1308061000168105: Detection of CNBP (CCHC-type zinc finger nucleic acid binding protein) 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 CNBP mutation detection test
• \Blood test\Whole blood CNBP mutation detection test
• \Body fluid analysis\Whole blood CNBP mutation detection test
• \Laboratory procedure\Laboratory test\...
• \Genetic test\Molecular genetic test\Whole blood CNBP mutation detection test
• \Blood test\Whole blood CNBP mutation detection test
• \Body fluid analysis\Whole blood CNBP mutation detection test

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

Descriptions:

Id	Description	Lang	Type	Status	Case?	Module
3334231000168117	Detection of CNBP (CCHC-type zinc finger nucleic acid binding protein) gene mutation in whole blood specimen (procedure)	en	Fully specified name	Active	Initial character case insensitive	SNOMED Clinical Terms Australian extension
3334241000168114	Whole blood CNBP mutation detection test	en	Synonym	Active	Initial character case insensitive	SNOMED Clinical Terms Australian extension
3334251000168111	Detection of CNBP (CCHC-type zinc finger nucleic acid binding protein) gene mutation in whole blood specimen	en	Synonym	Active	Initial character case insensitive	SNOMED Clinical Terms Australian extension
3334261000168113	Whole blood MD2 (myotonic dystrophy type 2) mutation detection test	en	Synonym	Active	Initial character case insensitive	SNOMED Clinical Terms Australian extension

Expanded Value Set

Reference Sets

Procedure foundation reference set

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