C0005129 - A rare, autosomal recessive bleeding disorder characterized by deficiency or absence of the Ib/IX/V complex on the surface of platelets. It results in thrombocytopenia, prolonged bleeding and the presence of giant platelets.

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Lang Dictionary CODE			LUI	preferred no	SUI	preference Yes / No	Terms, descriptions
							CUI C0005129

Russian	Medical Subject Headings Russian	D001606	L3341006	preferred	S3868487	Y	БЕРНАРА-СУЛЬЕ СИНДРОМ
Russian	Medical Subject Headings Russian	D001606	L0891111	no	S1094928	Y	BERNARA-SUL'E SINDROM
Russian	Medical Subject Headings Russian	D001606	L1521578	no	S1817487	Y	GIGANTSKIKH TROMBOTSITOV SINDROM
Russian	MDRRUS	10057473	L15784946	no	S19079270	Y	Синдром Бернара-Сулье
Russian	Medical Subject Headings Russian	D001606	L3344941	no	S3872420	Y	ГИГАНТСКИХ ТРОМБОЦИТОВ СИНДРОМ
	Medical Subject Headings				A0030074	AT38146048	A familial coagulation disorder characterized by a prolonged bleeding time, unusually large platelets, and impaired prothrombin consumption.
	Medical Subject Headings Czech				A13053230	AT156611351	Vzácné dědičné onemocnění s porušenou funkcí destiček (trombocytopatie). Porušena je adheze destiček (defekt membránových glykoproteinů Ib a IX). (cit. Velký lékařský slovník online, 2012 http://lekarske.slovniky.cz/ )
	NCI Thesaurus				A17680502	AT198147172	A rare, autosomal recessive bleeding disorder characterized by deficiency or absence of the Ib/IX/V complex on the surface of platelets. It results in thrombocytopenia, prolonged bleeding time and the presence of giant platelets.
	NCI National Institute of Child Health and Human Development				A17680502	AT224196113	A rare, autosomal recessive bleeding disorder characterized by deficiency or absence of the Ib/IX/V complex on the surface of platelets. It results in thrombocytopenia, prolonged bleeding and the presence of giant platelets.