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Human Disease

catecholaminergic polymorphic ventricular tachycardia 1

Term ID
DOID:0060675
Synonyms
  • arrhythmogenic right ventricular dysplasia 2
  • CVPT1
Definition
A catecholaminergic polymorphic ventricular tachycardia that is characterized by autosomal dominant inheritance and has_material_basis_in heterozygous mutation in the RYR2 gene on chromosome 1q43. (2)
References
Ontology
Human Disease   ( DOID:0060675 )
Relationships
is a type of
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Genes Involved
Zebrafish Models