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: C1836003
Disease: Facial diplegia
Facial diplegia 		42 0 6 0.14 0 0
CUI: C1854387
Disease: Type 1 muscle fiber predominance
Type 1 muscle fiber predominance 		44 0 6 0.13 0 0
CUI: C4024601
Disease: Weakness of long finger extensor muscles
Weakness of long finger extensor muscles 		18 0 3 0.13 0 0
CUI: C0497219
Disease: Hearing complaints (excluding H84-86)
Hearing complaints (excluding H84-86) 		1 0 1 0.12 0 0
CUI: C1836155
Disease: Myopathy, Myofibrillar, Zasp-Related
Myopathy, Myofibrillar, Zasp-Related 		1 0 1 0.12 0 0
CUI: C1836447
Disease: Nemaline myopathy 4
Nemaline myopathy 4 		1 0 1 0.12 0 0
CUI: C1853154
Disease: Nemaline Myopathy 7
Nemaline Myopathy 7 		1 0 1 0.12 0 0
CUI: C2750413
Disease: Cap Myopathy, Tpm2-Related
Cap Myopathy, Tpm2-Related 		1 0 1 0.12 0 0
CUI: C2750536
Disease: Nemaline Myopathy 3, With Intranuclear Rods
Nemaline Myopathy 3, With Intranuclear Rods 		1 0 1 0.12 0 0
CUI: C2750537
Disease: Myopathy, Actin, Congenital, With Cores
Myopathy, Actin, Congenital, With Cores 		1 0 1 0.12 0 0
CUI: C3152137
Disease: LEFT VENTRICULAR NONCOMPACTION 3
LEFT VENTRICULAR NONCOMPACTION 3 		1 0 1 0.12 0 0
CUI: C3807697
Disease: Bilateral foot drop
Bilateral foot drop 		1 0 1 0.12 0 0
CUI: C3807907
Disease: CAP MYOPATHY 2
CAP MYOPATHY 2 		1 0 1 0.12 0 0
CUI: C3808250
Disease: Reduced forced vital capacity
Reduced forced vital capacity 		10 0 2 0.12 0 0
CUI: C3810384
Disease: NEMALINE MYOPATHY 9
NEMALINE MYOPATHY 9 		1 0 1 0.12 0 0
CUI: C4015360
Disease: NEMALINE MYOPATHY 10
NEMALINE MYOPATHY 10 		1 0 1 0.12 0 0
CUI: C4022166
Disease: EMG: myokymic discharges
EMG: myokymic discharges 		1 0 1 0.12 0 0
CUI: C4024607
Disease: Exercise-induced leg cramps
Exercise-induced leg cramps 		1 0 1 0.12 0 0
CUI: C4225181
Disease: MYOPATHY, SCAPULOHUMEROPERONEAL
MYOPATHY, SCAPULOHUMEROPERONEAL 		1 0 1 0.12 0 0
CUI: C4225414
Disease: CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 24
CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 24 		1 0 1 0.12 0 0
CUI: C4721886
Disease: MYOPATHY, MYOFIBRILLAR, 4
MYOPATHY, MYOFIBRILLAR, 4 		1 0 1 0.12 0 0
CUI: C0086439
Disease: Hypokinesia
Hypokinesia 		47 0 6 0.12 0 0
CUI: C0206157
Disease: Myopathies, Nemaline
Myopathies, Nemaline 		47 0 6 0.12 0 0
CUI: C0476408
Disease: Reduced vital capacity
Reduced vital capacity 		29 0 4 0.12 0 0
CUI: C1864716
Disease: Intrinsic hand muscle atrophy
Intrinsic hand muscle atrophy 		11 0 2 0.12 0 0