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63321000000103: Germline whole genome sequencing targeting hypotonic infant panel for hypotonic infant with likely central cause (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
1089331000000116 Hypotonic infant with likely central cause germline WGS (whole genome sequencing) targeting hypotonic infant panel en Synonym Active Only initial character case insensitive SNOMED CT United Kingdom clinical extension module
1089341000000113 Germline whole genome sequencing targeting hypotonic infant panel for hypotonic infant with likely central cause (procedure) en Fully specified name Active Entire term 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 hypotonic infant panel for hypotonic infant with likely central cause (procedure) Is a Germline whole genome sequencing targeting hypotonic infant panel (procedure) true Inferred relationship Existential restriction modifier
Germline whole genome sequencing targeting hypotonic infant panel for hypotonic infant with likely central cause (procedure) Method Evaluation - action false Inferred relationship Existential restriction modifier
Germline whole genome sequencing targeting hypotonic infant panel for hypotonic infant with likely central cause (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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