MeSH Browser

MeSH Supplementary: Cardioencephalomyopathy, Fatal Infantile, due to Cytochrome C Oxidase Deficiency
Unique ID: C565784
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C565784
Entry Term(s): Cytochrome C Oxidase Deficiency, Fatal Infantile, with Cardioencephalomyopathy
Registry Numbers: 0
Heading Mapped to: *Cardiomyopathy, Hypertrophic; *Mitochondrial Encephalomyopathies; *Cytochrome-c Oxidase Deficiency
Frequency: 1
Note: mutation in SCO2
Date of Entry: 2012/11/05
Revision Date: 1955/01/01

Cardioencephalomyopathy, Fatal Infantile, due to Cytochrome C Oxidase Deficiency MeSH Supplementary Concept Data 2025