154794008: (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
240733018	(Hereditary haemolytic anaemia) or (haemoglobinopathy)	en	Synonym	Active	Initial character case insensitive	SNOMED CT core
240734012	(Hereditary hemolytic anemia) or (hemoglobinopathy)	en	Synonym	Active	Initial character case insensitive	SNOMED CT core
240735013	Anemia -heredit.hemol	en	Synonym	Active	Case insensitive	SNOMED CT core
240736014	Hereditary hemolytic anemia	en	Synonym	Active	Case insensitive	SNOMED CT core
240737017	Hereditary hemolytic anemias	en	Synonym	Active	Case insensitive	SNOMED CT core
240738010	Hereditary hemol.anaem	en	Synonym	Active	Case insensitive	SNOMED CT core
240739019	Hemoglobinopathy	en	Synonym	Active	Case insensitive	SNOMED CT core
240740017	Anaemia -heredit.haemol	en	Synonym	Active	Case insensitive	SNOMED CT core
240741018	Hereditary haemol.anaem	en	Synonym	Active	Case insensitive	SNOMED CT core
240742013	Hereditary haemolytic anaemias	en	Synonym	Active	Case insensitive	SNOMED CT core
240743015	Haemoglobinopathy	en	Synonym	Active	Case insensitive	SNOMED CT core
240744014	Hereditary haemolytic anaemia	en	Synonym	Active	Case insensitive	SNOMED CT core
2719112017	(Hereditary haemolytic anaemia) or (haemoglobinopathy) (disorder)	en	Fully specified name	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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