C0019069 - An X-linked recessive deficiency of coagulation factor VIII characterized by a tendency to bleed. Hemophilia A, the most common type of hemophilia, occurs in approximately 1 in 4,000 to 1 in 5,000 live male births.

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Lang Dictionary CODE			LUI	preferred no	SUI	preference Yes / No	Terms, descriptions
							CUI C0019069

Russian	Medical Subject Headings Russian	D006467	L3344205	preferred	S3871682	Y	ГЕМОФИЛИЯ A
Russian	Medical Subject Headings Russian	D006467	L0894167	no	S1097984	Y	GEMOFILIIA
Russian	Medical Subject Headings Russian	D006467	L1254995	no	S1496941	Y	GEMOFILIIA A
Russian	Medical Subject Headings Russian	D006467	L1519444	no	S1815353	Y	FAKTORA VIII NEDOSTATOCHNOST'
Russian	MDRRUS	10060613	L15712128	no	S19026970	N	Гемофилия A (дефицит фактора VIII)
Russian	MDRRUS	10018938	L15712128	no	S19026970	Y	Гемофилия A (дефицит фактора VIII)
Russian	MDRRUS	10060612	L15712131	no	S19026984	Y	Гемофилия типа A
Russian	MDRRUS	10010468	L15745050	no	S19024774	Y	Врожденное нарушение фактора VIII
Russian	MDRRUS	10018937	L15789314	no	S19026975	Y	Гемофилия A
Russian	Medical Subject Headings Russian	D006467	L3344204	no	S3871685	Y	ГЕМОФИЛИЯ
Russian	Medical Subject Headings Russian	D006467	L3373791	no	S3901268	Y	ФАКТОРА VIII НЕДОСТАТОЧНОСТЬ
	Medical Subject Headings				A0289960	AT38148311	The classic hemophilia resulting from a deficiency of factor VIII. It is an inherited disorder of blood coagulation characterized by a permanent tendency to hemorrhage.
	(CPTSP) CRISP Thesaurus				A1170645	AT51220912	classic hemophilia resulting from a deficiency of factor VIII; an inherited disorder of blood coagulation characterized by a permanent tendency to hemorrhage.
	Medical Subject Headings Czech				A13041390	AT231382774	Hemofilie způsobená nedostatkem koagulačního faktoru VIII (antihemofilického faktoru), nejčastější a nejtěžší typ hemofilie. (cit. Velký lékařský slovník online, 2017 http://lekarske.slovniky.cz)
	MSHNOR				A20206381	AT221512139	Den klassiske hemofili som skyldes mangel på factor VIII. Det er en arvelig blodlevringssykdom karakterisert ved en vedvarende blødningstendens.
	NCI Thesaurus				A7575405	AT213844686	An inherited deficiency of coagulation factor VIII characterized by the tendency to spontaneous or exaggerated post-traumatic hemorrhage. Inherited as an X-linked recessive disease, hemophilia A is the most common hemophilia, occurring in approximately 1 in 10,000 male births.
	NCI National Institute of Child Health and Human Development				A7575405	AT224190913	An X-linked recessive deficiency of coagulation factor VIII characterized by a tendency to bleed. Hemophilia A, the most common type of hemophilia, occurs in approximately 1 in 4,000 to 1 in 5,000 live male births.