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: C0033300
Disease: Progeria
Progeria 		1 0 1 0.33 0 0
CUI: C0037052
Disease: Sick Sinus Syndrome
Sick Sinus Syndrome 		1 0 1 0.33 0 0
CUI: C0079035
Disease: Bradyarrhythmia (disorder)
Bradyarrhythmia (disorder) 		1 0 1 0.33 0 0
CUI: C0264906
Disease: Second degree atrioventricular block
Second degree atrioventricular block 		1 0 1 0.33 0 0
CUI: C0392777
Disease: Poikiloderma
Poikiloderma 		1 0 1 0.33 0 0
CUI: C0410189
Disease: Muscular Dystrophy, Emery-Dreifuss
Muscular Dystrophy, Emery-Dreifuss 		1 0 1 0.33 0 0
CUI: C0410190
Disease: Autosomal Dominant Emery-Dreifuss Muscular Dystrophy (disorder)
Autosomal Dominant Emery-Dreifuss Muscular Dystrophy (disorder) 		1 0 1 0.33 0 0
CUI: C0428908
Disease: Sinus Node Dysfunction (disorder)
Sinus Node Dysfunction (disorder) 		1 0 1 0.33 0 0
CUI: C0432291
Disease: Mandibuloacral dysostosis
Mandibuloacral dysostosis 		1 0 1 0.33 0 0
CUI: C0796031
Disease: Malouf syndrome
Malouf syndrome 		1 0 1 0.33 0 0
CUI: C1720860
Disease: Familial Partial Lipodystrophy, Type 2
Familial Partial Lipodystrophy, Type 2 		1 0 1 0.33 0 0
CUI: C1832680
Disease: CARDIOMYOPATHY, DILATED, 1E
CARDIOMYOPATHY, DILATED, 1E 		1 0 1 0.33 0 0
CUI: C1834653
Disease: MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 1B (disorder)
MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 1B (disorder) 		1 0 1 0.33 0 0
CUI: C1837845
Disease: SICK SINUS SYNDROME 1, AUTOSOMAL RECESSIVE
SICK SINUS SYNDROME 1, AUTOSOMAL RECESSIVE 		1 8 1 0.33 1 9.1E-02
CUI: C1838527
Disease: LONG QT SYNDROME 3, ACQUIRED, SUSCEPTIBILITY TO (finding)
LONG QT SYNDROME 3, ACQUIRED, SUSCEPTIBILITY TO (finding) 		1 0 1 0.33 0 0
CUI: C1857829
Disease: Heart-hand syndrome, Slovenian type
Heart-hand syndrome, Slovenian type 		1 0 1 0.33 0 0
CUI: C1858672
Disease: GENERALIZED EPILEPSY WITH FEBRILE SEIZURES PLUS, TYPE 1
GENERALIZED EPILEPSY WITH FEBRILE SEIZURES PLUS, TYPE 1 		1 0 1 0.33 0 0
CUI: C1859062
Disease: LONG QT SYNDROME 3
LONG QT SYNDROME 3 		1 0 1 0.33 0 0
CUI: C1861983
Disease: Heart Block, Nonprogressive
Heart Block, Nonprogressive 		1 0 1 0.33 0 0
CUI: C1861984
Disease: Cardiac Conduction Defect, Nonprogressive
Cardiac Conduction Defect, Nonprogressive 		1 0 1 0.33 0 0
CUI: C2748541
Disease: Brugada Syndrome 5
Brugada Syndrome 5 		1 0 1 0.33 0 0
CUI: C2750035
Disease: Emery-Dreifuss Muscular Dystrophy 3
Emery-Dreifuss Muscular Dystrophy 3 		1 0 1 0.33 0 0
CUI: C2750285
Disease: Progeria Syndrome, Childhood-Onset
Progeria Syndrome, Childhood-Onset 		1 0 1 0.33 0 0
CUI: C2750785
Disease: MUSCULAR DYSTROPHY, CONGENITAL, LMNA-RELATED (disorder)
MUSCULAR DYSTROPHY, CONGENITAL, LMNA-RELATED (disorder) 		1 0 1 0.33 0 0
CUI: C2751898
Disease: Ventricular Fibrillation, Paroxysmal Familial, 1
Ventricular Fibrillation, Paroxysmal Familial, 1 		1 0 1 0.33 0 0