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Spinocerebellar ataxia type 7
1 OMIM reference -
1 associated gene
No signs/symptoms info
PROTEIN INTERACTIONS: 2
Semantic dementia
6 associated genes
No signs/symptoms info
Spinocerebellar ataxia type 7
Semantic dementia

ATXN7
(UniProt - OMIM)
 C9ORF72
(UniProt - OMIM)
CHMP2B
(UniProt - OMIM)
GRN
(UniProt - OMIM)
MAPT
(UniProt - OMIM)
PSEN1
(UniProt - OMIM)
VCP
(UniProt - OMIM)

INTERACTOME
ASSOCIATIONS
(click on a score value to see the evidence)
ATXN7
ATXN7
(0.68)
(0.63)
VCP
GRN


Citations in the biomedical literature:


Spinocerebellar ataxia type 7
ATXN7
Semantic dementia
C9ORF72 CHMP2B GRN MAPT PSEN1 VCP



Spinocerebellar ataxia type 7
Semantic dementia

Synonym(s):
- Autosomal dominant spinocerebellar ataxia type 7
- Cerebellar syndrome - pigmentary maculopathy
- SCA7
Synonym(s):
- Semantic primary progressive aphasia
- Semantic variant PPA
Classification (Orphanet):
- Rare eye disease
- 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: -
Average age onset: -
Average age of death: -
Type of inheritance: autosomal dominant
Epidemiological data:
Class of prevalence: -
Average age onset: adulthood
Average age of death: -
Type of inheritance: multigenic/multifactorial
External references:
1 OMIM reference -
No MeSH references
External references:
No OMIM references
No MeSH references
No signs/symptoms info available.