# infantile histiocytoid cardiomyopathy

> 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

**Wikidata**: [Q41516644](https://www.wikidata.org/wiki/Q41516644)  
**Source**: https://4ort.xyz/entity/infantile-histiocytoid-cardiomyopathy


## References

1. Monarch Disease Ontology release 2018-06-29
2. Disease Ontology
3. Human Phenotype Ontology release 2018-03-08
4. UniProt
5. [Identifiers.org](https://registry.identifiers.org/registry/doid)