| Descriptor English: | Hemophilia B | ||||||
| Descriptor Spanish: |
Hemofilia B
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| Descriptor Portuguese: | Hemofilia B | ||||||
| Descriptor French: | Hémophilie B | ||||||
| Entry term(s): |
Bs, Hemophilia Christmas Disease Deficiencies, F9 Deficiencies, Factor IX Deficiency, F9 Deficiency, Factor IX Disease, Christmas F9 Deficiencies F9 Deficiency Factor IX Deficiencies Factor IX Deficiency Haemophilia B Haemophilia Bs Hemophilia B Leyden Hemophilia B(M) Hemophilia Bs Hemophilia Bs (M) Plasma Thromboplastin Component Deficiency |
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| Tree number(s): |
C15.378.100.100.510 C15.378.100.141.510 C15.378.463.510 C16.320.099.510 C16.320.322.235 |
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| RDF Unique Identifier: | https://id.nlm.nih.gov/mesh/D002836 | ||||||
| Scope note: | A deficiency of blood coagulation factor IX inherited as an X-linked disorder. (Also known as Christmas Disease, after the first patient studied in detail, not the holy day.) Historical and clinical features resemble those in classic hemophilia (HEMOPHILIA A), but patients present with fewer symptoms. Severity of bleeding is usually similar in members of a single family. Many patients are asymptomatic until the hemostatic system is stressed by surgery or trauma. Treatment is similar to that for hemophilia A. (From Cecil Textbook of Medicine, 19th ed, p1008) |
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| Allowable Qualifiers: |
BL blood CF cerebrospinal fluid CI chemically induced CL classification CO complications DG diagnostic imaging DH diet therapy DI diagnosis DT drug therapy EC economics EH ethnology EM embryology EN enzymology EP epidemiology ET etiology GE genetics HI history IM immunology ME metabolism MI microbiology MO mortality NU nursing PA pathology PC prevention & control PP physiopathology PS parasitology PX psychology RH rehabilitation RT radiotherapy SU surgery TH therapy UR urine VE veterinary VI virology |
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| Public MeSH Note: | 1999; see CHRISTMAS DISEASE 1966-1998; for HEMOPHILIA B see CHRISTMAS DISEASE 1974-1998; for Hemophilia B Leyden see FACTOR IX 1990-2012 |
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| History Note: | 1999(1966) |
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| Related: |
Hemophilia A
MeSH | ||||||
| DeCS ID: | 2885 | ||||||
| Unique ID: | D002836 | ||||||
| NLM Classification: | WH 325 | ||||||
| Documents indexed in the Virtual Health Library (VHL): | Click here to access the VHL documents | ||||||
| Date Established: | 1999/01/01 | ||||||
| Date of Entry: | 1999/01/01 | ||||||
| Revision Date: | 2016/06/28 |
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Hemophilia B
- Preferred
| Concept UI |
M0004363 |
| Scope note | A deficiency of blood coagulation factor IX inherited as an X-linked disorder. (Also known as Christmas Disease, after the first patient studied in detail, not the holy day.) Historical and clinical features resemble those in classic hemophilia (HEMOPHILIA A), but patients present with fewer symptoms. Severity of bleeding is usually similar in members of a single family. Many patients are asymptomatic until the hemostatic system is stressed by surgery or trauma. Treatment is similar to that for hemophilia A. (From Cecil Textbook of Medicine, 19th ed, p1008) |
| Preferred term | Hemophilia B |
| Entry term(s) |
Bs, Hemophilia Christmas Disease Deficiencies, F9 Deficiencies, Factor IX Deficiency, F9 Deficiency, Factor IX Disease, Christmas F9 Deficiencies F9 Deficiency Factor IX Deficiencies Factor IX Deficiency Haemophilia B Haemophilia Bs Hemophilia B Leyden Hemophilia B(M) Hemophilia Bs Hemophilia Bs (M) Plasma Thromboplastin Component Deficiency |
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