|Name||Chromosome Xp11.3 deletion syndrome|
|NCBI Gene ID||100271686|
|Expression in Tissues and Cell Lines||
DELXP11.3 has 2 functional associations with biological entities spanning 1 categories (disease, phenotype or trait) extracted from 2 datasets.
Click the + buttons to view associations for DELXP11.3 from the datasets below.
If available, associations are ranked by standardized value
|CTD Gene-Disease Associations||diseases associated with DELXP11.3 gene/protein from the curated CTD Gene-Disease Associations dataset.|
|OMIM Gene-Disease Associations||phenotypes associated with DELXP11.3 gene from the curated OMIM Gene-Disease Associations dataset.|