Search Ontology:
Human Disease

restrictive cardiomyopathy 3

Term ID
DOID:0111427
Synonyms
  • familial restrictive cardiomyopathy 3
  • RCM3
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 )
Relationships
is a type of
Other Pages
Alliance (1)
Genes Involved
Zebrafish Models
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