevated hepatic transaminase', 'XPO:0101448', 'abnormal myelin accumulating cell', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(412683, 'HP:0002910', 'Elevated hepatic transaminase', 'XPO:0142057', 'abnormal desmosome', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(412684, 'HP:0002910', 'Elevated hepatic transaminase', 'XPO:0141790', 'abnormal cellular metabolic process', 0.5, 4.758907843651163, 1.5425478669479211, 'HP:0001939', 'Abnormality of metabolism/homeostasis'),
(412685, 'HP:0002910', 'Elevated hepatic transaminase', 'XPO:0131729', 'abnormal regulation of growth rate', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(412686, 'HP:0002910', 'Elevated hepatic transaminase', 'XPO:0141770', 'abnormal urate homeostasis', 0.5, 1.4755025719078136, 0.8589244937443028, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(412687, 'HP:0002910', 'Elevated hepatic transaminase', 'XPO:0141745', 'abnormal creatinine homeostasis', 0.5, 1.4755025719078136, 0.8589244937443028, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(412688, 'HP:0002910', 'Elevated hepatic transaminase', 'XPO:0100907', 'abnormal cytoplasm', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(412689, 'HP:0002828', 'Multiple joint contractures', 'XPO:0102728', 'abnormal tendon morphology', 0.423728813559322, 10.802658907487096, 2.1394854152705856, 'UPHENO:0021425', 'abnormal tendon morphology'),
(412690, 'HP:0002828', 'Multiple joint contractures', 'XPO:0128132', 'decreased size of the perichondrium', 0.4032258064516129, 6.985637650836012, 1.67832934054586, 'UPHENO:0002712', 'abnormal connective tissue'),
(412691, 'HP:0002828', 'Multiple joint contractures', 'XPO:0128816', 'decreased size of the tendon', 0.4307692307692308, 10.802658907487096, 2.15718637763189, 'UPHENO:0021425', 'abnormal tendon morphology'),
(412692, 'HP:0011684', 'Non-restrictive ventricular septal defect', 'XPO:0100837', 'abnormal atrioventricular canal', 0.4166666666666667, 10.504690711543915, 2.092117220220535, 'HP:0001671', 'Abnormal cardiac septum morphology'),
(412693, 'HP:0011684', 'Non-restrictive ventricular septal defect', 'XPO:0102877', 'abnormal ventricular outflow tract morphology', 0.41935483870967744, 9.40147820888365, 1.9855869101902717, 'UPHENO:0086866', 'abnormal cardiac ventricle morphology'),
(412694, 'HP:0011684', 'Non-restrictive ventricular septal defect', 'XPO:0102368', 'abnormal cardiac ventricle morphology', 0.41935483870967744, 9.40147820888365, 1.9855869101902717, 'UPHENO:0086866', 'abnormal cardiac ventricle morphology'),
(412695, 'HP:0011684', 'Non-restrictive ventricular septal defect', 'XPO:0141003', 'abnormally necrotic spiral septum', 0.4084507042253521, 10.504690711543915, 2.0713880174413553, 'UPHENO:0019888', 'abnormal cardiac septum morphology'),
(412696, 'HP:0011684', 'Non-restrictive ventricular septal defect', 'XPO:0103032', 'abnormal spiral septum morphology', 0.4461538461538462, 10.504690711543915, 2.1648806349570178, 'UPHENO:0019888', 'abnormal cardiac septum morphology'),
(412697, 'HP:0009293', 'Broad middle phalanx of the 4th finger', 'XPO:0103755', 'increased size of the forelimb digit', 0.4098360655737705, 7.492661022682715, 1.7523591852740201, 'HP:0001167', 'Abnormal finger morphology'),
(412698, 'HP:0009293', 'Broad middle phalanx of the 4th finger', 'XPO:0103609', 'abnormally increased number of forelimb digit in the regenerating forelimb', 0.4253731343283582, 7.774297771301195, 1.8185096673321148, 'HP:0005918', 'Abnormal finger phalanx morphology'),
(412699, 'HP:0009293', 'Broad middle phalanx of the 4th finger', 'XPO:0102746', 'abnormal forelimb digit 2 morphology', 0.4017094017094017, 7.492661022682715, 1.734898376457027, 'HP:0001167', 'Abnormal finger morphology'),
(412700, 'HP:0009293', 'Broad middle phalanx of the 4th finger', 'XPO:0102598', 'abnormal forelimb digit 3 morphology', 0.4017094017094017, 7.492661022682715, 1.734898376457027, 'HP:0001167', 'Abnormal finger morphology'),
(412701, 'HP:0009293', 'Broad middle phalanx of the 4th finger', 'XPO:0103634', 'abnormally increased number of forelimb digit', 0.4453125, 7.774297771301195, 1.8606428932717216, 'HP:0005918', 'Abnormal finger phalanx morphology'),
(412702, 'HP:0009293', 'Broad middle phalanx of the 4th finger', 'XPO:0115787', 'duplicated forelimb digit 3 in regenerating forelimb', 0.41007194244604317, 7.774297771301195, 1.7855031190763642, 'HP:0005918', 'Abnormal finger phalanx morphology'),
(412703, 'HP:0009293', 'Broad middle phalanx of the 4th finger', 'XPO:0115786', 'duplicated forelimb digit 2 in regenerating forelimb', 0.41007194244604317, 7.774297771301195, 1.7855031190763642, 'HP:0005918', 'Abnormal finger phalanx morphology'),
(412704, 'HP:0009293', 'Broad middle phalanx of the 4th finger', 'XPO:0115788', 'duplicated forelimb digit 4 in regenerating forelimb', 0.41007194244604317, 7.774297771301195, 1.7855031190763642, 'HP:0005918', 'Abnormal finger phalanx morphology'),
(412705, 'HP:0009293', 'Broad middle phalanx of the 4th finger', 'XPO:0102214', 'abnormal forelimb digit morphology', 0.40869565217391307, 7.492661022682715, 1.7499194219115835, 'HP:0001167', 'Abnormal finger morphology'),
(412706, 'HP:0009293', 'Broad middle phalanx of the 4th finger', 'XPO:0102529', 'abnormal forelimb digit 4 morphology', 0.4017094017094017, 7.492661022682715, 1.734898376457027, 'HP:0001167', 'Abnormal finger morphology'),
(412707, 'HP:0009293', 'Broad middle phalanx of the 4th finger', 'XPO:0115789', 'duplicated forelimb digit 5 in regenerating forelimb', 0.41007194244604317, 7.774297771301195, 1.7855031190763642, 'HP:0005918', 'Abnormal finger phalanx morphology'),
(412708, 'HP:0009293', 'Broad middle phalanx of the 4th finger', 'XPO:0102787', 'abnormal forelimb digit 5 morphology', 0.4017094017094017, 7.492661022682715, 1.734898376457027, 'HP:0001167', 'Abnormal finger morphology'),
(412709, 'HP:0500106', 'Isolated systolic hypertension', 'XPO:0100324', 'abnormal intersomitic vessel', 0.41025641025641024, 5.809304221129108, 1.5437954190396599, 'UPHENO:0002678', 'abnormal vasculature'),
(412710, 'HP:0500106', 'Isolated systolic hypertension', 'XPO:0100980', 'abnormal dorsal longitudinal anastomosing vessel - left branch', 0.42105263157894735, 5.809304221129108, 1.5639766078650594, 'UPHENO:0002678', 'abnormal vasculature'),
(412711, 'HP:0500106', 'Isolated systolic hypertension', 'XPO:0100987', 'abnormal larval aorta', 0.42105263157894735, 5.809304221129108, 1.5639766078650594, 'UPHENO:0002678', 'abnormal vasculature'),
(412712, 'HP:0500106', 'Isolated systolic hypertension', 'XPO:0100789', 'abnormal occipitovertebral artery', 0.42105263157894735, 5.809304221129108, 1.5639766078650594, 'UPHENO:0002678', 'abnormal vasculature'),
(412713, 'HP:0500106', 'Isolated systolic hypertension', 'XPO:0101585', 'abnormal dorsal longitudinal anastomosing vessel - right branch', 0.42105263157894735, 5.809304221129108, 1.5639766078650594, 'UPHENO:0002678', 'abnormal vasculature'),
(412714, 'HP:0500106', 'Isolated systolic hypertension', 'XPO:0100372', 'abnormal hematological system', 0.40625, 5.574066539846944, 1.5048137864243607, 'HP:0001871', 'Abnormality of blood and blood-forming tissues'),
(412715, 'HP:0500106', 'Isolated systolic hypertension', 'XPO:0100142', 'abnormal paired dorsal aorta', 0.41025641025641024, 5.809304221129108, 1.5437954190396599, 'UPHENO:0002678', 'abnormal vasculature'),
(412716, 'HP:0500106', 'Isolated systolic hypertension', 'XPO:0101243', 'abnormal vertebral artery', 0.42105263157894735, 5.809304221129108, 1.5639766078650594, 'UPHENO:0002678', 'abnormal vasculature'),
(412717, 'HP:0500106', 'Isolated systolic hypertension', 'XPO:0100080', 'abnormal aorta', 0.42105263157894735, 5.809304221129108, 1.5639766078650594, 'UPHENO:0002678', 'abnormal vasculature'),
(412718, 'HP:0500106', 'Isolated systolic hypertension', 'XPO:0100137', 'abnormal cardinal vein', 0.42105263157894735, 5.809304221129108, 1.5639766078650594, 'UPHENO:0002678', 'abnormal vasculature'),
(412719, 'HP:0500106', 'Isolated systolic hypertension', 'XPO:0100981', 'abnormal dorsal longitudinal anastomosing vessel', 0.43243243243243246, 5.809304221129108, 1.5849705218340364, 'UPHENO:0002678', 'abnormal vasculature'),
(412720, 'HP:0500106', 'Isolated systolic hypertension', 'XPO:0100522', 'abnormal subinterstitial vein', 0.42105263157894735, 5.809304221129108, 1.5639766078650594, 'UPHENO:0002678', 'abnormal vasculature'),
(412721, 'HP:0500106', 'Isolated systolic hypertension', 'XPO:0101206', 'abnormal ischiadic vein', 0.42105263157894735, 5.809304221129108, 1.5639766078650594, 'UPHENO:0002678', 'abnormal vasculature'),
(412722, 'HP:0500106', 'Isolated systolic hypertension', 'XPO:0100043', 'abnormal vein', 0.43243243243243246, 5.809304221129108, 1.5849705218340364, 'UPHENO:0002678', 'abnormal vasculature'),
(412723, 'HP:0500106', 'Isolated systolic hypertension', 'XPO:0100933', 'abnormal branchial vein', 0.42105263157894735, 5.809304221129108, 1.5639766078650594, 'UPHENO:0002678', 'abnormal vasculature'),
(412724, 'HP:0500106', 'Isolated systolic hypertension', 'XPO:0101557', 'abnormal Jacobsons vein', 0.42105263157894735, 5.809304221129108, 1.5639766078650594, 'UPHENO:0002678', 'abnormal vasculature'),
(412725, 'HP:0500106', 'Isolated systolic hypertension', 'XPO:0100076', 'abnormal artery', 0.43243243243243246, 5.809304221129108, 1.5849705218340364, 'UPHENO:0002678', 'abnormal vasculature'),
(412726, 'HP:0500106', 'Isolated systolic hypertension', 'XPO:0101524', 'abnormal ventral blood island border', 0.42857142857142855, 5.809304221129108, 1.5778788955605343, 'UPHENO:0002678', 'abnormal vasculature'),
(412727, 'HP:0500106', 'Isolated systolic hypertension', 'XPO:0101431', 'abnormal ischiadic artery', 0.42105263157894735, 5.809304221129108, 1.5639766078650594, 'UPHENO:0002678', 'abnormal vasculature'),
(412728, 'HP:0500106', 'Isolated systolic hypertension', 'XPO:0100780', 'abnormal vascular plexus', 0.43243243243243246, 5.809304221129108, 1.5849705218340364, 'UPHENO:0002678', 'abnormal vasculature'),
(412729, 'HP:0500106', 'Isolated systolic hypertension', 'XPO:0100659', 'abnormal anterior cardinal vein', 0.41025641025641024, 5.809304221129108, 1.5437954190396599, 'UPHENO:0002678', 'abnormal vasculature'),
(412730, 'HP:0500106', 'Isolated systolic hypertension', 'XPO:0100054', 'abnormal blood vessel', 0.4444444444444444, 5.809304221129108, 1.6068332169732154, 'UPHENO:0002678', 'abnormal vasculature'),
(412731, 'HP:0500106', 'Isolated systolic hypertension', 'XPO:0100792', 'abnormal capillary', 0.43243243243243246, 5.809304221129108, 1.5849705218340364, 'UPHENO:0002678', 'abnormal vasculature'),
(412732, 'HP:0500106', 'Isolated systolic hypertension', 'XPO:0101583', 'abnormal truncus arteriosus', 0.43243243243243246, 5.809304221129108, 1.5849705218340364, 'UPHENO:0002678', 'abnormal vasculature'),
(412733, 'HP:0031046', 'Absent soft palate', 'XPO:0126089', 'absent tongue', 0.4852941176470588, 7.884497199543557, 1.9560930733334743, 'UPHENO:0076786', 'abnormal oral cavity morphology'),
(412734, 'HP:0031046', 'Absent soft palate', 'XPO:0140626', 'abnormally necrotic tongue', 0.5223880597014925, 7.884497199543557, 2.0294746102849897, 'UPHENO:0076786', 'abnormal oral cavity morphology'),
(412735, 'HP:0031046', 'Absent soft palate', 'XPO:0102420', 'abnormal branchial arch 4 morphology', 0.40298507462686567, 5.725717590856133, 1.5190058362769763, 'UPHENO:0076803', 'abnormal digestive system morphology'),
(412736, 'HP:0031046', 'Absent soft palate', 'XPO:0102960', 'abnormal oral epithelium morphology', 0.4647887323943662, 7.312692920701687, 1.8435990000545652, 'UPHENO:0076800', 'abnormal mouth morphology'),
(412737, 'HP:0031046', 'Absent soft palate', 'XPO:0102203', 'abnormal branchial arch 1 morphology', 0.40298507462686567, 5.725717590856133, 1.5190058362769763, 'UPHENO:0076803', 'abnormal digestive system morphology'),
(412738, 'HP:0031046', 'Absent soft palate', 'XPO:0102204', 'abnormal branchial arch morphology', 0.421875, 5.725717590856133, 1.554199829057522, 'UPHENO:0076803', 'abnormal digestive system morphology'),
(412739, 'HP:0031046', 'Absent soft palate', 'XPO:0102261', 'abnormal branchial arch 2 morphology', 0.40298507462686567, 5.725717590856133, 1.5190058362769763, 'UPHENO:0076803', 'abnormal digestive system morphology'),
(412740, 'HP:0031046', 'Absent soft palate', 'XPO:0115393', 'abnormally decreased volume of oral cavity', 0.5072463768115942, 7.884497199543557, 1.99984565340669, 'UPHENO:0076786', 'abnormal oral cavity morphology'),
(412741, 'HP:0031046', 'Absent soft palate', 'XPO:0140897', 'abnormally necrotic lower jaw', 0.41975308641975306, 7.312692920701687, 1.752006114003148, 'UPHENO:0076800', 'abnormal mouth morphology'),
(412742, 'HP:0031046', 'Absent soft palate', 'XPO:0101816', 'abnormal tooth morphology', 0.43209876543209874, 7.884497199543557, 1.8457739585267778, 'UPHENO:0076786', 'abnormal oral cavity morphology'),
(412743, 'HP:0031046', 'Absent soft palate', 'XPO:0103352', 'decreased size of the mouth', 0.49295774647887325, 7.884497199543557, 1.971477611236298, 'UPHENO:0076786', 'abnormal oral cavity morphology'),
(412744, 'HP:0031046', 'Absent soft palate', 'XPO:0128105', 'decreased size of the tongue', 0.4666666666666667, 7.884497199543557, 1.9181845652735452, 'UPHENO:0076786', 'abnormal oral cavity morphology'),
(412745, 'HP:0031046', 'Absent soft palate', 'XPO:0127750', 'abnormally localised tongue', 0.5, 7.884497199543557, 1.9855096574360394, 'UPHENO:0076786', 'abnormal oral cavity morphology'),
(412746, 'HP:0031046', 'Absent soft palate', 'XPO:0131573', 'decreased size of the roof of mouth', 0.4583333333333333, 7.312692920701687, 1.830751463740579, 'UPHENO:0076800', 'abnormal mouth morphology'),
(412747, 'HP:0031046', 'Absent soft palate', 'XPO:0102279', 'abnormal mouth morphology', 0.532258064516129, 7.312692920701687, 1.9728760174865216, 'UPHENO:0076800', 'abnormal mouth morphology'),
(412748, 'HP:0031046', 'Absent soft palate', 'XPO:0130701', 'increased size of the upper jaw', 0.43373493975903615, 8.81758714901448, 1.9556317728288848, 'UPHENO:0087585', 'abnormal midface morphology'),
(412749, 'HP:0031046', 'Absent soft palate', 'XPO:0102735', 'abnormal pharyngeal mesenchyme morphology', 0.4090909090909091, 5.725717590856133, 1.5304701939081158, 'UPHENO:0076803', 'abnormal digestive system morphology'),
(412750, 'HP:0031046', 'Absent soft palate', 'XPO:0129585', 'increased size of the tongue', 0.4375, 7.884497199543557, 1.8572742190641387, 'UPHENO:0076786', 'abnormal oral cavity morphology'),
(412751, 'HP:0031046', 'Absent soft palate', 'XPO:0141009', 'abnormally necrotic oral epithelium', 0.4230769230769231, 7.312692920701687, 1.7589291117884391, 'UPHENO:0076800', 'abnormal mouth morphology'),
(412752, 'HP:0031046', 'Absent soft palate', 'XPO:0128880', 'decreased size of the lower jaw', 0.40963855421686746, 7.312692920701687, 1.7307688914087174, 'UPHENO:0076800', 'abnormal mouth morphology'),
(412753, 'HP:0031046', 'Absent soft palate', 'XPO:0128653', 'decreased size of the oral epithelium', 0.4125, 7.312692920701687, 1.7368033365322182, 'UPHENO:0076800', 'abnormal mouth morphology'),
(412754, 'HP:0031046', 'Absent soft palate', 'XPO:0140789', 'abnormally necrotic roof of mouth', 0.4714285714285714, 7.312692920701687, 1.856720866716972, 'UPHENO:0076800', 'abnormal mouth morphology'),
(412755, 'HP:0031046', 'Absent soft palate', 'XPO:0103138', 'abnormal upper jaw morphology', 0.47368421052631576, 8.81758714901448, 2.043710304184013, 'UPHENO:0087585', 'abnormal midface morphology'),
(412756, 'HP:0031046', 'Absent soft palate', 'XPO:0141311', 'abnormal roof of mouth morphology', 0.5076923076923077, 7.312692920701687, 1.9268103031581083, 'UPHENO:0076800', 'abnormal mouth morphology'),
(412757, 'HP:0031046', 'Absent soft palate', 'XPO:0103096', 'abnormal oral cavity morphology', 0.5645161290322581, 7.884497199543557, 2.1097217443189065, 'UPHENO:0076786', 'abnormal oral cavity morphology'),
(412758, 'HP:0031046', 'Absent soft palate', 'XPO:0115558', 'abnormally incomplete structure of mouth', 0.5238095238095238, 7.312692920701687, 1.9571556393291838, 'UPHENO:0076800', 'abnormal mouth morphology'),
(412759, 'HP:0031046', 'Absent soft palate', 'XPO:0103735', 'increased size of the mouth', 0.49295774647887325, 7.884497199543557, 1.971477611236298, 'UPHENO:0076786', 'abnormal oral cavity morphology'),
(412760, 'HP:0031046', 'Absent soft palate', 'XPO:0141830', 'increased width of mouth', 0.4605263157894737, 7.884497199543557, 1.9055231426456665, 'UPHENO:0076786', 'abnormal oral cavity morphology'),
(412761, 'HP:0031046', 'Absent soft palate', 'XPO:0131611', 'increased size of the roof of mouth', 0.4583333333333333, 7.312692920701687, 1.830751463740579, 'UPHENO:0076800', 'abnormal mouth morphology'),
(412762, 'HP:0031046', 'Absent soft palate', 'XPO:0139863', 'abnormally necrotic pharyngeal arch', 0.40298507462686567, 5.725717590856133, 1.5190058362769763, 'UPHENO:0076803', 'abnormal digestive system morphology'),
(412763, 'HP:0031046', 'Absent soft palate', 'XPO:0101567', 'abnormal tongue', 0.5714285714285714, 7.884497199543557, 2.122599107501873, 'UPHENO:0076786', 'abnormal oral cavity morphology'),
(412764, 'HP:0031046', 'Absent soft palate', 'XPO:0129225', 'decreased size of the upper jaw', 0.43373493975903615, 8.81758714901448, 1.9556317728288848, 'UPHENO:0087585', 'abnormal midface morphology'),
(412765, 'HP:0031046', 'Absent soft palate', 'XPO:0103828', 'decreased width of the mouth', 0.4605263157894737, 7.884497199543557, 1.9055231426456665, 'UPHENO:0076786', 'abnormal oral cavity morphology'),
(412766, 'HP:0031046', 'Absent soft palate', 'XPO:0130132', 'increased size of the oral epithelium', 0.4125, 7.312692920701687, 1.7368033365322182, 'UPHENO:0076800', 'abnormal mouth morphology'),
(412767, 'HP:0031046', 'Absent soft palate', 'XPO:0103199', 'abnormal tongue morphology', 0.5645161290322581, 7.884497199543557, 2.1097217443189065, 'UPHENO:0076786', 'abnormal oral cavity morphology'),
(412768, 'HP:0031046', 'Absent soft palate', 'XPO:0129152', 'decreased size of the oral cavity', 0.5223880597014925, 7.884497199543557, 2.0294746102849897, 'UPHENO:0076786', 'abnormal oral cavity morphology'),
(412769, 'HP:0031046', 'Absent soft palate', 'XPO:0140639', 'abnormally necrotic upper jaw', 0.4444444444444444, 8.81758714901448, 1.9796281524024186, 'UPHENO:0087585', 'abnormal midface morphology'),
(412770, 'HP:0031046', 'Absent soft palate', 'XPO:0101659', 'abnormal lower jaw morphology', 0.4473684210526316, 7.312692920701687, 1.8087199577538449, 'UPHENO:0076800', 'abnormal mouth morphology'),
(412771, 'HP:0031046', 'Absent soft palate', 'XPO:0102525', 'abnormal hyoid arch morphology', 0.4153846153846154, 5.725717590856133, 1.5421981063659433, 'UPHENO:0076803', 'abnormal digestive system morphology'),
(412772, 'HP:0031046', 'Absent soft palate', 'XPO:0102445', 'abnormal branchial arch 3 morphology', 0.4090909090909091, 5.725717590856133, 1.5304701939081158, 'UPHENO:0076803', 'abnormal digestive system morphology'),
(412773, 'HP:0031046', 'Absent soft palate', 'XPO:0130628', 'increased size of the oral cavity', 0.5223880597014925, 7.884497199543557, 2.0294746102849897, 'UPHENO:0076786', 'abnormal oral cavity morphology'),
(412774, 'HP:0031046', 'Absent soft palate', 'XPO:0130358', 'increased size of the lower jaw', 0.40963855421686746, 7.312692920701687, 1.7307688914087174, 'UPHENO:0076800', 'abnormal mouth morphology'),
(412775, 'HP:0031046', 'Absent soft palate', 'XPO:0102223', 'abnormal pharyngeal arch morphology', 0.43548387096774194, 5.725717590856133, 1.5790686053918375, 'UPHENO:0076803', 'abnormal digestive system morphology'),
(412776, 'HP:0030456', 'Abnormality of pattern onset/offset visual evoked potentials', 'XPO:0101230', 'abnormal iris', 0.40384615384615385, 6.02624522851634, 1.560024345217106, 'HP:0000478', 'Abnormality of the eye'),
(412777, 'HP:0030456', 'Abnormality of pattern onset/offset visual evoked potentials', 'XPO:0100002', 'abnormal head', 0.40540540540540543, 3.868794716113063, 1.2523698696136485, 'UPHENO:0002844', 'abnormal head'),
(412778, 'HP:0030456', 'Abnormality of pattern onset/offset visual evoked potentials', 'XPO:0101289', 'abnormal orbital region', 0.40425531914893614, 5.757493499662858, 1.5256137690136826, 'HP:0000315', 'Abnormality of the orbital region'),
(412779, 'HP:0030456', 'Abnormality of pattern onset/offset visual evoked potentials', 'XPO:0100564', 'abnormal central retina', 0.4117647058823529, 6.02624522851634, 1.5752444553449358, 'HP:0000478', 'Abnormality of the eye'),
(412780, 'HP:0030456', 'Abnormality of pattern onset/offset visual evoked potentials', 'XPO:0100844', 'abnormal lens transitional zone', 0.40384615384615385, 6.02624522851634, 1.560024345217106, 'HP:0000478', 'Abnormality of the eye'),
(412781, 'HP:0030456', 'Abnormality of pattern onset/offset visual evoked potentials', 'XPO:0101390', 'abnormal ciliary body', 0.40384615384615385, 6.02624522851634, 1.560024345217106, 'HP:0000478', 'Abnormality of the eye'),
(412782, 'HP:0030456', 'Abnormality of pattern onset/offset visual evoked potentials', 'XPO:0101578', 'abnormal pupil', 0.4117647058823529, 6.02624522851634, 1.5752444553449358, 'HP:0000478', 'Abnormality of the eye'),
(412783, 'HP:0030456', 'Abnormality of pattern onset/offset visual evoked potentials', 'XPO:0142052', 'abnormal nasal region', 0.40540540540540543, 3.868794716113063, 1.2523698696136485, 'UPHENO:0002844', 'abnormal head'),
(412784, 'HP:0030456', 'Abnormality of pattern onset/offset visual evoked potentials', 'XPO:0101416', 'abnormal cornea', 0.4117647058823529, 6.02624522851634, 1.5752444553449358, 'HP:0000478', 'Abnormality of the eye'),
(412785, 'HP:0030456', 'Abnormality of pattern onset/offset visual evoked potentials', 'XPO:0100918', 'abnormal lens', 0.42, 6.02624522851634, 1.590918915588366, 'HP:0000478', 'Abnormality of the eye'),
(412786, 'HP:0030456', 'Abnormality of pattern onset/offset visual evoked potentials', 'XPO:0100485', 'abnormal retina', 0.42, 6.02624522851634, 1.590918915588366, 'HP:0000478', 'Abnormality of the eye'),
(412787, 'HP:0030456', 'Abnormality of pattern onset/offset visual evoked potentials', 'XPO:0100881', 'abnormal sclera', 0.42, 6.02624522851634, 1.590918915588366, 'HP:0000478', 'Abnormality of the eye'),
(412788, 'HP:0030456', 'Abnormality of pattern onset/offset visual evoked potentials', 'XPO:0101554', 'abnormal peripheral retina', 0.4117647058823529, 6.02624522851634, 1.5752444553449358, 'HP:0000478', 'Abnormality of the eye'),
(412789, 'HP:0030456', 'Abnormality of pattern onset/offset visual evoked potentials', 'XPO:0101173', 'abnormal retinal layer', 0.45652173913043476, 6.02624522851634, 1.6586476274811248, 'HP:0000478', 'Abnormality of the eye'),
(412790, 'HP:0012745', 'Short palpebral fissure', 'XPO:0128178', 'decreased size of the conjunctiva', 0.4146341463414634, 9.23763525381927, 1.9570996417354842, 'HP:0030669', 'Abnormal ocular adnexa morphology'),
(412791, 'HP:0012745', 'Short palpebral fissure', 'XPO:0128568', 'decreased size of the optic disc', 0.4166666666666667, 6.575878401988876, 1.6552792314778892, 'UPHENO:0087924', 'abnormal camera-type eye morphology'),
(412792, 'HP:0012745', 'Short palpebral fissure', 'XPO:0129212', 'decreased size of the lower eyelid', 0.45569620253164556, 10.252047911556717, 2.161439173668527, 'HP:0000492', 'Abnormal eyelid morphology'),
(412793, 'HP:0012745', 'Short palpebral fissure', 'XPO:0131600', 'decreased size of the intercanthal region', 0.4067796610169492, 5.653868323764771, 1.5165350771332327, 'UPHENO:0012541', 'decreased size of the anatomical entity in the independent continuant'),
(412794, 'HP:0012745', 'Short palpebral fissure', 'XPO:0128582', 'decreased size of the head region', 0.4067796610169492, 5.653868323764771, 1.5165350771332327, 'UPHENO:0012541', 'decreased size of the anatomical entity in the independent continuant'),
(412795, 'HP:0012745', 'Short palpebral fissure', 'XPO:0130688', 'increased size of the lower eyelid', 0.41975308641975306, 10.252047911556717, 2.0744466136777575, 'HP:0000492', 'Abnormal eyelid morphology'),
(412796, 'HP:0012745', 'Short palpebral fissure', 'XPO:0103358', 'decreased size of the pharyngeal region', 0.42857142857142855, 5.653868323764771, 1.5566266169093397, 'UPHENO:0012541', 'decreased size of the anatomical entity in the independent continuant'),
(412797, 'HP:0012745', 'Short palpebral fissure', 'XPO:0102723', 'abnormal lower eyelid morphology', 0.44594594594594594, 10.252047911556717, 2.1381906378530235, 'HP:0000492', 'Abnormal eyelid morphology'),
(412798, 'HP:0012745', 'Short palpebral fissure', 'XPO:0140547', 'abnormally necrotic lower eyelid', 0.4125, 10.252047911556717, 2.056445905808647, 'HP:0000492', 'Abnormal eyelid morphology'),
(412799, 'HP:0009633', 'Osteolytic defect of the proximal phalanx of the thumb', 'XPO:0103634', 'abnormally increased number of forelimb digit', 0.4014084507042254, 7.774297771301195, 1.7665414865468982, 'HP:0005918', 'Abnormal finger phalanx morphology'),
(412800, 'HP:0010359', 'Aplasia/Hypoplasia of the phalanges of the 3rd toe', 'XPO:0141529', 'absent hindlimb digit 3 in the regenerating hindlimb', 0.41228070175438597, 10.299160507394836, 2.0606176553329347, 'HP:0006494', 'Aplasia/Hypoplasia involving bones of the feet'),
(412801, 'HP:0010359', 'Aplasia/Hypoplasia of the phalanges of the 3rd toe', 'XPO:0103289', 'absent hindlimb digit', 0.4519230769230769, 10.299160507394836, 2.1574124098619887, 'HP:0006494', 'Aplasia/Hypoplasia involving bones of the feet'),
(412802, 'HP:0010359', 'Aplasia/Hypoplasia of the phalanges of the 3rd toe', 'XPO:0103292', 'absent hindlimb digit 4', 0.4392523364485981, 10.299160507394836, 2.1269532943467073, 'HP:0006494', 'Aplasia/Hypoplasia involving bones of the feet'),
(412803, 'HP:0010359', 'Aplasia/Hypoplasia of the phalanges of the 3rd toe', 'XPO:0103589', 'abnormally decreased number of hindlimb digit', 0.415929203539823, 10.299160507394836, 2.0697153492617124, 'HP:0006494', 'Aplasia/Hypoplasia involving bones of the feet'),
(412804, 'HP:0010359', 'Aplasia/Hypoplasia of the phalanges of the 3rd toe', 'XPO:0103293', 'absent hindlimb digit 5', 0.4392523364485981, 10.299160507394836, 2.1269532943467073, 'HP:0006494', 'Aplasia/Hypoplasia involving bones of the feet'),
(412805, 'HP:0010359', 'Aplasia/Hypoplasia of the phalanges of the 3rd toe', 'XPO:0103908', 'absent hindlimb digit 1', 0.4392523364485981, 10.299160507394836, 2.1269532943467073, 'HP:0006494', 'Aplasia/Hypoplasia involving bones of the feet'),
(412806, 'HP:0010359', 'Aplasia/Hypoplasia of the phalanges of the 3rd toe', 'XPO:0103291', 'absent hindlimb digit 3', 0.4392523364485981, 10.299160507394836, 2.1269532943467073, 'HP:0006494', 'Aplasia/Hypoplasia involving bones of the feet'),
(412807, 'HP:0010359', 'Aplasia/Hypoplasia of the phalanges of the 3rd toe', 'XPO:0103290', 'absent hindlimb digit 2', 0.4392523364485981, 10.299160507394836, 2.1269532943467073, 'HP:0006494', 'Aplasia/Hypoplasia involving bones of the feet'),
(412808, 'HP:0010359', 'Aplasia/Hypoplasia of the phalanges of the 3rd toe', 'XPO:0141528', 'absent hindlimb digit 2 in the regenerating hindlimb', 0.41228070175438597, 10.299160507394836, 2.0606176553329347, 'HP:0006494', 'Aplasia/Hypoplasia involving bones of the feet'),
(412809, 'HP:0010359', 'Aplasia/Hypoplasia of the phalanges of the 3rd toe', 'XPO:0103571', 'decreased length of hindlimb digit', 0.40869565217391307, 10.299160507394836, 2.0516388864548123, 'HP:0006494', 'Aplasia/Hypoplasia involving bones of the feet'),
(412810, 'HP:0010359', 'Aplasia/Hypoplasia of the phalanges of the 3rd toe', 'XPO:0141524', 'absent hindlimb digit 1 in the regenerating hindlimb', 0.41228070175438597, 10.299160507394836, 2.0606176553329347, 'HP:0006494', 'Aplasia/Hypoplasia involving bones of the feet'),
(412811, 'HP:0010359', 'Aplasia/Hypoplasia of the phalanges of the 3rd toe', 'XPO:0102566', 'abnormal claw primordium morphology', 0.40425531914893614, 7.639349617137506, 1.7573410931194393, 'HP:0001780', 'Abnormal toe morphology'),
(412812, 'HP:0032904', 'Focal verbal automatism seizure', 'XPO:0100642', 'abnormal gustatory system', 0.40625, 3.94131651835137, 1.2653694462805098, 'UPHENO:0004523', 'abnormal nervous system'),
(412813, 'HP:0032904', 'Focal verbal automatism seizure', 'XPO:0100427', 'abnormal olfactory system', 0.40625, 3.94131651835137, 1.2653694462805098, 'UPHENO:0004523', 'abnormal nervous system'),
(412814, 'HP:0032904', 'Focal verbal automatism seizure', 'XPO:0100273', 'abnormal visual system', 0.40625, 3.94131651835137, 1.2653694462805098, 'UPHENO:0004523', 'abnormal nervous system'),
(412815, 'HP:0032904', 'Focal verbal automatism seizure', 'XPO:0107253', 'abnormal enteric nervous system', 0.41935483870967744, 3.94131651835137, 1.2856166430382838, 'UPHENO:0004523', 'abnormal nervous system'),
(412816, 'HP:0032904', 'Focal verbal automatism seizure', 'XPO:0100274', 'abnormal sensory system', 0.41935483870967744, 3.94131651835137, 1.2856166430382838, 'UPHENO:0004523', 'abnormal nervous system'),
(412817, 'HP:0032904', 'Focal verbal automatism seizure', 'XPO:0100587', 'abnormal vestibuloauditory system', 0.40625, 3.94131651835137, 1.2653694462805098, 'UPHENO:0004523', 'abnormal nervous system'),
(412818, 'HP:0032904', 'Focal verbal automatism seizure', 'XPO:0100032', 'abnormal nervous system', 0.43333333333333335, 3.94131651835137, 1.3068679445984308, 'UPHENO:0004523', 'abnormal nervous system'),
(412819, 'HP:0032904', 'Focal verbal automatism seizure', 'XPO:0100031', 'abnormal central nervous system', 0.41935483870967744, 3.94131651835137, 1.2856166430382838, 'UPHENO:0004523', 'abnormal nervous system'),
(412820, 'HP:0033961', 'Cortical radial artery intima/media multilamellation', 'XPO:0100271', 'abnormal mesonephric nephron', 0.40425531914893614, 6.880013295263146, 1.6677175931270638, 'HP:0000077', 'Abnormality of the kidney'),
(412821, 'HP:0033961', 'Cortical radial artery intima/media multilamellation', 'XPO:0103182', 'abnormal pronephric sinus morphology', 0.40350877192982454, 7.603795021646889, 1.7516272409365097, 'HP:0012210', 'Abnormal renal morphology'),
(412822, 'HP:0033961', 'Cortical radial artery intima/media multilamellation', 'XPO:0140552', 'abnormally necrotic kidney', 0.40350877192982454, 7.603795021646889, 1.7516272409365097, 'HP:0012210', 'Abnormal renal morphology'),
(412823, 'HP:0033961', 'Cortical radial artery intima/media multilamellation', 'XPO:0101717', 'abnormal mesonephric sinus morphology', 0.5476190476190477, 7.603795021646889, 2.040583982110201, 'HP:0012210', 'Abnormal renal morphology'),
(412824, 'HP:0033961', 'Cortical radial artery intima/media multilamellation', 'XPO:0126072', 'absent mesonephric sinus', 0.40425531914893614, 6.880013295263146, 1.6677175931270638, 'HP:0000077', 'Abnormality of the kidney'),
(412825, 'HP:0033961', 'Cortical radial artery intima/media multilamellation', 'XPO:0101701', 'abnormal urinary system morphology', 0.40476190476190477, 7.340144605965611, 1.7236620643091445, 'UPHENO:0087427', 'abnormal renal system morphology'),
(412826, 'HP:0033961', 'Cortical radial artery intima/media multilamellation', 'XPO:0100567', 'abnormal mesonephric collecting duct', 0.42592592592592593, 7.603795021646889, 1.7996259153351557, 'HP:0012210', 'Abnormal renal morphology'),
(412827, 'HP:0033961', 'Cortical radial artery intima/media multilamellation', 'XPO:0107387', 'abnormal embryonic kidney morphology', 0.45098039215686275, 7.603795021646889, 1.8517997895946297, 'HP:0012210', 'Abnormal renal morphology'),
(412828, 'HP:0033961', 'Cortical radial artery intima/media multilamellation', 'XPO:0102198', 'abnormal kidney morphology', 0.46938775510204084, 7.603795021646889, 1.8892136659115366, 'HP:0012210', 'Abnormal renal morphology'),
(412829, 'HP:0033961', 'Cortical radial artery intima/media multilamellation', 'XPO:0101779', 'abnormal mesonephric mesenchyme morphology', 0.46, 7.603795021646889, 1.870226111986882, 'HP:0012210', 'Abnormal renal morphology'),
(412830, 'HP:0033961', 'Cortical radial artery intima/media multilamellation', 'XPO:0126710', 'abnormally localised kidney', 0.4339622641509434, 7.603795021646889, 1.816524181984252, 'HP:0012210', 'Abnormal renal morphology'),
(412831, 'HP:0033961', 'Cortical radial artery intima/media multilamellation', 'XPO:0100566', 'abnormal kidney', 0.475, 6.880013295263146, 1.8077627928602786, 'HP:0000077', 'Abnormality of the kidney'),
(412832, 'HP:0033961', 'Cortical radial artery intima/media multilamellation', 'XPO:0100085', 'abnormal mesonephric sinus', 0.5277777777777778, 6.880013295263146, 1.9055492982485522, 'HP:0000077', 'Abnormality of the kidney'),
(412833, 'HP:0033961', 'Cortical radial artery intima/media multilamellation', 'XPO:0107301', 'abnormal adult kidney', 0.4634146341463415, 6.880013295263146, 1.7855808142300187, 'HP:0000077', 'Abnormality of the kidney'),
(412834, 'HP:0033961', 'Cortical radial artery intima/media multilamellation', 'XPO:0100778', 'abnormal mesonephric kidney', 0.41304347826086957, 6.880013295263146, 1.685747496500148, 'HP:0000077', 'Abnormality of the kidney'),
(412835, 'HP:0033961', 'Cortical radial artery intima/media multilamellation', 'XPO:0130678', 'increased size of the mesonephric sinus', 0.48936170212765956, 7.603795021646889, 1.9289909472112474, 'HP:0012210', 'Abnormal renal morphology'),
(412836, 'HP:0033961', 'Cortical radial artery intima/media multilamellation', 'XPO:0141643', 'neoplastic kidney', 0.4423076923076923, 7.603795021646889, 1.833907584586899, 'HP:0012210', 'Abnormal renal morphology'),
(412837, 'HP:0033961', 'Cortical radial artery intima/media multilamellation', 'XPO:0107388', 'abnormal adult kidney morphology', 0.45098039215686275, 7.603795021646889, 1.8517997895946297, 'HP:0012210', 'Abnormal renal morphology'),
(412838, 'HP:0033961', 'Cortical radial artery intima/media multilamellation', 'XPO:0100147', 'abnormal mesonephric mesenchyme', 0.48717948717948717, 6.880013295263146, 1.83079254667872, 'HP:0000077', 'Abnormality of the kidney'),
(412839, 'HP:0033961', 'Cortical radial artery intima/media multilamellation', 'XPO:0127733', 'abnormally localised mesonephric sinus', 0.4418604651162791, 6.880013295263146, 1.7435612620872136, 'HP:0000077', 'Abnormality of the kidney'),
(412840, 'HP:0033961', 'Cortical radial artery intima/media multilamellation', 'XPO:0140815', 'abnormally necrotic mesonephric mesenchyme', 0.4107142857142857, 7.603795021646889, 1.7671975670630444, 'HP:0012210', 'Abnormal renal morphology'),
(412841, 'HP:0033961', 'Cortical radial artery intima/media multilamellation', 'XPO:0126656', 'abnormally localised embryonic kidney', 0.41818181818181815, 7.603795021646889, 1.7831906312097294, 'HP:0012210', 'Abnormal renal morphology'),
(412842, 'HP:0033961', 'Cortical radial artery intima/media multilamellation', 'XPO:0141613', 'metaplastic kidney', 0.4318181818181818, 6.880013295263146, 1.7236341932224046, 'HP:0000077', 'Abnormality of the kidney'),
(412843, 'HP:0033961', 'Cortical radial artery intima/media multilamellation', 'XPO:0100069', 'abnormal urinary system', 0.42857142857142855, 6.355235291121788, 1.6503551943819923, 'HP:0000079', 'Abnormality of the urinary system'),
(412844, 'HP:0033961', 'Cortical radial artery intima/media multilamellation', 'XPO:0126885', 'abnormally localised adult kidney', 0.41818181818181815, 7.603795021646889, 1.7831906312097294, 'HP:0012210', 'Abnormal renal morphology'),
(412845, 'HP:0033961', 'Cortical radial artery intima/media multilamellation', 'XPO:0100761', 'abnormal ureter', 0.425, 6.828345551150745, 1.703539509151187, 'HP:0010935', 'Abnormality of the upper urinary tract'),
(412846, 'HP:0033961', 'Cortical radial artery intima/media multilamellation', 'XPO:0107300', 'abnormal embryonic kidney', 0.4634146341463415, 6.880013295263146, 1.7855808142300187, 'HP:0000077', 'Abnormality of the kidney'),
(412847, 'HP:0033961', 'Cortical radial artery intima/media multilamellation', 'XPO:0129202', 'decreased size of the mesonephric sinus', 0.48936170212765956, 7.603795021646889, 1.9289909472112474, 'HP:0012210', 'Abnormal renal morphology'),
(412848, 'HP:0012635', 'Iris hypoperfusion', 'XPO:0102411', 'abnormal optic choroid vascular plexus morphology', 0.4444444444444444, 9.773257991046536, 2.0841473600115, 'HP:0000553', 'Abnormal uvea morphology'),
(412849, 'HP:0012635', 'Iris hypoperfusion', 'XPO:0140375', 'abnormally necrotic lens', 0.40476190476190477, 9.014833150514745, 1.910199213986099, 'UPHENO:0021038', 'abnormal anterior segment of eyeball morphology'),
(412850, 'HP:0012635', 'Iris hypoperfusion', 'XPO:0102342', 'abnormal hyaloid vein morphology', 0.43529411764705883, 9.463856994035337, 2.029670239166096, 'HP:0008047', 'Abnormality of the vasculature of the eye'),
(412851, 'HP:0012635', 'Iris hypoperfusion', 'XPO:0129419', 'decreased size of the pupil', 0.47058823529411764, 11.539624501653302, 2.3303243401273113, 'HP:0000525', 'Abnormality iris morphology'),
(412852, 'HP:0012635', 'Iris hypoperfusion', 'XPO:0102862', 'abnormal iris morphology', 0.5063291139240507, 11.539624501653302, 2.417198347041132, 'HP:0000525', 'Abnormality iris morphology'),
(412853, 'HP:0012635', 'Iris hypoperfusion', 'XPO:0129532', 'increased size of the iris', 0.46511627906976744, 11.539624501653302, 2.3167363272654278, 'HP:0000525', 'Abnormality iris morphology'),
(412854, 'HP:0012635', 'Iris hypoperfusion', 'XPO:0103022', 'abnormal ciliary body morphology', 0.4268292682926829, 10.145960653167025, 2.081007679399005, 'UPHENO:0086817', 'abnormal anterior uvea morphology'),
(412855, 'HP:0012635', 'Iris hypoperfusion', 'XPO:0127230', 'abnormally localised hyaloid blood vessel', 0.5068493150684932, 9.463856994035337, 2.1901482678880395, 'UPHENO:0005090', 'abnormal vasculature of eye'),
(412856, 'HP:0012635', 'Iris hypoperfusion', 'XPO:0102947', 'abnormal hyaloid vascular plexus morphology', 0.44047619047619047, 9.463856994035337, 2.041715865624827, 'HP:0008047', 'Abnormality of the vasculature of the eye'),
(412857, 'HP:0012635', 'Iris hypoperfusion', 'XPO:0101315', 'abnormal hyaloid vascular plexus', 0.5606060606060606, 9.463856994035337, 2.30336614274962, 'HP:0008047', 'Abnormality of the vasculature of the eye'),
(412858, 'HP:0012635', 'Iris hypoperfusion', 'XPO:0100371', 'abnormal hyaloid blood vessel', 0.578125, 9.463856994035337, 2.339079375454514, 'HP:0008047', 'Abnormality of the vasculature of the eye'),
(412859, 'HP:0012635', 'Iris hypoperfusion', 'XPO:0102476', 'abnormal lens transitional zone morphology', 0.41975308641975306, 9.014833150514745, 1.9452516645636548, 'UPHENO:0021038', 'abnormal anterior segment of eyeball morphology'),
(412860, 'HP:0012635', 'Iris hypoperfusion', 'XPO:0100710', 'abnormal hyaloid vein', 0.5606060606060606, 9.463856994035337, 2.30336614274962, 'HP:0008047', 'Abnormality of the vasculature of the eye'),
(412861, 'HP:0012635', 'Iris hypoperfusion', 'XPO:0103048', 'abnormal cornea morphology', 0.40963855421686746, 9.014833150514745, 1.9216719850908865, 'UPHENO:0021038', 'abnormal anterior segment of eyeball morphology'),
(412862, 'HP:0012635', 'Iris hypoperfusion', 'XPO:0127563', 'abnormally localised retinal blood vessel', 0.42045454545454547, 9.463856994035337, 1.994773593838145, 'HP:0008047', 'Abnormality of the vasculature of the eye'),
(412863, 'HP:0012635', 'Iris hypoperfusion', 'XPO:0130893', 'increased size of the pupil', 0.47619047619047616, 11.539624501653302, 2.3441542795860455, 'HP:0000525', 'Abnormality iris morphology'),
(412864, 'HP:0012635', 'Iris hypoperfusion', 'XPO:0128564', 'decreased size of the hyaloid blood vessel', 0.43529411764705883, 9.463856994035337, 2.029670239166096, 'UPHENO:0005090', 'abnormal vasculature of eye'),
(412865, 'HP:0012635', 'Iris hypoperfusion', 'XPO:0140250', 'abnormally necrotic iris', 0.47619047619047616, 11.539624501653302, 2.3441542795860455, 'HP:0000525', 'Abnormality iris morphology'),
(412866, 'HP:0012635', 'Iris hypoperfusion', 'XPO:0103210', 'abnormal pupil morphology', 0.5063291139240507, 11.539624501653302, 2.417198347041132, 'HP:0000525', 'Abnormality iris morphology'),
(412867, 'HP:0012635', 'Iris hypoperfusion', 'XPO:0101359', 'abnormal hyaloid artery', 0.4625, 9.463856994035337, 2.0921361953136186, 'HP:0008047', 'Abnormality of the vasculature of the eye'),
(412868, 'HP:0012635', 'Iris hypoperfusion', 'XPO:0126243', 'absent optic choroid vascular plexus', 0.4567901234567901, 9.463856994035337, 2.079181667070679, 'UPHENO:0005090', 'abnormal vasculature of eye'),
(412869, 'HP:0012635', 'Iris hypoperfusion', 'XPO:0100779', 'abnormal optic choroid vascular plexus', 0.5692307692307692, 9.463856994035337, 2.321016716140737, 'UPHENO:0005090', 'abnormal vasculature of eye'),
(412870, 'HP:0012635', 'Iris hypoperfusion', 'XPO:0127645', 'abnormally localised hyaloid vein', 0.4805194805194805, 9.463856994035337, 2.1325026720931706, 'HP:0008047', 'Abnormality of the vasculature of the eye'),
(412871, 'HP:0012635', 'Iris hypoperfusion', 'XPO:0125990', 'absent hyaloid vein', 0.4625, 9.463856994035337, 2.0921361953136186, 'HP:0008047', 'Abnormality of the vasculature of the eye'),
(412872, 'HP:0012635', 'Iris hypoperfusion', 'XPO:0102550', 'abnormal lens morphology', 0.43037974683544306, 9.014833150514745, 1.969721200851099, 'UPHENO:0021038', 'abnormal anterior segment of eyeball morphology'),
(412873, 'HP:0012635', 'Iris hypoperfusion', 'XPO:0100329', 'abnormal retinal blood vessel', 0.47435897435897434, 9.463856994035337, 2.1187886862947445, 'UPHENO:0005090', 'abnormal vasculature of eye'),
(412874, 'HP:0012635', 'Iris hypoperfusion', 'XPO:0139722', 'abnormally necrotic hyaloid blood vessel', 0.4457831325301205, 9.463856994035337, 2.0539785336312946, 'HP:0008047', 'Abnormality of the vasculature of the eye'),
(412875, 'HP:0012635', 'Iris hypoperfusion', 'XPO:0125589', 'absent hyaloid blood vessel', 0.4868421052631579, 9.463856994035337, 2.1464864460055706, 'UPHENO:0005090', 'abnormal vasculature of eye'),
(412876, 'HP:0012635', 'Iris hypoperfusion', 'XPO:0126122', 'absent hyaloid vascular plexus', 0.4567901234567901, 9.463856994035337, 2.079181667070679, 'HP:0008047', 'Abnormality of the vasculature of the eye'),
(412877, 'HP:0012635', 'Iris hypoperfusion', 'XPO:0127907', 'abnormally localised optic choroid vascular plexus', 0.4868421052631579, 9.463856994035337, 2.1464864460055706, 'HP:0008047', 'Abnormality of the vasculature of the eye'),
(412878, 'HP:0012635', 'Iris hypoperfusion', 'XPO:0140754', 'abnormally necrotic optic choroid vascular plexus', 0.40816326530612246, 9.773257991046536, 1.9972693594767605, 'HP:0000553', 'Abnormal uvea morphology'),
(412879, 'HP:0012635', 'Iris hypoperfusion', 'XPO:0127566', 'abnormally localised hyaloid artery', 0.40217391304347827, 9.463856994035337, 1.9509270616235455, 'HP:0008047', 'Abnormality of the vasculature of the eye'),
(412880, 'HP:0012635', 'Iris hypoperfusion', 'XPO:0127783', 'abnormally localised hyaloid vascular plexus', 0.47435897435897434, 9.463856994035337, 2.1187886862947445, 'HP:0008047', 'Abnormality of the vasculature of the eye'),
(412881, 'HP:0012635', 'Iris hypoperfusion', 'XPO:0102003', 'abnormal hyaloid blood vessel morphology', 0.4805194805194805, 9.463856994035337, 2.1325026720931706, 'UPHENO:0005090', 'abnormal vasculature of eye'),
(412882, 'HP:0012635', 'Iris hypoperfusion', 'XPO:0128052', 'decreased size of the iris', 0.46511627906976744, 11.539624501653302, 2.3167363272654278, 'HP:0000525', 'Abnormality iris morphology'),
(412883, 'HP:0012635', 'Iris hypoperfusion', 'XPO:0130044', 'increased size of the hyaloid blood vessel', 0.43529411764705883, 9.463856994035337, 2.029670239166096, 'HP:0008047', 'Abnormality of the vasculature of the eye'),
(412884, 'HP:0008940', 'Generalized lymphadenopathy', 'XPO:0129487', 'increased size of the anatomical structure', 0.41025641025641024, 5.972749669260594, 1.565362206861726, 'UPHENO:0065599', 'increased size of the anatomical entity in independent continuant'),
(412885, 'HP:0008940', 'Generalized lymphadenopathy', 'XPO:0130378', 'increased size of the dorsal lymph space', 0.44680851063829785, 6.786309419308587, 1.741315825567528, 'UPHENO:0087123', 'abnormal immune system morphology'),
(412886, 'HP:0008940', 'Generalized lymphadenopathy', 'XPO:0129582', 'increased size of the portion of organism substance', 0.41025641025641024, 5.972749669260594, 1.565362206861726, 'UPHENO:0065599', 'increased size of the anatomical entity in independent continuant'),
(412887, 'HP:0008940', 'Generalized lymphadenopathy', 'XPO:0129515', 'increased size of the larval immune system', 0.40384615384615385, 6.786309419308587, 1.6554833003681126, 'UPHENO:0087123', 'abnormal immune system morphology'),
(412888, 'HP:0008940', 'Generalized lymphadenopathy', 'XPO:0102553', 'abnormal dorsal caudal lymphatic vessel morphology', 0.4067796610169492, 8.696350005340756, 1.8808238373801138, 'UPHENO:0075774', 'abnormal lymphatic part of lymphoid system'),
(412889, 'HP:0008940', 'Generalized lymphadenopathy', 'XPO:0101013', 'abnormal ventral caudal lymphatic vessel', 0.425531914893617, 8.696350005340756, 1.923687726830363, 'UPHENO:0075774', 'abnormal lymphatic part of lymphoid system'),
(412890, 'HP:0008940', 'Generalized lymphadenopathy', 'XPO:0130463', 'increased size of the ventral caudal lymphatic vessel', 0.4153846153846154, 8.696350005340756, 1.9006130595727444, 'UPHENO:0075774', 'abnormal lymphatic part of lymphoid system'),
(412891, 'HP:0008940', 'Generalized lymphadenopathy', 'XPO:0129516', 'increased size of the immune system', 0.42857142857142855, 6.786309419308587, 1.7054085500433094, 'UPHENO:0087123', 'abnormal immune system morphology'),
(412892, 'HP:0008940', 'Generalized lymphadenopathy', 'XPO:0100921', 'abnormal dorsal caudal lymphatic vessel', 0.425531914893617, 8.696350005340756, 1.923687726830363, 'UPHENO:0075774', 'abnormal lymphatic part of lymphoid system'),
(412893, 'HP:0008940', 'Generalized lymphadenopathy', 'XPO:0129982', 'increased size of the anatomical line', 0.41025641025641024, 5.972749669260594, 1.565362206861726, 'UPHENO:0065599', 'increased size of the anatomical entity in independent continuant'),
(412894, 'HP:0008940', 'Generalized lymphadenopathy', 'XPO:0102645', 'abnormal ventral caudal lymphatic vessel morphology', 0.4067796610169492, 8.696350005340756, 1.8808238373801138, 'UPHENO:0075774', 'abnormal lymphatic part of lymphoid system'),
(412895, 'HP:0008940', 'Generalized lymphadenopathy', 'XPO:0130442', 'increased size of the dorsal caudal lymphatic vessel', 0.4153846153846154, 8.696350005340756, 1.9006130595727444, 'UPHENO:0075774', 'abnormal lymphatic part of lymphoid system'),
(412896, 'HP:0008940', 'Generalized lymphadenopathy', 'XPO:0129794', 'increased size of the adult immune system', 0.40384615384615385, 6.786309419308587, 1.6554833003681126, 'UPHENO:0087123', 'abnormal immune system morphology'),
(412897, 'HP:0008940', 'Generalized lymphadenopathy', 'XPO:0129643', 'increased size of the lymphatic system', 0.42857142857142855, 6.786309419308587, 1.7054085500433094, 'UPHENO:0087123', 'abnormal immune system morphology'),
(412898, 'HP:0008940', 'Generalized lymphadenopathy', 'XPO:0130939', 'increased size of the anterior lymph sac', 0.40384615384615385, 6.786309419308587, 1.6554833003681126, 'UPHENO:0087123', 'abnormal immune system morphology'),
(412899, 'HP:0008940', 'Generalized lymphadenopathy', 'XPO:0100922', 'abnormal lymph vessel', 0.43478260869565216, 8.696350005340756, 1.944484955316575, 'UPHENO:0075774', 'abnormal lymphatic part of lymphoid system'),
(412900, 'HP:0008940', 'Generalized lymphadenopathy', 'XPO:0129751', 'increased size of the lymph vessel', 0.43548387096774194, 8.696350005340756, 1.9460524565427664, 'UPHENO:0075774', 'abnormal lymphatic part of lymphoid system'),
(412901, 'HP:0008940', 'Generalized lymphadenopathy', 'XPO:0102554', 'abnormal lymph vessel morphology', 0.42105263157894735, 8.696350005340756, 1.913536269549213, 'UPHENO:0075774', 'abnormal lymphatic part of lymphoid system'),
(412902, 'HP:0031982', 'Abnormal putamen morphology', 'XPO:0102174', 'abnormal pallium morphology', 0.4264705882352941, 8.02346099791745, 1.8498027277157947, 'HP:0002060', 'Abnormal cerebral morphology'),
(412903, 'HP:0031982', 'Abnormal putamen morphology', 'XPO:0100590', 'abnormal hypothalamus', 0.421875, 6.667568321314008, 1.677164388351466, 'HP:0100547', 'Abnormal forebrain morphology'),
(412904, 'HP:0031982', 'Abnormal putamen morphology', 'XPO:0100263', 'abnormal prethalamus', 0.4153846153846154, 6.667568321314008, 1.6642131181731699, 'HP:0100547', 'Abnormal forebrain morphology'),
(412905, 'HP:0031982', 'Abnormal putamen morphology', 'XPO:0101797', 'abnormal lateral pallium morphology', 0.42028985507246375, 8.02346099791745, 1.8363494384224073, 'HP:0002060', 'Abnormal cerebral morphology'),
(412906, 'HP:0031982', 'Abnormal putamen morphology', 'XPO:0101595', 'abnormal prosomere 4', 0.4090909090909091, 6.667568321314008, 1.6515573214369805, 'HP:0100547', 'Abnormal forebrain morphology'),
(412907, 'HP:0031982', 'Abnormal putamen morphology', 'XPO:0102389', 'abnormal bed nucleus of the stria terminalis morphology', 0.40540540540540543, 8.651717009412357, 1.872819489874467, 'UPHENO:0087531', 'abnormal cerebral hemisphere morphology'),
(412908, 'HP:0031982', 'Abnormal putamen morphology', 'XPO:0102357', 'abnormal subpallium morphology', 0.4264705882352941, 8.02346099791745, 1.8498027277157947, 'HP:0002060', 'Abnormal cerebral morphology'),
(412909, 'HP:0031982', 'Abnormal putamen morphology', 'XPO:0100575', 'abnormal diencephalon', 0.42857142857142855, 6.667568321314008, 1.6904228111816126, 'HP:0100547', 'Abnormal forebrain morphology'),
(412910, 'HP:0031982', 'Abnormal putamen morphology', 'XPO:0101663', 'abnormal central nervous system morphology', 0.40384615384615385, 5.483278994082134, 1.4880863994491305, 'HP:0002011', 'Morphological central nervous system abnormality'),
(412911, 'HP:0031982', 'Abnormal putamen morphology', 'XPO:0103178', 'abnormal dorsal pallium morphology', 0.42028985507246375, 8.02346099791745, 1.8363494384224073, 'HP:0002060', 'Abnormal cerebral morphology'),
(412912, 'HP:0031982', 'Abnormal putamen morphology', 'XPO:0100962', 'abnormal dorsal thalamus', 0.4153846153846154, 6.667568321314008, 1.6642131181731699, 'HP:0100547', 'Abnormal forebrain morphology'),
(412913, 'HP:0031982', 'Abnormal putamen morphology', 'XPO:0103200', 'abnormal prosomere 5 morphology', 0.4027777777777778, 8.02346099791745, 1.7976851200440698, 'HP:0002060', 'Abnormal cerebral morphology'),
(412914, 'HP:0031982', 'Abnormal putamen morphology', 'XPO:0101140', 'abnormal ventrolateral thalamic nucleus', 0.40298507462686567, 6.667568321314008, 1.639185931352649, 'HP:0100547', 'Abnormal forebrain morphology'),
(412915, 'HP:0031982', 'Abnormal putamen morphology', 'XPO:0101805', 'abnormal pallidum morphology', 0.4084507042253521, 8.02346099791745, 1.810300608993995, 'HP:0002060', 'Abnormal cerebral morphology'),
(412916, 'HP:0031982', 'Abnormal putamen morphology', 'XPO:0101588', 'abnormal central nucleus of the thalamus', 0.40298507462686567, 6.667568321314008, 1.639185931352649, 'HP:0100547', 'Abnormal forebrain morphology'),
(412917, 'HP:0031982', 'Abnormal putamen morphology', 'XPO:0100988', 'abnormal habenula', 0.4090909090909091, 6.667568321314008, 1.6515573214369805, 'HP:0100547', 'Abnormal forebrain morphology'),
(412918, 'HP:0031982', 'Abnormal putamen morphology', 'XPO:0101268', 'abnormal lateral hypothalamic nucleus', 0.40298507462686567, 6.667568321314008, 1.639185931352649, 'HP:0100547', 'Abnormal forebrain morphology'),
(412919, 'HP:0031982', 'Abnormal putamen morphology', 'XPO:0100195', 'abnormal retromammillary area', 0.4153846153846154, 6.667568321314008, 1.6642131181731699, 'HP:0100547', 'Abnormal forebrain morphology'),
(412920, 'HP:0031982', 'Abnormal putamen morphology', 'XPO:0107380', 'abnormal dorsal telencephalon morphology', 0.4264705882352941, 8.02346099791745, 1.8498027277157947, 'HP:0002060', 'Abnormal cerebral morphology'),
(412921, 'HP:0031982', 'Abnormal putamen morphology', 'XPO:0101851', 'abnormal basal ganglion morphology', 0.4142857142857143, 8.02346099791745, 1.8231854734408677, 'HP:0002060', 'Abnormal cerebral morphology'),
(412922, 'HP:0031982', 'Abnormal putamen morphology', 'XPO:0102604', 'abnormal ventral pallidum morphology', 0.4027777777777778, 8.02346099791745, 1.7976851200440698, 'HP:0002060', 'Abnormal cerebral morphology'),
(412923, 'HP:0031982', 'Abnormal putamen morphology', 'XPO:0102442', 'abnormal medial pallium morphology', 0.42028985507246375, 8.02346099791745, 1.8363494384224073, 'HP:0002060', 'Abnormal cerebral morphology'),
(412924, 'HP:0031982', 'Abnormal putamen morphology', 'XPO:0140554', 'abnormally necrotic central amygdala', 0.40229885057471265, 11.189682030596343, 2.121696542676503, 'UPHENO:0088139', 'abnormal basal ganglion morphology'),
(412925, 'HP:0031982', 'Abnormal putamen morphology', 'XPO:0102066', 'abnormal ventral pallium morphology', 0.42028985507246375, 8.02346099791745, 1.8363494384224073, 'HP:0002060', 'Abnormal cerebral morphology'),
(412926, 'HP:0031982', 'Abnormal putamen morphology', 'XPO:0101123', 'abnormal third ventricle', 0.4090909090909091, 6.667568321314008, 1.6515573214369805, 'HP:0100547', 'Abnormal forebrain morphology'),
(412927, 'HP:0031982', 'Abnormal putamen morphology', 'XPO:0100194', 'abnormal preoptic area', 0.4090909090909091, 6.667568321314008, 1.6515573214369805, 'HP:0100547', 'Abnormal forebrain morphology'),
(412928, 'HP:0031982', 'Abnormal putamen morphology', 'XPO:0100695', 'abnormal zona limitans intrathalamica', 0.4153846153846154, 6.667568321314008, 1.6642131181731699, 'HP:0100547', 'Abnormal forebrain morphology'),
(412929, 'HP:0031982', 'Abnormal putamen morphology', 'XPO:0140421', 'abnormally necrotic anterior entopeduncular region', 0.42028985507246375, 8.02346099791745, 1.8363494384224073, 'HP:0002060', 'Abnormal cerebral morphology'),
(412930, 'HP:0031982', 'Abnormal putamen morphology', 'XPO:0102826', 'abnormal anterior commissure morphology', 0.42028985507246375, 8.02346099791745, 1.8363494384224073, 'HP:0002060', 'Abnormal cerebral morphology'),
(412931, 'HP:0031982', 'Abnormal putamen morphology', 'XPO:0101987', 'abnormal striatum morphology', 0.4084507042253521, 8.02346099791745, 1.810300608993995, 'HP:0002060', 'Abnormal cerebral morphology'),
(412932, 'HP:0031982', 'Abnormal putamen morphology', 'XPO:0102191', 'abnormal telencephalon morphology', 0.43283582089552236, 8.02346099791745, 1.8635560972122107, 'HP:0002060', 'Abnormal cerebral morphology'),
(412933, 'HP:0031982', 'Abnormal putamen morphology', 'XPO:0115310', 'abnormally incomplete structure of forebrain', 0.40298507462686567, 6.667568321314008, 1.639185931352649, 'HP:0100547', 'Abnormal forebrain morphology'),
(412934, 'HP:0031982', 'Abnormal putamen morphology', 'XPO:0102007', 'abnormal anterior entopeduncular region morphology', 0.4393939393939394, 8.02346099791745, 1.8776208710622537, 'HP:0002060', 'Abnormal cerebral morphology'),
(412935, 'HP:0031982', 'Abnormal putamen morphology', 'XPO:0100951', 'abnormal adenohypophysis', 0.40298507462686567, 6.667568321314008, 1.639185931352649, 'HP:0100547', 'Abnormal forebrain morphology'),
(412936, 'HP:0031982', 'Abnormal putamen morphology', 'XPO:0102200', 'abnormal telencephalon septum morphology', 0.4027777777777778, 8.02346099791745, 1.7976851200440698, 'HP:0002060', 'Abnormal cerebral morphology'),
(412937, 'HP:0031982', 'Abnormal putamen morphology', 'XPO:0100998', 'abnormal rostral tuberal region', 0.40298507462686567, 6.667568321314008, 1.639185931352649, 'HP:0100547', 'Abnormal forebrain morphology'),
(412938, 'HP:0031982', 'Abnormal putamen morphology', 'XPO:0101293', 'abnormal posterior hypothalamus', 0.4153846153846154, 6.667568321314008, 1.6642131181731699, 'HP:0100547', 'Abnormal forebrain morphology'),
(412939, 'HP:0031982', 'Abnormal putamen morphology', 'XPO:0129372', 'decreased size of the anterior entopeduncular region', 0.4084507042253521, 8.02346099791745, 1.810300608993995, 'HP:0002060', 'Abnormal cerebral morphology'),
(412940, 'HP:0031982', 'Abnormal putamen morphology', 'XPO:0101053', 'abnormal anterior hypothalamus', 0.4153846153846154, 6.667568321314008, 1.6642131181731699, 'HP:0100547', 'Abnormal forebrain morphology'),
(412941, 'HP:0031982', 'Abnormal putamen morphology', 'XPO:0102249', 'abnormal forebrain morphology', 0.4090909090909091, 6.667568321314008, 1.6515573214369805, 'HP:0100547', 'Abnormal forebrain morphology'),
(412942, 'HP:0031982', 'Abnormal putamen morphology', 'XPO:0102238', 'abnormal basal forebrain morphology', 0.4264705882352941, 8.02346099791745, 1.8498027277157947, 'HP:0002060', 'Abnormal cerebral morphology'),
(412943, 'HP:0031982', 'Abnormal putamen morphology', 'XPO:0101496', 'abnormal subcommissural organ', 0.4153846153846154, 6.667568321314008, 1.6642131181731699, 'HP:0100547', 'Abnormal forebrain morphology'),
(412944, 'HP:0031982', 'Abnormal putamen morphology', 'XPO:0100656', 'abnormal ventral hypothalamic nucleus', 0.40298507462686567, 6.667568321314008, 1.639185931352649, 'HP:0100547', 'Abnormal forebrain morphology'),
(412945, 'HP:0031982', 'Abnormal putamen morphology', 'XPO:0100698', 'abnormal optic stalk', 0.4090909090909091, 6.667568321314008, 1.6515573214369805, 'HP:0100547', 'Abnormal forebrain morphology'),
(412946, 'HP:0031982', 'Abnormal putamen morphology', 'XPO:0100971', 'abnormal prethalamus basal plate', 0.40298507462686567, 6.667568321314008, 1.639185931352649, 'HP:0100547', 'Abnormal forebrain morphology'),
(412947, 'HP:0031982', 'Abnormal putamen morphology', 'XPO:0100763', 'abnormal pretectum', 0.421875, 6.667568321314008, 1.677164388351466, 'HP:0100547', 'Abnormal forebrain morphology'),
(412948, 'HP:0031982', 'Abnormal putamen morphology', 'XPO:0102760', 'abnormal dorsal pallidum morphology', 0.4027777777777778, 8.02346099791745, 1.7976851200440698, 'HP:0002060', 'Abnormal cerebral morphology'),
(412949, 'HP:0031982', 'Abnormal putamen morphology', 'XPO:0101117', 'abnormal tuberal region', 0.4090909090909091, 6.667568321314008, 1.6515573214369805, 'HP:0100547', 'Abnormal forebrain morphology'),
(412950, 'HP:0031982', 'Abnormal putamen morphology', 'XPO:0102978', 'abnormal prosomere 6 morphology', 0.4027777777777778, 8.02346099791745, 1.7976851200440698, 'HP:0002060', 'Abnormal cerebral morphology'),
(412951, 'HP:0031982', 'Abnormal putamen morphology', 'XPO:0130846', 'increased size of the anterior entopeduncular region', 0.4084507042253521, 8.02346099791745, 1.810300608993995, 'HP:0002060', 'Abnormal cerebral morphology'),
(412952, 'HP:0031982', 'Abnormal putamen morphology', 'XPO:0100157', 'abnormal optic tract', 0.421875, 6.667568321314008, 1.677164388351466, 'HP:0100547', 'Abnormal forebrain morphology'),
(412953, 'HP:0031982', 'Abnormal putamen morphology', 'XPO:0100315', 'abnormal neurohypophysis', 0.40298507462686567, 6.667568321314008, 1.639185931352649, 'HP:0100547', 'Abnormal forebrain morphology'),
(412954, 'HP:0031982', 'Abnormal putamen morphology', 'XPO:0100611', 'abnormal hypophysis', 0.4090909090909091, 6.667568321314008, 1.6515573214369805, 'HP:0100547', 'Abnormal forebrain morphology'),
(412955, 'HP:0031982', 'Abnormal putamen morphology', 'XPO:0102696', 'abnormal accessory olfactory bulb morphology', 0.40540540540540543, 8.651717009412357, 1.872819489874467, 'UPHENO:0087531', 'abnormal cerebral hemisphere morphology'),
(412956, 'HP:0031982', 'Abnormal putamen morphology', 'XPO:0101106', 'abnormal caudal tuberal region', 0.40298507462686567, 6.667568321314008, 1.639185931352649, 'HP:0100547', 'Abnormal forebrain morphology'),
(412957, 'HP:0031982', 'Abnormal putamen morphology', 'XPO:0100729', 'abnormal thalamus', 0.421875, 6.667568321314008, 1.677164388351466, 'HP:0100547', 'Abnormal forebrain morphology'),
(412958, 'HP:0031982', 'Abnormal putamen morphology', 'XPO:0102968', 'abnormal medial ganglionic eminence morphology', 0.4142857142857143, 8.02346099791745, 1.8231854734408677, 'HP:0002060', 'Abnormal cerebral morphology'),
(412959, 'HP:0031982', 'Abnormal putamen morphology', 'XPO:0103040', 'abnormal nucleus of the diagonal band morphology', 0.4027777777777778, 8.02346099791745, 1.7976851200440698, 'HP:0002060', 'Abnormal cerebral morphology'),
(412960, 'HP:0031982', 'Abnormal putamen morphology', 'XPO:0142058', 'abnormal cerebrospinal fluid morphology', 0.4117647058823529, 5.483278994082134, 1.502604659339613, 'HP:0002011', 'Morphological central nervous system abnormality'),
(412961, 'HP:0031982', 'Abnormal putamen morphology', 'XPO:0101986', 'abnormal amygdala morphology', 0.4142857142857143, 8.02346099791745, 1.8231854734408677, 'HP:0002060', 'Abnormal cerebral morphology'),
(412962, 'HP:0031982', 'Abnormal putamen morphology', 'XPO:0101186', 'abnormal optic chiasm', 0.421875, 6.667568321314008, 1.677164388351466, 'HP:0100547', 'Abnormal forebrain morphology'),
(412963, 'HP:0031982', 'Abnormal putamen morphology', 'XPO:0101284', 'abnormal ventromedial thalamic nucleus', 0.40298507462686567, 6.667568321314008, 1.639185931352649, 'HP:0100547', 'Abnormal forebrain morphology'),
(412964, 'HP:0031982', 'Abnormal putamen morphology', 'XPO:0139879', 'abnormally necrotic telencephalon', 0.4027777777777778, 8.02346099791745, 1.7976851200440698, 'HP:0002060', 'Abnormal cerebral morphology'),
(412965, 'HP:0031982', 'Abnormal putamen morphology', 'XPO:0101970', 'abnormal lateral ganglionic eminence morphology', 0.4142857142857143, 8.02346099791745, 1.8231854734408677, 'HP:0002060', 'Abnormal cerebral morphology'),
(412966, 'HP:0031982', 'Abnormal putamen morphology', 'XPO:0101075', 'abnormal mammilary region', 0.4090909090909091, 6.667568321314008, 1.6515573214369805, 'HP:0100547', 'Abnormal forebrain morphology'),
(412967, 'HP:0031982', 'Abnormal putamen morphology', 'XPO:0101564', 'abnormal anterior thalamic nucleus', 0.40298507462686567, 6.667568321314008, 1.639185931352649, 'HP:0100547', 'Abnormal forebrain morphology'),
(412968, 'HP:0031982', 'Abnormal putamen morphology', 'XPO:0101354', 'abnormal eminentia thalami', 0.421875, 6.667568321314008, 1.677164388351466, 'HP:0100547', 'Abnormal forebrain morphology'),
(412969, 'HP:0031982', 'Abnormal putamen morphology', 'XPO:0101795', 'abnormal central amygdala morphology', 0.43209876543209874, 11.189682030596343, 2.1988742099079746, 'UPHENO:0088139', 'abnormal basal ganglion morphology'),
(412970, 'HP:0031982', 'Abnormal putamen morphology', 'XPO:0101526', 'abnormal infundibulum', 0.4090909090909091, 6.667568321314008, 1.6515573214369805, 'HP:0100547', 'Abnormal forebrain morphology'),
(412971, 'HP:0100718', 'Uterine rupture', 'XPO:0131304', 'abnormally decreased number of primary oogonium', 0.410958904109589, 8.550271745852811, 1.874516019274003, 'UPHENO:0076766', 'abnormal internal female genitalia morphology'),
(412972, 'HP:0100718', 'Uterine rupture', 'XPO:0131086', 'abnormally increased number of primary oogonium', 0.4225352112676056, 8.550271745852811, 1.9007342998245065, 'UPHENO:0076766', 'abnormal internal female genitalia morphology'),
(412973, 'HP:0100718', 'Uterine rupture', 'XPO:0100765', 'abnormal male genitalia', 0.4782608695652174, 7.005035523447265, 1.8303645486020337, 'HP:0012243', 'Abnormal reproductive system morphology'),
(412974, 'HP:0100718', 'Uterine rupture', 'XPO:0140359', 'abnormally necrotic ovary', 0.40540540540540543, 8.550271745852811, 1.861807289558681, 'UPHENO:0076766', 'abnormal internal female genitalia morphology'),
(412975, 'HP:0100718', 'Uterine rupture', 'XPO:0129864', 'increased size of the genital system', 0.41509433962264153, 7.005035523447265, 1.705212771075354, 'HP:0012243', 'Abnormal reproductive system morphology'),
(412976, 'HP:0100718', 'Uterine rupture', 'XPO:0127828', 'abnormally localised follicle layer', 0.44776119402985076, 8.550271745852811, 1.9566501696017997, 'UPHENO:0076766', 'abnormal internal female genitalia morphology'),
(412977, 'HP:0100718', 'Uterine rupture', 'XPO:0128383', 'decreased size of the female genitalia', 0.43859649122807015, 8.209234828017744, 1.897509312555765, 'UPHENO:0087974', 'abnormal female reproductive system morphology'),
(412978, 'HP:0100718', 'Uterine rupture', 'XPO:0125273', 'absent primary oogonium', 0.4166666666666667, 8.550271745852811, 1.8874886032606055, 'UPHENO:0076766', 'abnormal internal female genitalia morphology'),
(412979, 'HP:0100718', 'Uterine rupture', 'XPO:0140069', 'abnormally necrotic follicle layer', 0.4411764705882353, 8.550271745852811, 1.9422097495908242, 'UPHENO:0076766', 'abnormal internal female genitalia morphology'),
(412980, 'HP:0100718', 'Uterine rupture', 'XPO:0102864', 'abnormal female genitalia morphology', 0.5102040816326531, 8.209234828017744, 2.0465544498829207, 'UPHENO:0087974', 'abnormal female reproductive system morphology'),
(412981, 'HP:0100718', 'Uterine rupture', 'XPO:0131177', 'abnormally increased number of follicle cell', 0.43478260869565216, 8.550271745852811, 1.9280844003099589, 'UPHENO:0076766', 'abnormal internal female genitalia morphology'),
(412982, 'HP:0100718', 'Uterine rupture', 'XPO:0128384', 'decreased size of the genital system', 0.41509433962264153, 7.005035523447265, 1.705212771075354, 'HP:0012243', 'Abnormal reproductive system morphology'),
(412983, 'HP:0100718', 'Uterine rupture', 'XPO:0131395', 'abnormally decreased number of follicle cell', 0.4225352112676056, 8.550271745852811, 1.9007342998245065, 'UPHENO:0076766', 'abnormal internal female genitalia morphology'),
(412984, 'HP:0100718', 'Uterine rupture', 'XPO:0101752', 'abnormal genital system morphology', 0.4782608695652174, 7.005035523447265, 1.8303645486020337, 'UPHENO:0020950', 'abnormal reproductive system morphology'),
(412985, 'HP:0100718', 'Uterine rupture', 'XPO:0101910', 'abnormal follicle cell morphology', 0.45454545454545453, 8.550271745852811, 1.971417550192202, 'UPHENO:0076766', 'abnormal internal female genitalia morphology'),
(412986, 'HP:0100718', 'Uterine rupture', 'XPO:0100036', 'abnormal ovary', 0.5357142857142857, 8.550271745852811, 2.1402109057269514, 'UPHENO:0076766', 'abnormal internal female genitalia morphology'),
(412987, 'HP:0100718', 'Uterine rupture', 'XPO:0125335', 'absent female genitalia', 0.4444444444444444, 7.960567433004586, 1.8809651698594156, 'UPHENO:0005170', 'abnormal female reproductive system'),
(412988, 'HP:0100718', 'Uterine rupture', 'XPO:0126691', 'abnormally localised ovary', 0.43478260869565216, 8.550271745852811, 1.9280844003099589, 'UPHENO:0076766', 'abnormal internal female genitalia morphology'),
(412989, 'HP:0100718', 'Uterine rupture', 'XPO:0101232', 'abnormal female genitalia', 0.5454545454545454, 7.960567433004586, 2.083777265143704, 'UPHENO:0005170', 'abnormal female reproductive system'),
(412990, 'HP:0100718', 'Uterine rupture', 'XPO:0125071', 'absent ovary', 0.4166666666666667, 8.550271745852811, 1.8874886032606055, 'UPHENO:0076766', 'abnormal internal female genitalia morphology'),
(412991, 'HP:0100718', 'Uterine rupture', 'XPO:0126899', 'abnormally localised primary oogonium', 0.43478260869565216, 8.550271745852811, 1.9280844003099589, 'UPHENO:0076766', 'abnormal internal female genitalia morphology'),
(412992, 'HP:0100718', 'Uterine rupture', 'XPO:0141148', 'abnormally necrotic oviduct', 0.423728813559322, 8.209234828017744, 1.8650708656525155, 'UPHENO:0087974', 'abnormal female reproductive system morphology'),
(412993, 'HP:0100718', 'Uterine rupture', 'XPO:0130087', 'increased size of the oviduct', 0.4098360655737705, 8.209234828017744, 1.8342411246305543, 'UPHENO:0087974', 'abnormal female reproductive system morphology'),
(412994, 'HP:0100718', 'Uterine rupture', 'XPO:0101668', 'abnormal ovary morphology', 0.45454545454545453, 8.550271745852811, 1.971417550192202, 'UPHENO:0076766', 'abnormal internal female genitalia morphology'),
(412995, 'HP:0100718', 'Uterine rupture', 'XPO:0125782', 'absent oviduct', 0.4067796610169492, 7.960567433004586, 1.7994990752707185, 'UPHENO:0005170', 'abnormal female reproductive system'),
(412996, 'HP:0100718', 'Uterine rupture', 'XPO:0127432', 'abnormally localised oviduct', 0.42105263157894735, 7.960567433004586, 1.8307970577123633, 'UPHENO:0005170', 'abnormal female reproductive system'),
(412997, 'HP:0100718', 'Uterine rupture', 'XPO:0130654', 'increased size of the follicle layer', 0.42857142857142855, 8.550271745852811, 1.9142628285567427, 'UPHENO:0076766', 'abnormal internal female genitalia morphology'),
(412998, 'HP:0100718', 'Uterine rupture', 'XPO:0102260', 'abnormal primary oogonium morphology', 0.4411764705882353, 8.550271745852811, 1.9422097495908242, 'UPHENO:0076766', 'abnormal internal female genitalia morphology'),
(412999, 'HP:0100718', 'Uterine rupture', 'XPO:0102596', 'abnormal follicle layer morphology', 0.47619047619047616, 8.550271745852811, 2.0178101928119068, 'UPHENO:0076766', 'abnormal internal female genitalia morphology'),
(413000, 'HP:0100718', 'Uterine rupture', 'XPO:0140839', 'abnormally necrotic female genitalia', 0.45454545454545453, 8.209234828017744, 1.9317014200884415, 'UPHENO:0087974', 'abnormal female reproductive system morphology'),
(413001, 'HP:0100718', 'Uterine rupture', 'XPO:0102894', 'abnormal oviduct morphology', 0.4716981132075472, 8.209234828017744, 1.967811113713319, 'UPHENO:0087974', 'abnormal female reproductive system morphology'),
(413002, 'HP:0100718', 'Uterine rupture', 'XPO:0126964', 'abnormally localised female genitalia', 0.4528301886792453, 7.960567433004586, 1.8986272021335104, 'UPHENO:0005170', 'abnormal female reproductive system'),
(413003, 'HP:0100718', 'Uterine rupture', 'XPO:0125540', 'absent follicle cell', 0.42857142857142855, 8.550271745852811, 1.9142628285567427, 'UPHENO:0076766', 'abnormal internal female genitalia morphology'),
(413004, 'HP:0100718', 'Uterine rupture', 'XPO:0100964', 'abnormal follicle layer', 0.5172413793103449, 8.550271745852811, 2.1029870069268566, 'UPHENO:0076766', 'abnormal internal female genitalia morphology'),
(413005, 'HP:0100718', 'Uterine rupture', 'XPO:0126166', 'absent follicle layer', 0.4411764705882353, 8.550271745852811, 1.9422097495908242, 'UPHENO:0076766', 'abnormal internal female genitalia morphology'),
(413006, 'HP:0100718', 'Uterine rupture', 'XPO:0101262', 'abnormal oviduct', 0.5, 7.960567433004586, 1.9950648401749487, 'UPHENO:0005170', 'abnormal female reproductive system'),
(413007, 'HP:0100718', 'Uterine rupture', 'XPO:0129863', 'increased size of the female genitalia', 0.43859649122807015, 8.209234828017744, 1.897509312555765, 'UPHENO:0087974', 'abnormal female reproductive system morphology'),
(413008, 'HP:0100718', 'Uterine rupture', 'XPO:0102270', 'abnormal polar body morphology', 0.43137254901960786, 7.005035523447265, 1.7383267902561792, 'HP:0012243', 'Abnormal reproductive system morphology'),
(413009, 'HP:0100718', 'Uterine rupture', 'XPO:0100278', 'abnormal follicle cell', 0.5, 8.550271745852811, 2.067640170079505, 'UPHENO:0076766', 'abnormal internal female genitalia morphology'),
(413010, 'HP:0100718', 'Uterine rupture', 'XPO:0102397', 'abnormal male genitalia morphology', 0.4230769230769231, 7.005035523447265, 1.7215309684419309, 'HP:0012243', 'Abnormal reproductive system morphology'),
(413011, 'HP:0100718', 'Uterine rupture', 'XPO:0139867', 'abnormally necrotic genital system', 0.43137254901960786, 7.005035523447265, 1.7383267902561792, 'UPHENO:0020950', 'abnormal reproductive system morphology'),
(413012, 'HP:0100718', 'Uterine rupture', 'XPO:0100628', 'abnormal primary oogonium', 0.4918032786885246, 8.550271745852811, 2.0506222661154023, 'UPHENO:0076766', 'abnormal internal female genitalia morphology'),
(413013, 'HP:0100718', 'Uterine rupture', 'XPO:0141099', 'abnormally necrotic follicle cell', 0.42857142857142855, 8.550271745852811, 1.9142628285567427, 'UPHENO:0076766', 'abnormal internal female genitalia morphology'),
(413014, 'HP:0100718', 'Uterine rupture', 'XPO:0128607', 'decreased size of the oviduct', 0.4098360655737705, 8.209234828017744, 1.8342411246305543, 'UPHENO:0087974', 'abnormal female reproductive system morphology'),
(413015, 'HP:0100718', 'Uterine rupture', 'XPO:0127178', 'abnormally localised follicle cell', 0.44776119402985076, 8.550271745852811, 1.9566501696017997, 'UPHENO:0076766', 'abnormal internal female genitalia morphology'),
(413016, 'HP:0100718', 'Uterine rupture', 'XPO:0129178', 'decreased size of the follicle layer', 0.42857142857142855, 8.550271745852811, 1.9142628285567427, 'UPHENO:0076766', 'abnormal internal female genitalia morphology'),
(413017, 'HP:0100718', 'Uterine rupture', 'XPO:0140488', 'abnormally necrotic primary oogonium', 0.410958904109589, 8.550271745852811, 1.874516019274003, 'UPHENO:0076766', 'abnormal internal female genitalia morphology'),
(413018, 'HP:0032244', 'Decreased serum thromboxane B2', 'XPO:0141917', 'abnormal tryptophan metabolic process', 0.5217391304347826, 9.119292702704945, 2.1812592337660224, 'HP:0004354', 'Abnormal circulating carboxylic acid concentration'),
(413019, 'HP:0032244', 'Decreased serum thromboxane B2', 'XPO:0141843', 'abnormal alanine metabolic process', 0.5294117647058824, 9.119292702704945, 2.1972393685278124, 'HP:0004354', 'Abnormal circulating carboxylic acid concentration'),
(413020, 'HP:0032244', 'Decreased serum thromboxane B2', 'XPO:0141893', 'abnormal isoleucine metabolic process', 0.5217391304347826, 9.119292702704945, 2.1812592337660224, 'HP:0004354', 'Abnormal circulating carboxylic acid concentration'),
(413021, 'HP:0032244', 'Decreased serum thromboxane B2', 'XPO:0141847', 'abnormal arginine metabolic process', 0.5217391304347826, 9.119292702704945, 2.1812592337660224, 'HP:0004354', 'Abnormal circulating carboxylic acid concentration'),
(413022, 'HP:0032244', 'Decreased serum thromboxane B2', 'XPO:0141848', 'abnormal proline metabolic process', 0.5217391304347826, 9.119292702704945, 2.1812592337660224, 'HP:0004354', 'Abnormal circulating carboxylic acid concentration'),
(413023, 'HP:0032244', 'Decreased serum thromboxane B2', 'XPO:0141882', 'abnormal gamma-aminobutyric acid metabolic process', 0.5606060606060606, 10.553838360873003, 2.4323950640802856, 'UPHENO:0050484', 'abnormal monocarboxylic acid metabolic process'),
(413024, 'HP:0032244', 'Decreased serum thromboxane B2', 'XPO:0141858', 'abnormal serine family amino acid metabolic process', 0.5294117647058824, 9.119292702704945, 2.1972393685278124, 'HP:0004354', 'Abnormal circulating carboxylic acid concentration'),
(413025, 'HP:0032244', 'Decreased serum thromboxane B2', 'XPO:0141868', 'abnormal asparagine metabolic process', 0.5217391304347826, 9.119292702704945, 2.1812592337660224, 'HP:0004354', 'Abnormal circulating carboxylic acid concentration'),
(413026, 'HP:0032244', 'Decreased serum thromboxane B2', 'XPO:0141888', 'abnormal threonine metabolic process', 0.5217391304347826, 9.119292702704945, 2.1812592337660224, 'HP:0004354', 'Abnormal circulating carboxylic acid concentration'),
(413027, 'HP:0032244', 'Decreased serum thromboxane B2', 'XPO:0141869', 'abnormal alpha-amino acid metabolic process', 0.5454545454545454, 9.119292702704945, 2.2302824162022348, 'HP:0004354', 'Abnormal circulating carboxylic acid concentration'),
(413028, 'HP:0032244', 'Decreased serum thromboxane B2', 'XPO:0141857', 'abnormal glycine metabolic process', 0.5142857142857142, 9.119292702704945, 2.1656227652550926, 'HP:0004354', 'Abnormal circulating carboxylic acid concentration'),
(413029, 'HP:0032244', 'Decreased serum thromboxane B2', 'XPO:0141887', 'abnormal histidine metabolic process', 0.5217391304347826, 9.119292702704945, 2.1812592337660224, 'HP:0004354', 'Abnormal circulating carboxylic acid concentration'),
(413030, 'HP:0032244', 'Decreased serum thromboxane B2', 'XPO:0141889', 'abnormal homoserine metabolic process', 0.5142857142857142, 9.119292702704945, 2.1656227652550926, 'HP:0004354', 'Abnormal circulating carboxylic acid concentration'),
(413031, 'HP:0032244', 'Decreased serum thromboxane B2', 'XPO:0141853', 'abnormal glutamate metabolic process', 0.5070422535211268, 9.119292702704945, 2.1503178189510224, 'HP:0004354', 'Abnormal circulating carboxylic acid concentration'),
(413032, 'HP:0032244', 'Decreased serum thromboxane B2', 'XPO:0141896', 'abnormal lysine metabolic process', 0.5217391304347826, 9.119292702704945, 2.1812592337660224, 'HP:0004354', 'Abnormal circulating carboxylic acid concentration'),
(413033, 'HP:0032244', 'Decreased serum thromboxane B2', 'XPO:0141912', 'abnormal D-serine metabolic process', 0.5142857142857142, 9.119292702704945, 2.1656227652550926, 'HP:0004354', 'Abnormal circulating carboxylic acid concentration'),
(413034, 'HP:0032244', 'Decreased serum thromboxane B2', 'XPO:0141873', 'abnormal tricarboxylic acid metabolic process', 0.5555555555555556, 9.119292702704945, 2.250838449050702, 'HP:0004354', 'Abnormal circulating carboxylic acid concentration'),
(413035, 'HP:0032244', 'Decreased serum thromboxane B2', 'XPO:0141895', 'abnormal leucine metabolic process', 0.5217391304347826, 9.119292702704945, 2.1812592337660224, 'HP:0004354', 'Abnormal circulating carboxylic acid concentration'),
(413036, 'HP:0032244', 'Decreased serum thromboxane B2', 'XPO:0141918', 'abnormal tyrosine metabolic process', 0.5217391304347826, 9.119292702704945, 2.1812592337660224, 'HP:0004354', 'Abnormal circulating carboxylic acid concentration'),
(413037, 'HP:0032244', 'Decreased serum thromboxane B2', 'XPO:0141922', 'abnormal valine metabolic process', 0.5217391304347826, 9.119292702704945, 2.1812592337660224, 'HP:0004354', 'Abnormal circulating carboxylic acid concentration'),
(413038, 'HP:0032244', 'Decreased serum thromboxane B2', 'XPO:0141913', 'abnormal L-serine metabolic process', 0.5142857142857142, 9.119292702704945, 2.1656227652550926, 'HP:0004354', 'Abnormal circulating carboxylic acid concentration'),
(413039, 'HP:0032244', 'Decreased serum thromboxane B2', 'XPO:0141905', 'abnormal ornithine metabolic process', 0.5294117647058824, 9.119292702704945, 2.1972393685278124, 'HP:0004354', 'Abnormal circulating carboxylic acid concentration'),
(413040, 'HP:0100209', 'Pseudoepiphysis of the distal phalanx of the 5th toe', 'XPO:0102566', 'abnormal claw primordium morphology', 0.40186915887850466, 7.639349617137506, 1.752146970153439, 'UPHENO:0088132', 'abnormal pedal digit morphology'),
(413041, 'HP:0034797', 'Hepatic hemophagocytosis', 'XPO:0101921', 'abnormal chondroblast morphology', 0.41304347826086957, 5.43643956286526, 1.4984945466703803, 'HP:0025461', 'Abnormal cell morphology'),
(413042, 'HP:0034797', 'Hepatic hemophagocytosis', 'XPO:0103080', 'abnormal myelin accumulating cell morphology', 0.41304347826086957, 5.43643956286526, 1.4984945466703803, 'HP:0025461', 'Abnormal cell morphology'),
(413043, 'HP:0034797', 'Hepatic hemophagocytosis', 'XPO:0102386', 'abnormal electrically active cell morphology', 0.41304347826086957, 5.43643956286526, 1.4984945466703803, 'HP:0025461', 'Abnormal cell morphology'),
(413044, 'HP:0034797', 'Hepatic hemophagocytosis', 'XPO:0103150', 'abnormal B cell morphology', 0.43137254901960786, 6.786309419308587, 1.7109727036522004, 'UPHENO:0087123', 'abnormal immune system morphology'),
(413045, 'HP:0034797', 'Hepatic hemophagocytosis', 'XPO:0101636', 'abnormal cell morphology', 0.4318181818181818, 5.43643956286526, 1.532172786470543, 'HP:0025461', 'Abnormal cell morphology'),
(413046, 'HP:0034797', 'Hepatic hemophagocytosis', 'XPO:0139951', 'abnormally necrotic lymphocyte', 0.41509433962264153, 6.786309419308587, 1.6783797624145764, 'UPHENO:0087123', 'abnormal immune system morphology'),
(413047, 'HP:0034797', 'Hepatic hemophagocytosis', 'XPO:0102109', 'abnormal pericyte morphology', 0.41304347826086957, 5.43643956286526, 1.4984945466703803, 'HP:0025461', 'Abnormal cell morphology'),
(413048, 'HP:0034797', 'Hepatic hemophagocytosis', 'XPO:0102929', 'abnormal barrier cell morphology', 0.41304347826086957, 5.43643956286526, 1.4984945466703803, 'HP:0025461', 'Abnormal cell morphology'),
(413049, 'HP:0034797', 'Hepatic hemophagocytosis', 'XPO:0102336', 'abnormal Merkel cell morphology', 0.41304347826086957, 5.43643956286526, 1.4984945466703803, 'HP:0025461', 'Abnormal cell morphology'),
(413050, 'HP:0034797', 'Hepatic hemophagocytosis', 'XPO:0102165', 'abnormal melanoblast morphology', 0.41304347826086957, 5.43643956286526, 1.4984945466703803, 'HP:0025461', 'Abnormal cell morphology'),
(413051, 'HP:0034797', 'Hepatic hemophagocytosis', 'XPO:0102764', 'abnormal apoptotic cell morphology', 0.41304347826086957, 5.43643956286526, 1.4984945466703803, 'HP:0025461', 'Abnormal cell morphology'),
(413052, 'HP:0034797', 'Hepatic hemophagocytosis', 'XPO:0102958', 'abnormal cementoblast morphology', 0.41304347826086957, 5.43643956286526, 1.4984945466703803, 'HP:0025461', 'Abnormal cell morphology'),
(413053, 'HP:0034797', 'Hepatic hemophagocytosis', 'XPO:0102347', 'abnormal ciliated cell morphology', 0.41304347826086957, 5.43643956286526, 1.4984945466703803, 'HP:0025461', 'Abnormal cell morphology'),
(413054, 'HP:0034797', 'Hepatic hemophagocytosis', 'XPO:0103219', 'abnormal hemangioblast morphology', 0.42, 5.574066539846944, 1.5300679549404714, 'UPHENO:0004459', 'abnormal hematopoietic system'),
(413055, 'HP:0034797', 'Hepatic hemophagocytosis', 'XPO:0102636', 'abnormal acid secreting cell morphology', 0.41304347826086957, 5.43643956286526, 1.4984945466703803, 'HP:0025461', 'Abnormal cell morphology'),
(413056, 'HP:0034797', 'Hepatic hemophagocytosis', 'XPO:0102181', 'abnormal mitotic cell morphology', 0.41304347826086957, 5.43643956286526, 1.4984945466703803, 'HP:0025461', 'Abnormal cell morphology'),
(413057, 'HP:0034797', 'Hepatic hemophagocytosis', 'XPO:0102965', 'abnormal barrier epithelial cell morphology', 0.41304347826086957, 5.43643956286526, 1.4984945466703803, 'HP:0025461', 'Abnormal cell morphology'),
(413058, 'HP:0034797', 'Hepatic hemophagocytosis', 'XPO:0102081', 'abnormal lymphocyte morphology', 0.4489795918367347, 6.786309419308587, 1.7455413009032348, 'UPHENO:0087123', 'abnormal immune system morphology'),
(413059, 'HP:0034797', 'Hepatic hemophagocytosis', 'XPO:0102869', 'abnormal mucus secreting cell morphology', 0.41304347826086957, 5.43643956286526, 1.4984945466703803, 'HP:0025461', 'Abnormal cell morphology'),
(413060, 'HP:0034797', 'Hepatic hemophagocytosis', 'XPO:0101804', 'abnormal stem cell morphology', 0.41304347826086957, 5.43643956286526, 1.4984945466703803, 'HP:0025461', 'Abnormal cell morphology'),
(413061, 'HP:0034797', 'Hepatic hemophagocytosis', 'XPO:0101969', 'abnormal zygote morphology', 0.41304347826086957, 5.43643956286526, 1.4984945466703803, 'HP:0025461', 'Abnormal cell morphology'),
(413062, 'HP:0034797', 'Hepatic hemophagocytosis', 'XPO:0102739', 'abnormal erythroid cell morphology', 0.42, 5.574066539846944, 1.5300679549404714, 'HP:0001871', 'Abnormality of blood and blood-forming tissues'),
(413063, 'HP:0034797', 'Hepatic hemophagocytosis', 'XPO:0102873', 'abnormal nucleate erythrocyte morphology', 0.41304347826086957, 5.43643956286526, 1.4984945466703803, 'HP:0025461', 'Abnormal cell morphology'),
(413064, 'HP:0034797', 'Hepatic hemophagocytosis', 'XPO:0139717', 'abnormally necrotic cell', 0.40425531914893614, 5.43643956286526, 1.4824674062251753, 'HP:0025461', 'Abnormal cell morphology'),
(413065, 'HP:0034797', 'Hepatic hemophagocytosis', 'XPO:0103067', 'abnormal paracrine cell morphology', 0.41304347826086957, 5.43643956286526, 1.4984945466703803, 'HP:0025461', 'Abnormal cell morphology'),
(413066, 'HP:0034797', 'Hepatic hemophagocytosis', 'XPO:0141478', 'abnormally necrotic lymphoblast', 0.41509433962264153, 6.786309419308587, 1.6783797624145764, 'UPHENO:0087123', 'abnormal immune system morphology'),
(413067, 'HP:0034797', 'Hepatic hemophagocytosis', 'XPO:0103005', 'abnormal oxygen accumulating cell morphology', 0.41304347826086957, 5.43643956286526, 1.4984945466703803, 'HP:0025461', 'Abnormal cell morphology'),
(413068, 'HP:0034797', 'Hepatic hemophagocytosis', 'XPO:0102423', 'abnormal multiciliated cell precursor morphology', 0.41304347826086957, 5.43643956286526, 1.4984945466703803, 'HP:0025461', 'Abnormal cell morphology'),
(413069, 'HP:0034797', 'Hepatic hemophagocytosis', 'XPO:0102715', 'abnormal T cell morphology', 0.43137254901960786, 6.786309419308587, 1.7109727036522004, 'UPHENO:0087123', 'abnormal immune system morphology'),
(413070, 'HP:0034797', 'Hepatic hemophagocytosis', 'XPO:0141503', 'abnormal lymphoblast morphology', 0.4489795918367347, 6.786309419308587, 1.7455413009032348, 'UPHENO:0087123', 'abnormal immune system morphology'),
(413071, 'HP:0034797', 'Hepatic hemophagocytosis', 'XPO:0103167', 'abnormal absorptive cell morphology', 0.41304347826086957, 5.43643956286526, 1.4984945466703803, 'HP:0025461', 'Abnormal cell morphology'),
(413072, 'HP:0034797', 'Hepatic hemophagocytosis', 'XPO:0102323', 'abnormal keratin accumulating cell morphology', 0.41304347826086957, 5.43643956286526, 1.4984945466703803, 'HP:0025461', 'Abnormal cell morphology'),
(413073, 'HP:0034797', 'Hepatic hemophagocytosis', 'XPO:0103099', 'abnormal alkali secreting cell morphology', 0.41304347826086957, 5.43643956286526, 1.4984945466703803, 'HP:0025461', 'Abnormal cell morphology'),
(413074, 'HP:0034797', 'Hepatic hemophagocytosis', 'XPO:0102446', 'abnormal natural killer cell morphology', 0.41509433962264153, 6.786309419308587, 1.6783797624145764, 'UPHENO:0087123', 'abnormal immune system morphology'),
(413075, 'HP:0034797', 'Hepatic hemophagocytosis', 'XPO:0102285', 'abnormal myoblast morphology', 0.41304347826086957, 5.43643956286526, 1.4984945466703803, 'HP:0025461', 'Abnormal cell morphology'),
(413076, 'HP:0034797', 'Hepatic hemophagocytosis', 'XPO:0102434', 'abnormal exocrine cell morphology', 0.41304347826086957, 5.43643956286526, 1.4984945466703803, 'HP:0025461', 'Abnormal cell morphology'),
(413077, 'HP:0034797', 'Hepatic hemophagocytosis', 'XPO:0103082', 'abnormal myeloid cell morphology', 0.42, 5.574066539846944, 1.5300679549404714, 'UPHENO:0004459', 'abnormal hematopoietic system'),
(413078, 'HP:0034797', 'Hepatic hemophagocytosis', 'XPO:0101658', 'abnormal germ cell morphology', 0.41304347826086957, 5.43643956286526, 1.4984945466703803, 'HP:0025461', 'Abnormal cell morphology'),
(413079, 'HP:0034797', 'Hepatic hemophagocytosis', 'XPO:0101917', 'abnormal progenitor cell morphology', 0.41304347826086957, 5.43643956286526, 1.4984945466703803, 'HP:0025461', 'Abnormal cell morphology'),
(413080, 'HP:0003546', 'Exercise intolerance', 'XPO:0141816', 'abnormal ligase activity', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(413081, 'HP:0003546', 'Exercise intolerance', 'XPO:0101366', 'abnormal morula cell', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(413082, 'HP:0003546', 'Exercise intolerance', 'XPO:0100610', 'abnormal appendage', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(413083, 'HP:0003546', 'Exercise intolerance', 'XPO:0141963', 'absent cilium motility in pronephric nephrostome', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(413084, 'HP:0003546', 'Exercise intolerance', 'XPO:0107253', 'abnormal enteric nervous system', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(413085, 'HP:0003546', 'Exercise intolerance', 'XPO:0101463', 'abnormal right-ventral blastomere', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(413086, 'HP:0003546', 'Exercise intolerance', 'XPO:0101040', 'abnormal axial mesoderm', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(413087, 'HP:0003546', 'Exercise intolerance', 'XPO:0100894', 'abnormal nucleus', 0.47619047619047616, 1.8210412618256888, 0.9312156064152277, 'HP:0000118', 'Phenotypic abnormality'),
(413088, 'HP:0003546', 'Exercise intolerance', 'XPO:0132054', 'abnormal development of portion of organism substance', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(413089, 'HP:0003546', 'Exercise intolerance', 'XPO:0101411', 'abnormal marginal zone (sensu neural)', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(413090, 'HP:0003546', 'Exercise intolerance', 'XPO:0101480', 'abnormal stage V oocyte', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(413091, 'HP:0003546', 'Exercise intolerance', 'XPO:0141724', 'abnormal prevention of polyspermy', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(413092, 'HP:0003546', 'Exercise intolerance', 'XPO:0100533', 'abnormal melanoblast', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(413093, 'HP:0003546', 'Exercise intolerance', 'XPO:0100754', 'abnormal electrically active cell', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(413094, 'HP:0003546', 'Exercise intolerance', 'XPO:0131714', 'abnormal establishment of tissue polarity', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(413095, 'HP:0003546', 'Exercise intolerance', 'XPO:0141841', 'abnormality of whole organism mass', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(413096, 'HP:0003546', 'Exercise intolerance', 'XPO:0141786', 'abnormal pigment metabolic process', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(413097, 'HP:0003546', 'Exercise intolerance', 'XPO:0101212', 'abnormal glomeral mesenchyme', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(413098, 'HP:0003546', 'Exercise intolerance', 'XPO:0101451', 'abnormal dorsal lymph space', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(413099, 'HP:0003546', 'Exercise intolerance', 'XPO:0133401', 'absent determination of left/right symmetry in lateral plate mesoderm', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(413100, 'HP:0003546', 'Exercise intolerance', 'XPO:0141767', 'abnormal temperature homeostasis', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(413101, 'HP:0003546', 'Exercise intolerance', 'XPO:0100991', 'abnormal iliac process primordium', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(413102, 'HP:0003546', 'Exercise intolerance', 'XPO:0141272', 'absent surface breathing', 0.5714285714285714, 1.4755025719078136, 0.918228907628411, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(413103, 'HP:0003546', 'Exercise intolerance', 'XPO:0100915', 'abnormal dermal system', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(413104, 'HP:0003546', 'Exercise intolerance', 'XPO:0100031', 'abnormal central nervous system', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(413105, 'HP:0003546', 'Exercise intolerance', 'XPO:0100394', 'abnormal marginal zone', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(413106, 'HP:0003546', 'Exercise intolerance', 'XPO:0115391', 'abnormally undifferentiated alimentary system', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(413107, 'HP:0003546', 'Exercise intolerance', 'XPO:0131669', 'abnormal Roux spot', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(413108, 'HP:0003546', 'Exercise intolerance', 'XPO:0100295', 'abnormal extracellular matrix', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(413109, 'HP:0003546', 'Exercise intolerance', 'XPO:0100791', 'abnormal multiciliated cell precursor', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(413110, 'HP:0003546', 'Exercise intolerance', 'XPO:0131666', 'abnormal adherens junction', 0.47619047619047616, 1.8210412618256888, 0.9312156064152277, 'HP:0000118', 'Phenotypic abnormality'),
(413111, 'HP:0003546', 'Exercise intolerance', 'XPO:0131740', 'abnormal detection of nodal flow', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(413112, 'HP:0003546', 'Exercise intolerance', 'XPO:0101061', 'abnormal plasma membrane', 0.47619047619047616, 1.8210412618256888, 0.9312156064152277, 'HP:0000118', 'Phenotypic abnormality'),
(413113, 'HP:0003546', 'Exercise intolerance', 'XPO:0141267', 'abnormal resting posture', 0.5714285714285714, 1.4755025719078136, 0.918228907628411, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(413114, 'HP:0003546', 'Exercise intolerance', 'XPO:0131730', 'abnormal regulation of protein folding', 0.47058823529411764, 1.4755025719078136, 0.8332791557971614, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(413115, 'HP:0003546', 'Exercise intolerance', 'XPO:0131480', 'absent mating behavior', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(413116, 'HP:0003546', 'Exercise intolerance', 'XPO:0141775', 'abnormal nitrogen compound metabolic process', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(413117, 'HP:0003546', 'Exercise intolerance', 'XPO:0101072', 'abnormal mitochondrial cloud', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(413118, 'HP:0003546', 'Exercise intolerance', 'XPO:0101435', 'abnormal paracrine cell', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(413119, 'HP:0003546', 'Exercise intolerance', 'XPO:0131469', 'abnormal heart process', 0.47058823529411764, 1.4755025719078136, 0.8332791557971614, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(413120, 'HP:0003546', 'Exercise intolerance', 'XPO:0131479', 'absent social behavior', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(413121, 'HP:0003546', 'Exercise intolerance', 'XPO:0133340', 'abnormal cell adhesion', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(413122, 'HP:0003546', 'Exercise intolerance', 'XPO:0131472', 'absent vocalization behavior', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(413123, 'HP:0003546', 'Exercise intolerance', 'XPO:0100231', 'abnormal compound organ', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(413124, 'HP:0003546', 'Exercise intolerance', 'XPO:0100218', 'abnormal epithelial cell', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(413125, 'HP:0003546', 'Exercise intolerance', 'XPO:0101220', 'abnormal centriole', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(413126, 'HP:0003546', 'Exercise intolerance', 'XPO:0131975', 'abnormal development of anatomical line', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(413127, 'HP:0003546', 'Exercise intolerance', 'XPO:0103783', 'absent hatching behavior', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(413128, 'HP:0003546', 'Exercise intolerance', 'XPO:0131719', 'abnormal activation of meiosis', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(413129, 'HP:0003546', 'Exercise intolerance', 'XPO:0141264', 'abnormal schooling behavior', 0.5714285714285714, 1.4755025719078136, 0.918228907628411, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(413130, 'HP:0003546', 'Exercise intolerance', 'XPO:0100422', 'abnormal notochord', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(413131, 'HP:0003546', 'Exercise intolerance', 'XPO:0115508', 'abnormally peramorphic growth of whole organism', 0.47058823529411764, 1.4755025719078136, 0.8332791557971614, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(413132, 'HP:0003546', 'Exercise intolerance', 'XPO:0107272', 'abnormal axial region', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(413133, 'HP:0003546', 'Exercise intolerance', 'XPO:0100546', 'abnormal whole organism', 0.5, 1.4755025719078136, 0.8589244937443028, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(413134, 'HP:0003546', 'Exercise intolerance', 'XPO:0100258', 'abnormal organ part', 0.5, 1.4755025719078136, 0.8589244937443028, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(413135, 'HP:0003546', 'Exercise intolerance', 'XPO:0101448', 'abnormal myelin accumulating cell', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(413136, 'HP:0003546', 'Exercise intolerance', 'XPO:0101141', 'abnormal Keller explant', 0.5, 1.4755025719078136, 0.8589244937443028, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(413137, 'HP:0003546', 'Exercise intolerance', 'XPO:0100172', 'abnormal stem cell', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(413138, 'HP:0003546', 'Exercise intolerance', 'XPO:0100006', 'abnormal anatomical structure', 0.5333333333333333, 1.4755025719078136, 0.8870934026456857, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(413139, 'HP:0003546', 'Exercise intolerance', 'XPO:0107260', 'abnormal anterior-posterior axis', 0.47058823529411764, 1.4755025719078136, 0.8332791557971614, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(413140, 'HP:0003546', 'Exercise intolerance', 'XPO:0100842', 'abnormal left-dorsal blastomere', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(413141, 'HP:0003546', 'Exercise intolerance', 'XPO:0107263', 'abnormal anatomical side', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(413142, 'HP:0003546', 'Exercise intolerance', 'XPO:0100585', 'abnormal elastica externa', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(413143, 'HP:0003546', 'Exercise intolerance', 'XPO:0101373', 'abnormal oxygen accumulating cell', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(413144, 'HP:0003546', 'Exercise intolerance', 'XPO:0100293', 'abnormal duct', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(413145, 'HP:0003546', 'Exercise intolerance', 'XPO:0141276', 'decreased surface breathing', 0.5333333333333333, 1.4755025719078136, 0.8870934026456857, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(413146, 'HP:0003546', 'Exercise intolerance', 'XPO:0100823', 'abnormal blood', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(413147, 'HP:0003546', 'Exercise intolerance', 'XPO:0101519', 'abnormal hypobranchial placode', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(413148, 'HP:0003546', 'Exercise intolerance', 'XPO:0131700', 'abnormal BMP signaling pathway', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(413149, 'HP:0003546', 'Exercise intolerance', 'XPO:0141814', 'abnormal lyase activity', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(413150, 'HP:0003546', 'Exercise intolerance', 'XPO:0100745', 'abnormal anterior lymph sac', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(413151, 'HP:0003546', 'Exercise intolerance', 'XPO:0100643', 'abnormal thoracic region', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(413152, 'HP:0003546', 'Exercise intolerance', 'XPO:0101311', 'abnormal bottle cell', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(413153, 'HP:0003546', 'Exercise intolerance', 'XPO:0100277', 'abnormal blastocoel', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(413154, 'HP:0003546', 'Exercise intolerance', 'XPO:0100232', 'abnormal lymphatic system', 0.47619047619047616, 1.8210412618256888, 0.9312156064152277, 'HP:0000118', 'Phenotypic abnormality'),
(413155, 'HP:0003546', 'Exercise intolerance', 'XPO:0101110', 'abnormal cell-free extract', 0.5, 1.4755025719078136, 0.8589244937443028, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(413156, 'HP:0003546', 'Exercise intolerance', 'XPO:0141817', 'abnormal demethylase activity', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(413157, 'HP:0003546', 'Exercise intolerance', 'XPO:0141961', 'absent cilium motility in mucociliary epithelium', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(413158, 'HP:0003546', 'Exercise intolerance', 'XPO:0107339', 'abnormal yolk platelet', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(413159, 'HP:0003546', 'Exercise intolerance', 'XPO:0133388', 'absent insulin receptor signaling pathway', 0.47058823529411764, 1.4755025719078136, 0.8332791557971614, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(413160, 'HP:0003546', 'Exercise intolerance', 'XPO:0141809', 'abnormal catalytic activity', 0.47058823529411764, 1.4755025719078136, 0.8332791557971614, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(413161, 'HP:0003546', 'Exercise intolerance', 'XPO:0116429', 'abnormal behavior', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(413162, 'HP:0003546', 'Exercise intolerance', 'XPO:0141892', 'abnormal inositol metabolic process', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(413163, 'HP:0003546', 'Exercise intolerance', 'XPO:0141968', 'absent cilium motility in ciliated cell', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(413164, 'HP:0003546', 'Exercise intolerance', 'XPO:0107261', 'abnormal dorsal-ventral axis', 0.47058823529411764, 1.4755025719078136, 0.8332791557971614, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(413165, 'HP:0003546', 'Exercise intolerance', 'XPO:0131476', 'absent mechanosensory behavior', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(413166, 'HP:0003546', 'Exercise intolerance', 'XPO:0128000', 'absent behavior', 0.47058823529411764, 1.4755025719078136, 0.8332791557971614, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(413167, 'HP:0003546', 'Exercise intolerance', 'XPO:0100704', 'abnormal Merkel cell', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(413168, 'HP:0003546', 'Exercise intolerance', 'XPO:0100887', 'abnormal right-dorsal blastomere', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(413169, 'HP:0003546', 'Exercise intolerance', 'XPO:0100481', 'abnormal anatomical line', 0.5333333333333333, 1.4755025719078136, 0.8870934026456857, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(413170, 'HP:0003546', 'Exercise intolerance', 'XPO:0100003', 'abnormal organism subdivision', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(413171, 'HP:0003546', 'Exercise intolerance', 'XPO:0141776', 'abnormal metabolic process', 0.5555555555555556, 1.8210412618256888, 1.005827813247954, 'HP:0000118', 'Phenotypic abnormality'),
(413172, 'HP:0003546', 'Exercise intolerance', 'XPO:0100573', 'abnormal extraembryonic structure', 0.47058823529411764, 1.4755025719078136, 0.8332791557971614, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(413173, 'HP:0003546', 'Exercise intolerance', 'XPO:0141811', 'abnormal oxidoreductase activity', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(413174, 'HP:0003546', 'Exercise intolerance', 'XPO:0141815', 'abnormal isomerase activity', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(413175, 'HP:0003546', 'Exercise intolerance', 'XPO:0101497', 'abnormal ciliary axoneme', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(413176, 'HP:0003546', 'Exercise intolerance', 'XPO:0100026', 'abnormal germ cell', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(413177, 'HP:0003546', 'Exercise intolerance', 'XPO:0141600', 'absent metamorphosis', 0.47058823529411764, 1.4755025719078136, 0.8332791557971614, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(413178, 'HP:0003546', 'Exercise intolerance', 'XPO:0100282', 'abnormal pelvic girdle primordium', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(413179, 'HP:0003546', 'Exercise intolerance', 'XPO:0131705', 'abnormal chemotaxis', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(413180, 'HP:0003546', 'Exercise intolerance', 'XPO:0141266', 'abnormal surface breathing', 0.5714285714285714, 1.4755025719078136, 0.918228907628411, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(413181, 'HP:0003546', 'Exercise intolerance', 'XPO:0100724', 'abnormal kinetochore', 0.47619047619047616, 1.8210412618256888, 0.9312156064152277, 'HP:0000118', 'Phenotypic abnormality'),
(413182, 'HP:0003546', 'Exercise intolerance', 'XPO:0107269', 'abnormal right side', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(413183, 'HP:0003546', 'Exercise intolerance', 'XPO:0100317', 'abnormal respiratory system', 0.47619047619047616, 1.8210412618256888, 0.9312156064152277, 'HP:0000118', 'Phenotypic abnormality'),
(413184, 'HP:0003546', 'Exercise intolerance', 'XPO:0100501', 'abnormal urogenital system', 0.47619047619047616, 1.8210412618256888, 0.9312156064152277, 'HP:0000118', 'Phenotypic abnormality'),
(413185, 'HP:0003546', 'Exercise intolerance', 'XPO:0103624', 'absent anterior/posterior pattern specification in midgut', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(413186, 'HP:0003546', 'Exercise intolerance', 'XPO:0107270', 'abnormal proximal-distal axis', 0.47058823529411764, 1.4755025719078136, 0.8332791557971614, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(413187, 'HP:0003546', 'Exercise intolerance', 'XPO:0100674', 'abnormal secondary oogonium', 0.47619047619047616, 1.8210412618256888, 0.9312156064152277, 'HP:0000118', 'Phenotypic abnormality'),
(413188, 'HP:0003546', 'Exercise intolerance', 'XPO:0101406', 'abnormal cleavage furrow', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(413189, 'HP:0003546', 'Exercise intolerance', 'XPO:0141960', 'absent cilium motility in brain', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(413190, 'HP:0003546', 'Exercise intolerance', 'XPO:0100784', 'abnormal left blastomere', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(413191, 'HP:0003546', 'Exercise intolerance', 'XPO:0131729', 'abnormal regulation of growth rate', 0.47058823529411764, 1.4755025719078136, 0.8332791557971614, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(413192, 'HP:0003546', 'Exercise intolerance', 'XPO:0100028', 'abnormal anatomical cluster', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(413193, 'HP:0003546', 'Exercise intolerance', 'XPO:0100289', 'abnormal chondroblast', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(413194, 'HP:0003546', 'Exercise intolerance', 'XPO:0100265', 'abnormal sensory epithelial cell', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(413195, 'HP:0003546', 'Exercise intolerance', 'XPO:0107312', 'abnormal filopodium', 0.47619047619047616, 1.8210412618256888, 0.9312156064152277, 'HP:0000118', 'Phenotypic abnormality'),
(413196, 'HP:0003546', 'Exercise intolerance', 'XPO:0100852', 'abnormal interdigital region', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(413197, 'HP:0003546', 'Exercise intolerance', 'XPO:0107284', 'abnormal migrating myoblast', 0.47619047619047616, 1.8210412618256888, 0.9312156064152277, 'HP:0000118', 'Phenotypic abnormality'),
(413198, 'HP:0003546', 'Exercise intolerance', 'XPO:0141754', 'abnormal homeostatic process', 0.47058823529411764, 1.4755025719078136, 0.8332791557971614, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(413199, 'HP:0003546', 'Exercise intolerance', 'XPO:0100762', 'abnormal intersomitic region', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(413200, 'HP:0003546', 'Exercise intolerance', 'XPO:0100515', 'abnormal somatic stem cell', 0.47619047619047616, 1.8210412618256888, 0.9312156064152277, 'HP:0000118', 'Phenotypic abnormality'),
(413201, 'HP:0003546', 'Exercise intolerance', 'XPO:0141788', 'abnormal hormone biosynthetic process', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(413202, 'HP:0003546', 'Exercise intolerance', 'XPO:0141794', 'abnormal prosthetic group metabolic process', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(413203, 'HP:0003546', 'Exercise intolerance', 'XPO:0100337', 'abnormal zygote', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(413204, 'HP:0003546', 'Exercise intolerance', 'XPO:0100070', 'abnormal anatomical system', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(413205, 'HP:0003546', 'Exercise intolerance', 'XPO:0131481', 'absent feeding behavior', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(413206, 'HP:0003546', 'Exercise intolerance', 'XPO:0100162', 'abnormal presumptive rhombomere', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(413207, 'HP:0003546', 'Exercise intolerance', 'XPO:0100108', 'abnormal cell part', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(413208, 'HP:0003546', 'Exercise intolerance', 'XPO:0141860', 'abnormal malate-aspartate shuttle', 0.47619047619047616, 1.8210412618256888, 0.9312156064152277, 'HP:0000118', 'Phenotypic abnormality'),
(413209, 'HP:0003546', 'Exercise intolerance', 'XPO:0141743', 'abnormal chemical homeostasis within a tissue', 0.5714285714285714, 1.4755025719078136, 0.918228907628411, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(413210, 'HP:0003546', 'Exercise intolerance', 'XPO:0131715', 'abnormal fibroblast growth factor receptor signaling pathway', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(413211, 'HP:0003546', 'Exercise intolerance', 'XPO:0107278', 'abnormal medial region', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(413212, 'HP:0003546', 'Exercise intolerance', 'XPO:0100626', 'abnormal primordial germ cell', 0.47619047619047616, 1.8210412618256888, 0.9312156064152277, 'HP:0000118', 'Phenotypic abnormality'),
(413213, 'HP:0003546', 'Exercise intolerance', 'XPO:0131675', 'abnormal spindle microtubule', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(413214, 'HP:0003546', 'Exercise intolerance', 'XPO:0101264', 'abnormal mitotic spindle', 0.47619047619047616, 1.8210412618256888, 0.9312156064152277, 'HP:0000118', 'Phenotypic abnormality'),
(413215, 'HP:0003546', 'Exercise intolerance', 'XPO:0142057', 'abnormal desmosome', 0.47619047619047616, 1.8210412618256888, 0.9312156064152277, 'HP:0000118', 'Phenotypic abnormality'),
(413216, 'HP:0003546', 'Exercise intolerance', 'XPO:0100667', 'abnormal vegetal yolk mass', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(413217, 'HP:0003546', 'Exercise intolerance', 'XPO:0141778', 'abnormal biosynthetic process', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(413218, 'HP:0003546', 'Exercise intolerance', 'XPO:0101004', 'abnormal acid secreting cell', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(413219, 'HP:0003546', 'Exercise intolerance', 'XPO:0141760', 'abnormal multicellular organismal homeostasis', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(413220, 'HP:0003546', 'Exercise intolerance', 'XPO:0100081', 'abnormal anatomical entity in vitro', 0.5333333333333333, 1.4755025719078136, 0.8870934026456857, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(413221, 'HP:0003546', 'Exercise intolerance', 'XPO:0131677', 'abnormal actin filament', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(413222, 'HP:0003546', 'Exercise intolerance', 'XPO:0101535', 'abnormal absorptive cell', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(413223, 'HP:0003546', 'Exercise intolerance', 'XPO:0101078', 'abnormal mucous gland', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(413224, 'HP:0003546', 'Exercise intolerance', 'XPO:0101174', 'abnormal articular system', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(413225, 'HP:0003546', 'Exercise intolerance', 'XPO:0100416', 'abnormal ligament', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(413226, 'HP:0003546', 'Exercise intolerance', 'XPO:0141715', 'abnormal septum', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(413227, 'HP:0003546', 'Exercise intolerance', 'XPO:0142056', 'abnormal main body axis', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(413228, 'HP:0003546', 'Exercise intolerance', 'XPO:00000000', 'Xenopus phenotype', 0.6153846153846154, 1.4755025719078136, 0.9528911704452407, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(413229, 'HP:0003546', 'Exercise intolerance', 'XPO:0131685', 'abnormal cortical actin cytoskeleton', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(413230, 'HP:0003546', 'Exercise intolerance', 'XPO:0101109', 'abnormal egg cell-free extract', 0.47058823529411764, 1.4755025719078136, 0.8332791557971614, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(413231, 'HP:0003546', 'Exercise intolerance', 'XPO:0141271', 'increased surface breathing', 0.5333333333333333, 1.4755025719078136, 0.8870934026456857, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(413232, 'HP:0003546', 'Exercise intolerance', 'XPO:0101132', 'abnormal apoptotic cell', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(413233, 'HP:0003546', 'Exercise intolerance', 'XPO:0116494', 'absent biological process', 0.5333333333333333, 1.4755025719078136, 0.8870934026456857, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(413234, 'HP:0003546', 'Exercise intolerance', 'XPO:0100715', 'abnormal ciliated cell', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(413235, 'HP:0003546', 'Exercise intolerance', 'XPO:0141904', 'abnormal glucosamine metabolic process', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(413236, 'HP:0003546', 'Exercise intolerance', 'XPO:0100344', 'abnormal portion of organism substance', 0.5333333333333333, 1.4755025719078136, 0.8870934026456857, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(413237, 'HP:0003546', 'Exercise intolerance', 'XPO:0100308', 'abnormal early embryonic cell', 0.47619047619047616, 1.8210412618256888, 0.9312156064152277, 'HP:0000118', 'Phenotypic abnormality'),
(413238, 'HP:0003546', 'Exercise intolerance', 'XPO:0101157', 'abnormal female organism', 0.47058823529411764, 1.4755025719078136, 0.8332791557971614, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(413239, 'HP:0003546', 'Exercise intolerance', 'XPO:0101168', 'abnormal circulating cell', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(413240, 'HP:0003546', 'Exercise intolerance', 'XPO:0141880', 'abnormal ethanolamine metabolic process', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(413241, 'HP:0003546', 'Exercise intolerance', 'XPO:0101221', 'abnormal larval immune system', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(413242, 'HP:0003546', 'Exercise intolerance', 'XPO:0141813', 'abnormal hydrolase activity', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(413243, 'HP:0003546', 'Exercise intolerance', 'XPO:0101547', 'abnormal lampbrush chromosome', 0.47619047619047616, 1.8210412618256888, 0.9312156064152277, 'HP:0000118', 'Phenotypic abnormality'),
(413244, 'HP:0003546', 'Exercise intolerance', 'XPO:0131474', 'absent behavioral response to pain', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(413245, 'HP:0003546', 'Exercise intolerance', 'XPO:0101468', 'abnormal stage I oocyte', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(413246, 'HP:0003546', 'Exercise intolerance', 'XPO:0100545', 'abnormal male organism', 0.47058823529411764, 1.4755025719078136, 0.8332791557971614, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(413247, 'HP:0003546', 'Exercise intolerance', 'XPO:0101071', 'abnormal endoplasmic reticulum', 0.47619047619047616, 1.8210412618256888, 0.9312156064152277, 'HP:0000118', 'Phenotypic abnormality'),
(413248, 'HP:0003546', 'Exercise intolerance', 'XPO:0141798', 'abnormal lipid metabolic process', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(413249, 'HP:0003546', 'Exercise intolerance', 'XPO:0101228', 'abnormal mesenchymal stem cell', 0.47619047619047616, 1.8210412618256888, 0.9312156064152277, 'HP:0000118', 'Phenotypic abnormality'),
(413250, 'HP:0003546', 'Exercise intolerance', 'XPO:0100025', 'abnormal oocyte', 0.47619047619047616, 1.8210412618256888, 0.9312156064152277, 'HP:0000118', 'Phenotypic abnormality'),
(413251, 'HP:0003546', 'Exercise intolerance', 'XPO:0100014', 'abnormal tissue', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(413252, 'HP:0003546', 'Exercise intolerance', 'XPO:0141810', 'abnormal cyclase activity', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(413253, 'HP:0003546', 'Exercise intolerance', 'XPO:0141965', 'absent cilium motility in alimentary system', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(413254, 'HP:0003546', 'Exercise intolerance', 'XPO:0101302', 'abnormal subcortical cytoplasm', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(413255, 'HP:0003546', 'Exercise intolerance', 'XPO:0101297', 'abnormal barrier cell', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(413256, 'HP:0003546', 'Exercise intolerance', 'XPO:0115512', 'abnormally semi-erect whole organism', 0.47058823529411764, 1.4755025719078136, 0.8332791557971614, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(413257, 'HP:0003546', 'Exercise intolerance', 'XPO:0141772', 'abnormal water homeostasis', 0.5714285714285714, 1.4755025719078136, 0.918228907628411, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(413258, 'HP:0003546', 'Exercise intolerance', 'XPO:0131738', 'abnormal Wnt signaling pathway', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(413259, 'HP:0003546', 'Exercise intolerance', 'XPO:0100653', 'abnormal myoblast', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(413260, 'HP:0003546', 'Exercise intolerance', 'XPO:0101570', 'abnormal forelimb region', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(413261, 'HP:0003546', 'Exercise intolerance', 'XPO:0141787', 'abnormal hormone metabolic process', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(413262, 'HP:0003546', 'Exercise intolerance', 'XPO:0100363', 'abnormal cardiovascular system', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(413263, 'HP:0003546', 'Exercise intolerance', 'XPO:0141911', 'abnormal ribose phosphate metabolic process', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(413264, 'HP:0003546', 'Exercise intolerance', 'XPO:0100002', 'abnormal head', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(413265, 'HP:0003546', 'Exercise intolerance', 'XPO:0100665', 'abnormal egg jelly', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(413266, 'HP:0003546', 'Exercise intolerance', 'XPO:0100493', 'abnormal liver and biliary system', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(413267, 'HP:0003546', 'Exercise intolerance', 'XPO:0100888', 'abnormal microtubule', 0.47619047619047616, 1.8210412618256888, 0.9312156064152277, 'HP:0000118', 'Phenotypic abnormality'),
(413268, 'HP:0003546', 'Exercise intolerance', 'XPO:0141796', 'abnormal demethylation', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(413269, 'HP:0003546', 'Exercise intolerance', 'XPO:0141771', 'abnormal urea homeostasis', 0.5714285714285714, 1.4755025719078136, 0.918228907628411, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(413270, 'HP:0003546', 'Exercise intolerance', 'XPO:0142052', 'abnormal nasal region', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(413271, 'HP:0003546', 'Exercise intolerance', 'XPO:0100205', 'abnormal limb segment', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(413272, 'HP:0003546', 'Exercise intolerance', 'XPO:0101409', 'abnormal perivitelline space', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(413273, 'HP:0003546', 'Exercise intolerance', 'XPO:0107288', 'abnormal larval alimentary system', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(413274, 'HP:0003546', 'Exercise intolerance', 'XPO:0141777', 'abnormal catabolic process', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(413275, 'HP:0003546', 'Exercise intolerance', 'XPO:0100728', 'abnormal cell condensation', 0.47058823529411764, 1.4755025719078136, 0.8332791557971614, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(413276, 'HP:0003546', 'Exercise intolerance', 'XPO:0131728', 'abnormal regulation of cell size', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(413277, 'HP:0003546', 'Exercise intolerance', 'XPO:0107271', 'abnormal apical region', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(413278, 'HP:0003546', 'Exercise intolerance', 'XPO:0100285', 'abnormal progenitor cell', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(413279, 'HP:0003546', 'Exercise intolerance', 'XPO:0141962', 'absent cilium motility in pronephric kidney', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(413280, 'HP:0003546', 'Exercise intolerance', 'XPO:0100192', 'abnormal epithelium', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(413281, 'HP:0003546', 'Exercise intolerance', 'XPO:0100060', 'abnormal regenerating tissue', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(413282, 'HP:0003546', 'Exercise intolerance', 'XPO:0141315', 'abnormal anatomical region', 0.47058823529411764, 1.4755025719078136, 0.8332791557971614, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(413283, 'HP:0003546', 'Exercise intolerance', 'XPO:0141714', 'abnormal anterior notochord', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(413284, 'HP:0003546', 'Exercise intolerance', 'XPO:0101575', 'abnormal vitelline membrane', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(413285, 'HP:0003546', 'Exercise intolerance', 'XPO:0100164', 'abnormal neural nucleus', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(413286, 'HP:0003546', 'Exercise intolerance', 'XPO:0141795', 'abnormal glycosylation', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(413287, 'HP:0003546', 'Exercise intolerance', 'XPO:0141744', 'abnormal chemical homeostasis', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(413288, 'HP:0003546', 'Exercise intolerance', 'XPO:0107273', 'abnormal basal region', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(413289, 'HP:0003546', 'Exercise intolerance', 'XPO:0100900', 'abnormal angioblast', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(413290, 'HP:0003546', 'Exercise intolerance', 'XPO:0141907', 'abnormal putrescine metabolic process', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(413291, 'HP:0003546', 'Exercise intolerance', 'XPO:0141784', 'abnormal cellular hormone metabolic process', 0.5714285714285714, 1.4755025719078136, 0.918228907628411, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(413292, 'HP:0003546', 'Exercise intolerance', 'XPO:0100551', 'abnormal oocyte cortex', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(413293, 'HP:0003546', 'Exercise intolerance', 'XPO:0100742', 'abnormal musculoskeletal system', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(413294, 'HP:0003546', 'Exercise intolerance', 'XPO:0131482', 'absent locomotory behavior', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(413295, 'HP:0003546', 'Exercise intolerance', 'XPO:0133403', 'abnormal developmental process', 0.47058823529411764, 1.4755025719078136, 0.8332791557971614, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(413296, 'HP:0003546', 'Exercise intolerance', 'XPO:0141770', 'abnormal urate homeostasis', 0.5714285714285714, 1.4755025719078136, 0.918228907628411, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(413297, 'HP:0003546', 'Exercise intolerance', 'XPO:0131745', 'abnormal axis elongation', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(413298, 'HP:0003546', 'Exercise intolerance', 'XPO:0107264', 'abnormal anterior side', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(413299, 'HP:0003546', 'Exercise intolerance', 'XPO:0131722', 'abnormal determination of left/right symmetry', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(413300, 'HP:0003546', 'Exercise intolerance', 'XPO:0100274', 'abnormal sensory system', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(413301, 'HP:0003546', 'Exercise intolerance', 'XPO:0100574', 'abnormal gastrula cell', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(413302, 'HP:0003546', 'Exercise intolerance', 'XPO:0100225', 'abnormal endocrine system', 0.47619047619047616, 1.8210412618256888, 0.9312156064152277, 'HP:0000118', 'Phenotypic abnormality'),
(413303, 'HP:0003546', 'Exercise intolerance', 'XPO:0107285', 'abnormal flexural organ', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(413304, 'HP:0003546', 'Exercise intolerance', 'XPO:0101176', 'abnormal non-ciliated epithelial cell', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(413305, 'HP:0003546', 'Exercise intolerance', 'XPO:0100912', 'abnormal trabecula', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(413306, 'HP:0003546', 'Exercise intolerance', 'XPO:0141748', 'abnormal gas homeostasis', 0.5714285714285714, 1.4755025719078136, 0.918228907628411, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(413307, 'HP:0003546', 'Exercise intolerance', 'XPO:0141791', 'abnormal primary metabolic process', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(413308, 'HP:0003546', 'Exercise intolerance', 'XPO:0100114', 'abnormal peripheral nervous system', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(413309, 'HP:0003546', 'Exercise intolerance', 'XPO:0100429', 'abnormal spermatid', 0.47619047619047616, 1.8210412618256888, 0.9312156064152277, 'HP:0000118', 'Phenotypic abnormality'),
(413310, 'HP:0003546', 'Exercise intolerance', 'XPO:0100402', 'abnormal zeugopod', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(413311, 'HP:0003546', 'Exercise intolerance', 'XPO:0101498', 'abnormal stage II oocyte', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(413312, 'HP:0003546', 'Exercise intolerance', 'XPO:0100581', 'abnormal immune system', 0.47619047619047616, 1.8210412618256888, 0.9312156064152277, 'HP:0000118', 'Phenotypic abnormality'),
(413313, 'HP:0003546', 'Exercise intolerance', 'XPO:0100023', 'abnormal mesenchyme', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(413314, 'HP:0003546', 'Exercise intolerance', 'XPO:0141898', 'abnormal maltose metabolic process', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(413315, 'HP:0003546', 'Exercise intolerance', 'XPO:0100976', 'abnormal multiciliated cell', 0.47619047619047616, 1.8210412618256888, 0.9312156064152277, 'HP:0000118', 'Phenotypic abnormality'),
(413316, 'HP:0003546', 'Exercise intolerance', 'XPO:0101096', 'abnormal tendon', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(413317, 'HP:0003546', 'Exercise intolerance', 'XPO:0101461', 'abnormal sperm entry point', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(413318, 'HP:0003546', 'Exercise intolerance', 'XPO:0100372', 'abnormal hematological system', 0.47619047619047616, 1.8210412618256888, 0.9312156064152277, 'HP:0000118', 'Phenotypic abnormality'),
(413319, 'HP:0003546', 'Exercise intolerance', 'XPO:0101200', 'abnormal joint region', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(413320, 'HP:0003546', 'Exercise intolerance', 'XPO:0141718', 'abnormal posterior notochord', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(413321, 'HP:0003546', 'Exercise intolerance', 'XPO:0107268', 'abnormal left side', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(413322, 'HP:0003546', 'Exercise intolerance', 'XPO:0101237', 'abnormal mucus secreting cell', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(413323, 'HP:0003546', 'Exercise intolerance', 'XPO:0100902', 'abnormal spermatocyte', 0.47619047619047616, 1.8210412618256888, 0.9312156064152277, 'HP:0000118', 'Phenotypic abnormality'),
(413324, 'HP:0003546', 'Exercise intolerance', 'XPO:0107258', 'abnormal anatomical axis', 0.5, 1.4755025719078136, 0.8589244937443028, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(413325, 'HP:0003546', 'Exercise intolerance', 'XPO:0141975', 'abnormal cilium motility', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(413326, 'HP:0003546', 'Exercise intolerance', 'XPO:0131694', 'abnormal RNA polymerase II activity', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(413327, 'HP:0003546', 'Exercise intolerance', 'XPO:0141964', 'absent cilium motility in olfactory pit', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(413328, 'HP:0003546', 'Exercise intolerance', 'XPO:0131703', 'abnormal cell division', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(413329, 'HP:0003546', 'Exercise intolerance', 'XPO:0100437', 'abnormal proepicardium', 0.47619047619047616, 1.8210412618256888, 0.9312156064152277, 'HP:0000118', 'Phenotypic abnormality'),
(413330, 'HP:0003546', 'Exercise intolerance', 'XPO:0141790', 'abnormal cellular metabolic process', 0.47619047619047616, 1.8210412618256888, 0.9312156064152277, 'HP:0000118', 'Phenotypic abnormality'),
(413331, 'HP:0003546', 'Exercise intolerance', 'XPO:0100307', 'abnormal blastomere', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(413332, 'HP:0003546', 'Exercise intolerance', 'XPO:0100010', 'abnormal multicellular anatomical structure', 0.47058823529411764, 1.4755025719078136, 0.8332791557971614, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(413333, 'HP:0003546', 'Exercise intolerance', 'XPO:0101241', 'abnormal nucleate erythrocyte', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(413334, 'HP:0003546', 'Exercise intolerance', 'XPO:0100781', 'abnormal presumptive ectoderm', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(413335, 'HP:0003546', 'Exercise intolerance', 'XPO:0100599', 'abnormal adult immune system', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(413336, 'HP:0003546', 'Exercise intolerance', 'XPO:0101283', 'abnormal left-ventral blastomere', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(413337, 'HP:0003546', 'Exercise intolerance', 'XPO:0131711', 'abnormal establishment of cell polarity', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(413338, 'HP:0003546', 'Exercise intolerance', 'XPO:0101472', 'abnormal zygote cortex', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(413339, 'HP:0003546', 'Exercise intolerance', 'XPO:0100251', 'abnormal proteinaceous extracellular matrix', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(413340, 'HP:0003546', 'Exercise intolerance', 'XPO:0100856', 'abnormal simple organ', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(413341, 'HP:0003546', 'Exercise intolerance', 'XPO:0101240', 'abnormal ciliated non-epidermal cell', 0.47619047619047616, 1.8210412618256888, 0.9312156064152277, 'HP:0000118', 'Phenotypic abnormality'),
(413342, 'HP:0003546', 'Exercise intolerance', 'XPO:0100807', 'abnormal matrix-based tissue', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(413343, 'HP:0003546', 'Exercise intolerance', 'XPO:0133397', 'abnormal insulin receptor signaling pathway', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(413344, 'HP:0003546', 'Exercise intolerance', 'XPO:0100135', 'abnormal surface structure', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(413345, 'HP:0003546', 'Exercise intolerance', 'XPO:0131723', 'abnormal pathway-restricted SMAD protein phosphorylation', 0.5714285714285714, 1.4755025719078136, 0.918228907628411, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(413346, 'HP:0003546', 'Exercise intolerance', 'XPO:0101503', 'abnormal organ cortex', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(413347, 'HP:0003546', 'Exercise intolerance', 'XPO:0141781', 'abnormal secondary metabolic process', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(413348, 'HP:0003546', 'Exercise intolerance', 'XPO:0100084', 'abnormal anatomical group', 0.47058823529411764, 1.4755025719078136, 0.8332791557971614, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(413349, 'HP:0003546', 'Exercise intolerance', 'XPO:0141745', 'abnormal creatinine homeostasis', 0.5714285714285714, 1.4755025719078136, 0.918228907628411, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(413350, 'HP:0003546', 'Exercise intolerance', 'XPO:0100104', 'abnormal embryonic structure', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(413351, 'HP:0003546', 'Exercise intolerance', 'XPO:0141499', 'abnormal tadpole', 0.47058823529411764, 1.4755025719078136, 0.8332791557971614, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(413352, 'HP:0003546', 'Exercise intolerance', 'XPO:0100386', 'abnormal limb', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(413353, 'HP:0003546', 'Exercise intolerance', 'XPO:0141738', 'abnormal carbon dioxide homeostasis', 0.5714285714285714, 1.4755025719078136, 0.918228907628411, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(413354, 'HP:0003546', 'Exercise intolerance', 'XPO:0115509', 'abnormally semi-viable whole organism', 0.47058823529411764, 1.4755025719078136, 0.8332791557971614, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(413355, 'HP:0003546', 'Exercise intolerance', 'XPO:0107259', 'abnormal animal-vegetal axis', 0.47058823529411764, 1.4755025719078136, 0.8332791557971614, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(413356, 'HP:0003546', 'Exercise intolerance', 'XPO:0100415', 'abnormal secretory epithelial cell', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(413357, 'HP:0003546', 'Exercise intolerance', 'XPO:0100458', 'abnormal autopod', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(413358, 'HP:0003546', 'Exercise intolerance', 'XPO:0100989', 'abnormal right blastomere', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(413359, 'HP:0003546', 'Exercise intolerance', 'XPO:0100549', 'abnormal mitotic cell', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(413360, 'HP:0003546', 'Exercise intolerance', 'XPO:0141783', 'abnormal collagen metabolic process', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(413361, 'HP:0003546', 'Exercise intolerance', 'XPO:0100587', 'abnormal vestibuloauditory system', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(413362, 'HP:0003546', 'Exercise intolerance', 'XPO:0141792', 'abnormal small molecule metabolic process', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(413363, 'HP:0003546', 'Exercise intolerance', 'XPO:0142051', 'abnormal cerebrospinal fluid', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(413364, 'HP:0003546', 'Exercise intolerance', 'XPO:0100917', 'abnormal stage III oocyte', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(413365, 'HP:0003546', 'Exercise intolerance', 'XPO:0100176', 'abnormal stage VI oocyte', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(413366, 'HP:0003546', 'Exercise intolerance', 'XPO:0131477', 'absent visual behavior', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(413367, 'HP:0003546', 'Exercise intolerance', 'XPO:0101569', 'abnormal activin-induced ectoderm', 0.5, 1.4755025719078136, 0.8589244937443028, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(413368, 'HP:0003546', 'Exercise intolerance', 'XPO:0141782', 'abnormal methylation', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(413369, 'HP:0003546', 'Exercise intolerance', 'XPO:0101467', 'abnormal alkali secreting cell', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(413370, 'HP:0003546', 'Exercise intolerance', 'XPO:0100009', 'abnormal multi-tissue structure', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(413371, 'HP:0003546', 'Exercise intolerance', 'XPO:0100239', 'abnormal acellular anatomical structure', 0.47058823529411764, 1.4755025719078136, 0.8332791557971614, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(413372, 'HP:0003546', 'Exercise intolerance', 'XPO:0141877', 'abnormal 2-deoxyribose 1-phosphate metabolic process', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(413373, 'HP:0003546', 'Exercise intolerance', 'XPO:0100423', 'abnormal process', 0.47058823529411764, 1.4755025719078136, 0.8332791557971614, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(413374, 'HP:0003546', 'Exercise intolerance', 'XPO:0115758', 'abnormally decreased mobility of melanoblast', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(413375, 'HP:0003546', 'Exercise intolerance', 'XPO:0100377', 'abnormal connective tissue', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(413376, 'HP:0003546', 'Exercise intolerance', 'XPO:0100004', 'abnormal cell', 0.5263157894736842, 1.8210412618256888, 0.9790009036675816, 'HP:0000118', 'Phenotypic abnormality'),
(413377, 'HP:0003546', 'Exercise intolerance', 'XPO:0107267', 'abnormal ventral side', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(413378, 'HP:0003546', 'Exercise intolerance', 'XPO:0100899', 'abnormal secondary spermatogonium', 0.47619047619047616, 1.8210412618256888, 0.9312156064152277, 'HP:0000118', 'Phenotypic abnormality'),
(413379, 'HP:0003546', 'Exercise intolerance', 'XPO:0100062', 'abnormal anatomical space', 0.47058823529411764, 1.4755025719078136, 0.8332791557971614, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(413380, 'HP:0003546', 'Exercise intolerance', 'XPO:0100069', 'abnormal urinary system', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(413381, 'HP:0003546', 'Exercise intolerance', 'XPO:0133402', 'absent determination of left/right symmetry in alimentary system', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(413382, 'HP:0003546', 'Exercise intolerance', 'XPO:0101023', 'abnormal ultimobranchial body', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(413383, 'HP:0003546', 'Exercise intolerance', 'XPO:0141789', 'abnormal hormone catabolic process', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(413384, 'HP:0003546', 'Exercise intolerance', 'XPO:0101362', 'abnormal vegetal cortex', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(413385, 'HP:0003546', 'Exercise intolerance', 'XPO:0100339', 'abnormal circumblastoporal collar', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(413386, 'HP:0003546', 'Exercise intolerance', 'XPO:0100511', 'abnormal stylopod', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(413387, 'HP:0003546', 'Exercise intolerance', 'XPO:0100151', 'abnormal primordium', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(413388, 'HP:0003546', 'Exercise intolerance', 'XPO:0131475', 'absent olfactory behavior', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(413389, 'HP:0003546', 'Exercise intolerance', 'XPO:0100557', 'abnormal prime meridian', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(413390, 'HP:0003546', 'Exercise intolerance', 'XPO:0101347', 'abnormal hindlimb region', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(413391, 'HP:0003546', 'Exercise intolerance', 'XPO:0141797', 'abnormal hydrogen metabolic process', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(413392, 'HP:0003546', 'Exercise intolerance', 'XPO:0100642', 'abnormal gustatory system', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(413393, 'HP:0003546', 'Exercise intolerance', 'XPO:0100956', 'abnormal centrosome', 0.47619047619047616, 1.8210412618256888, 0.9312156064152277, 'HP:0000118', 'Phenotypic abnormality'),
(413394, 'HP:0003546', 'Exercise intolerance', 'XPO:0131765', 'abnormal development of anatomical region', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(413395, 'HP:0003546', 'Exercise intolerance', 'XPO:0141265', 'abnormal escape behavior', 0.5714285714285714, 1.4755025719078136, 0.918228907628411, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(413396, 'HP:0003546', 'Exercise intolerance', 'XPO:0116433', 'abnormal axis specification', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(413397, 'HP:0003546', 'Exercise intolerance', 'XPO:0116434', 'abnormal biological process', 0.5333333333333333, 1.4755025719078136, 0.8870934026456857, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(413398, 'HP:0003546', 'Exercise intolerance', 'XPO:0101333', 'abnormal barrier epithelial cell', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(413399, 'HP:0003546', 'Exercise intolerance', 'XPO:0101326', 'abnormal cementoblast', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(413400, 'HP:0003546', 'Exercise intolerance', 'XPO:0100268', 'abnormal circulatory system', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(413401, 'HP:0003546', 'Exercise intolerance', 'XPO:0100152', 'abnormal alimentary system', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(413402, 'HP:0003546', 'Exercise intolerance', 'XPO:0107276', 'abnormal dorsal region', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(413403, 'HP:0003546', 'Exercise intolerance', 'XPO:0100640', 'abnormal notochordal sheath', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(413404, 'HP:0003546', 'Exercise intolerance', 'XPO:0100384', 'abnormal amputated tissue', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(413405, 'HP:0003546', 'Exercise intolerance', 'XPO:0141818', 'abnormal peptidoglycan muralytic activity', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(413406, 'HP:0003546', 'Exercise intolerance', 'XPO:0107265', 'abnormal posterior side', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(413407, 'HP:0003546', 'Exercise intolerance', 'XPO:0141812', 'abnormal transferase activity', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(413408, 'HP:0003546', 'Exercise intolerance', 'XPO:0100392', 'abnormal cilium', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(413409, 'HP:0003546', 'Exercise intolerance', 'XPO:0141263', 'abnormal visually guided collision avoidance behavior', 0.5714285714285714, 1.4755025719078136, 0.918228907628411, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(413410, 'HP:0003546', 'Exercise intolerance', 'XPO:0131725', 'abnormal phosphorylation of RNA polymerase II C-terminal domain', 0.5714285714285714, 1.4755025719078136, 0.918228907628411, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(413411, 'HP:0003546', 'Exercise intolerance', 'XPO:0100638', 'abnormal polar body', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(413412, 'HP:0003546', 'Exercise intolerance', 'XPO:0100913', 'abnormal Brachets cleft', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(413413, 'HP:0003546', 'Exercise intolerance', 'XPO:0100999', 'abnormal serous membrane', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(413414, 'HP:0003546', 'Exercise intolerance', 'XPO:0100531', 'abnormal proliferative region', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(413415, 'HP:0003546', 'Exercise intolerance', 'XPO:0100427', 'abnormal olfactory system', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(413416, 'HP:0003546', 'Exercise intolerance', 'XPO:0101405', 'abnormal ring structure', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(413417, 'HP:0003546', 'Exercise intolerance', 'XPO:0101389', 'abnormal wedge region', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(413418, 'HP:0003546', 'Exercise intolerance', 'XPO:0100547', 'abnormal blastomere V2', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(413419, 'HP:0003546', 'Exercise intolerance', 'XPO:0131798', 'abnormal development of anatomical space', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(413420, 'HP:0003546', 'Exercise intolerance', 'XPO:0141871', 'abnormal cadaverine transport', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(413421, 'HP:0003546', 'Exercise intolerance', 'XPO:0100477', 'abnormal pericyte', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(413422, 'HP:0003546', 'Exercise intolerance', 'XPO:0101136', 'abnormal ooplasm', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(413423, 'HP:0003546', 'Exercise intolerance', 'XPO:0131760', 'abnormal development of anatomical structure', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(413424, 'HP:0003546', 'Exercise intolerance', 'XPO:0100417', 'abnormal dense regular connective tissue', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(413425, 'HP:0003546', 'Exercise intolerance', 'XPO:0100503', 'abnormal blastomere D2', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(413426, 'HP:0003546', 'Exercise intolerance', 'XPO:0101513', 'abnormal basal body', 0.47619047619047616, 1.8210412618256888, 0.9312156064152277, 'HP:0000118', 'Phenotypic abnormality'),
(413427, 'HP:0003546', 'Exercise intolerance', 'XPO:0141959', 'absent cilium motility in floor plate', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(413428, 'HP:0003546', 'Exercise intolerance', 'XPO:0100721', 'abnormal centromere', 0.47619047619047616, 1.8210412618256888, 0.9312156064152277, 'HP:0000118', 'Phenotypic abnormality'),
(413429, 'HP:0003546', 'Exercise intolerance', 'XPO:0101113', 'abnormal stage IV oocyte', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(413430, 'HP:0003546', 'Exercise intolerance', 'XPO:0100907', 'abnormal cytoplasm', 0.47619047619047616, 1.8210412618256888, 0.9312156064152277, 'HP:0000118', 'Phenotypic abnormality'),
(413431, 'HP:0003546', 'Exercise intolerance', 'XPO:0141958', 'absent cilium motility in left-right organizer', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(413432, 'HP:0003546', 'Exercise intolerance', 'XPO:0115505', 'dead whole organism', 0.47058823529411764, 1.4755025719078136, 0.8332791557971614, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
