| 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 | |
| Subsets |
DO_rare_slim |
| Parent Relationships |
is_a monogenic disease |