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: C4021910
Disease: Narrow foramen obturatorium
Narrow foramen obturatorium 		6 0 6 0.67 0 0
CUI: C0159060
Disease: Abnormal bowel sounds
Abnormal bowel sounds 		5 0 5 0.56 0 0
CUI: C4022020
Disease: Mucosal telangiectasiae
Mucosal telangiectasiae 		16 0 6 0.32 0 0
CUI: C0748540
Disease: Scleroderma, Limited
Scleroderma, Limited 		17 0 6 0.30 0 0
CUI: C0020546
Disease: Hypertensive crisis
Hypertensive crisis 		19 0 5 0.22 0 0
CUI: C0028961
Disease: Oliguria
Oliguria 		24 0 5 0.18 0 0
CUI: C1384606
Disease: Dyspareunia
Dyspareunia 		37 0 5 0.12 0 0
CUI: C0042171
Disease: Uveoparotid Fever
Uveoparotid Fever 		1 0 1 0.11 0 0
CUI: C0155568
Disease: Rheumatic aortic regurgitation
Rheumatic aortic regurgitation 		1 0 1 0.11 0 0
CUI: C0274295
Disease: Brisket disease
Brisket disease 		1 0 1 0.11 0 0
CUI: C0279983
Disease: Malignant Childhood Hemangiopericytoma
Malignant Childhood Hemangiopericytoma 		1 0 1 0.11 0 0
CUI: C0334542
Disease: Hemangiopericytoma, Malignant
Hemangiopericytoma, Malignant 		1 0 1 0.11 0 0
CUI: C1274865
Disease: Scleroderma-like secondary cutaneous sclerosis
Scleroderma-like secondary cutaneous sclerosis 		1 0 1 0.11 0 0
CUI: C1737267
Disease: Acute pulmonary congestion
Acute pulmonary congestion 		1 0 1 0.11 0 0
CUI: C2675861
Disease: Lipodystrophy, Congenital Generalized, Type 3
Lipodystrophy, Congenital Generalized, Type 3 		1 0 1 0.11 0 0
CUI: C2676770
Disease: Birk-Barel Mental Retardation Dysmorphism Syndrome
Birk-Barel Mental Retardation Dysmorphism Syndrome 		1 0 1 0.11 0 0
CUI: C2677097
Disease: SYSTEMIC LUPUS ERYTHEMATOSUS, SUSCEPTIBILITY TO, 10 (finding)
SYSTEMIC LUPUS ERYTHEMATOSUS, SUSCEPTIBILITY TO, 10 (finding) 		1 0 1 0.11 0 0
CUI: C2677100
Disease: Inflammatory Bowel Disease 14
Inflammatory Bowel Disease 14 		1 0 1 0.11 0 0
CUI: C3277426
Disease: Lack of facial subcutaneous fat
Lack of facial subcutaneous fat 		1 0 1 0.11 0 0
CUI: C3496177
Disease: Atypical psychosis
Atypical psychosis 		1 0 1 0.11 0 0
CUI: C3554046
Disease: LETHAL CONGENITAL CONTRACTURE SYNDROME 4
LETHAL CONGENITAL CONTRACTURE SYNDROME 4 		1 0 1 0.11 0 0
CUI: C3805917
Disease: Elevated pulmonary artery pressure
Elevated pulmonary artery pressure 		1 0 1 0.11 0 0
CUI: C3807567
Disease: PARTIAL LIPODYSTROPHY, CONGENITAL CATARACTS, AND NEURODEGENERATION SYNDROME
PARTIAL LIPODYSTROPHY, CONGENITAL CATARACTS, AND NEURODEGENERATION SYNDROME 		1 0 1 0.11 0 0
CUI: C4017076
Disease: SYSTEMIC LUPUS ERYTHEMATOSUS, ASSOCIATION WITH SUSCEPTIBILITY TO, 10
SYSTEMIC LUPUS ERYTHEMATOSUS, ASSOCIATION WITH SUSCEPTIBILITY TO, 10 		1 0 1 0.11 0 0
CUI: C4023544
Disease: Incisor macrodontia
Incisor macrodontia 		1 0 1 0.11 0 0