205794007: (Multiple system congenital anomalies NEC) or (Prader-Willi syndrome) or (Noonan's syndrome) (disorder)

• (Multiple system congenital anomalies NEC) or (Prader-Willi syndrome) or (Noonan's syndrome)

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

Descriptions:

Id	Description	Lang	Type	Status	Case?	Module
2750701016	(Multiple system congenital anomalies NEC) or (Prader-Willi syndrome) or (Noonan's syndrome) (disorder)	en	Fully specified name	Active	Initial character case insensitive	SNOMED CT core
315578014	(Multiple system congenital anomalies NEC) or (Prader-Willi syndrome) or (Noonan's syndrome)	en	Synonym	Active	Initial character case insensitive	SNOMED CT core
315579018	Prader-Willi Syndrome	en	Synonym	Active	Case sensitive	SNOMED CT core
315580015	Prader-Willi syndrome	en	Synonym	Active	Case sensitive	SNOMED CT core
315581016	Prader - Willi syndrome	en	Synonym	Active	Case sensitive	SNOMED CT core
315582011	Multiple system congenital anomalies NEC	en	Synonym	Active	Initial character case insensitive	SNOMED CT core
315583018	Noonan's syndrome	en	Synonym	Active	Case sensitive	SNOMED CT core

Expanded Value Set

Reference Sets

Concept inactivation indicator reference set

Description inactivation indicator reference set

POSSIBLY EQUIVALENT TO association reference set

REPLACED BY association reference set

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