267556002: (Hereditary haemolytic anaemia) or (haemoglobinopathy) (disorder)

• (Hereditary haemolytic anaemia) or (haemoglobinopathy)

Status: retired, Primitive. Date: 31-Jan 2002. Module: SNOMED CT core

Descriptions:

Id	Description	Lang	Type	Status	Case?	Module
2733563012	(Hereditary haemolytic anaemia) or (haemoglobinopathy) (disorder)	en	Fully specified name	Active	Initial character case insensitive	SNOMED CT core
399291014	(Hereditary hemolytic anemia) or (hemoglobinopathy)	en	Synonym	Active	Initial character case insensitive	SNOMED CT core
399292019	Anaemia -heredit.haemol	en	Synonym	Active	Case insensitive	SNOMED CT core
399293012	Hereditary haemol.anaem	en	Synonym	Active	Case insensitive	SNOMED CT core
399294018	Hereditary haemolytic anaemias	en	Synonym	Active	Case insensitive	SNOMED CT core
399295017	Hereditary haemolytic anaemia	en	Synonym	Active	Case insensitive	SNOMED CT core
399296016	Haemoglobinopathy	en	Synonym	Active	Case insensitive	SNOMED CT core
399297013	Anemia -heredit.hemol	en	Synonym	Active	Case insensitive	SNOMED CT core
399298015	Hemoglobinopathy	en	Synonym	Active	Case insensitive	SNOMED CT core
399299011	Hereditary hemol.anaem	en	Synonym	Active	Case insensitive	SNOMED CT core
399300015	Hereditary hemolytic anemia	en	Synonym	Active	Case insensitive	SNOMED CT core
399301016	Hereditary hemolytic anemias	en	Synonym	Active	Case insensitive	SNOMED CT core
399302011	(Hereditary haemolytic anaemia) or (haemoglobinopathy)	en	Synonym	Active	Initial character case insensitive	SNOMED CT core

Expanded Value Set

Reference Sets

Concept inactivation indicator reference set

POSSIBLY EQUIVALENT TO association reference set

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