63381000000102: Germline whole genome sequencing targeting childhood onset hereditary ataxia and cerebellar anomalies panel for cerebellar anomalies (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 cerebellar anomalies (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 cerebellar anomalies (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
1089451000000116	Cerebellar anomalies 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
1089461000000118	Germline whole genome sequencing targeting childhood onset hereditary ataxia and cerebellar anomalies panel for cerebellar anomalies (procedure)	en	Fully specified name	Active	Entire term case insensitive	SNOMED CT United Kingdom clinical extension module

Expanded Value Set

This concept is not in any reference sets

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