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1 OMIM reference -
1 associated gene
No signs/symptoms info
PROTEIN INTERACTIONS: 1
7 OMIM references -
5 associated genes
No signs/symptoms info
Juvenile Huntington disease
Posterior polar cataract

HTT CHMP4B
CRYAB
EPHA2
GJA3
PITX3


INTERACTOME
ASSOCIATIONS

(click on a score value to see the evidence)
HTT
(0.63)
CHMP4B



Citations in the biomedical literature:


Juvenile Huntington disease
HTT
Posterior polar cataract
CHMP4B CRYAB EPHA2 GJA3 PITX3



Juvenile Huntington disease
Posterior polar cataract

Synonym(s):
- JHD
- Juvenile Huntington chorea

Synonym(s):
- Posterior subcapsular cataract

Classification (Orphanet):
- Rare genetic disease
- Rare neurologic disease
Classification (Orphanet):
- Rare developmental defect during embryogenesis
- Rare eye disease
- Rare genetic disease

Classification (ICD10):
- Diseases of the nervous system -
Classification (ICD10):
- Congenital malformations, deformations and chromosomal abnormalities -

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:
(no data available)

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

No signs/symptoms info available.