Visualize Submit Comment
Metadata
ID DOID:0080198
Name infantile histiocytoid cardiomyopathy
Definition An intrinsic cardiomyopathy characterized by the presence of characteristic pale granular foamy histiocyte-like cells within the myocardium and has_material_basis_in a mutation in the gene encoding mitochondrial cytochrome b.
https://www.ncbi.nlm.nih.gov/pubmed/10960495
Xrefs

GARD:9511

OMIM:500000

Parent Relationships

is_a intrinsic cardiomyopathy

Add an item to the term tracker