Source: CLINVAR ×
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: C0007196
Disease: Restrictive cardiomyopathy
Restrictive cardiomyopathy 		6 0 3 6.5E-02 0 0
CUI: C0085298
Disease: Sudden Cardiac Death
Sudden Cardiac Death 		6 5 3 6.5E-02 1 2.2E-03
CUI: C0234182
Disease: Gowers sign
Gowers sign 		7 0 3 6.4E-02 0 0
CUI: C3495498
Disease: Cardiomyopathy, Familial Hypertrophic, 1 (disorder)
Cardiomyopathy, Familial Hypertrophic, 1 (disorder) 		7 0 3 6.4E-02 0 0
CUI: C0039070
Disease: Syncope
Syncope 		8 12 3 6.2E-02 1 2.2E-03
CUI: C0018808
Disease: Heart murmur
Heart murmur 		11 10 3 5.9E-02 1 2.2E-03
CUI: C0699743
Disease: Congenital muscular dystrophy (disorder)
Congenital muscular dystrophy (disorder) 		12 0 3 5.8E-02 0 0
CUI: C4021726
Disease: EMG: myopathic abnormalities
EMG: myopathic abnormalities 		13 0 3 5.7E-02 0 0
CUI: C1836296
Disease: Muscle Weakness Lower Limb
Muscle Weakness Lower Limb 		15 0 3 5.5E-02 0 0
CUI: C0856863
Disease: Broad-based gait
Broad-based gait 		19 0 3 5.1E-02 0 0
CUI: C1836150
Disease: Gait imbalance
Gait imbalance 		20 0 3 5.0E-02 0 0
CUI: C1844806
Disease: Weight less than 3rd percentile
Weight less than 3rd percentile 		22 27 3 4.8E-02 1 2.1E-03
CUI: C0004239
Disease: Atrial Flutter
Atrial Flutter 		2 0 2 4.7E-02 0 0
CUI: C0151517
Disease: Complete atrioventricular block
Complete atrioventricular block 		2 0 2 4.7E-02 0 0
CUI: C0340477
Disease: Re-entrant atrioventricular tachycardia
Re-entrant atrioventricular tachycardia 		2 0 2 4.7E-02 0 0
CUI: C0428974
Disease: Supraventricular arrhythmia
Supraventricular arrhythmia 		2 1 2 4.7E-02 1 2.3E-03
CUI: C1835928
Disease: CARDIOMYOPATHY, DILATED, 1P
CARDIOMYOPATHY, DILATED, 1P 		2 3 2 4.7E-02 3 6.8E-03
CUI: C1836118
Disease: LEFT VENTRICULAR NONCOMPACTION 2
LEFT VENTRICULAR NONCOMPACTION 2 		2 0 2 4.7E-02 0 0
CUI: C1837148
Disease: MYOPIA 6 (disorder)
MYOPIA 6 (disorder) 		2 0 2 4.7E-02 0 0
CUI: C1837342
Disease: MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 2J
MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 2J 		2 230 2 4.7E-02 33 5.2E-02
CUI: C1838244
Disease: TIBIAL MUSCULAR DYSTROPHY, TARDIVE
TIBIAL MUSCULAR DYSTROPHY, TARDIVE 		2 17 2 4.7E-02 1 2.2E-03
CUI: C1857777
Disease: Arrhythmogenic Right Ventricular Dysplasia, Familial, 10
Arrhythmogenic Right Ventricular Dysplasia, Familial, 10 		2 27 2 4.7E-02 1 2.1E-03
CUI: C1858424
Disease: Cardioencephalomyopathy, Fatal Infantile, due to Cytochrome C Oxidase Deficiency
Cardioencephalomyopathy, Fatal Infantile, due to Cytochrome C Oxidase Deficiency 		2 0 2 4.7E-02 0 0
CUI: C1858763
Disease: Cardiomyopathy, Dilated, 1g
Cardiomyopathy, Dilated, 1g 		2 306 2 4.7E-02 41 5.8E-02
CUI: C1861065
Disease: CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 9
CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 9 		2 7 2 4.7E-02 1 2.2E-03