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: C0003516
Disease: Aortopulmonary Septal Defect
Aortopulmonary Septal Defect 		1 0 1 1.00 0 0
CUI: C0263579
Disease: Pigmented hairy epidermal nevus
Pigmented hairy epidermal nevus 		1 0 1 1.00 0 0
CUI: C1858042
Disease: Becker Nevus Syndrome
Becker Nevus Syndrome 		1 0 1 1.00 0 0
CUI: C0011992
Disease: Infantile Diarrhea
Infantile Diarrhea 		2 0 1 0.50 0 0
CUI: C0266833
Disease: Visceral Myopathy, Familial
Visceral Myopathy, Familial 		2 0 1 0.50 0 0
CUI: C1290162
Disease: Disorder of smooth muscle
Disorder of smooth muscle 		2 0 1 0.50 0 0
CUI: C1527298
Disease: Dysentery, Bacillary
Dysentery, Bacillary 		2 0 1 0.50 0 0
CUI: C1837819
Disease: Cerebrofrontofacial Syndrome
Cerebrofrontofacial Syndrome 		2 0 1 0.50 0 0
CUI: C1844696
Disease: OTOPALATODIGITAL SYNDROME, TYPE II
OTOPALATODIGITAL SYNDROME, TYPE II 		2 0 1 0.50 0 0
CUI: C1846339
Disease: Externally rotated hips
Externally rotated hips 		2 0 1 0.50 0 0
CUI: C3711377
Disease: Intranuclear Rod Myopathy
Intranuclear Rod Myopathy 		2 0 1 0.50 0 0
CUI: C3711389
Disease: Actin-Accumulation Myopathy
Actin-Accumulation Myopathy 		2 0 1 0.50 0 0
CUI: C3839205
Disease: Signet-ring stromal tumor
Signet-ring stromal tumor 		2 0 1 0.50 0 0
CUI: C4477072
Disease: Iris flocculi
Iris flocculi 		2 0 1 0.50 0 0
CUI: C0014040
Disease: Encephalitis Lethargica
Encephalitis Lethargica 		3 0 1 0.33 0 0
CUI: C0270992
Disease: Secondary myopathy
Secondary myopathy 		3 0 1 0.33 0 0
CUI: C1853623
Disease: Fryns-Aftimos Syndrome
Fryns-Aftimos Syndrome 		3 1 1 0.33 1 0.50
CUI: C0154254
Disease: Polyclonal hypergammaglobulinemia
Polyclonal hypergammaglobulinemia 		4 0 1 0.25 0 0
CUI: C0265283
Disease: Atelosteogenesis, type 1
Atelosteogenesis, type 1 		4 0 1 0.25 0 0
CUI: C0270969
Disease: Zebra body myopathy
Zebra body myopathy 		4 0 1 0.25 0 0
CUI: C0751656
Disease: Nemaline Myopathy, Autosomal Dominant
Nemaline Myopathy, Autosomal Dominant 		4 0 1 0.25 0 0
CUI: C1628319
Disease: Lattice corneal dystrophy Type II
Lattice corneal dystrophy Type II 		4 0 1 0.25 0 0
CUI: C1855722
Disease: Iris Coloboma with Ptosis, Hypertelorism, and Mental Retardation
Iris Coloboma with Ptosis, Hypertelorism, and Mental Retardation 		4 30 1 0.25 2 6.7E-02
CUI: C3151201
Disease: MULTISYSTEMIC SMOOTH MUSCLE DYSFUNCTION SYNDROME
MULTISYSTEMIC SMOOTH MUSCLE DYSFUNCTION SYNDROME 		4 0 1 0.25 0 0
CUI: C4076349
Disease: Chronic alcoholic liver disease
Chronic alcoholic liver disease 		4 0 1 0.25 0 0