281022002: Family history of complete trisomy 21 syndrome (situation)

• SNOMED CT Concept\Situation with explicit context\...
• \Finding with explicit context\Family history of clinical finding\Family history of disorder\...
• \Family history of development disorder\Family history of complete trisomy 21 syndrome
• \Family history of congenital disease\Family history of chromosomal anomaly\Family history of complete trisomy 21 syndrome
• \Family history with explicit context\Family history of clinical finding\Family history of disorder\...
• \Family history of development disorder\Family history of complete trisomy 21 syndrome
• \Family history of congenital disease\Family history of chromosomal anomaly\Family history of complete trisomy 21 syndrome

Status: current, Defined. Date: 31-Jul 2005. Module: SNOMED CT core

Descriptions:

Id	Description	Lang	Type	Status	Case?	Module
2551221011	Mongol child	en	Synonym	Inactive	Initial character case insensitive	SNOMED CT core
2610500015	Down's child in family (situation)	en	Fully specified name	Inactive	Case sensitive	SNOMED CT core
2840602013	Down child in family	en	Synonym	Inactive	Case sensitive	SNOMED CT core
3285396017	Family history of trisomy 21 down syndrome	en	Synonym	Inactive	Case insensitive	SNOMED CT core
418918013	Down's child in family	en	Synonym	Inactive	Case sensitive	SNOMED CT core
418919017	Mongol child in family	en	Synonym	Inactive	Initial character case insensitive	SNOMED CT core
4546420012	Family history of complete trisomy 21 syndrome	en	Synonym	Active	Case insensitive	SNOMED CT core
4546421011	Family history of complete trisomy 21 syndrome (situation)	en	Fully specified name	Active	Case insensitive	SNOMED CT core
4546422016	Family history of Down syndrome	en	Synonym	Active	Initial character case insensitive	SNOMED CT core
674507018	Down's child in family (context-dependent category)	en	Fully specified name	Inactive	Case sensitive	SNOMED CT core

Expanded Value Set

Reference Sets

Situation with explicit context foundation reference set

Problem/Diagnosis reference set

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