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

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

INTERACTOME
ASSOCIATIONS
(click on a score value to see the evidence)
ETFB
(0.63)
HTT


Citations in the biomedical literature:


Multiple acyl-CoA dehydrogenation deficiency, mild type
ETFA ETFB ETFDH
Huntington disease
HTT



Multiple acyl-CoA dehydrogenation deficiency, mild type
Huntington disease

Synonym(s):
(no synonyms)

Synonym(s):
- Huntington chorea
Classification (Orphanet):
- Inborn errors of metabolism
- Rare cardiac disease
- Rare genetic disease
- Rare neurologic disease
Classification (Orphanet):
- 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: 1-9 / 100 000
Average age onset: variable
Average age of death: any age
Type of inheritance: autosomal dominant
External references:
No OMIM references
No MeSH references
External references:
1 OMIM reference -
1 MeSH reference: D006816
Huntington disease

Frequent
- Abnormal cry / voice / phonation disorder / nasal speech
- Autosomal dominant inheritance
- Cortical atrophy without hydrocephaly / cerebral hemiatrophy / subcortical atrophy
- EEG anomalies
- Hypertonia / spasticity / rigidity / stiffness
- Movement disorder
- Psychic / behavioural troubles
- Psychic / psychomotor regression / dementia / intellectual decline



Multiple acyl-CoA dehydrogenation deficiency, mild type

(no data available)