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Histiocytoid cardiomyopathy
2 OMIM references -
1 associated gene
2 connected diseases
No signs/symptoms info
Disease Type of connection
Isolated CoQ-cytochrome C reductase deficiency
Leber hereditary optic neuropathy
Synonym(s):
- Foamy myocardial transformation of infancy
- Infantile cardiomyopathy with histiocytoid change
- Infantile xanthomatous cardiomyopathy
- Oncocytic cardiomyopathy
Classification (Orphanet):
- Rare cardiac disease
- Rare genetic disease
Classification (ICD10):
- Diseases of the circulatory system -
Epidemiological data:
Class of prevalence: <1 / 1 000 000
Average age onset: neonatal/infancy
Average age of death: before age 5
Type of inheritance: autosomal recessive
External references:
2 OMIM references -
1 MeSH reference: C535584
Gene symbol UniProt reference OMIM reference
MT-CYB P00156516020
No signs/symptoms info available.