Fatal infantile cytochrome C oxidase deficiency

Disease Export to PDF
Name:
Fatal infantile cytochrome C oxidase deficiency
Description:
Fatal infantile cytochrome C oxidase deficiency is a very rare mitochondrial disease characterized clinically by cardioencephalomyopathy resulting in death in infancy.
ORPHAcode:
1561
Synonyms:
Fatal infantile COX deficiency
Fatal infantile cardioencephalomyopathy due to cytochrome C oxidase deficiency
XREF(s):
Analyte(s):
Created:
13 May 2019 - 01:02
Changed:
22 Jun 2023 - 16:14