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63341000000105: Germline whole genome sequencing targeting craniosynostosis panel for rare syndromic craniosynostosis or isolated multisuture synostosis (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
1089371000000119 Germline whole genome sequencing targeting craniosynostosis panel for rare syndromic craniosynostosis or isolated multisuture synostosis (procedure) en Fully specified name Active Entire term case insensitive SNOMED CT United Kingdom clinical extension module
1089381000000117 Rare syndromic craniosynostosis or isolated multisuture synostosis germline WGS (whole genome sequencing) targeting craniosynostosis panel en Synonym Active Only initial character case insensitive SNOMED CT United Kingdom clinical extension module


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Germline whole genome sequencing targeting craniosynostosis panel for rare syndromic craniosynostosis or isolated multisuture synostosis (procedure) Method Evaluation - action false Inferred relationship Existential restriction modifier
Germline whole genome sequencing targeting craniosynostosis panel for rare syndromic craniosynostosis or isolated multisuture synostosis (procedure) Is a Germline whole genome sequencing targeting craniosynostosis panel (procedure) true Inferred relationship Existential restriction modifier
Germline whole genome sequencing targeting craniosynostosis panel for rare syndromic craniosynostosis or isolated multisuture synostosis (procedure) Method Evaluation - action true Inferred relationship Existential restriction modifier 1

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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