FHIR © HL7.org  |  Server Home  |  FHIR Server FHIR Server 3.7.4-SNAPSHOT  |  FHIR Version n/a  User: [n/a]

685061000119108: Hemoglobin C beta plus thalassemia (disorder)


Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 01-Sep 2023. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
5256345016 Haemoglobin C beta plus thalassaemia en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
5256346015 Hemoglobin C beta plus thalassemia (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
5256347012 Hemoglobin C beta plus thalassemia en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
5256345016 Haemoglobin C beta plus thalassaemia en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
5256346015 Hemoglobin C beta plus thalassemia (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
5256347012 Hemoglobin C beta plus thalassemia en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Haemoglobin C beta plus thalassaemia Is a Hemoglobin C beta thalassemia (disorder) true Inferred relationship Existential restriction modifier (core metadata concept)
Haemoglobin C beta plus thalassaemia Interprets Measurement of total haemoglobin concentration true Inferred relationship Existential restriction modifier (core metadata concept) 2
Haemoglobin C beta plus thalassaemia Has interpretation Below reference range true Inferred relationship Existential restriction modifier (core metadata concept) 2
Haemoglobin C beta plus thalassaemia Occurrence Congenital true Inferred relationship Existential restriction modifier (core metadata concept) 1
Haemoglobin C beta plus thalassaemia Finding site Erythrocyte true Inferred relationship Existential restriction modifier (core metadata concept) 1
Haemoglobin C beta plus thalassaemia Is a Thalassemia with other hemoglobinopathy (disorder) true Inferred relationship Existential restriction modifier (core metadata concept)

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

Back to Start