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Autosomal recessive cerebellar ataxia with late-onset spasticity
1 associated gene
No signs/symptoms info
PROTEIN INTERACTIONS: 1
Hereditary cerebral hemorrhage with amyloidosis, Flemish type
1 OMIM reference -
1 associated gene
No signs/symptoms info
Autosomal recessive cerebellar ataxia with late-onset spasticity
Hereditary cerebral hemorrhage with amyloidosis, Flemish type

GBA2
(UniProt - OMIM)
 APP
(UniProt - OMIM)

INTERACTOME
ASSOCIATIONS
(click on a score value to see the evidence)
GBA2
(0.56)
APP


Citations in the biomedical literature:


Autosomal recessive cerebellar ataxia with late-onset spasticity
GBA2
Hereditary cerebral hemorrhage with amyloidosis, Flemish type
APP



Autosomal recessive cerebellar ataxia with late-onset spasticity
Hereditary cerebral hemorrhage with amyloidosis, Flemish type

Synonym(s):
- Autosomal recessive cerebellar ataxia due to GBA2 deficiency
Synonym(s):
- HCHWA, Flemish type
Classification (Orphanet):
- Inborn errors of metabolism
- 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: <1 / 1 000 000
Average age onset: childhood
Average age of death: -
Type of inheritance: autosomal recessive
Epidemiological data:
(no data available)
External references:
No OMIM references
No MeSH references
External references:
1 OMIM reference -
No MeSH references
No signs/symptoms info available.