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Metadata
ID DOID:12259
Name hemophilia B
Definition 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.
http://www.nlm.nih.gov/medlineplus/ency/article/000539.htm
Xrefs

CSP2005:0438-3499

GARD:8732

ICD10CM:D67

ICD9CM:286.1

ICD9CM_2006:286.1

MESH:D002836

MTHICD9_2006:286.1

NCI:C26721

OMIM:306900

SNOMEDCT_US_2018_03_01:41788008

UMLS_CUI:C0008533

Subsets

NCIthesaurus

Synonyms

Congenital factor IX deficiency [EXACT]

Congenital factor IX disorder [EXACT]

deficiency, functional factor IX [EXACT]

factor IX deficiency [EXACT]

Parent Relationships

is_a inherited blood coagulation disease

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