63361000000106: Germline whole genome sequencing targeting childhood onset hereditary ataxia and cerebellar anomalies panel for childhood onset hereditary ataxia (procedure)

• SNOMED CT Concept\Procedure\...
• \Procedure by method\Evaluation procedure\Laboratory test\Genetic test\Molecular genetic test\Whole genome sequencing (procedure)\Germline whole genome sequencing (procedure)\Germline whole genome sequencing targeting childhood onset hereditary ataxia and cerebellar anomalies panel (procedure)\Germline whole genome sequencing targeting childhood onset hereditary ataxia and cerebellar anomalies panel for childhood onset hereditary ataxia (procedure)
• \Laboratory procedure\Laboratory test\Genetic test\Molecular genetic test\Whole genome sequencing (procedure)\Germline whole genome sequencing (procedure)\Germline whole genome sequencing targeting childhood onset hereditary ataxia and cerebellar anomalies panel (procedure)\Germline whole genome sequencing targeting childhood onset hereditary ataxia and cerebellar anomalies panel for childhood onset hereditary ataxia (procedure)

Status: current, Not sufficiently defined by necessary conditions definition status. Date: 01-Jun 2019. Module: SNOMED CT United Kingdom clinical extension module

Descriptions:

Id	Description	Lang	Type	Status	Case?	Module
1089411000000115	Childhood onset hereditary ataxia germline WGS (whole genome sequencing) targeting childhood onset hereditary ataxia and cerebellar anomalies panel	en	Synonym	Active	Only initial character case insensitive	SNOMED CT United Kingdom clinical extension module
1089421000000114	Germline whole genome sequencing targeting childhood onset hereditary ataxia and cerebellar anomalies panel for childhood onset hereditary ataxia (procedure)	en	Fully specified name	Active	Entire term case insensitive	SNOMED CT United Kingdom clinical extension module

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