OBO ID: DOID:0111426
Term Name: restrictive cardiomyopathy 2 Search Ontology:
Synonyms:
  • familial restrictive cardiomyopathy 2
  • RCM2
Definition: A restrictive cardiomyopathy that has_material_basis_in variation in a region on chromosome 10q23.3. https://www.ncbi.nlm.nih.gov/pubmed/16061566
References:
Ontology: Human Disease   ( DOID:0111426 )
Relationships
is a type of:
OTHER restrictive cardiomyopathy 2 PAGES
GENES INVOLVED No data available
ZEBRAFISH MODELS No data available
PHENOTYPE No data available

CITATIONS: None
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