North West Genomic Medicine Service Alliance
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DRAFT Implementation Guide

This is for collaboration and discussion purposes and is subject to change.

North West Genomic Medicine Service Alliance - Local Development build (v0.0.1) built by the FHIR (HL7® FHIR® Standard) Build Tools. See the Directory of published versions

ConceptMap: LOINC to SNOMED UK edition

Official URL: https://nw-gmsa.github.io/ConceptMap/LOINCtoSNOMEDUK Version: 0.0.1
Draft as of 2025-06-19 Computable Name:

For demonstration purposes only - THIS HAS NOT BEEN VALIDATED

For Implementation Guide see SNOMED CT Implementation Guide for the LOINC Ontology

Mapping from (not specified) to SNOMED CT Reference Set (All of SNOMED CT)


Group 1 Mapping from Logical Observation Identifiers, Names and Codes (LOINC) to http://snomed.info/sct|http://snomed.info/sct/83821000000107

Source Concept DetailsRelationshipTarget Concept Details
Codes from Logical Observation Identifiers, Names and Codes (LOINC)Codes from http://snomed.info/sct|http://snomed.info/sct/83821000000107
785-6MCH [Entitic mass] by Automated countis related to1022471000000107
787-2MCV [Entitic mean volume] in Red Blood Cells by Automated countis related to1022491000000106
is related to1491000237105