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 )