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: C4316789
Disease: Partial lipodystrophy
Partial lipodystrophy 		14 0 6 0.21 0 0
CUI: C0854110
Disease: Insulin-resistant diabetes mellitus
Insulin-resistant diabetes mellitus 		21 0 5 0.14 0 0
CUI: C1720860
Disease: Familial Partial Lipodystrophy, Type 2
Familial Partial Lipodystrophy, Type 2 		16 0 4 0.12 0 0
CUI: C3160761
Disease: Diabetic dyslipidaemia
Diabetic dyslipidaemia 		28 0 5 0.11 0 0
CUI: C1720859
Disease: Familial Partial Lipodystrophy, Type 1
Familial Partial Lipodystrophy, Type 1 		9 0 3 0.11 0 0
CUI: C4505390
Disease: Heroin Smoking
Heroin Smoking 		10 0 3 0.11 0 0
CUI: C0920563
Disease: Insulin Sensitivity
Insulin Sensitivity 		62 0 8 0.11 0 0
CUI: C0151691
Disease: Decreased HDL cholesterol concentration
Decreased HDL cholesterol concentration 		12 0 3 1.0E-01 0 0
CUI: C1136321
Disease: HIV-Associated Lipodystrophy Syndrome
HIV-Associated Lipodystrophy Syndrome 		12 0 3 1.0E-01 0 0
CUI: C0948242
Disease: Nuchal bleb, familial
Nuchal bleb, familial 		24 0 4 9.8E-02 0 0
CUI: C4531217
Disease: Peripheral arterial calcification
Peripheral arterial calcification 		2 0 2 9.5E-02 0 0
CUI: C0271693
Disease: Acquired generalized lipodystrophy
Acquired generalized lipodystrophy 		3 0 2 9.1E-02 0 0
CUI: C1261982
Disease: Chondrosis
Chondrosis 		3 0 2 9.1E-02 0 0
CUI: C4024615
Disease: Adipose tissue loss
Adipose tissue loss 		3 0 2 9.1E-02 0 0
CUI: C0271694
Disease: Familial partial lipodystrophy
Familial partial lipodystrophy 		28 0 4 8.9E-02 0 0
CUI: C2675519
Disease: Hypoadiponectinemia
Hypoadiponectinemia 		16 0 3 8.8E-02 0 0
CUI: C0271695
Disease: Rabson-Mendenhall Syndrome
Rabson-Mendenhall Syndrome 		4 0 2 8.7E-02 0 0
CUI: C1834674
Disease: BETHLEM MYOPATHY 1
BETHLEM MYOPATHY 1 		17 0 3 8.6E-02 0 0
CUI: C2712907
Disease: obsolete Combined hyperlipidemia
obsolete Combined hyperlipidemia 		17 0 3 8.6E-02 0 0
CUI: C2936179
Disease: Obesity, Visceral
Obesity, Visceral 		55 0 6 8.6E-02 0 0
CUI: C0263420
Disease: Hyperkeratosis lenticularis perstans
Hyperkeratosis lenticularis perstans 		18 0 3 8.3E-02 0 0
CUI: C2675518
Disease: Adiponectin Deficiency
Adiponectin Deficiency 		5 0 2 8.3E-02 0 0
CUI: C4551514
Disease: Hemophagocytic Lymphohistiocytosis, Familial, 1
Hemophagocytic Lymphohistiocytosis, Familial, 1 		5 0 2 8.3E-02 0 0
CUI: C0342336
Disease: Insulin resistance - type A
Insulin resistance - type A 		6 0 2 8.0E-02 0 0
CUI: C1720862
Disease: Congenital Generalized Lipodystrophy Type 1
Congenital Generalized Lipodystrophy Type 1 		6 0 2 8.0E-02 0 0