Begreppsinformation
Congenital, Hereditary, and Neonatal Diseases and Abnormalities
Genetic Diseases, Inborn
Genetic Diseases, X-Linked
Congenital, Hereditary, and Neonatal Diseases and Abnormalities
Genetic Diseases, Inborn
Blood Coagulation Disorders, Inherited
Föredragen term
Hemophilia B
Typ
-
Topical Descriptor
Överordnat begrepp
Hänvisningstermer
- 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 (M)
- Plasma Thromboplastin Component Deficiency
Användningsanmärkning
- 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)
Anmärkning om ändringshistoria
- 1999(1966)
Termer på andra språk
-
finska
-
B-hemofilia
-
Christmas disease
-
Christmasin tauti
-
deficientia hereditaria factoris IX
-
haemophilia B
-
hyytymistekijä IX:n perinnöllinen puute
-
hyytymistekijä IX:n puute
-
hyytymistekijä IX:n puutos
-
hyytymistekijä IX:n vajaatoiminta
-
morbus Christmas
-
plasman tromboplastiinikomponentin puute
-
PTC-puute
-
svenska
URI
http://www.yso.fi/onto/mesh/D002836
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