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Multiple acyl-CoA dehydrogenation deficiency, mild type
3 associated genes
No signs/symptoms info
PROTEIN INTERACTIONS: 1
Acute fatty liver of pregnancy
1 associated gene
No signs/symptoms info
Multiple acyl-CoA dehydrogenation deficiency, mild type
Acute fatty liver of pregnancy

ETFA
(UniProt - OMIM)
 HADHA
(UniProt - OMIM)
ETFB
(UniProt - OMIM)
ETFDH
(UniProt - OMIM)

INTERACTOME
ASSOCIATIONS
(click on a score value to see the evidence)
ETFA
(0.49)
HADHA


Citations in the biomedical literature:


Multiple acyl-CoA dehydrogenation deficiency, mild type
ETFA ETFB ETFDH
Acute fatty liver of pregnancy
HADHA



Multiple acyl-CoA dehydrogenation deficiency, mild type
Acute fatty liver of pregnancy

Synonym(s):
(no synonyms)

Synonym(s):
- AFLP
Classification (Orphanet):
- Inborn errors of metabolism
- Rare cardiac disease
- Rare genetic disease
- Rare neurologic disease
Classification (Orphanet):
- Rare gynecologic or obstetric disease
- Rare hepatic disease
Classification (ICD10):
(no data available)
Classification (ICD10):
- Pregnancy, childbirth and the puerperium -
Epidemiological data:
(no data available)
Epidemiological data:
Class of prevalence: -
Average age onset: adulthood
Average age of death: -
Type of inheritance: multigenic/multifactorial
External references:
No OMIM references
No MeSH references
External references:
No OMIM references
1 MeSH reference: C537957
No signs/symptoms info available.