Cytoscape Web
Click node...

Autosomal dominant spastic paraplegia type 3
1 OMIM reference -
1 associated gene
1 connected disease
No signs/symptoms info
Disease Type of connection
Hereditary sensory and autonomic neuropathy type 1
Synonym(s):
- Strümpell disease
Classification (Orphanet):
- Rare genetic disease
- Rare neurologic disease
Classification (ICD10):
- Diseases of the nervous system -
Epidemiological data:
(no data available)
External references:
1 OMIM reference -
1 MeSH reference: C536864
Gene symbol UniProt reference OMIM reference
ATL1 Q8WXF7606439
No signs/symptoms info available.