| Dataset | OMIM Gene-Disease Associations |
| Category | disease or phenotype associations |
| Type | phenotype |
| 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://www.omim.org/entry/306900 |
| Similar Terms | |
| Downloads & Tools |
1 genes associated with the hemophilia b phenotype from the curated OMIM Gene-Disease Associations dataset.
| Symbol | Name |
|---|---|
| F9 | coagulation factor IX |
