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Autosomal dominant spastic ataxia 1
1 OMIM reference -
1 associated gene
5 connected diseases
No signs/symptoms info
Disease Type of connection
Adult-onset proximal spinal muscular atrophy, autosomal dominant
Amyotrophic lateral sclerosis
Cystic fibrosis
CADDS
Severe motor and intellectual disabilities-sensorineural deafness-dystonia syndrome
Synonym(s):
- SPAX1
Classification (Orphanet):
- Rare genetic disease
- Rare neurologic disease
Classification (ICD10):
- Diseases of the nervous system -
Epidemiological data:
Class of prevalence: unknown
Average age onset: childhood
Average age of death: -
Type of inheritance: autosomal dominant
External references:
1 OMIM reference -
No MeSH references
Gene symbol UniProt reference OMIM reference
VAMP1 P23763185880
No signs/symptoms info available.