Search Ontology:
Human Disease

X-linked dilated cardiomyopathy

Term ID
DOID:0110461
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 Pages
Alliance (1)
Genes Involved
Zebrafish Models
Citations
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