191239005: (Red cell: [constitutional aplasia or hypoplasia] or [congenital pure aplasia] or [congenital hypoplasia]) or (Blackfan - Diamond syndrome) (disorder)

• (Red cell: [constitutional aplasia or hypoplasia] or [congenital pure aplasia] or [congenital hypoplasia]) or (Blackfan - Diamond syndrome)

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

Descriptions:

Id	Description	Lang	Type	Status	Case?	Module
2712614016	(Red cell: [constitutional aplasia or hypoplasia] or [congenital pure aplasia] or [congenital hypoplasia]) or (Blackfan - Diamond syndrome) (disorder)	en	Fully specified name	Active	Initial character case insensitive	SNOMED CT core
294172015	Congenital pure red cell aplasia	en	Synonym	Active	Case insensitive	SNOMED CT core
294173013	Constitutional red cell aplasia and hypoplasia	en	Synonym	Active	Case insensitive	SNOMED CT core
294174019	Constitutional red cell hypoplasia	en	Synonym	Active	Case insensitive	SNOMED CT core
294175018	Blackfan - Diamond syndrome	en	Synonym	Active	Case sensitive	SNOMED CT core
294176017	Congenital red cell hypoplasia	en	Synonym	Active	Case insensitive	SNOMED CT core
294177014	(Red cell: [constitutional aplasia or hypoplasia] or [congenital pure aplasia] or [congenital hypoplasia]) or (Blackfan - Diamond syndrome)	en	Synonym	Active	Initial character case insensitive	SNOMED CT core

Expanded Value Set

Reference Sets

Australian dialect reference set

Concept inactivation indicator reference set

POSSIBLY EQUIVALENT TO association reference set

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