|Name||spastic paraplegia 18 (autosomal dominant)|
|NCBI Gene ID||140906|
|Expression in Tissues and Cell Lines||
SPG18 has 1 functional associations with biological entities spanning 1 categories (disease, phenotype or trait) extracted from 1 datasets.
Click the + buttons to view associations for SPG18 from the datasets below.
If available, associations are ranked by standardized value
|CTD Gene-Disease Associations||diseases associated with SPG18 gene/protein from the curated CTD Gene-Disease Associations dataset.|