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1 associated gene
No signs/symptoms info
PROTEIN INTERACTIONS: 1
1 OMIM reference -
1 associated gene
3 signs/symptoms
Machado-Joseph disease type 3
Hereditary cerebral hemorrhage with amyloidosis, Arctic type

ATXN3 APP


INTERACTOME
ASSOCIATIONS

(click on a score value to see the evidence)
ATXN3
(0.56)
APP



Citations in the biomedical literature:


Machado-Joseph disease type 3
ATXN3
Hereditary cerebral hemorrhage with amyloidosis, Arctic type
APP



Machado-Joseph disease type 3
Hereditary cerebral hemorrhage with amyloidosis, Arctic type

Synonym(s):
- SCA3, Machado type

Synonym(s):
- HCHWA, Arctic type

Classification (Orphanet):
- Rare genetic disease
- Rare neurologic disease
Classification (Orphanet):
- Rare genetic disease
- Rare neurologic disease
- Rare systemic or rheumatologic disease

Classification (ICD10):
- Diseases of the nervous system -
Classification (ICD10):
(no data available)

Epidemiological data:
Class of prevalence: unknown
Average age onset: adulthood
Average age of death: -
Type of inheritance: autosomal dominant
Epidemiological data:
(no data available)

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

Hereditary cerebral hemorrhage with amyloidosis, Arctic type

Very frequent
- Autosomal dominant inheritance
- Psychic / behavioural troubles
- Psychic / psychomotor regression / dementia / intellectual decline



Machado-Joseph disease type 3

(no data available)