Search Ontology:
Human Disease

infantile histiocytoid cardiomyopathy

Term ID
DOID:0080198
Synonyms
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
Ontology
Human Disease   ( DOID:0080198 )
Relationships
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Genes Involved
Zebrafish Models