1308151000168107: Detection of MECP2 (methyl-CpG binding protein 2) gene mutation in whole blood specimen (procedure)

• SNOMED CT Concept\Procedure\...
• \Procedure by method\Evaluation procedure\Laboratory test\...
• \Genetic test\Molecular genetic test\Whole blood MECP2 mutation detection test
• \Blood test\Whole blood MECP2 mutation detection test
• \Body fluid analysis\Whole blood MECP2 mutation detection test
• \Laboratory procedure\Laboratory test\...
• \Genetic test\Molecular genetic test\Whole blood MECP2 mutation detection test
• \Blood test\Whole blood MECP2 mutation detection test
• \Body fluid analysis\Whole blood MECP2 mutation detection test

Status: current, Primitive. Date: 31-May 2019. Module: SNOMED Clinical Terms Australian extension

Descriptions:

Id	Description	Lang	Type	Status	Case?	Module
3334611000168113	Detection of MECP2 (methyl-CpG binding protein 2) gene mutation in whole blood specimen (procedure)	en	Fully specified name	Active	Initial character case insensitive	SNOMED Clinical Terms Australian extension
3334621000168118	Whole blood MECP2 mutation detection test	en	Synonym	Active	Initial character case insensitive	SNOMED Clinical Terms Australian extension
3334631000168115	Detection of MECP2 (methyl-CpG binding protein 2) gene mutation in whole blood specimen	en	Synonym	Active	Initial character case insensitive	SNOMED Clinical Terms Australian extension
3334641000168112	Whole blood MECP2 mutation detection test for Rett syndrome	en	Synonym	Active	Initial character case insensitive	SNOMED Clinical Terms Australian extension

Expanded Value Set

Reference Sets

Procedure foundation reference set

Australian dialect reference set

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