|Name||alpha-thalassemia/mental retardation syndrome, type 1|
|NCBI Gene ID||8129|
|Expression in Tissues and Cell Lines||
HBHR 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 HBHR from the datasets below.
If available, associations are ranked by standardized value
|CTD Gene-Disease Associations||diseases associated with HBHR gene/protein from the curated CTD Gene-Disease Associations dataset.|
|OMIM Gene-Disease Associations||phenotypes associated with HBHR gene from the curated OMIM Gene-Disease Associations dataset.|