Search Ontology:
Human Disease

restrictive cardiomyopathy 1

Term ID
DOID:0111425
Synonyms
  • familial restrictive cardiomyopathy 1
  • RCM1
Definition
A restrictive cardiomyopathy that has_material_basis_in heterozygous mutation in the TNNI3 gene on chromosome 19q13.42. https://www.ncbi.nlm.nih.gov/pubmed/12531876
References
Ontology
Human Disease   ( DOID:0111425 )
Relationships
is a type of
Other Pages
Alliance (1)
Genes Involved
Zebrafish Models
Citations
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