OBO ID: DOID:12259
Term Name: hemophilia B Search Ontology:
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
  • NCI:C26721
  • OMIM:306900
  • SNOMEDCT_US_2023_03_01:41788008
  • UMLS_CUI:C0008533
Ontology: Human Disease   ( DOID:12259 )
Relationships
is a type of:
OTHER hemophilia B PAGES
GENES INVOLVED
Human Gene Zebrafish Ortholog OMIM Term OMIM Phenotype ID
F9 Hemophilia B 306900
ZEBRAFISH MODELS No data available
PHENOTYPE No data available

CITATIONS: None
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