1426351000168106: Detection of common CFTR (cystic fibrosis transmembrane conductance regulator) gene mutations in whole blood specimen (procedure)

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

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

Descriptions:

Id	Description	Lang	Type	Status	Case?	Module
4289671000168115	Detection of common CFTR (cystic fibrosis transmembrane conductance regulator) gene mutations in whole blood specimen (procedure)	en	Fully specified name	Active	Initial character case insensitive	SNOMED Clinical Terms Australian extension
4289681000168117	Whole blood common CFTR mutations detection test	en	Synonym	Active	Initial character case insensitive	SNOMED Clinical Terms Australian extension
4289691000168119	Detection of common CFTR (cystic fibrosis transmembrane conductance regulator) gene mutations in whole blood specimen	en	Synonym	Active	Initial character case insensitive	SNOMED Clinical Terms Australian extension
4289701000168119	Detection of common CFTR mutations in whole blood for cystic fibrosis	en	Synonym	Active	Initial character case insensitive	SNOMED Clinical Terms Australian extension

Expanded Value Set

Reference Sets

Procedure foundation reference set

Description inactivation indicator reference set

REFERS TO concept association reference set

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