Associated Disease N. genes N. variants N. of shared genes JI g p-value g N. of shared variants JI v p-value v
Abnormality of skeletal muscle fiber size
8 0 6 0.33 0 0
Loss of subcutaneous adipose tissue in limbs
11 0 6 0.29 0 0
CUI: C4025887
Disease: Abnormal oral cavity morphology
Abnormal oral cavity morphology
12 0 6 0.27 0 0
Lipodystrophy, not elsewhere classified
4 0 4 0.25 0 0
CUI: C0235986
Disease: Growth hormone excess
Growth hormone excess
20 0 6 0.20 0 0
CUI: C2265792
Disease: Skeletal muscle hypertrophy
Skeletal muscle hypertrophy
21 0 6 0.19 0 0
CUI: C1837795
Disease: Prominent umbilicus
Prominent umbilicus
3 0 3 0.19 0 0
CUI: C0011859
Disease: Lipoatrophic Diabetes Mellitus
Lipoatrophic Diabetes Mellitus
11 0 4 0.17 0 0
CUI: C1560305
Disease: Prolonged QTc interval
Prolonged QTc interval
25 0 6 0.17 0 0
CUI: C1963217
Disease: Prolonged QTc Interval, CTCAE
Prolonged QTc Interval, CTCAE
25 0 6 0.17 0 0
Progressive proximal muscle weakness
28 0 6 0.16 0 0
CUI: C1866241
Disease: Broad foot
Broad foot
30 0 6 0.15 0 0
CUI: C4551838
Disease: Talipes transversoplanus
Talipes transversoplanus
30 0 6 0.15 0 0
Congenital Generalized Lipodystrophy Type 2
9 0 3 0.14 0 0
CUI: C0005937
Disease: Bone Cysts
Bone Cysts
35 0 6 0.13 0 0
CUI: C0426870
Disease: Large hand
Large hand
35 0 6 0.13 0 0
CUI: C4317112
Disease: Generalized Lipodystrophy
Generalized Lipodystrophy
18 0 4 0.13 0 0
Familial Partial Lipodystrophy, Type 3
10 0 3 0.13 0 0
CUI: C0271694
Disease: Familial partial lipodystrophy
Familial partial lipodystrophy
28 0 5 0.13 0 0
CUI: C0028949
Disease: Oligomenorrhea
Oligomenorrhea
37 0 6 0.13 0 0
CUI: C1850830
Disease: Exercise-induced myalgia
Exercise-induced myalgia
37 0 6 0.13 0 0
Cutis Laxa, Autosomal Recessive, Type I
2 0 2 0.12 0 0
CUI: C0432336
Disease: Cutis laxa, recessive, type I
Cutis laxa, recessive, type I
2 0 2 0.12 0 0
Generalized muscular appearance from birth
2 0 2 0.12 0 0
CUI: C2315541
Disease: Diverticulum of renal calyx
Diverticulum of renal calyx
2 0 2 0.12 0 0