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Fatal infantile cytochrome C oxidase deficiency
2 OMIM references -
5 associated genes
No signs/symptoms info
PROTEIN INTERACTIONS: 1
Dopa-responsive dystonia due to sepiapterin reductase deficiency
1 OMIM reference -
1 associated gene
No signs/symptoms info
Fatal infantile cytochrome C oxidase deficiency
Dopa-responsive dystonia due to sepiapterin reductase deficiency

COX10
(UniProt - OMIM)
 SPR
(UniProt - OMIM)
COX15
(UniProt - OMIM)
SCO1
(UniProt - OMIM)
SCO2
(UniProt - OMIM)
SURF1
(UniProt - OMIM)

INTERACTOME
ASSOCIATIONS
(click on a score value to see the evidence)
SCO2
(0.49)
SPR


Citations in the biomedical literature:


Fatal infantile cytochrome C oxidase deficiency
COX10 COX15 SCO1 SCO2 SURF1
Dopa-responsive dystonia due to sepiapterin reductase deficiency
SPR



Fatal infantile cytochrome C oxidase deficiency
Dopa-responsive dystonia due to sepiapterin reductase deficiency

Synonym(s):
- Fatal infantile COX deficiency
- Fatal infantile cardioencephalomyopathy due to cytochrome c oxidase deficiency
Synonym(s):
- Autosomal recessive sepiapterin reductase-deficient DRD
- DRD autosomique récessive par déficit en sépiaptérine réductase
- DRD due to SRD
- SPR deficiency
- Sepiapterin reductase deficiency
Classification (Orphanet):
- Inborn errors of metabolism
- Rare genetic disease
Classification (Orphanet):
- Inborn errors of metabolism
- Rare genetic disease
- Rare neurologic disease
Classification (ICD10):
- Diseases of the nervous system -
Classification (ICD10):
- Diseases of the nervous system -
Epidemiological data:
(no data available)
Epidemiological data:
Class of prevalence: <1 / 1 000 000
Average age onset: neonatal/infancy
Average age of death: normal
Type of inheritance: autosomal recessive
External references:
2 OMIM references -
No MeSH references
External references:
1 OMIM reference -
No MeSH references
No signs/symptoms info available.