OBO ID: DOID:0110461
Term Name: X-linked dilated cardiomyopathy Search Ontology:
Synonyms:
  • CMD3B
  • DMD-related dilated cardiomyopathy
Definition: A dilated cardiomyopathy that has_material_basis_in mutation in the gene encoding dystrophin (DMD) on chromosome Xp21, without skeletal muscle weakness or wasting. (3)
References:
Ontology: Human Disease   ( DOID:0110461 )
Relationships
is a type of:
OTHER X-linked dilated cardiomyopathy PAGES
GENES INVOLVED
Human Gene Zebrafish Ortholog OMIM Term OMIM Phenotype ID
DMD Cardiomyopathy, dilated, 3B 302045
ZEBRAFISH MODELS No data available
PHENOTYPE No data available

CITATIONS: None
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