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Spinocerebellar ataxia type 7
1 OMIM reference -
1 associated gene
No signs/symptoms info
PROTEIN INTERACTIONS: 1
Von Willebrand disease type 1
1 OMIM reference -
1 associated gene
No signs/symptoms info
Spinocerebellar ataxia type 7
Von Willebrand disease type 1

ATXN7
(UniProt - OMIM)
 VWF
(UniProt - OMIM)

INTERACTOME
ASSOCIATIONS
(click on a score value to see the evidence)
ATXN7
(0.63)
VWF


Citations in the biomedical literature:


Spinocerebellar ataxia type 7
ATXN7
Von Willebrand disease type 1
VWF



Spinocerebellar ataxia type 7
Von Willebrand disease type 1

Synonym(s):
- Autosomal dominant spinocerebellar ataxia type 7
- Cerebellar syndrome - pigmentary maculopathy
- SCA7
Synonym(s):
- Willebrand disease type 1
Classification (Orphanet):
- Rare eye disease
- Rare genetic disease
- Rare neurologic disease
Classification (Orphanet):
- Rare genetic disease
- Rare hematologic disease
Classification (ICD10):
- Diseases of the nervous system -
Classification (ICD10):
- Diseases of the blood and blood-forming organs and certain disorders involving the immune mechanism -
Epidemiological data:
Class of prevalence: -
Average age onset: -
Average age of death: -
Type of inheritance: autosomal dominant
Epidemiological data:
Class of prevalence: 1-5 / 10 000
Average age onset: variable
Average age of death: -
Type of inheritance: autosomal dominant
External references:
1 OMIM reference -
No MeSH references
External references:
1 OMIM reference -
1 MeSH reference: D056725
No signs/symptoms info available.