OBO ID: DOID:0110444
Term Name: dilated cardiomyopathy 1X Search Ontology:
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 dilated cardiomyopathy 1X PAGES
GENES INVOLVED
Human Gene Zebrafish Ortholog OMIM Term OMIM Phenotype ID
FKTN Cardiomyopathy, dilated, 1X 611615
ZEBRAFISH MODELS No data available
PHENOTYPE No data available

CITATIONS: None
Your Input Welcome
We welcome your input and comments. Please use this form to recommend updates to the information in ZFIN. We appreciate as much detail as possible and references as appropriate. We will review your comments promptly.
Please check the highlighted fields and try again.
Thank you for submitting comments. Your input has been emailed to ZFIN curators who may contact you if additional information is required.
Oops. Something went wrong. Please try again later.