Search Ontology:
Human Disease

catecholaminergic polymorphic ventricular tachycardia 2

Term ID
DOID:0060676
Synonyms
  • CVPT2
Definition
A catecholaminergic polymorphic ventricular tachycardia that is characterized by autosomal recessive inheritance and has_material_basis_in homozygous or compound heterozygous mutation in the CASQ2 gene on chromosome 1p13. https://www.ncbi.nlm.nih.gov/pubmed/11401939
References
Ontology
Human Disease   ( DOID:0060676 )
Relationships
is a type of
Other Pages
Alliance (1)
Genes Involved
Zebrafish Models
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