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: C0857898
Disease: Abnormal circulating aldosterone
Abnormal circulating aldosterone 		2 0 2 0.18 0 0
CUI: C4024883
Disease: Hyperextensible skin of face
Hyperextensible skin of face 		2 2 2 0.18 2 3.7E-02
CUI: C0476369
Disease: Echocardiogram abnormal
Echocardiogram abnormal 		3 1 2 0.17 1 1.9E-02
CUI: C1846672
Disease: MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 2I
MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 2I 		3 52 2 0.17 2 1.9E-02
CUI: C0546817
Disease: Fluid overload
Fluid overload 		4 0 2 0.15 0 0
CUI: C1850438
Disease: Postural hypotension with compensatory tachycardia
Postural hypotension with compensatory tachycardia 		4 2 2 0.15 2 3.7E-02
CUI: C1858593
Disease: Limb-girdle muscular dystrophy, type 2E
Limb-girdle muscular dystrophy, type 2E 		5 0 2 0.14 0 0
CUI: C4021124
Disease: Adrenocorticotropic hormone excess
Adrenocorticotropic hormone excess 		5 0 2 0.14 0 0
CUI: C4022858
Disease: Elevated aldolase level
Elevated aldolase level 		5 3 2 0.14 2 3.6E-02
CUI: C4554215
Disease: Duchenne or Becker muscular dystrophy
Duchenne or Becker muscular dystrophy 		7 0 2 0.12 0 0
CUI: C1845155
Disease: Exercise-induced myoglobinuria
Exercise-induced myoglobinuria 		8 2 2 0.12 2 3.7E-02
CUI: C1855580
Disease: Exercise-induced muscle fatigue
Exercise-induced muscle fatigue 		18 3 3 0.12 1 1.8E-02
CUI: C0741933
Disease: cardiac symptom
cardiac symptom 		9 0 2 0.11 0 0
CUI: C1845206
Disease: Decreased circulating renin level
Decreased circulating renin level 		9 0 2 0.11 0 0
CUI: C2936332
Disease: Alpha-Sarcoglycanopathies
Alpha-Sarcoglycanopathies 		9 0 2 0.11 0 0
CUI: C2936331
Disease: Sarcoglycanopathies
Sarcoglycanopathies 		20 0 3 0.11 0 0
CUI: C0085570
Disease: Hypokalemic alkalosis
Hypokalemic alkalosis 		10 0 2 0.11 0 0
CUI: C0264789
Disease: Familial cardiomyopathy
Familial cardiomyopathy 		10 0 2 0.11 0 0
CUI: C1389118
Disease: Peroneal muscle atrophy
Peroneal muscle atrophy 		10 0 2 0.11 0 0
CUI: C0750403
Disease: Proximal weakness
Proximal weakness 		11 0 2 1.0E-01 0 0
CUI: C1847766
Disease: Shoulder girdle muscle atrophy
Shoulder girdle muscle atrophy 		12 0 2 9.5E-02 0 0
CUI: C4021740
Disease: Increased circulating ACTH level
Increased circulating ACTH level 		12 0 2 9.5E-02 0 0
CUI: C0016724
Disease: Froehlich's Syndrome
Froehlich's Syndrome 		1 0 1 9.1E-02 0 0
CUI: C0264955
Disease: Idiopathic arterial calcification of infancy
Idiopathic arterial calcification of infancy 		1 0 1 9.1E-02 0 0
CUI: C0267494
Disease: Chilaiditi Syndrome
Chilaiditi Syndrome 		1 0 1 9.1E-02 0 0