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: C4024612
Disease: Tibialis muscle weakness
Tibialis muscle weakness
5 0 4 0.12 0 0
CUI: C0427149
Disease: Gait, Drop Foot
Gait, Drop Foot
51 5 9 0.12 1 4.5E-02
CUI: C0544966
Disease: Autophagic vaculoes (finding)
Autophagic vaculoes (finding)
6 0 4 0.12 0 0
CUI: C0427055
Disease: Facial Paresis
Facial Paresis
44 0 8 0.12 0 0
CUI: C0427064
Disease: Pelvic girdle weakness
Pelvic girdle weakness
16 0 5 0.12 0 0
CUI: C0240953
Disease: Winged scapula
Winged scapula
73 0 11 0.12 0 0
Nemaline Myopathy, Autosomal Recessive
7 0 4 0.12 0 0
Fatty replacement of skeletal muscle
17 4 5 0.12 1 4.8E-02
CUI: C1843057
Disease: Calf muscle hypertrophy
Calf muscle hypertrophy
46 0 8 0.12 0 0
Limb-girdle muscular dystrophy type 2A
18 0 5 0.11 0 0
Weakness of long finger extensor muscles
18 0 5 0.11 0 0
CUI: C4021727
Disease: EMG: neuropathic changes
EMG: neuropathic changes
28 0 6 0.11 0 0
CUI: C0427065
Disease: Distal muscle weakness
Distal muscle weakness
117 0 15 0.11 0 0
CUI: C1533847
Disease: Disorder of skeletal muscle
Disorder of skeletal muscle
29 0 6 0.11 0 0
CUI: C1836450
Disease: Distal lower limb muscle weakness
Distal lower limb muscle weakness
49 11 8 0.11 1 3.6E-02
CUI: C1843637
Disease: Neck flexor weakness
Neck flexor weakness
30 0 6 0.11 0 0
CUI: C0221629
Disease: Proximal muscle weakness
Proximal muscle weakness
112 0 14 0.11 0 0
Increased endomysial connective tissue
10 0 4 0.11 0 0
CARDIOMYOPATHY, FAMILIAL RESTRICTIVE, 1 (disorder)
21 0 5 0.11 0 0
CUI: C0750403
Disease: Proximal weakness
Proximal weakness
11 0 4 0.11 0 0
Respiratory insufficiency due to muscle weakness
85 0 11 0.10 0 0
Proximal muscle weakness in upper limbs
22 0 5 0.10 0 0
CUI: C0558845
Disease: Reflex, Ankle, Absent
Reflex, Ankle, Absent
33 0 6 0.10 0 0
CUI: C0206157
Disease: Myopathies, Nemaline
Myopathies, Nemaline
47 0 7 9.9E-02 0 0
CUI: C0333751
Disease: Muscle fiber atrophy
Muscle fiber atrophy
25 0 5 9.8E-02 0 0