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: C1837764
Disease: Loss of subcutaneous adipose tissue in limbs
Loss of subcutaneous adipose tissue in limbs 		11 0 6 0.23 0 0
CUI: C4023051
Disease: Abnormality of skeletal muscle fiber size
Abnormality of skeletal muscle fiber size 		8 0 5 0.21 0 0
CUI: C2265792
Disease: Skeletal muscle hypertrophy
Skeletal muscle hypertrophy 		21 0 7 0.20 0 0
CUI: C1720861
Disease: Familial Partial Lipodystrophy, Type 3
Familial Partial Lipodystrophy, Type 3 		10 0 5 0.19 0 0
CUI: C1837792
Disease: Insulin-resistant diabetes mellitus at puberty
Insulin-resistant diabetes mellitus at puberty 		5 0 4 0.18 0 0
CUI: C4317112
Disease: Generalized Lipodystrophy
Generalized Lipodystrophy 		18 0 6 0.18 0 0
CUI: C1837767
Disease: Loss of facial adipose tissue
Loss of facial adipose tissue 		6 0 4 0.17 0 0
CUI: C1720859
Disease: Familial Partial Lipodystrophy, Type 1
Familial Partial Lipodystrophy, Type 1 		9 0 4 0.15 0 0
CUI: C0221032
Disease: Familial generalized lipodystrophy
Familial generalized lipodystrophy 		49 0 9 0.15 0 0
CUI: C0271694
Disease: Familial partial lipodystrophy
Familial partial lipodystrophy 		28 0 6 0.14 0 0
CUI: C4025887
Disease: Abnormal oral cavity morphology
Abnormal oral cavity morphology 		12 0 4 0.14 0 0
CUI: C0494360
Disease: Lipodystrophy, not elsewhere classified
Lipodystrophy, not elsewhere classified 		4 0 3 0.14 0 0
CUI: C1857710
Disease: Progeroid facial appearance
Progeroid facial appearance 		14 0 4 0.13 0 0
CUI: C0038449
Disease: Stricture of artery
Stricture of artery 		16 0 4 0.12 0 0
CUI: C1720860
Disease: Familial Partial Lipodystrophy, Type 2
Familial Partial Lipodystrophy, Type 2 		16 0 4 0.12 0 0
CUI: C0028949
Disease: Oligomenorrhea
Oligomenorrhea 		37 0 6 0.12 0 0
CUI: C1837802
Disease: Decreased serum leptin
Decreased serum leptin 		8 0 3 0.12 0 0
CUI: C0014390
Disease: Entropion
Entropion 		18 0 4 0.11 0 0
CUI: C1720863
Disease: Congenital Generalized Lipodystrophy Type 2
Congenital Generalized Lipodystrophy Type 2 		9 0 3 0.11 0 0
CUI: C0235986
Disease: Growth hormone excess
Growth hormone excess 		20 0 4 0.11 0 0
CUI: C1836646
Disease: Dermal translucency
Dermal translucency 		10 0 3 0.11 0 0
CUI: C0000889
Disease: Acanthosis Nigricans
Acanthosis Nigricans 		64 0 8 0.10 0 0
CUI: C0241267
Disease: Absence of subcutaneous fat
Absence of subcutaneous fat 		11 0 3 0.10 0 0
CUI: C0037301
Disease: Skin Wrinkling
Skin Wrinkling 		12 0 3 1.0E-01 0 0
CUI: C0426870
Disease: Large hand
Large hand 		35 0 5 9.8E-02 0 0