Source: ALL
Associated Disease N. genes N. variants N. of shared genes JI g p-value g N. of shared variants JI v p-value v
CUI: C0393907
Disease: Axonal sensorimotor neuropathy
Axonal sensorimotor neuropathy 		0 2 0 0 1 9.1E-02
CUI: C0344482
Disease: Hypoplasia of corpus callosum
Hypoplasia of corpus callosum 		385 0 1 2.0E-03 0 0
CUI: C0018777
Disease: Conductive hearing loss
Conductive hearing loss 		291 0 1 2.4E-03 0 0
CUI: C0005890
Disease: Body Height
Body Height 		1903 0 5 2.5E-03 0 0
CUI: C0424503
Disease: Dysmorphic facies
Dysmorphic facies 		271 0 1 2.5E-03 0 0
CUI: C1314691
Disease: Age at menarche
Age at menarche 		267 0 1 2.6E-03 0 0
CUI: C1854114
Disease: Short nose
Short nose 		265 0 1 2.6E-03 0 0
CUI: C0202239
Disease: Uric acid measurement (procedure)
Uric acid measurement (procedure) 		264 0 1 2.6E-03 0 0
CUI: C0008924
Disease: Cleft upper lip
Cleft upper lip 		255 0 1 2.7E-03 0 0
CUI: C0489786
Disease: Height
Height 		249 0 1 2.7E-03 0 0
CUI: C0266470
Disease: Cerebellar Hypoplasia
Cerebellar Hypoplasia 		226 0 1 2.9E-03 0 0
CUI: C0200665
Disease: Platelet mean volume determination (procedure)
Platelet mean volume determination (procedure) 		223 0 1 2.9E-03 0 0
CUI: C0020608
Disease: Hypodontia
Hypodontia 		218 0 1 2.9E-03 0 0
CUI: C1387005
Disease: Penis agenesis
Penis agenesis 		217 0 1 2.9E-03 0 0
CUI: C0005612
Disease: Birth Weight
Birth Weight 		214 0 1 3.0E-03 0 0
CUI: C0040420
Disease: Tonometry
Tonometry 		206 0 1 3.0E-03 0 0
CUI: C1527304
Disease: Allergic Reaction
Allergic Reaction 		197 0 1 3.1E-03 0 0
CUI: C0543888
Disease: Epileptic encephalopathy
Epileptic encephalopathy 		187 0 1 3.2E-03 0 0
CUI: C0221356
Disease: Brachycephaly
Brachycephaly 		186 0 1 3.2E-03 0 0
CUI: C1836047
Disease: Long face
Long face 		182 0 1 3.3E-03 0 0
CUI: C0399526
Disease: Class III malocclusion
Class III malocclusion 		181 0 1 3.3E-03 0 0
CUI: C1837249
Disease: Malformations of Cortical Development, Group II
Malformations of Cortical Development, Group II 		180 0 1 3.3E-03 0 0
CUI: C1854113
Disease: Prominent nasal bridge
Prominent nasal bridge 		180 0 1 3.3E-03 0 0
CUI: C0235659
Disease: Reduced fetal movement
Reduced fetal movement 		169 0 1 3.4E-03 0 0
CUI: C2267233
Disease: Neonatal Hypotonia
Neonatal Hypotonia 		169 0 1 3.4E-03 0 0