OBO ID: DOID:0111427 |
Term Name: | restrictive cardiomyopathy 3 | Search Ontology: | |
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Definition: | A restrictive cardiomyopathy that has_material_basis_in heterozygous mutation in the TNNT2 gene on chromosome 1q32.1. https://www.ncbi.nlm.nih.gov/pubmed/16651346 | ||
References: | |||
Ontology: | Human Disease ( DOID:0111427 ) |
OTHER restrictive cardiomyopathy 3 PAGES
ZEBRAFISH MODELS
No data available
PHENOTYPE
No data available
CITATIONS: None
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