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: C1836767
Disease: Proximal lower limb amyotrophy
Proximal lower limb amyotrophy
15 0 7 0.37 0 0
CUI: C1834481
Disease: CARDIOMYOPATHY, DILATED, 1S
CARDIOMYOPATHY, DILATED, 1S
9 0 5 0.33 0 0
CUI: C1389118
Disease: Peroneal muscle atrophy
Peroneal muscle atrophy
8 0 4 0.27 0 0
CUI: C3277184
Disease: Decreased patellar reflex
Decreased patellar reflex
8 0 4 0.27 0 0
CUI: C0428974
Disease: Supraventricular arrhythmia
Supraventricular arrhythmia
13 0 5 0.26 0 0
CUI: C1836057
Disease: Muscle fiber splitting
Muscle fiber splitting
13 0 5 0.26 0 0
CUI: C3805969
Disease: Scapular muscle atrophy
Scapular muscle atrophy
4 0 3 0.25 0 0
CUI: C0340427
Disease: Familial dilated cardiomyopathy
Familial dilated cardiomyopathy
10 0 4 0.24 0 0
CUI: C0546264
Disease: Congenital Fiber Type Disproportion
Congenital Fiber Type Disproportion
6 45 3 0.21 1 1.2E-02
Type 1 fibers relatively smaller than type 2 fibers
6 0 3 0.21 0 0
CUI: C0686353
Disease: Muscular Dystrophies, Limb-Girdle
Muscular Dystrophies, Limb-Girdle
21 0 5 0.19 0 0
CUI: C0231666
Disease: Wrist-Drop
Wrist-Drop
2 0 2 0.18 0 0
Re-entrant atrioventricular tachycardia
2 0 2 0.18 0 0
X-Linked Emery-Dreifuss Muscular Dystrophy
2 0 2 0.18 0 0
CUI: C1836118
Disease: LEFT VENTRICULAR NONCOMPACTION 2
LEFT VENTRICULAR NONCOMPACTION 2
2 0 2 0.18 0 0
MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 2J
2 0 2 0.18 0 0
CUI: C1838244
Disease: TIBIAL MUSCULAR DYSTROPHY, TARDIVE
TIBIAL MUSCULAR DYSTROPHY, TARDIVE
2 0 2 0.18 0 0
CUI: C1843697
Disease: Axial muscle weakness
Axial muscle weakness
28 0 6 0.18 0 0
CUI: C1853932
Disease: Rimmed vacuoles on biopsy
Rimmed vacuoles on biopsy
28 0 6 0.18 0 0
CUI: C1858763
Disease: Cardiomyopathy, Dilated, 1g
Cardiomyopathy, Dilated, 1g
2 306 2 0.18 1 2.9E-03
CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 9
2 0 2 0.18 0 0
Hereditary Myopathy with Early Respiratory Failure
2 0 2 0.18 0 0
Myopathy, Early-Onset, with Fatal Cardiomyopathy
2 0 2 0.18 0 0
CUI: C2678065
Disease: Myofibrillar Myopathy
Myofibrillar Myopathy
15 15 4 0.18 1 1.9E-02
CUI: C4023180
Disease: Type 1 muscle fiber atrophy
Type 1 muscle fiber atrophy
15 0 4 0.18 0 0