FB2025_05 , released December 11, 2025
FB2025_05 , released December 11, 2025
CV Term Report
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General Information
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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 Genes
 hemophilia B       1
 for disease ribbon | hemophilia B       1
 model of | hemophilia B       1
Spanning Tree (Parents/Children)
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X-linked monogenic disease
 |__X-linked recessive disease__
blood coagulation disease       |
 |__hemophilia__________________|
                                hemophilia B  1 rec.
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Is a hemophilia
X-linked recessive disease
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Synonyms
  • "Congenital factor IX deficiency" EXACT
    "Congenital factor IX disorder" EXACT
    "deficiency, functional factor IX" EXACT
    "factor IX deficiency" EXACT
Secondary IDs
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GARD:8732
ICD10CM:D67
ICD9CM:286.1
MESH:D002836
MIM:306900
NCI:C26721
SNOMEDCT_US_2023_03_01:41788008
UMLS_CUI:C0008533