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234392002: Hemoglobin E/beta thalassemia disease (disorder)


Status: current, Primitive. Date: 31-Jan 2002. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
351167019 Hemoglobin E/beta thalassemia disease en Synonym Active Initial character case insensitive SNOMED CT core
351168012 Double heterozygous for Hb E and beta thalassaemia en Synonym Active Initial character case insensitive SNOMED CT core
351169016 Haemoglobin E/beta thalassaemia disease en Synonym Active Initial character case insensitive SNOMED CT core
351170015 Double heterozygous for Hb E and beta thalassemia en Synonym Active Initial character case insensitive SNOMED CT core
622704011 Hemoglobin E/beta thalassemia disease (disorder) en Fully specified name Active Initial character case insensitive SNOMED CT core


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Haemoglobin E/beta thalassaemia disease Is a Beta thalassaemia true Inferred relationship Some
Haemoglobin E/beta thalassaemia disease Is a Autosomal recessive hereditary disorder true Inferred relationship Some
Haemoglobin E/beta thalassaemia disease Interprets Measurement of total haemoglobin concentration true Inferred relationship Some 2
Haemoglobin E/beta thalassaemia disease Has interpretation Below reference range true Inferred relationship Some 2
Haemoglobin E/beta thalassaemia disease Finding site Haematopoietic system structure false Inferred relationship Some
Haemoglobin E/beta thalassaemia disease Finding site Body system structure false Inferred relationship Some
Haemoglobin E/beta thalassaemia disease Has definitional manifestation Red blood cell finding false Inferred relationship Some
Haemoglobin E/beta thalassaemia disease Is a Haemoglobin E disease true Inferred relationship Some
Haemoglobin E/beta thalassaemia disease Finding site Haematopoietic system structure false Inferred relationship Some
Haemoglobin E/beta thalassaemia disease Finding site Erythrocyte false Inferred relationship Some
Haemoglobin E/beta thalassaemia disease Occurrence Congenital true Inferred relationship Some 1
Haemoglobin E/beta thalassaemia disease Finding site Erythrocyte true Inferred relationship Some 1

Inbound Relationships Type Active Source Characteristic Refinability Group
Sickle cell-delta beta^0^-thalassaemia Is a False Haemoglobin E/beta thalassaemia disease Inferred relationship Some

Reference Sets

Australian emergency department reference set

Clinical finding foundation reference set

Problem/Diagnosis reference set

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