| Dataset | CTD Gene-Disease Associations |
| Category | disease or phenotype associations |
| Type | disease |
| Description | OMIM mapping confirmed by DO. [SN]. (Human Disease Ontology, DOID_9631) |
| External Link | http://ctdbase.org/detail.go?type=disease&acc=MESH:D010381 |
| Similar Terms | |
| Downloads & Tools |
1 genes/proteins associated with the disease Pelger-Huet Anomaly from the curated CTD Gene-Disease Associations dataset.
| Symbol | Name | Standardized Value |
|---|---|---|
| LBR | lamin B receptor | 2.88009 |
