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Very long chain acyl-CoA dehydrogenase deficiency
1 OMIM reference -
1 associated gene
7 connected diseases
No signs/symptoms info
Disease Type of connection
Familial gastric cancer
Gastric linitis plastica
Familial isolated congenital asplenia
Hereditary hyperekplexia
Sulfite oxidase deficiency due to molybdenum cofactor deficiency type C
Congenital analbuminemia
Richieri Costa-Pereira syndrome
Synonym(s):
- VLCAD deficiency
- VLCADD
Classification (Orphanet):
- Inborn errors of metabolism
- Rare cardiac disease
- Rare genetic disease
- Rare neurologic disease
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
External references:
1 OMIM reference -
No MeSH references
Gene symbol UniProt reference OMIM reference
ACADVL P49748609575
No signs/symptoms info available.