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: C0013882
Disease: Elephantiasis
Elephantiasis 		0 6 0 0 1 1.5E-02
CUI: C0014067
Disease: Occipital Encephalocele
Occipital Encephalocele 		0 9 0 0 1 1.5E-02
CUI: C0035085
Disease: Renal infarction
Renal infarction 		0 1 0 0 1 1.7E-02
CUI: C0042485
Disease: Venous Insufficiency
Venous Insufficiency 		0 1 0 0 1 1.7E-02
CUI: C0268066
Disease: Hepatic hemosiderosis
Hepatic hemosiderosis 		0 1 0 0 1 1.7E-02
CUI: C2697788
Disease: Interleukin 8 Measurement
Interleukin 8 Measurement 		0 5 0 0 1 1.6E-02
CUI: C3495893
Disease: Congenital thrombophilia
Congenital thrombophilia 		0 1 0 0 1 1.7E-02
CUI: C3875381
Disease: Homozygous methylenetetrahydrofolate reductase mutation
Homozygous methylenetetrahydrofolate reductase mutation 		0 1 0 0 1 1.7E-02
CUI: C4022560
Disease: Splanchnic vein thrombosis
Splanchnic vein thrombosis 		0 2 0 0 1 1.6E-02
CUI: C0016202
Disease: Flatfoot
Flatfoot 		285 0 1 2.0E-03 0 0
CUI: C1854114
Disease: Short nose
Short nose 		265 0 1 2.1E-03 0 0
CUI: C0266435
Disease: Congenital hypoplasia of penis
Congenital hypoplasia of penis 		237 0 1 2.2E-03 0 0
CUI: C0086437
Disease: Joint laxity
Joint laxity 		224 0 1 2.3E-03 0 0
CUI: C0854723
Disease: Retinal Dystrophies
Retinal Dystrophies 		219 0 1 2.3E-03 0 0
CUI: C0029089
Disease: Ophthalmoplegia
Ophthalmoplegia 		216 0 1 2.3E-03 0 0
CUI: C1862475
Disease: Abnormality of retinal pigmentation
Abnormality of retinal pigmentation 		215 0 1 2.3E-03 0 0
CUI: C0333068
Disease: Flexion contracture
Flexion contracture 		210 0 1 2.3E-03 0 0
CUI: C0020224
Disease: Polyhydramnios
Polyhydramnios 		208 0 1 2.4E-03 0 0
CUI: C0040420
Disease: Tonometry
Tonometry 		206 0 1 2.4E-03 0 0
CUI: C4049796
Disease: Abnormality of cardiovascular system morphology
Abnormality of cardiovascular system morphology 		198 0 1 2.4E-03 0 0
CUI: C3494422
Disease: Retrognathia
Retrognathia 		191 0 1 2.5E-03 0 0
CUI: C0152421
Disease: Macrotia
Macrotia 		188 0 1 2.5E-03 0 0
CUI: C1837249
Disease: Malformations of Cortical Development, Group II
Malformations of Cortical Development, Group II 		180 0 1 2.5E-03 0 0
CUI: C1854113
Disease: Prominent nasal bridge
Prominent nasal bridge 		180 0 1 2.5E-03 0 0
CUI: C0001807
Disease: Aggressive behavior
Aggressive behavior 		176 0 1 2.5E-03 0 0