268359006: (Congenital anomaly NOS) or (thyroglossal cyst) or (situs inversus) or (Marfan's syndrome) or (tuberose sclerosis) (disorder)

• (Congenital anomaly NOS) or (thyroglossal cyst) or (situs inversus) or (Marfan's syndrome) or (tuberose sclerosis)

Status: retired, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2002. Module: SNOMED CT core

Descriptions:

Id	Description	Lang	Type	Status	Case?	Module
401220017	(Congenital anomaly NOS) or (thyroglossal cyst) or (situs inversus) or (Marfan's syndrome) or (tuberose sclerosis)	en	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
401221018	Thyroglossal cyst	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
401222013	Congenital anomaly NOS	en	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
401223015	Tuberous sclerosis	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
401224014	Tuberose sclerosis	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
401225010	Situs inversus	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
401226011	Marfan's syndrome	en	Synonym (core metadata concept)	Active	Entire term case sensitive (core metadata concept)	SNOMED CT core
2716925013	(Congenital anomaly NOS) or (thyroglossal cyst) or (situs inversus) or (Marfan's syndrome) or (tuberose sclerosis) (disorder)	en	Fully specified name	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core

Expanded Value Set

Reference Sets

Concept inactivation indicator reference set

POSSIBLY EQUIVALENT TO association reference set (foundation metadata concept)

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