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Diseases
Genes (581)
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RYR2
Ventricular Tachycardia, Catecholaminergic Polymorphic, 2
TTPA
Familial Isolated Vitamin E Deficiency
F12
Factor Xii Deficiency
TRDN
Ventricular Tachycardia, Catecholaminergic Polymorphic, 2
CALM1
Ventricular Tachycardia, Catecholaminergic Polymorphic, 2
SLC12A6
Andermann Syndrome
CASQ2
Ventricular Tachycardia, Catecholaminergic Polymorphic, 2
PQBP1
Renpenning's Syndrome
MED12
Fg Syndrome
SLC17A5
Salla Disease
PMM2
Pmm2 Deficiency
FAM20A
Enamel-Renal Syndrome
NGLY1
Ngly1 Deficiency
UBE3B
Kaufman Oculocerebrofacial Syndrome
IFIH1
Singleton Merten Syndrome
ACTG2
Berdon Syndrome
TECRL
Ventricular Tachycardia, Catecholaminergic Polymorphic, 2
FLNA
Intestinal Neuronal Dysplasia
Fg Syndrome
TRNL1
Merrf Syndrome
DMPK
Myotonic Dystrophy