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| Term | hemophilia B | ID (Ontology) | DOID:12259 (Human Disease) | |||||||||
| Definition | 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. | |||||||||||
| Also Known As | "Congenital factor IX deficiency" ; "Congenital factor IX disorder" ; "deficiency, functional factor IX" (for all, see Synonyms field below) | |||||||||||
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Full annotation statements including this term (annotations to child terms are NOT included), and relevant FlyBase records
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X-linked monogenic disease |__X-linked recessive disease__ blood coagulation disease | |__hemophilia__________________| hemophilia B 1 rec. |
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hemophilia X-linked recessive disease |
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GARD:8732 ICD10CM:D67 ICD9CM:286.1 MESH:D002836 MIM:306900 NCI:C26721 SNOMEDCT_US_2025_09_01:41788008 UMLS_CUI:C0008533 |
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