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62981000000108: Germline whole genome sequencing targeting skeletal dysplasia panel (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
1088651000000110 Germline whole genome sequencing targeting skeletal dysplasia panel (procedure) en Fully specified name Active Entire term case insensitive SNOMED CT United Kingdom clinical extension module
1088661000000113 Germline WGS (whole genome sequencing) targeting skeletal dysplasia panel en Synonym Active Only initial character case insensitive SNOMED CT United Kingdom clinical extension module


1 descendants. Search Descendants:

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Germline whole genome sequencing targeting skeletal dysplasia panel (procedure) Method Evaluation - action false Inferred relationship Existential restriction modifier
Germline whole genome sequencing targeting skeletal dysplasia panel (procedure) Is a Germline whole genome sequencing (procedure) true Inferred relationship Existential restriction modifier
Germline whole genome sequencing targeting skeletal dysplasia panel (procedure) Method Evaluation - action true Inferred relationship Existential restriction modifier 1

Inbound Relationships Type Active Source Characteristic Refinability Group
Germline whole genome sequencing targeting skeletal dysplasia panel for skeletal dysplasia (procedure) Is a True Germline whole genome sequencing targeting skeletal dysplasia panel (procedure) Inferred relationship Existential restriction modifier

This concept is not in any reference sets

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