|Name||Chromosome 19p13.13 deletion syndrome|
|Synonyms||C19DELP13.13, DUP19P13.13, C19DUPP13.13|
|NCBI Gene ID||100526791|
|Expression in Tissues and Cell Lines||
DEL19P13.13 has 2 functional associations with biological entities spanning 1 categories (disease, phenotype or trait) extracted from 1 datasets.
Click the + buttons to view associations for DEL19P13.13 from the datasets below.
If available, associations are ranked by standardized value
|OMIM Gene-Disease Associations||phenotypes associated with DEL19P13.13 gene from the curated OMIM Gene-Disease Associations dataset.|