FHIR © HL7.org  |  Server Home  |  FHIR Server FHIR Server 3.7.10  |  FHIR Version n/a  User: [n/a]

1129151000000106: National Health Service Sickle Cell and Thalassaemia Screening Programme thalassaemia screening result consistent with homozygous haemoglobin variant not clinically significant (situation)


Status: current, Not sufficiently defined by necessary conditions definition status. Date: 01-Oct 2019. Module: SNOMED CT United Kingdom clinical extension module

Descriptions:

Id Description Lang Type Status Case? Module
1858841000000118 National Health Service Sickle Cell and Thalassaemia Screening Programme thalassaemia screening result consistent with homozygous haemoglobin variant not clinically significant (situation) en Fully specified name Active Entire term case sensitive SNOMED CT United Kingdom clinical extension module
1858851000000115 NHS Sickle Cell and Thalassaemia Screening Programme thalassaemia screening result consistent with homozygous haemoglobin variant not clinically significant en Synonym Active Entire term case sensitive SNOMED CT United Kingdom clinical extension module


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
National Health Service Sickle Cell and Thalassaemia Screening Programme thalassaemia screening result consistent with homozygous haemoglobin variant not clinically significant (situation) Subject relationship context Subject of record true Inferred relationship Existential restriction modifier 1
National Health Service Sickle Cell and Thalassaemia Screening Programme thalassaemia screening result consistent with homozygous haemoglobin variant not clinically significant (situation) Temporal context Current or specified time true Inferred relationship Existential restriction modifier 1
National Health Service Sickle Cell and Thalassaemia Screening Programme thalassaemia screening result consistent with homozygous haemoglobin variant not clinically significant (situation) Associated finding Homozygous hemoglobinopathy true Inferred relationship Existential restriction modifier 1
National Health Service Sickle Cell and Thalassaemia Screening Programme thalassaemia screening result consistent with homozygous haemoglobin variant not clinically significant (situation) Finding context Probably present true Inferred relationship Existential restriction modifier 1
National Health Service Sickle Cell and Thalassaemia Screening Programme thalassaemia screening result consistent with homozygous haemoglobin variant not clinically significant (situation) Is a Possible clinical finding true Inferred relationship Existential restriction modifier

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

Back to Start