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: C1096488
Disease: Hereditary factor IX deficiency disease without inhibitor
Hereditary factor IX deficiency disease without inhibitor 		1 0 1 1.9E-02 0 0
CUI: C1332887
Disease: Central Nervous System Melanocytic Neoplasm
Central Nervous System Melanocytic Neoplasm 		1 0 1 1.9E-02 0 0
CUI: C1334557
Disease: Malignant Adult Brain Neoplasm
Malignant Adult Brain Neoplasm 		1 0 1 1.9E-02 0 0
CUI: C1510961
Disease: Atypical neurofibroma
Atypical neurofibroma 		1 0 1 1.9E-02 0 0
CUI: C1513718
Disease: Mucin-Producing Intrahepatic Cholangiocarcinoma
Mucin-Producing Intrahepatic Cholangiocarcinoma 		1 0 1 1.9E-02 0 0
CUI: C1720732
Disease: Subretinal fluid (finding)
Subretinal fluid (finding) 		1 0 1 1.9E-02 0 0
CUI: C1832162
Disease: HYPOTRICHOSIS, CONGENITAL, WITH JUVENILE MACULAR DYSTROPHY
HYPOTRICHOSIS, CONGENITAL, WITH JUVENILE MACULAR DYSTROPHY 		1 0 1 1.9E-02 0 0
CUI: C1833999
Disease: Retinal pigmentary degeneration
Retinal pigmentary degeneration 		1 0 1 1.9E-02 0 0
CUI: C1835042
Disease: Melanoma astrocytoma syndrome
Melanoma astrocytoma syndrome 		1 0 1 1.9E-02 0 0
CUI: C1835044
Disease: MELANOMA, CUTANEOUS MALIGNANT, SUSCEPTIBILITY TO, 2
MELANOMA, CUTANEOUS MALIGNANT, SUSCEPTIBILITY TO, 2 		1 0 1 1.9E-02 0 0
CUI: C1838547
Disease: MELANOMA-PANCREATIC CANCER SYNDROME
MELANOMA-PANCREATIC CANCER SYNDROME 		1 0 1 1.9E-02 0 0
CUI: C1840455
Disease: Mild myopia
Mild myopia 		1 0 1 1.9E-02 0 0
CUI: C1844776
Disease: CONE-ROD DYSTROPHY, X-LINKED, 1
CONE-ROD DYSTROPHY, X-LINKED, 1 		1 0 1 1.9E-02 0 0
CUI: C1849198
Disease: Opacification of the corneal epithelium
Opacification of the corneal epithelium 		1 0 1 1.9E-02 0 0
CUI: C1851481
Disease: Erythrokeratodermia with ataxia
Erythrokeratodermia with ataxia 		1 0 1 1.9E-02 0 0
CUI: C1852429
Disease: Cataract, Variable Zonular Pulverulent
Cataract, Variable Zonular Pulverulent 		1 0 1 1.9E-02 0 0
CUI: C1857041
Disease: Ectodermal dysplasia, ectrodactyly, and macular dystrophy
Ectodermal dysplasia, ectrodactyly, and macular dystrophy 		1 3 1 1.9E-02 1 1.6E-02
CUI: C1857780
Disease: JOUBERT SYNDROME 5
JOUBERT SYNDROME 5 		1 45 1 1.9E-02 2 2.0E-02
CUI: C1857821
Disease: LEBER CONGENITAL AMAUROSIS 10 (disorder)
LEBER CONGENITAL AMAUROSIS 10 (disorder) 		1 17 1 1.9E-02 1 1.3E-02
CUI: C1859231
Disease: Hypoplastic olfactory lobes
Hypoplastic olfactory lobes 		1 0 1 1.9E-02 0 0
CUI: C1866422
Disease: RETINITIS PIGMENTOSA 19
RETINITIS PIGMENTOSA 19 		1 22 1 1.9E-02 6 8.0E-02
CUI: C1970161
Disease: MECKEL SYNDROME, TYPE 4
MECKEL SYNDROME, TYPE 4 		1 26 1 1.9E-02 1 1.2E-02
CUI: C1970573
Disease: MACULAR DEGENERATION, AGE-RELATED, 2, SUSCEPTIBILITY TO
MACULAR DEGENERATION, AGE-RELATED, 2, SUSCEPTIBILITY TO 		1 2 1 1.9E-02 1 1.7E-02
CUI: C2673648
Disease: Hypomagnesemia 4, Renal
Hypomagnesemia 4, Renal 		1 0 1 1.9E-02 0 0
CUI: C2675210
Disease: CONE-ROD DYSTROPHY 12 (disorder)
CONE-ROD DYSTROPHY 12 (disorder) 		1 6 1 1.9E-02 1 1.6E-02