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Autosomal dominant spastic paraplegia type 12
1 OMIM reference -
1 associated gene
1 connected disease
No signs/symptoms info
Disease Type of connection
Fanconi anemia
Synonym(s):
- SPG12
Classification (Orphanet):
- Rare genetic disease
- Rare neurologic disease
Classification (ICD10):
- Diseases of the nervous system -
Epidemiological data:
Class of prevalence: <1 / 1 000 000
Average age onset: -
Average age of death: -
Type of inheritance: autosomal dominant
External references:
1 OMIM reference -
1 MeSH reference: C537484
Gene symbol UniProt reference OMIM reference
RTN2 O75298603183
No signs/symptoms info available.