Search Ontology:
Human Disease

restrictive cardiomyopathy 2

Term ID
DOID:0111426
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 Pages
Alliance (1)
Genes Involved
Zebrafish Models
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