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Diseases
Genes (723)
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MYO15A
Deafness, Autosomal Recessive 3
RYR2
Ventricular Tachycardia, Catecholaminergic Polymorphic, 3
LIPA
Lysosomal Acid Lipase Deficiency
PHKG2
Glycogen Storage Disease Type Ix
Phosphorylase Kinase Deficiency
Glycogen Storage Disease Ixc
Mauriac Syndrome
GATA2
Monomac
PIK3CD
Cholera
Activated Pi3k Delta Syndrome
SLC20A2
Primary Familial Brain Calcification
TRDN
Ventricular Tachycardia, Catecholaminergic Polymorphic, 3
CALM1
Ventricular Tachycardia, Catecholaminergic Polymorphic, 3
PDGFRB
Primary Familial Brain Calcification
CASQ2
Ventricular Tachycardia, Catecholaminergic Polymorphic, 3
TNNI3K
Cardiac Conduction Disease With Or Without Dilated Cardiomyopathy
HPS4
Hermansky-Pudlak Syndrome 4
HPS3
Hermansky-Pudlak Syndrome 4
BLOC1S3
Hermansky-Pudlak Syndrome 4
MYH6
Sick Sinus Syndrome
DTNBP1
Hermansky-Pudlak Syndrome 4
BLOC1S6
Hermansky-Pudlak Syndrome 4
HPS6
Hermansky-Pudlak Syndrome 4
HPS5
Hermansky-Pudlak Syndrome 4