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Very long chain acyl-CoA dehydrogenase deficiency
1 OMIM reference -
1 associated gene
No signs/symptoms info
PROTEIN INTERACTIONS: 1
Sulfite oxidase deficiency due to molybdenum cofactor deficiency type C
1 OMIM reference -
1 associated gene
No signs/symptoms info
Very long chain acyl-CoA dehydrogenase deficiency
Sulfite oxidase deficiency due to molybdenum cofactor deficiency type C

ACADVL
(UniProt - OMIM)
 GPHN
(UniProt - OMIM)

INTERACTOME
ASSOCIATIONS
(click on a score value to see the evidence)
ACADVL
(0.63)
GPHN


Citations in the biomedical literature:


Very long chain acyl-CoA dehydrogenase deficiency
ACADVL
Sulfite oxidase deficiency due to molybdenum cofactor deficiency type C
GPHN



Very long chain acyl-CoA dehydrogenase deficiency
Sulfite oxidase deficiency due to molybdenum cofactor deficiency type C

Synonym(s):
- VLCAD deficiency
- VLCADD
Synonym(s):
- Combined deficiency of sulfite oxidase, xanthine dehydrogenase and aldehyde oxidase type C
- MOCOD type C
Classification (Orphanet):
- Inborn errors of metabolism
- Rare cardiac disease
- Rare genetic disease
- Rare neurologic disease
Classification (Orphanet):
- Inborn errors of metabolism
- Rare genetic disease
Classification (ICD10):
- Endocrine, nutritional and metabolic diseases -
Classification (ICD10):
- Endocrine, nutritional and metabolic diseases -
Epidemiological data:
Class of prevalence: 1-9 / 100 000
Average age onset: neonatal/infancy
Average age of death: before age 5
Type of inheritance: autosomal recessive
Epidemiological data:
(no data available)
External references:
1 OMIM reference -
No MeSH references
External references:
1 OMIM reference -
No MeSH references
No signs/symptoms info available.