111578003: Hereditary nonspherocytic hemolytic anemia due to aldolase A deficiency (disorder)

Status: retired, Primitive. Date: 31-Jan 2022. Module: SNOMED CT core

Descriptions:

Id	Description	Lang	Type	Status	Case?	Module
1208635014	HNSHA due to aldolase A deficiency	en	Synonym	Active	Case sensitive	SNOMED CT core
199731010	Fructose 1,6-biphosphate aldolase A deficiency	en	Synonym	Active	Initial character case insensitive	SNOMED CT core
199732015	Aldolase A deficiency	en	Synonym	Active	Initial character case insensitive	SNOMED CT core
2618713012	Hereditary nonspherocytic haemolytic anaemia (HNSHA) due to aldolase A deficiency	en	Synonym	Active	Initial character case insensitive	SNOMED CT core
2618714018	Hereditary nonspherocytic hemolytic anemia (HNSHA) due to aldolase A deficiency	en	Synonym	Active	Initial character case insensitive	SNOMED CT core
2913901014	Hereditary nonspherocytic hemolytic anemia due to aldolase A deficiency (disorder)	en	Fully specified name	Active	Initial character case insensitive	SNOMED CT core
2914382018	Hereditary nonspherocytic hemolytic anemia due to aldolase A deficiency	en	Synonym	Active	Initial character case insensitive	SNOMED CT core
3780590017	Hereditary nonspherocytic haemolytic anaemia due to aldolase A deficiency	en	Synonym	Active	Initial character case insensitive	SNOMED CT core

Expanded Value Set

Reference Sets

Concept inactivation indicator reference set

REPLACED BY association reference set

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