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Juvenile Huntington disease
1 OMIM reference -
1 associated gene
No signs/symptoms info
PROTEIN INTERACTIONS: 1
Autosomal dominant intermediate Charcot-Marie-Tooth disease type B
1 OMIM reference -
1 associated gene
No signs/symptoms info
Juvenile Huntington disease
Autosomal dominant intermediate Charcot-Marie-Tooth disease type B

HTT
(UniProt - OMIM)
 DNM2
(UniProt - OMIM)

INTERACTOME
ASSOCIATIONS
(click on a score value to see the evidence)
HTT
(0.63)
DNM2


Citations in the biomedical literature:


Juvenile Huntington disease
HTT
Autosomal dominant intermediate Charcot-Marie-Tooth disease type B
DNM2



Juvenile Huntington disease
Autosomal dominant intermediate Charcot-Marie-Tooth disease type B

Synonym(s):
- JHD
- Juvenile Huntington chorea
Synonym(s):
- CMTDIB
Classification (Orphanet):
- Rare genetic disease
- Rare neurologic disease
Classification (Orphanet):
- Rare genetic disease
- Rare neurologic disease
Classification (ICD10):
- Diseases of the nervous system -
Classification (ICD10):
- Diseases of the nervous system -
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: -
Average age onset: -
Average age of death: -
Type of inheritance: autosomal dominant
External references:
1 OMIM reference -
No MeSH references
External references:
1 OMIM reference -
No MeSH references
No signs/symptoms info available.