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: C0428977
Disease: Bradycardia
Bradycardia 		63 0 13 0.12 0 0
CUI: C4023051
Disease: Abnormality of skeletal muscle fiber size
Abnormality of skeletal muscle fiber size 		8 0 7 0.11 0 0
CUI: C0235986
Disease: Growth hormone excess
Growth hormone excess 		20 0 8 0.11 0 0
CUI: C4551472
Disease: Hypertrophic obstructive cardiomyopathy
Hypertrophic obstructive cardiomyopathy 		233 90 29 0.11 1 1.0E-02
CUI: C1837764
Disease: Loss of subcutaneous adipose tissue in limbs
Loss of subcutaneous adipose tissue in limbs 		11 0 7 0.11 0 0
CUI: C0949658
Disease: Cardiomyopathy, Hypertrophic, Familial
Cardiomyopathy, Hypertrophic, Familial 		83 355 14 0.11 1 2.8E-03
CUI: C0038449
Disease: Stricture of artery
Stricture of artery 		16 0 7 0.10 0 0
CUI: C0221032
Disease: Familial generalized lipodystrophy
Familial generalized lipodystrophy 		49 0 10 0.10 0 0
CUI: C1866241
Disease: Broad foot
Broad foot 		30 0 8 9.8E-02 0 0
CUI: C4551838
Disease: Talipes transversoplanus
Talipes transversoplanus 		30 0 8 9.8E-02 0 0
CUI: C0036529
Disease: Myocardial Diseases, Secondary
Myocardial Diseases, Secondary 		101 0 14 9.5E-02 0 0
CUI: C0267176
Disease: Gastroparesis with diabetes mellitus
Gastroparesis with diabetes mellitus 		21 0 7 9.5E-02 0 0
CUI: C2265792
Disease: Skeletal muscle hypertrophy
Skeletal muscle hypertrophy 		21 0 7 9.5E-02 0 0
CUI: C0011859
Disease: Lipoatrophic Diabetes Mellitus
Lipoatrophic Diabetes Mellitus 		11 0 6 9.2E-02 0 0
CUI: C0005937
Disease: Bone Cysts
Bone Cysts 		35 0 8 9.2E-02 0 0
CUI: C4025887
Disease: Abnormal oral cavity morphology
Abnormal oral cavity morphology 		12 0 6 9.1E-02 0 0
CUI: C0451718
Disease: Non-obstructive reflux-associated chronic pyelonephritis (disorder)
Non-obstructive reflux-associated chronic pyelonephritis (disorder) 		13 0 6 9.0E-02 0 0
CUI: C3495566
Disease: Reflux nephropathy (disorder)
Reflux nephropathy (disorder) 		13 0 6 9.0E-02 0 0
CUI: C0393626
Disease: Opsoclonus-Myoclonus Syndrome
Opsoclonus-Myoclonus Syndrome 		14 0 6 8.8E-02 0 0
CUI: C0000889
Disease: Acanthosis Nigricans
Acanthosis Nigricans 		64 0 10 8.8E-02 0 0
CUI: C0271694
Disease: Familial partial lipodystrophy
Familial partial lipodystrophy 		28 0 7 8.6E-02 0 0
CUI: C4543929
Disease: Primary osteosarcoma
Primary osteosarcoma 		28 0 7 8.6E-02 0 0
CUI: C1280433
Disease: Lipoatrophy
Lipoatrophy 		106 0 13 8.5E-02 0 0
CUI: C1849300
Disease: Widely patent fontanelles and sutures
Widely patent fontanelles and sutures 		17 0 6 8.5E-02 0 0
CUI: C1145628
Disease: Autonomic nervous system disorders
Autonomic nervous system disorders 		73 0 10 8.1E-02 0 0