Search Ontology:
Human Disease

dilated cardiomyopathy 1X

Term ID
DOID:0110444
Synonyms
  • CMD1X
  • dilated cardiomyopathy with mild or no proximal muscle weakness
Definition
A dilated cardiomyopathy that has_material_basis_in mutation in the FKTN gene on chromosome 9q31. https://www.ncbi.nlm.nih.gov/pubmed/17036286
References
Ontology
Human Disease   ( DOID:0110444 )
Relationships
is a type of
Other Pages
Alliance (1)
Genes Involved
Zebrafish Models
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