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: C1836050
Disease: Filaminopathy, autosomal dominant
Filaminopathy, autosomal dominant
1 38 1 1.00 36 0.80
CUI: C1862133
Disease: Decreased finger mobility
Decreased finger mobility
1 0 1 1.00 0 0
CUI: C3279722
Disease: MYOPATHY, DISTAL, 4
MYOPATHY, DISTAL, 4
1 38 1 1.00 36 0.80
CARDIOMYOPATHY, FAMILIAL RESTRICTIVE, 5
1 2 1 1.00 2 4.7E-02
CUI: C4476982
Disease: Two-raphe bicuspid aortic valve
Two-raphe bicuspid aortic valve
1 0 1 1.00 0 0
Abnormal morphology of left ventricular trabeculae
1 0 1 1.00 0 0
CUI: C1839512
Disease: Limited knee flexion
Limited knee flexion
2 0 1 0.50 0 0
Abnormal ventricular septum morphology
2 0 1 0.50 0 0
Muscle fiber cytoplasmatic inclusion bodies
2 0 1 0.50 0 0
CUI: C4477022
Disease: Finger flexor weakness
Finger flexor weakness
2 0 1 0.50 0 0
Familial restrictive cardiomyopathy (disorder)
3 0 1 0.33 0 0
Abnormal peripheral nervous system morphology
4 0 1 0.25 0 0
CUI: C0348616
Disease: Other restrictive cardiomyopathy
Other restrictive cardiomyopathy
5 0 1 0.20 0 0
CUI: C4021581
Disease: Distal upper limb amyotrophy
Distal upper limb amyotrophy
8 0 1 0.12 0 0
CUI: C0393524
Disease: Cerebellar Ataxia, Late Onset
Cerebellar Ataxia, Late Onset
9 0 1 0.11 0 0
CUI: C4021779
Disease: Abnormality of the calf musculature
Abnormality of the calf musculature
9 0 1 0.11 0 0
CUI: C0264789
Disease: Familial cardiomyopathy
Familial cardiomyopathy
10 0 1 1.0E-01 0 0
CUI: C1864716
Disease: Intrinsic hand muscle atrophy
Intrinsic hand muscle atrophy
11 0 1 9.1E-02 0 0
CUI: C1858033
Disease: Asymmetry of the thorax
Asymmetry of the thorax
12 0 1 8.3E-02 0 0
CUI: C4021866
Disease: obsolete Abnormal heart morphology
obsolete Abnormal heart morphology
12 0 1 8.3E-02 0 0
CUI: C1836057
Disease: Muscle fiber splitting
Muscle fiber splitting
13 0 1 7.7E-02 0 0
CUI: C3150620
Disease: Distal upper limb muscle weakness
Distal upper limb muscle weakness
13 0 1 7.7E-02 0 0
Fatiguable weakness of proximal limb muscles
14 0 1 7.1E-02 0 0
CUI: C3279725
Disease: Hip flexor weakness
Hip flexor weakness
16 0 1 6.2E-02 0 0
Limb-girdle muscular dystrophy type 2A
18 0 1 5.6E-02 0 0