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63681000000109: Tumour and germline whole genome sequencing for paediatric fibrolamellar hepatocellular carcinoma (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
1090101000000116 Paediatric FLHCC (fibrolamellar hepatocellular carcinoma) tumour and germline WGS (whole genome sequencing) en Synonym Active Only initial character case insensitive SNOMED CT United Kingdom clinical extension module
1090111000000119 Tumour and germline whole genome sequencing for paediatric fibrolamellar hepatocellular carcinoma (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
Tumour and germline whole genome sequencing for paediatric fibrolamellar hepatocellular carcinoma (procedure) Method Evaluation - action false Inferred relationship Existential restriction modifier
Tumour and germline whole genome sequencing for paediatric fibrolamellar hepatocellular carcinoma (procedure) Is a Tumour and germline whole genome sequencing (procedure) true Inferred relationship Existential restriction modifier
Tumour and germline whole genome sequencing for paediatric fibrolamellar hepatocellular carcinoma (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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