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hemophilia B

^ http://purl.obolibrary.org/obo/DOID_12259


An inherited 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. [ url:http://www.nlm.nih.gov/medlineplus/ency/article/000539.htm ]

Synonyms: factor IX deficiency, Congenital factor IX deficiency, Congenital factor IX disorder, deficiency, functional factor IX

Term info

database cross reference
  • OMIM:306900
  • NCI:C26721
  • SNOMEDCT_US_2016_03_01:154817006
  • ICD10CM:D67
  • SNOMEDCT_US_2016_03_01:41788008
  • SNOMEDCT_US_2016_03_01:234443007
  • MESH:D002836
  • UMLS_CUI:C0008533
  • ICD9CM:286.1
comment

OMIM mapping confirmed by DO. [SN].

has obo namespace

disease_ontology

id

DOID:12259

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