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: C3839205
Disease: Signet-ring stromal tumor
Signet-ring stromal tumor 		2 0 1 0.20 0 0
CUI: C4225429
Disease: Ehlers-Danlos syndrome classic type
Ehlers-Danlos syndrome classic type 		2 0 1 0.20 0 0
CUI: C4289994
Disease: Adenosine Deaminase 2 Deficiency
Adenosine Deaminase 2 Deficiency 		2 0 1 0.20 0 0
CUI: C4293700
Disease: Subcutaneous spheroids
Subcutaneous spheroids 		2 0 1 0.20 0 0
CUI: C0014040
Disease: Encephalitis Lethargica
Encephalitis Lethargica 		3 0 1 0.17 0 0
CUI: C0220679
Disease: Ehlers-Danlos Syndrome, Autosomal Dominant, Type Unspecified
Ehlers-Danlos Syndrome, Autosomal Dominant, Type Unspecified 		3 0 1 0.17 0 0
CUI: C0270992
Disease: Secondary myopathy
Secondary myopathy 		3 0 1 0.17 0 0
CUI: C0338586
Disease: Vertebral Artery Dissection
Vertebral Artery Dissection 		3 0 1 0.17 0 0
CUI: C1853623
Disease: Fryns-Aftimos Syndrome
Fryns-Aftimos Syndrome 		3 0 1 0.17 0 0
CUI: C4021962
Disease: Genital hernia
Genital hernia 		3 0 1 0.17 0 0
CUI: C4732796
Disease: Apical hypertrophic cardiomyopathy
Apical hypertrophic cardiomyopathy 		10 0 2 0.17 0 0
CUI: C0154254
Disease: Polyclonal hypergammaglobulinemia
Polyclonal hypergammaglobulinemia 		4 0 1 0.14 0 0
CUI: C0265283
Disease: Atelosteogenesis, type 1
Atelosteogenesis, type 1 		4 0 1 0.14 0 0
CUI: C0268335
Disease: Ehlers-Danlos syndrome type 1
Ehlers-Danlos syndrome type 1 		4 0 1 0.14 0 0
CUI: C0268336
Disease: Ehlers-Danlos syndrome type 2
Ehlers-Danlos syndrome type 2 		4 0 1 0.14 0 0
CUI: C0270969
Disease: Zebra body myopathy
Zebra body myopathy 		4 0 1 0.14 0 0
CUI: C0431401
Disease: Gillespie syndrome
Gillespie syndrome 		4 0 1 0.14 0 0
CUI: C0751656
Disease: Nemaline Myopathy, Autosomal Dominant
Nemaline Myopathy, Autosomal Dominant 		4 0 1 0.14 0 0
CUI: C1628319
Disease: Lattice corneal dystrophy Type II
Lattice corneal dystrophy Type II 		4 0 1 0.14 0 0
CUI: C1855722
Disease: Iris Coloboma with Ptosis, Hypertelorism, and Mental Retardation
Iris Coloboma with Ptosis, Hypertelorism, and Mental Retardation 		4 0 1 0.14 0 0
CUI: C4076349
Disease: Chronic alcoholic liver disease
Chronic alcoholic liver disease 		4 0 1 0.14 0 0
CUI: C4293686
Disease: Periventricular white matter hyperdensities
Periventricular white matter hyperdensities 		4 0 1 0.14 0 0
CUI: C4538407
Disease: EHLERS-DANLOS SYNDROME, CLASSIC TYPE, 2
EHLERS-DANLOS SYNDROME, CLASSIC TYPE, 2 		4 0 1 0.14 0 0
CUI: C0877854
Disease: Cerebral Arteriosclerosis
Cerebral Arteriosclerosis 		5 0 1 0.12 0 0
CUI: C1300346
Disease: Desmoplastic fibroblastoma
Desmoplastic fibroblastoma 		5 0 1 0.12 0 0