Source: CURATED ×
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: C1720859
Disease: Familial Partial Lipodystrophy, Type 1
Familial Partial Lipodystrophy, Type 1 		7 0 7 1.00 0 0
CUI: C1720860
Disease: Familial Partial Lipodystrophy, Type 2
Familial Partial Lipodystrophy, Type 2 		7 0 7 1.00 0 0
CUI: C0271694
Disease: Familial partial lipodystrophy
Familial partial lipodystrophy 		8 0 7 0.88 0 0
CUI: C0011859
Disease: Lipoatrophic Diabetes Mellitus
Lipoatrophic Diabetes Mellitus 		4 0 2 0.22 0 0
CUI: C0221032
Disease: Familial generalized lipodystrophy
Familial generalized lipodystrophy 		6 0 2 0.18 0 0
CUI: C0030625
Disease: Passive Cutaneous Anaphylaxis
Passive Cutaneous Anaphylaxis 		1 0 1 0.14 0 0
CUI: C0037188
Disease: Sinoatrial Block
Sinoatrial Block 		1 0 1 0.14 0 0
CUI: C0796031
Disease: Malouf syndrome
Malouf syndrome 		1 0 1 0.14 0 0
CUI: C0796083
Disease: Najjar syndrome
Najjar syndrome 		1 0 1 0.14 0 0
CUI: C1836302
Disease: Carotid Intimal Medial Thickness 1
Carotid Intimal Medial Thickness 1 		1 0 1 0.14 0 0
CUI: C1854154
Disease: Charcot-Marie-Tooth disease, Type 2B1
Charcot-Marie-Tooth disease, Type 2B1 		1 0 1 0.14 0 0
CUI: C1857829
Disease: Heart-hand syndrome, Slovenian type
Heart-hand syndrome, Slovenian type 		1 0 1 0.14 0 0
CUI: C2675861
Disease: Lipodystrophy, Congenital Generalized, Type 3
Lipodystrophy, Congenital Generalized, Type 3 		1 0 1 0.14 0 0
CUI: C2750035
Disease: Emery-Dreifuss Muscular Dystrophy 3
Emery-Dreifuss Muscular Dystrophy 3 		1 0 1 0.14 0 0
CUI: C2750785
Disease: MUSCULAR DYSTROPHY, CONGENITAL, LMNA-RELATED (disorder)
MUSCULAR DYSTROPHY, CONGENITAL, LMNA-RELATED (disorder) 		1 0 1 0.14 0 0
CUI: C3151268
Disease: LIPODYSTROPHY, FAMILIAL PARTIAL, TYPE 4
LIPODYSTROPHY, FAMILIAL PARTIAL, TYPE 4 		1 0 1 0.14 0 0
CUI: C3278384
Disease: HYPOINSULINEMIC HYPOGLYCEMIA WITH HEMIHYPERTROPHY
HYPOINSULINEMIC HYPOGLYCEMIA WITH HEMIHYPERTROPHY 		1 0 1 0.14 0 0
CUI: C3807567
Disease: PARTIAL LIPODYSTROPHY, CONGENITAL CATARACTS, AND NEURODEGENERATION SYNDROME
PARTIAL LIPODYSTROPHY, CONGENITAL CATARACTS, AND NEURODEGENERATION SYNDROME 		1 0 1 0.14 0 0
CUI: C3808940
Disease: LIPODYSTROPHY, FAMILIAL PARTIAL, TYPE 5
LIPODYSTROPHY, FAMILIAL PARTIAL, TYPE 5 		1 0 1 0.14 0 0
CUI: C3809192
Disease: PULMONARY HYPERTENSION, PRIMARY, 3
PULMONARY HYPERTENSION, PRIMARY, 3 		1 0 1 0.14 0 0
CUI: C4014869
Disease: LIPODYSTROPHY, FAMILIAL PARTIAL, TYPE 6
LIPODYSTROPHY, FAMILIAL PARTIAL, TYPE 6 		1 0 1 0.14 0 0
CUI: C4275075
Disease: Atypical Werner syndrome
Atypical Werner syndrome 		1 0 1 0.14 0 0
CUI: C4316789
Disease: Partial lipodystrophy
Partial lipodystrophy 		1 0 1 0.14 0 0
CUI: C4750858
Disease: LMNA-related cardiocutaneous progeria syndrome
LMNA-related cardiocutaneous progeria syndrome 		1 0 1 0.14 0 0
CUI: C0004245
Disease: Atrioventricular Block
Atrioventricular Block 		2 0 1 0.12 0 0