C0008533 - An X-linked recessive deficiency of coagulation factor IX characterized by a tendency to bleed. Hemophilia B occurs in approximately 1 in 20,000 live male births.

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Lang Dictionary CODE			LUI	preferred no	SUI	preference Yes / No	Terms, descriptions
							CUI C0008533

Russian	Medical Subject Headings Russian	D002836	L3344206	preferred	S3871683	Y	ГЕМОФИЛИЯ B
Russian	Medical Subject Headings Russian	D002836	L0894168	no	S1097985	Y	GEMOFILIIA B
Russian	Medical Subject Headings Russian	D002836	L15161298	no	S18460446	Y	ФАКТОРА IX ДЕФИЦИТ
Russian	Medical Subject Headings Russian	D002836	L15169737	no	S18439240	Y	FAKTORA IX DEFITSIT
Russian	Medical Subject Headings Russian	D002836	L1527091	no	S1823000	Y	KRISTMASA BOLEZN'
Russian	MDRRUS	10008793	L15722362	no	S19021038	Y	Болезнь Кристмаса (дефицит фактора IX)
Russian	MDRRUS	10016077	L15726101	no	S19050162	N	Недостаточность фактора IX
Russian	MDRRUS	10016077	L15726101	no	S19050162	Y	Недостаточность фактора IX
Russian	MDRRUS	10018939	L15756422	no	S19026976	N	Гемофилия B (дефицит фактора IX)
Russian	MDRRUS	10060614	L15756422	no	S19026976	Y	Гемофилия B (дефицит фактора IX)
Russian	MDRRUS	10010467	L15767145	no	S19024773	Y	Врожденное нарушение фактора IX
Russian	MDRRUS	10082788	L16092735	no	S19403090	Y	Гемофилия B
Russian	MDRRUS	10082786	L16134862	no	S19403353	Y	Дефицит фактора свертывания крови B
Russian	Medical Subject Headings Russian	D002836	L3353891	no	S3881373	Y	КРИСТМАСА БОЛЕЗНЬ
	Medical Subject Headings				A0067190	AT38147243	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)
	(CPTSP) CRISP Thesaurus				A1303602	AT51220203	deficiency of blood coagulation factor IX inherited as an X-linked disorder; clinical features resemble those in hemophilia A, but patients present with fewer symptoms.
	Medical Subject Headings Czech				A13040919	AT231378383	Hemofilie způsobená nedostatkem koagulačního faktoru IX (antihemofilického faktoru). Je méně častá než h. A, je rovněž recesivně vázaná na X chromozom. (cit. Velký lékařský slovník online, 2017 http://lekarske.slovniky.cz)
	NCI Thesaurus				A7571013	AT198016760	An X-linked inherited bleeding disorder caused by deficiency of the coagulation factor IX.
	NCI National Institute of Child Health and Human Development				A7571013	AT224191880	An X-linked recessive deficiency of coagulation factor IX characterized by a tendency to bleed. Hemophilia B occurs in approximately 1 in 20,000 live male births.