Search Ontology:
Human Disease
infantile histiocytoid cardiomyopathy
- Term ID
- DOID:0080198
- Synonyms
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- 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
- References
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- GARD:9511
- MIM:500000
- Ontology
- Human Disease ( DOID:0080198 )
- is a type of
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Genes Involved
Zebrafish Models