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Multiple acyl-CoA dehydrogenation deficiency, mild type
3 associated genes
No signs/symptoms info
COMMON GENES: 3
PROTEIN INTERACTIONS: 1
Multiple acyl-CoA dehydrogenation deficiency, severe neonatal type
3 associated genes
No signs/symptoms info
Multiple acyl-CoA dehydrogenation deficiency, mild type
Multiple acyl-CoA dehydrogenation deficiency, severe neonatal type

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

COMMON
GENES 		ETFA
ETFB
ETFDH
INTERACTOME
ASSOCIATIONS
(click on a score value to see the evidence)
ETFA
(0.91)
ETFB


Citations in the biomedical literature:


Multiple acyl-CoA dehydrogenation deficiency, mild type
ETFA ETFB ETFDH
Multiple acyl-CoA dehydrogenation deficiency, severe neonatal type



Multiple acyl-CoA dehydrogenation deficiency, mild type
Multiple acyl-CoA dehydrogenation deficiency, severe neonatal type

Classification (Orphanet):
- Inborn errors of metabolism
- Rare cardiac disease
- Rare genetic disease
- Rare neurologic disease
Classification (Orphanet):
- Inborn errors of metabolism
- Rare cardiac disease
- Rare genetic disease
- Rare neurologic disease
Classification (ICD10):
(no data available)
Classification (ICD10):
(no data available)
Epidemiological data:
(no data available)
Epidemiological data:
(no data available)
External references:
No OMIM references
No MeSH references
External references:
No OMIM references
No MeSH references
No signs/symptoms info available.