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: C1837323
Disease: Decreased Achilles reflex
Decreased Achilles reflex
7 0 5 0.33 0 0
CUI: C0751336
Disease: Distal Muscular Dystrophies
Distal Muscular Dystrophies
31 0 10 0.29 0 0
CUI: C4021523
Disease: Upper limb amyotrophy
Upper limb amyotrophy
9 0 4 0.22 0 0
CUI: C3805969
Disease: Scapular muscle atrophy
Scapular muscle atrophy
4 0 3 0.21 0 0
CUI: C1851542
Disease: Limited hip movement
Limited hip movement
10 0 4 0.21 0 0
CUI: C4024612
Disease: Tibialis muscle weakness
Tibialis muscle weakness
5 0 3 0.20 0 0
Limb-girdle muscular dystrophy type 2A
18 0 5 0.19 0 0
CUI: C0410266
Disease: Contracture of hamstring(s)
Contracture of hamstring(s)
6 0 3 0.19 0 0
CUI: C0544966
Disease: Autophagic vaculoes (finding)
Autophagic vaculoes (finding)
6 0 3 0.19 0 0
CUI: C3150620
Disease: Distal upper limb muscle weakness
Distal upper limb muscle weakness
13 0 4 0.18 0 0
CUI: C1850808
Disease: Miyoshi myopathy
Miyoshi myopathy
7 0 3 0.18 0 0
CUI: C4551973
Disease: Miyoshi Muscular Dystrophy 1
Miyoshi Muscular Dystrophy 1
7 0 3 0.18 0 0
CUI: C1853932
Disease: Rimmed vacuoles on biopsy
Rimmed vacuoles on biopsy
28 0 6 0.17 0 0
CUI: C4021727
Disease: EMG: neuropathic changes
EMG: neuropathic changes
28 0 6 0.17 0 0
CUI: C0221054
Disease: Welander Distal Myopathy
Welander Distal Myopathy
8 0 3 0.17 0 0
CUI: C1836767
Disease: Proximal lower limb amyotrophy
Proximal lower limb amyotrophy
15 0 4 0.17 0 0
CUI: C3277184
Disease: Decreased patellar reflex
Decreased patellar reflex
8 0 3 0.17 0 0
CUI: C0427064
Disease: Pelvic girdle weakness
Pelvic girdle weakness
16 0 4 0.16 0 0
CUI: C0231666
Disease: Wrist-Drop
Wrist-Drop
2 0 2 0.15 0 0
CUI: C0586738
Disease: Calf muscle weakness
Calf muscle weakness
2 0 2 0.15 0 0
CUI: C1450052
Disease: Tibial Muscular Dystrophy
Tibial Muscular Dystrophy
2 0 2 0.15 0 0
CUI: C4477022
Disease: Finger flexor weakness
Finger flexor weakness
2 0 2 0.15 0 0
CUI: C0264789
Disease: Familial cardiomyopathy
Familial cardiomyopathy
10 0 3 0.15 0 0
CUI: C1389118
Disease: Peroneal muscle atrophy
Peroneal muscle atrophy
10 0 3 0.15 0 0
Increased variability in muscle fiber diameter
50 0 8 0.15 0 0