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Multiple acyl-CoA dehydrogenation deficiency, mild type
3 associated genes
No signs/symptoms info
PROTEIN INTERACTIONS: 1
Estrogen resistance syndrome
1 OMIM reference -
1 associated gene
No signs/symptoms info
Multiple acyl-CoA dehydrogenation deficiency, mild type
Estrogen resistance syndrome

ETFA
(UniProt - OMIM)
 ESR1
(UniProt - OMIM)
ETFB
(UniProt - OMIM)
ETFDH
(UniProt - OMIM)

INTERACTOME
ASSOCIATIONS
(click on a score value to see the evidence)
ETFA
(0.63)
ESR1


Citations in the biomedical literature:


Multiple acyl-CoA dehydrogenation deficiency, mild type
ETFA ETFB ETFDH
Estrogen resistance syndrome
ESR1



Multiple acyl-CoA dehydrogenation deficiency, mild type
Estrogen resistance syndrome

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