63291000000108: Germline whole genome sequencing targeting intellectual disability panel for intellectual disability using microarray, fragile X and sequencing (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 intellectual disability panel (procedure)\Germline whole genome sequencing targeting intellectual disability panel for intellectual disability using microarray, fragile X and sequencing (procedure)
• \Laboratory procedure\Laboratory test\Genetic test\Molecular genetic test\Whole genome sequencing (procedure)\Germline whole genome sequencing (procedure)\Germline whole genome sequencing targeting intellectual disability panel (procedure)\Germline whole genome sequencing targeting intellectual disability panel for intellectual disability using microarray, fragile X and sequencing (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
1089271000000112	Intellectual disability germline WGS (whole genome sequencing) using microarray, fragile X and sequencing targeting intellectual disability panel	en	Synonym	Active	Only initial character case insensitive	SNOMED CT United Kingdom clinical extension module
1089281000000114	Germline whole genome sequencing targeting intellectual disability panel for intellectual disability using microarray, fragile X and sequencing (procedure)	en	Fully specified name	Active	Only initial character case insensitive	SNOMED CT United Kingdom clinical extension module

Expanded Value Set

This concept is not in any reference sets

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