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1 OMIM reference -
1 associated gene
No signs/symptoms info
PROTEIN INTERACTIONS: 1
1 OMIM reference -
1 associated gene
No signs/symptoms info
Juvenile Huntington disease
Long chain 3-hydroxyacyl-CoA dehydrogenase deficiency

HTT HADHA


INTERACTOME
ASSOCIATIONS

(click on a score value to see the evidence)
HTT
(0.63)
HADHA



Citations in the biomedical literature:


Juvenile Huntington disease
HTT
Long chain 3-hydroxyacyl-CoA dehydrogenase deficiency
HADHA



Juvenile Huntington disease
Long chain 3-hydroxyacyl-CoA dehydrogenase deficiency

Synonym(s):
- JHD
- Juvenile Huntington chorea

Synonym(s):
- LCHAD deficiency
- LCHADD

Classification (Orphanet):
- Rare genetic disease
- Rare neurologic disease
Classification (Orphanet):
- Inborn errors of metabolism
- Rare cardiac disease
- Rare endocrine disease
- Rare eye disease
- Rare genetic disease
- Rare neurologic disease

Classification (ICD10):
- Diseases of the nervous system -
Classification (ICD10):
- Endocrine, nutritional and metabolic diseases -

Epidemiological data:
Class of prevalence: 1-9 / 1 000 000
Average age onset: adolescence / young
Average age of death: -
Type of inheritance: autosomal dominant
Epidemiological data:
Class of prevalence: 1-9 / 100 000
Average age onset: neonatal/infancy
Average age of death: before age 5
Type of inheritance: autosomal recessive

External references:
1 OMIM reference -
No MeSH references
External references:
1 OMIM reference -
No MeSH references

No signs/symptoms info available.