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: C0750863
Disease: Finding of creatine kinase level
Finding of creatine kinase level
2 2 2 6.9E-02 2 3.9E-02
Antiphospholipid antibodies measurement
6 0 2 6.1E-02 0 0
CUI: C0546125
Disease: Nemaline Myopathy, Childhood Onset
Nemaline Myopathy, Childhood Onset
7 0 2 5.9E-02 0 0
CUI: C3710589
Disease: Cap Myopathy
Cap Myopathy
9 0 2 5.6E-02 0 0
CUI: C4025729
Disease: Neuromuscular dysphagia
Neuromuscular dysphagia
12 0 2 5.1E-02 0 0
CUI: C1837262
Disease: Increased muscle lipid content
Increased muscle lipid content
14 0 2 4.9E-02 0 0
Fatiguable weakness of proximal limb muscles
14 0 2 4.9E-02 0 0
Fatigable weakness of bulbar muscles
14 0 2 4.9E-02 0 0
CUI: C0039106
Disease: Pigmented villonodular synovitis
Pigmented villonodular synovitis
15 0 2 4.8E-02 0 0
CUI: C3808039
Disease: Nemaline bodies
Nemaline bodies
15 0 2 4.8E-02 0 0
CUI: C1866021
Disease: Increased connective tissue
Increased connective tissue
16 0 2 4.7E-02 0 0
Activated Partial Thromboplastin Time measurement
17 44 2 4.5E-02 1 1.1E-02
Fatty replacement of skeletal muscle
17 0 2 4.5E-02 0 0
CUI: C0587246
Disease: Muscle weakness of limb
Muscle weakness of limb
42 0 3 4.4E-02 0 0
Rapidly progressive glomerulonephritis
19 0 2 4.3E-02 0 0
CUI: C4024921
Disease: Lower limb amyotrophy
Lower limb amyotrophy
19 0 2 4.3E-02 0 0
CUI: C1838114
Disease: Generalized limb muscle atrophy
Generalized limb muscle atrophy
21 0 2 4.2E-02 0 0
CUI: C0202202
Disease: Protein measurement
Protein measurement
75 422 4 4.0E-02 1 2.1E-03
CUI: C1857790
Disease: Thoracic scoliosis
Thoracic scoliosis
23 0 2 4.0E-02 0 0
Increased variability in muscle fiber diameter
50 0 3 3.9E-02 0 0
Progressive proximal muscle weakness
28 0 2 3.6E-02 0 0
CUI: C4021727
Disease: EMG: neuropathic changes
EMG: neuropathic changes
28 0 2 3.6E-02 0 0
CUI: C0476408
Disease: Reduced vital capacity
Reduced vital capacity
29 0 2 3.6E-02 0 0
CUI: C0006157
Disease: Breech Presentation
Breech Presentation
30 0 2 3.5E-02 0 0
CUI: C2931687
Disease: Dysferlinopathy
Dysferlinopathy
30 0 2 3.5E-02 0 0