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63621000000108: Tumour and germline whole genome sequencing for paediatric central nervous system high-grade neuroepithelial tumour with MN1 proto-oncogene transcriptional regulator alteration (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
1089981000000118 Paediatric CNS (central nervous system) high-grade neuroepithelial tumour with MN1 alteration tumour and germline WGS (whole genome sequencing) en Synonym Active Only initial character case insensitive SNOMED CT United Kingdom clinical extension module
1089991000000116 Tumour and germline whole genome sequencing for paediatric central nervous system high-grade neuroepithelial tumour with MN1 proto-oncogene transcriptional regulator alteration (procedure) en Fully specified name 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
Tumour and germline whole genome sequencing for paediatric central nervous system high-grade neuroepithelial tumour with MN1 proto-oncogene transcriptional regulator alteration (procedure) Method Evaluation - action false Inferred relationship Existential restriction modifier
Tumour and germline whole genome sequencing for paediatric central nervous system high-grade neuroepithelial tumour with MN1 proto-oncogene transcriptional regulator alteration (procedure) Is a Tumour and germline whole genome sequencing (procedure) true Inferred relationship Existential restriction modifier
Tumour and germline whole genome sequencing for paediatric central nervous system high-grade neuroepithelial tumour with MN1 proto-oncogene transcriptional regulator alteration (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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