1407691000168102: Detection of HBA1 (hemoglobin subunit alpha 1) and HBA2 (hemoglobin subunit alpha 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 HBA1 and HBA2 mutation detection test
• \Laboratory procedure\Laboratory test\Genetic test\Molecular genetic test\Whole blood HBA1 and HBA2 mutation detection test

Status: current, Primitive. Date: 30-Nov 2019. Module: SNOMED Clinical Terms Australian extension

Descriptions:

Id	Description	Lang	Type	Status	Case?	Module
4247391000168111	Detection of HBA1 (hemoglobin subunit alpha 1) and HBA2 (hemoglobin subunit alpha 2) gene mutation in whole blood specimen (procedure)	en	Fully specified name	Active	Initial character case insensitive	SNOMED Clinical Terms Australian extension
4247401000168113	Detection of HBA1 (haemoglobin subunit alpha 1) and HBA2 (haemoglobin subunit alpha 2) gene mutation in whole blood specimen	en	Synonym	Active	Initial character case insensitive	SNOMED Clinical Terms Australian extension
4247411000168111	Whole blood HBA1 and HBA2 mutation detection test	en	Synonym	Active	Initial character case insensitive	SNOMED Clinical Terms Australian extension
4247421000168116	Whole blood HBA1 and HBA2 mutation detection test for alpha thalassaemia	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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