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: C0018794
Disease: Heart Block
Heart Block 		1 0 1 1.0E-01 0 0
CUI: C0033300
Disease: Progeria
Progeria 		1 0 1 1.0E-01 0 0
CUI: C0037052
Disease: Sick Sinus Syndrome
Sick Sinus Syndrome 		1 0 1 1.0E-01 0 0
CUI: C0079035
Disease: Bradyarrhythmia (disorder)
Bradyarrhythmia (disorder) 		1 0 1 1.0E-01 0 0
CUI: C0205700
Disease: Asymmetric Septal Hypertrophy
Asymmetric Septal Hypertrophy 		1 0 1 1.0E-01 0 0
CUI: C0221347
Disease: Acrocyanosis
Acrocyanosis 		1 0 1 1.0E-01 0 0
CUI: C0264886
Disease: Conduction disorder of the heart
Conduction disorder of the heart 		1 0 1 1.0E-01 0 0
CUI: C0264906
Disease: Second degree atrioventricular block
Second degree atrioventricular block 		1 0 1 1.0E-01 0 0
CUI: C0270960
Disease: Congenital myopathy (disorder)
Congenital myopathy (disorder) 		1 0 1 1.0E-01 0 0
CUI: C0392777
Disease: Poikiloderma
Poikiloderma 		1 0 1 1.0E-01 0 0
CUI: C0410189
Disease: Muscular Dystrophy, Emery-Dreifuss
Muscular Dystrophy, Emery-Dreifuss 		1 0 1 1.0E-01 0 0
CUI: C0410190
Disease: Autosomal Dominant Emery-Dreifuss Muscular Dystrophy (disorder)
Autosomal Dominant Emery-Dreifuss Muscular Dystrophy (disorder) 		1 0 1 1.0E-01 0 0
CUI: C0428908
Disease: Sinus Node Dysfunction (disorder)
Sinus Node Dysfunction (disorder) 		1 0 1 1.0E-01 0 0
CUI: C0432291
Disease: Mandibuloacral dysostosis
Mandibuloacral dysostosis 		1 0 1 1.0E-01 0 0
CUI: C0796031
Disease: Malouf syndrome
Malouf syndrome 		1 0 1 1.0E-01 0 0
CUI: C1720860
Disease: Familial Partial Lipodystrophy, Type 2
Familial Partial Lipodystrophy, Type 2 		1 0 1 1.0E-01 0 0
CUI: C1832243
Disease: CARDIOMYOPATHY, DILATED, 1D (disorder)
CARDIOMYOPATHY, DILATED, 1D (disorder) 		1 0 1 1.0E-01 0 0
CUI: C1832680
Disease: CARDIOMYOPATHY, DILATED, 1E
CARDIOMYOPATHY, DILATED, 1E 		1 0 1 1.0E-01 0 0
CUI: C1834653
Disease: MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 1B (disorder)
MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 1B (disorder) 		1 0 1 1.0E-01 0 0
CUI: C1837845
Disease: SICK SINUS SYNDROME 1, AUTOSOMAL RECESSIVE
SICK SINUS SYNDROME 1, AUTOSOMAL RECESSIVE 		1 0 1 1.0E-01 0 0
CUI: C1838527
Disease: LONG QT SYNDROME 3, ACQUIRED, SUSCEPTIBILITY TO (finding)
LONG QT SYNDROME 3, ACQUIRED, SUSCEPTIBILITY TO (finding) 		1 0 1 1.0E-01 0 0
CUI: C1842160
Disease: MYOPATHY, MYOSIN STORAGE (disorder)
MYOPATHY, MYOSIN STORAGE (disorder) 		1 14 1 1.0E-01 1 2.2E-02
CUI: C1850709
Disease: Myopathy, Hyaline Body, Autosomal Recessive
Myopathy, Hyaline Body, Autosomal Recessive 		1 11 1 1.0E-01 1 2.4E-02
CUI: C1857829
Disease: Heart-hand syndrome, Slovenian type
Heart-hand syndrome, Slovenian type 		1 0 1 1.0E-01 0 0
CUI: C1859062
Disease: LONG QT SYNDROME 3
LONG QT SYNDROME 3 		1 0 1 1.0E-01 0 0