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Multiple acyl-CoA dehydrogenation deficiency, mild type
3 associated genes
No signs/symptoms info
PROTEIN INTERACTIONS: 1
Mitochondrial trifunctional protein deficiency
1 OMIM reference -
2 associated genes
No signs/symptoms info
Multiple acyl-CoA dehydrogenation deficiency, mild type
Mitochondrial trifunctional protein deficiency

ETFA
(UniProt - OMIM)
 HADHA
(UniProt - OMIM)
ETFB
(UniProt - OMIM)
 HADHB
(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
Mitochondrial trifunctional protein deficiency
HADHA HADHB



Multiple acyl-CoA dehydrogenation deficiency, mild type
Mitochondrial trifunctional protein deficiency

Synonym(s):
(no synonyms)

Synonym(s):
- TFP deficiency
- TFPD
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):
- Diseases of the nervous system -
Epidemiological data:
(no data available)
Epidemiological data:
Class of prevalence: <1 / 1 000 000
Average age onset: neonatal/infancy
Average age of death: before age 5
Type of inheritance: autosomal recessive
External references:
No OMIM references
No MeSH references
External references:
1 OMIM reference -
1 MeSH reference: D024741
No signs/symptoms info available.