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Diseases
Genes (912)
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SCN5A
Premature Ventricular Contraction
Cardiomyopathy, Dilated, 1e
Ventricular Tachycardia, Catecholaminergic Polymorphic, 4
Ventricular Fibrillation, Paroxysmal Familial, 1
TTN
Premature Ventricular Contraction
Cardiomyopathy, Dilated, 1e
Limb–girdle Muscular Dystrophy
CACNA1F
Oguchi Disease 1
X-Linked Congenital Stationary Night Blindness
Achromatopsia
CNGA3
Color Blindness
X-Linked Congenital Stationary Night Blindness
Achromatopsia
Oligocone Trichromacy
PAX3
Waardenburg Syndrome Type I
Heterochromia Iridum
CNGB3
Color Blindness
Achromatopsia
GNAT2
Color Blindness
Achromatopsia
ATF6
Color Blindness
Achromatopsia
RYR2
Premature Ventricular Contraction
Ventricular Tachycardia, Catecholaminergic Polymorphic, 4
Ventricular Fibrillation, Paroxysmal Familial, 1
PDE6H
Color Blindness
Achromatopsia
LMNA
Premature Ventricular Contraction
Cardiomyopathy, Dilated, 1e
Limb–girdle Muscular Dystrophy
CYP4V2
Bietti Crystalline Dystrophy
LAMP2
Danon Disease
SAG
Oguchi Disease 1
X-Linked Congenital Stationary Night Blindness
DES
Cardiomyopathy, Dilated, 1e
Limb–girdle Muscular Dystrophy
NAA10
Premature Ventricular Contraction
Ogden Syndrome
SLC45A2
Oculocutaneous Albinism Type 4
Ocular Albinism, X-Linked
PDE6C
Achromatopsia
TRDN
Premature Ventricular Contraction
Ventricular Tachycardia, Catecholaminergic Polymorphic, 4
GPR143
Ocular Albinism, X-Linked