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Spinocerebellar ataxia type 1 with axonal neuropathy
1 OMIM reference -
1 associated gene
No signs/symptoms info
PROTEIN INTERACTIONS: 1
Ataxia-telangiectasia variant
1 associated gene
No signs/symptoms info
Spinocerebellar ataxia type 1 with axonal neuropathy
Ataxia-telangiectasia variant

TDP1
(UniProt - OMIM)
 ATM
(UniProt - OMIM)

INTERACTOME
ASSOCIATIONS
(click on a score value to see the evidence)
TDP1
(0.83)
ATM


Citations in the biomedical literature:


Spinocerebellar ataxia type 1 with axonal neuropathy
TDP1
Ataxia-telangiectasia variant
ATM



Spinocerebellar ataxia type 1 with axonal neuropathy
Ataxia-telangiectasia variant

Synonym(s):
- SCAN1
Synonym(s):
- v-AT
Classification (Orphanet):
- 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:
(no data available)
Epidemiological data:
(no data available)
External references:
1 OMIM reference -
No MeSH references
External references:
No OMIM references
No MeSH references
No signs/symptoms info available.