Search Ontology:
Human Disease

hemophilia B

Term ID
DOID:12259
Synonyms
  • Congenital factor IX deficiency
  • Congenital factor IX disorder
  • deficiency, functional factor IX
  • factor IX deficiency
Definition
A 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. http://www.nlm.nih.gov/medlineplus/ency/article/000539.htm
References
  • GARD:8732
  • ICD10CM:D67
  • ICD9CM:286.1
  • MESH:D002836
  • MIM:306900
  • NCI:C26721
  • SNOMEDCT_US_2023_03_01:41788008
  • UMLS_CUI:C0008533
Ontology
Human Disease   ( DOID:12259 )
Relationships
is a type of
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Genes Involved
Zebrafish Models