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: C0030625
Disease: Passive Cutaneous Anaphylaxis
Passive Cutaneous Anaphylaxis 		1 0 1 0.12 0 0
CUI: C0037188
Disease: Sinoatrial Block
Sinoatrial Block 		1 0 1 0.12 0 0
CUI: C0274295
Disease: Brisket disease
Brisket disease 		1 0 1 0.12 0 0
CUI: C0338822
Disease: Cycloid psychosis
Cycloid psychosis 		1 0 1 0.12 0 0
CUI: C0344688
Disease: Patent Ductus Venosus
Patent Ductus Venosus 		1 0 1 0.12 0 0
CUI: C0345183
Disease: Congenital constriction of pylorus
Congenital constriction of pylorus 		1 0 1 0.12 0 0
CUI: C0796031
Disease: Malouf syndrome
Malouf syndrome 		1 0 1 0.12 0 0
CUI: C0796083
Disease: Najjar syndrome
Najjar syndrome 		1 0 1 0.12 0 0
CUI: C1332575
Disease: Bone Epithelioid Hemangioma
Bone Epithelioid Hemangioma 		1 0 1 0.12 0 0
CUI: C1832250
Disease: OBESITY, MODIFIER OF
OBESITY, MODIFIER OF 		1 0 1 0.12 0 0
CUI: C1832251
Disease: BODY MASS INDEX, MODIFIER OF
BODY MASS INDEX, MODIFIER OF 		1 0 1 0.12 0 0
CUI: C1832253
Disease: INTIMAL MEDIAL THICKNESS OF INTERNAL CAROTID ARTERY, MODIFIER OF
INTIMAL MEDIAL THICKNESS OF INTERNAL CAROTID ARTERY, MODIFIER OF 		1 0 1 0.12 0 0
CUI: C1835380
Disease: Labial pseudohypertrophy
Labial pseudohypertrophy 		1 0 1 0.12 0 0
CUI: C1835389
Disease: Increased intramuscular fat
Increased intramuscular fat 		1 0 1 0.12 0 0
CUI: C1836302
Disease: Carotid Intimal Medial Thickness 1
Carotid Intimal Medial Thickness 1 		1 0 1 0.12 0 0
CUI: C1857829
Disease: Heart-hand syndrome, Slovenian type
Heart-hand syndrome, Slovenian type 		1 0 1 0.12 0 0
CUI: C2675074
Disease: Enlarged peripheral nerve
Enlarged peripheral nerve 		1 0 1 0.12 0 0
CUI: C2675861
Disease: Lipodystrophy, Congenital Generalized, Type 3
Lipodystrophy, Congenital Generalized, Type 3 		1 0 1 0.12 0 0
CUI: C2750035
Disease: Emery-Dreifuss Muscular Dystrophy 3
Emery-Dreifuss Muscular Dystrophy 3 		1 0 1 0.12 0 0
CUI: C2750069
Disease: Lipodystrophy, Congenital Generalized, Type 4
Lipodystrophy, Congenital Generalized, Type 4 		1 0 1 0.12 0 0
CUI: C2750285
Disease: Progeria Syndrome, Childhood-Onset
Progeria Syndrome, Childhood-Onset 		1 0 1 0.12 0 0
CUI: C2750785
Disease: MUSCULAR DYSTROPHY, CONGENITAL, LMNA-RELATED (disorder)
MUSCULAR DYSTROPHY, CONGENITAL, LMNA-RELATED (disorder) 		1 0 1 0.12 0 0
CUI: C3277426
Disease: Lack of facial subcutaneous fat
Lack of facial subcutaneous fat 		1 0 1 0.12 0 0
CUI: C3805917
Disease: Elevated pulmonary artery pressure
Elevated pulmonary artery pressure 		1 0 1 0.12 0 0
CUI: C3807567
Disease: PARTIAL LIPODYSTROPHY, CONGENITAL CATARACTS, AND NEURODEGENERATION SYNDROME
PARTIAL LIPODYSTROPHY, CONGENITAL CATARACTS, AND NEURODEGENERATION SYNDROME 		1 0 1 0.12 0 0