Cardioencephalomyopathy, Fatal Infantile, due to Cytochrome C Oxidase Deficiency [Supplementary Concept]

mutation in SCO2

Date introduced: November 5, 2012

MeSH Unique ID: C565784

Heading Mapped to:

• Cardiomyopathy, Hypertrophic
• Mitochondrial Encephalomyopathies
• Cytochrome-c Oxidase Deficiency

Entry Terms:

• Cytochrome C Oxidase Deficiency, Fatal Infantile, with Cardioencephalomyopathy