205492005: (Osteogenesis imperfecta) or (Vrolik's disease) or (syndromes: [Adair-Dighton] or [Lobstein's] or [Van der Hoeve's]) (disorder)

• (Osteogenesis imperfecta) or (Vrolik's disease) or (syndromes: [Adair-Dighton] or [Lobstein's] or [Van der Hoeve's])

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

Descriptions:

Id	Description	Lang	Type	Status	Case?	Module
2731588012	(Osteogenesis imperfecta) or (Vrolik's disease) or (syndromes: [Adair-Dighton] or [Lobstein's] or [Van der Hoeve's]) (disorder)	en	Fully specified name	Active	Initial character case insensitive	SNOMED CT core
315111015	(Osteogenesis imperfecta) or (Vrolik's disease) or (syndromes: [Adair-Dighton] or [Lobstein's] or [Van der Hoeve's])	en	Synonym	Active	Initial character case insensitive	SNOMED CT core
315112010	Eddowe's syndrome	en	Synonym	Active	Case sensitive	SNOMED CT core
315113017	Lobstein's syndrome	en	Synonym	Active	Case sensitive	SNOMED CT core
315114011	Vrolik's disease	en	Synonym	Active	Case sensitive	SNOMED CT core
315115012	Adair-Dighton syndrome	en	Synonym	Active	Case sensitive	SNOMED CT core
315116013	Van der Hoeve's syndrome	en	Synonym	Active	Initial character case insensitive	SNOMED CT core
315117016	Osteogenesis imperfecta	en	Synonym	Active	Case insensitive	SNOMED CT core
590866019	(Osteogenesis imperfecta) or (Vrolik's disease) or (syndromes: [Adair-Dighton] or [Lobstein's] or [Van der Hoeve's])	en	Fully specified name	Inactive	Case sensitive	SNOMED CT core

Expanded Value Set

Reference Sets

Concept inactivation indicator reference set

POSSIBLY EQUIVALENT TO association reference set

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