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: C4023180
Disease: Type 1 muscle fiber atrophy
Type 1 muscle fiber atrophy
16 0 2 4.9E-02 0 0
Ventricular Arrhythmia by ECG Finding
17 0 2 4.8E-02 0 0
CUI: C1840333
Disease: Barakat syndrome
Barakat syndrome
17 0 2 4.8E-02 0 0
CUI: C1883529
Disease: Ventricular Arrhythmia, CTCAE 3.0
Ventricular Arrhythmia, CTCAE 3.0
17 0 2 4.8E-02 0 0
CUI: C4553764
Disease: Ventricular Arrhythmia, CTCAE 5.0
Ventricular Arrhythmia, CTCAE 5.0
17 0 2 4.8E-02 0 0
CUI: C0855329
Disease: Electrocardiogram change
Electrocardiogram change
18 0 2 4.7E-02 0 0
CUI: C0007196
Disease: Restrictive cardiomyopathy
Restrictive cardiomyopathy
41 0 3 4.6E-02 0 0
CUI: C0264886
Disease: Conduction disorder of the heart
Conduction disorder of the heart
41 0 3 4.6E-02 0 0
CUI: C0027125
Disease: Myotonia
Myotonia
19 0 2 4.5E-02 0 0
CUI: C0263505
Disease: Alopecia universalis
Alopecia universalis
19 0 2 4.5E-02 0 0
CUI: C0428974
Disease: Supraventricular arrhythmia
Supraventricular arrhythmia
19 0 2 4.5E-02 0 0
Amelogenesis imperfecta nephrocalcinosis
19 0 2 4.5E-02 0 0
X-Linked Emery-Dreifuss Muscular Dystrophy
20 0 2 4.4E-02 0 0
CUI: C4551647
Disease: Long QT Syndrome 1
Long QT Syndrome 1
20 0 2 4.4E-02 0 0
CUI: C4721508
Disease: Hamman-Rich Disease
Hamman-Rich Disease
20 0 2 4.4E-02 0 0
CUI: C0233488
Disease: Feeling despair
Feeling despair
21 0 2 4.3E-02 0 0
CARDIOMYOPATHY, FAMILIAL RESTRICTIVE, 1 (disorder)
21 0 2 4.3E-02 0 0
CUI: C2265792
Disease: Skeletal muscle hypertrophy
Skeletal muscle hypertrophy
21 0 2 4.3E-02 0 0
CUI: C0027443
Disease: Natal Teeth
Natal Teeth
22 0 2 4.3E-02 0 0
Proximal muscle weakness in upper limbs
22 0 2 4.3E-02 0 0
CUI: C0549399
Disease: Low density lipoprotein increased
Low density lipoprotein increased
23 0 2 4.2E-02 0 0
Familial Idiopathic Pulmonary Fibrosis
23 0 2 4.2E-02 0 0
CUI: C0240479
Disease: Neck muscle weakness
Neck muscle weakness
49 0 3 4.1E-02 0 0
CUI: C1096616
Disease: Contralateral breast cancer
Contralateral breast cancer
24 0 2 4.1E-02 0 0
CUI: C1846228
Disease: Absence of pubertal development
Absence of pubertal development
24 0 2 4.1E-02 0 0