OBO ID: DOID:0060676 |
Term Name: | catecholaminergic polymorphic ventricular tachycardia 2 | Search Ontology: | |
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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 | ||
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Ontology: | Human Disease ( DOID:0060676 ) |
OTHER catecholaminergic polymorphic ventricular tachycardia 2 PAGES
ZEBRAFISH MODELS
No data available
PHENOTYPE
No data available
CITATIONS: None
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