234396004: congenitale methemoglobinemie met afwijkend methemoglobine (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)\Hereditary haemoglobinopathy due to globin chain mutation\Congenital methemoglobinemia with abnormal methemoglobins

\Red blood cell disorder\Hereditary red blood cell disorder (disorder)\Hereditary hemoglobinopathy (disorder)\Hereditary haemoglobinopathy due to globin chain mutation\Congenital methemoglobinemia with abnormal methemoglobins
\Red blood cell disorder\Hemoglobinopathy\Hereditary hemoglobinopathy (disorder)\Hereditary haemoglobinopathy due to globin chain mutation\Congenital methemoglobinemia with abnormal methemoglobins
\Red blood cell disorder\Hemoglobinopathy\Methemoglobinemia\Congenital methemoglobinemia\Congenital methemoglobinemia with abnormal methemoglobins

\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)\Hereditary haemoglobinopathy due to globin chain mutation\Congenital methemoglobinemia with abnormal methemoglobins
\Disease\Disorder of foetus and/or newborn\Congenital disease (disorder)\Hereditary hemoglobinopathy (disorder)\Hereditary haemoglobinopathy due to globin chain mutation\Congenital methemoglobinemia with abnormal methemoglobins
\Disease\Disorder of foetus and/or newborn\Congenital disease (disorder)\Congenital methemoglobinemia\Congenital methemoglobinemia with abnormal methemoglobins
\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)\Hereditary haemoglobinopathy due to globin chain mutation\Congenital methemoglobinemia with abnormal methemoglobins
\Disease\Disorder of cellular component of blood (disorder)\Red blood cell disorder\Hereditary red blood cell disorder (disorder)\Hereditary hemoglobinopathy (disorder)\Hereditary haemoglobinopathy due to globin chain mutation\Congenital methemoglobinemia with abnormal methemoglobins
\Disease\Disorder of cellular component of blood (disorder)\Red blood cell disorder\Hemoglobinopathy\Hereditary hemoglobinopathy (disorder)\Hereditary haemoglobinopathy due to globin chain mutation\Congenital methemoglobinemia with abnormal methemoglobins
\Disease\Disorder of cellular component of blood (disorder)\Red blood cell disorder\Hemoglobinopathy\Methemoglobinemia\Congenital methemoglobinemia\Congenital methemoglobinemia with abnormal methemoglobins
\Disease\Disorder of body system\Hematological disorder (disorder)\Red blood cell disorder\Hereditary red blood cell disorder (disorder)\Hereditary hemoglobinopathy (disorder)\Hereditary haemoglobinopathy due to globin chain mutation\Congenital methemoglobinemia with abnormal methemoglobins
\Disease\Disorder of body system\Hematological disorder (disorder)\Red blood cell disorder\Hemoglobinopathy\Hereditary hemoglobinopathy (disorder)\Hereditary haemoglobinopathy due to globin chain mutation\Congenital methemoglobinemia with abnormal methemoglobins
\Disease\Disorder of body system\Hematological disorder (disorder)\Red blood cell disorder\Hemoglobinopathy\Methemoglobinemia\Congenital methemoglobinemia\Congenital methemoglobinemia with abnormal methemoglobins
\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)\Hereditary haemoglobinopathy due to globin chain mutation\Congenital methemoglobinemia with abnormal methemoglobins

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
Congenital methemoglobinemia with abnormal methemoglobins	Is a	Congenital methemoglobinemia	true	Inferred relationship	Some
Congenital methemoglobinemia with abnormal methemoglobins	Finding site	Hematopoietic system structure	false	Inferred relationship	Some
Congenital methemoglobinemia with abnormal methemoglobins	Finding site	Erythrocyte	false	Inferred relationship	Some
Congenital methemoglobinemia with abnormal methemoglobins	Finding site	Hematopoietic system structure	false	Inferred relationship	Some
Congenital methemoglobinemia with abnormal methemoglobins	Occurrence	Congenital	false	Inferred relationship	Some
Congenital methemoglobinemia with abnormal methemoglobins	Has definitional manifestation	Red blood cell finding	false	Inferred relationship	Some
Congenital methemoglobinemia with abnormal methemoglobins	Is a	Hereditary haemoglobinopathy due to globin chain mutation	true	Inferred relationship	Some
Congenital methemoglobinemia with abnormal methemoglobins	Finding site	Body system structure	false	Inferred relationship	Some
Congenital methemoglobinemia with abnormal methemoglobins	Occurrence	Congenital	true	Inferred relationship	Some	1
Congenital methemoglobinemia with abnormal methemoglobins	Finding site	Erythrocyte	true	Inferred relationship	Some	1

Inbound Relationships

Type

Active

Source

Characteristic

Refinability

Group

This concept is not in any reference sets

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Id	Description	Lang	Type	Status	Case?	Module
351177017	Congenital methemoglobinemia with abnormal methemoglobins	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
351178010	Congenital methaemoglobinaemia with abnormal methaemoglobins	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
622708014	Congenital methemoglobinemia with abnormal methemoglobins (disorder)	en	Fully specified name	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
6448311000146116	congenitale methemoglobinemie met afwijkend methemoglobine	nl	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT Netherlands NRC maintained module (core metadata concept)
6448321000146114	aangeboren methemoglobinemie met abnormaal methemoglobine	nl	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT Netherlands NRC maintained module (core metadata concept)
6448331000146111	congenitale methemoglobinemie met afwijkend methemoglobine (aandoening)	nl	Fully specified name	Active	Entire term case insensitive (core metadata concept)	SNOMED CT Netherlands NRC maintained module (core metadata concept)