46248003: Hemoglobin E trait (disorder)

SNOMED CT Concept\Clinical finding (finding)\...

\Finding of blood, lymphatics and immune system\Disorder of cellular component of blood (disorder)\...

\Hereditary disorder of cellular element of blood (disorder)\Hereditary red blood cell disorder (disorder)\Hereditary hemoglobinopathy (disorder)\...

\Hereditary hemoglobinopathy due to globin chain mutation\Hemoglobin E trait

\Heterozygous hemoglobinopathy\Hemoglobin E trait

\Red blood cell disorder\Hereditary red blood cell disorder (disorder)\Hereditary hemoglobinopathy (disorder)\Hereditary hemoglobinopathy due to globin chain mutation\Hemoglobin E trait
\Red blood cell disorder\Hereditary red blood cell disorder (disorder)\Hereditary hemoglobinopathy (disorder)\Heterozygous hemoglobinopathy\Hemoglobin E trait
\Red blood cell disorder\Hemoglobinopathy\Hereditary hemoglobinopathy (disorder)\Hereditary hemoglobinopathy due to globin chain mutation\Hemoglobin E trait
\Red blood cell disorder\Hemoglobinopathy\Hereditary hemoglobinopathy (disorder)\Heterozygous hemoglobinopathy\Hemoglobin E trait

Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2002. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module

77120014 Hemoglobin E trait en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core

77121013 Hemoglobin E-A disorder en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core

494476010 Haemoglobin E trait en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core

494477018 Haemoglobin E-A disorder en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core

494478011 Heterozygous for Hb E en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core

783576010 Hemoglobin E trait (disorder) en Fully specified name Active Entire term case sensitive (core metadata concept) SNOMED CT core

981461000241112 trait d'hémoglobine E fr Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module

981471000241116 trait d'HbE fr Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module

981481000241119 hémoglobinose E hétérozygote fr Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
Hemoglobin E trait	Is a	Hereditary hemoglobinopathy due to globin chain mutation	true	Inferred relationship	Some
Hemoglobin E trait	Finding site	Erythrocyte	false	Inferred relationship	Some
Hemoglobin E trait	Finding site	Hematopoietic system structure	false	Inferred relationship	Some
Hemoglobin E trait	Finding site	Hematopoietic system structure	false	Inferred relationship	Some
Hemoglobin E trait	Finding site	Body system structure	false	Inferred relationship	Some
Hemoglobin E trait	Has definitional manifestation	Red blood cell finding	false	Inferred relationship	Some
Hemoglobin E trait	Is a	Heterozygous hemoglobinopathy	true	Inferred relationship	Some
Hemoglobin E trait	Occurrence	Congenital	true	Inferred relationship	Some	1
Hemoglobin E trait	Finding site	Erythrocyte	true	Inferred relationship	Some	1

Inbound Relationships

Type

Active

Source

Characteristic

Refinability

Group

This concept is not in any reference sets