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Spinocerebellar ataxia with axonal neuropathy type 2
2 OMIM references -
2 associated genes
No signs/symptoms info
PROTEIN INTERACTIONS: 1
Hereditary cerebral hemorrhage with amyloidosis, Flemish type
1 OMIM reference -
1 associated gene
No signs/symptoms info
Spinocerebellar ataxia with axonal neuropathy type 2
Hereditary cerebral hemorrhage with amyloidosis, Flemish type

PIK3R5
(UniProt - OMIM)
 APP
(UniProt - OMIM)
SETX
(UniProt - OMIM)

INTERACTOME
ASSOCIATIONS
(click on a score value to see the evidence)
PIK3R5
(0.56)
APP


Citations in the biomedical literature:


Spinocerebellar ataxia with axonal neuropathy type 2
PIK3R5 SETX
Hereditary cerebral hemorrhage with amyloidosis, Flemish type
APP



Spinocerebellar ataxia with axonal neuropathy type 2
Hereditary cerebral hemorrhage with amyloidosis, Flemish type

Synonym(s):
- AOA2
- Ataxia - oculomotor apraxia type 2
- SCAN 2
- SCAR1
Synonym(s):
- HCHWA, Flemish type
Classification (Orphanet):
- Rare eye disease
- 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: -
Average age onset: childhood
Average age of death: -
Type of inheritance: autosomal recessive
Epidemiological data:
(no data available)
External references:
2 OMIM references -
No MeSH references
External references:
1 OMIM reference -
No MeSH references
No signs/symptoms info available.