98011000119108: Family history of butyrylcholinesterase deficiency (situation)

• SNOMED CT Concept\Situation with explicit context\...
• \Finding with explicit context\Family history of clinical finding\Family history of disorder\FH: Metabolic disorder\FH: Butyrylcholinesterase deficiency
• \Family history with explicit context\Family history of clinical finding\Family history of disorder\FH: Metabolic disorder\FH: Butyrylcholinesterase deficiency

Status: current, Defined. Date: 31-Jul 2015. Module: SNOMED CT core

Descriptions:

Id	Description	Lang	Type	Status	Case?	Module
3042477014	Family history of pseudocholinesterase deficiency	en	Synonym	Active	Case insensitive	SNOMED CT core
3788091010	Family history of butyrylcholinesterase deficiency	en	Synonym	Active	Case insensitive	SNOMED CT core
3788092015	Family history of butyrylcholinesterase deficiency (situation)	en	Fully specified name	Active	Case insensitive	SNOMED CT core
4353161000168119	FH: Butyrylcholinesterase deficiency	en	Synonym	Active	Case sensitive	SNOMED Clinical Terms Australian extension

Expanded Value Set

Reference Sets

Situation with explicit context foundation reference set

Problem/Diagnosis reference set

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