| Dataset | CTD Gene-Disease Associations |
| Category | disease or phenotype associations |
| Type | disease |
| Description | An inherited blood coagulation disease that has_material_basis_in Factor IX deficiency, which makes coagulation much more prolonged. The disease is inherited as an X-linked recessive trait. (Human Disease Ontology, DOID_12259) |
| External Link | http://ctdbase.org/detail.go?type=disease&acc=MESH:D002836 |
| Similar Terms | |
| Downloads & Tools |
1 genes/proteins associated with the disease Hemophilia B from the curated CTD Gene-Disease Associations dataset.
| Symbol | Name | Standardized Value |
|---|---|---|
| F9 | coagulation factor IX | 2.88009 |
