Hemophilia B
Disease ID: disease_node_2097
Connections displayed (default: 10).
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| Dbxref | GARD:8732, ICD10CM:D67, ICD9CM:286.1, MESH:D002836, MIM:306900, NCI:C26721, SNOMEDCT_US_2023_03_01:41788008, UMLS_CUI:C0008533 |
|---|---|
| Subclassof | DOID_0080012, DOID_0061030 |
| Data Source | DOID, MESH |
| Synonyms | Congenital factor IX deficiency, Congenital factor IX disorder, deficiency, functional factor IX, factor IX deficiency |
| Mesh Id | D002836 |
| Mesh Label | Hemophilia B |
| Mesh Subclassof | D020147, D040181, D025861, D006474 |
| Doid Label | hemophilia B |
| Doid Description | A hemophilia that has_material_basis_in Factor IX deficiency, which makes coagulation much more prolonged. The disease is inherited as an X-linked recessive trait. OMIM mapping confirmed by DO. [SN]. |
| Has Material Basis In | GENO_0000149 |
| Disease Node Id | disease_node_2097 |
| Doid Id | DOID_12259 |
| Label | Hemophilia B |
- Outgoing r'ship
SUBCLASS_OFto/from X-Linked Recessive Disease(ID:disease_node_13254) (Disease) - Outgoing r'ship
SUBCLASS_OFto/from Hemophilia(ID:disease_node_15603) (Disease)