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Diseases
Genes (773)
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RYR2
Ventricular Tachycardia, Catecholaminergic Polymorphic, 2
TTPA
Familial Isolated Vitamin E Deficiency
ATP7B
Wilson's Disease
TRDN
Ventricular Tachycardia, Catecholaminergic Polymorphic, 2
CALM1
Ventricular Tachycardia, Catecholaminergic Polymorphic, 2
CASQ2
Ventricular Tachycardia, Catecholaminergic Polymorphic, 2
PQBP1
Renpenning's Syndrome
MED12
Fg Syndrome
SLC20A2
Cyclopia
Primary Familial Brain Calcification
FAM20A
Enamel-Renal Syndrome
PDGFRB
Primary Familial Brain Calcification
UBE3B
Kaufman Oculocerebrofacial Syndrome
IFIH1
Singleton Merten Syndrome
TNF
Familial Isolated Vitamin E Deficiency
Renpenning's Syndrome
Wilson's Disease
Pleural Effusion
Myotonic Dystrophy
TECRL
Ventricular Tachycardia, Catecholaminergic Polymorphic, 2
ACTG2
Berdon Syndrome
FLNA
Aneurysm Of Sinus Of Valsalva
Intestinal Neuronal Dysplasia
Fg Syndrome
DMPK
Myotonic Dystrophy
ASS1
Citrullinemia Type I
PDGFB
Primary Familial Brain Calcification