123773003: heterozygote hemoglobinopathie (aandoening)

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)\Heterozygous hemoglobinopathy

\Red blood cell disorder\Hereditary red blood cell disorder (disorder)\Hereditary hemoglobinopathy (disorder)\Heterozygous hemoglobinopathy
\Red blood cell disorder\Hemoglobinopathy\Hereditary hemoglobinopathy (disorder)\Heterozygous hemoglobinopathy

\Disease\Genetic disease\Hereditary disease\Hereditary disorder by system\Hereditary disorder of cellular element of blood (disorder)\Hereditary red blood cell disorder (disorder)\Hereditary hemoglobinopathy (disorder)\Heterozygous hemoglobinopathy
\Disease\Disorder of foetus and/or newborn\Congenital disease (disorder)\Hereditary hemoglobinopathy (disorder)\Heterozygous hemoglobinopathy
\Disease\Disorder of cellular component of blood (disorder)\Hereditary disorder of cellular element of blood (disorder)\Hereditary red blood cell disorder (disorder)\Hereditary hemoglobinopathy (disorder)\Heterozygous hemoglobinopathy
\Disease\Disorder of cellular component of blood (disorder)\Red blood cell disorder\Hereditary red blood cell disorder (disorder)\Hereditary hemoglobinopathy (disorder)\Heterozygous hemoglobinopathy
\Disease\Disorder of cellular component of blood (disorder)\Red blood cell disorder\Hemoglobinopathy\Hereditary hemoglobinopathy (disorder)\Heterozygous hemoglobinopathy
\Disease\Disorder of body system\Hematological disorder (disorder)\Red blood cell disorder\Hereditary red blood cell disorder (disorder)\Hereditary hemoglobinopathy (disorder)\Heterozygous hemoglobinopathy
\Disease\Disorder of body system\Hematological disorder (disorder)\Red blood cell disorder\Hemoglobinopathy\Hereditary hemoglobinopathy (disorder)\Heterozygous hemoglobinopathy
\Disease\Disorder of body system\Hereditary disorder by system\Hereditary disorder of cellular element of blood (disorder)\Hereditary red blood cell disorder (disorder)\Hereditary hemoglobinopathy (disorder)\Heterozygous hemoglobinopathy

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

Descriptions:

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
Heterozygous hemoglobinopathy	Is a	Hemoglobinopathy	false	Inferred relationship	Some
Heterozygous hemoglobinopathy	Finding site	Erythrocyte	false	Inferred relationship	Some
Heterozygous hemoglobinopathy	Finding site	Hematopoietic system structure	false	Inferred relationship	Some
Heterozygous hemoglobinopathy	Finding site	Hematopoietic system structure	false	Inferred relationship	Some
Heterozygous hemoglobinopathy	Has definitional manifestation	Red blood cell finding	false	Inferred relationship	Some
Heterozygous hemoglobinopathy	Is a	Hereditary hemoglobinopathy (disorder)	true	Inferred relationship	Some
Heterozygous hemoglobinopathy	Finding site	Body system structure	false	Inferred relationship	Some
Heterozygous hemoglobinopathy	Occurrence	Congenital	true	Inferred relationship	Some	1
Heterozygous hemoglobinopathy	Finding site	Erythrocyte	true	Inferred relationship	Some	1

Inbound Relationships	Type	Active	Source	Characteristic	Refinability	Group
Sickle cell trait	Is a	True	Heterozygous hemoglobinopathy	Inferred relationship	Some
Hemoglobin E trait	Is a	True	Heterozygous hemoglobinopathy	Inferred relationship	Some
Hemoglobin D trait	Is a	True	Heterozygous hemoglobinopathy	Inferred relationship	Some
Hemoglobin C trait	Is a	True	Heterozygous hemoglobinopathy	Inferred relationship	Some
Hemoglobin O-Arab trait (disorder)	Is a	True	Heterozygous hemoglobinopathy	Inferred relationship	Some

Reference Sets

GB English

US English

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Id	Description	Lang	Type	Status	Case?	Module
192262014	Heterozygous hemoglobinopathy	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
203428015	Trait hemoglobinopathy	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
203429011	Trait haemoglobinopathy	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
203430018	Heterozygous haemoglobinopathy	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
726899017	Heterozygous hemoglobinopathy (disorder)	en	Fully specified name	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
6498221000146111	heterozygote hemoglobinopathie	nl	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT Netherlands NRC maintained module (core metadata concept)
6498231000146113	heterozygote hemoglobinopathie (aandoening)	nl	Fully specified name	Active	Entire term case insensitive (core metadata concept)	SNOMED CT Netherlands NRC maintained module (core metadata concept)
6498241000146117	dragerschap van hemoglobinopathie	nl	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT Netherlands NRC maintained module (core metadata concept)