160321003: Family history: Sickle cell trait (situation)

• SNOMED CT Concept\Situation with explicit context\...
• \Finding with explicit context\Family history of clinical finding\Family history of disorder\...
• \Family history of hereditary disease\FH: Sickle cell trait
• \Family history of congenital disease\FH: Sickle cell trait
• \FH: Blood disorder\Family history of haemoglobinopathy\FH: Sickle cell trait
• \Family history with explicit context\Family history of clinical finding\Family history of disorder\...
• \Family history of hereditary disease\FH: Sickle cell trait
• \Family history of congenital disease\FH: Sickle cell trait
• \FH: Blood disorder\Family history of haemoglobinopathy\FH: Sickle cell trait

Status: current, Defined. Date: 31-Jul 2004. Module: SNOMED CT core

Descriptions:

Id	Description	Lang	Type	Status	Case?	Module
249837019	FH: Sickle cell trait	en	Synonym	Active	Case sensitive	SNOMED CT core
249838012	Family history of sickle cell trait	en	Synonym	Active	Case insensitive	SNOMED CT core
2607062014	Family history: Sickle cell trait (situation)	en	Fully specified name	Active	Initial character case insensitive	SNOMED CT core
2666201011	Family history: Sickle cell trait	en	Synonym	Active	Initial character case insensitive	SNOMED CT core

Expanded Value Set

Reference Sets

Situation with explicit context foundation reference set

Problem/Diagnosis reference set

Description inactivation indicator reference set

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