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63431000000108: Germline whole genome sequencing targeting childhood onset white matter disorders panel for childhood onset leukodystrophy (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
1089561000000119 Germline whole genome sequencing targeting childhood onset white matter disorders panel for childhood onset leukodystrophy (procedure) en Fully specified name Active Entire term case insensitive SNOMED CT United Kingdom clinical extension module
1089571000000114 Childhood onset leukodystrophy germline WGS (whole genome sequencing) targeting childhood onset white matter disorders 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 childhood onset white matter disorders panel for childhood onset leukodystrophy (procedure) Is a Germline whole genome sequencing targeting childhood onset white matter disorders panel (procedure) true Inferred relationship Existential restriction modifier
Germline whole genome sequencing targeting childhood onset white matter disorders panel for childhood onset leukodystrophy (procedure) Method Evaluation - action false Inferred relationship Existential restriction modifier
Germline whole genome sequencing targeting childhood onset white matter disorders panel for childhood onset leukodystrophy (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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