234396004: Congenital methemoglobinemia with abnormal methemoglobins (disorder)

SNOMED CT Concept\Clinical finding\...

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

\Hereditary disorder of cellular element of blood\Hereditary red blood cell disorder\Hereditary hemoglobinopathy\Hereditary hemoglobinopathy due to globin chain mutation\Congenital methemoglobinemia with abnormal methemoglobins

\Red blood cell disorder\Hereditary red blood cell disorder\Hereditary hemoglobinopathy\Hereditary hemoglobinopathy due to globin chain mutation\Congenital methemoglobinemia with abnormal methemoglobins
\Red blood cell disorder\Hemoglobinopathy\Hereditary hemoglobinopathy\Hereditary hemoglobinopathy 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\Hereditary red blood cell disorder\Hereditary hemoglobinopathy\Hereditary hemoglobinopathy due to globin chain mutation\Congenital methemoglobinemia with abnormal methemoglobins
\Disease\Disorder of cellular component of blood\Hereditary disorder of cellular element of blood\Hereditary red blood cell disorder\Hereditary hemoglobinopathy\Hereditary hemoglobinopathy due to globin chain mutation\Congenital methemoglobinemia with abnormal methemoglobins
\Disease\Disorder of cellular component of blood\Red blood cell disorder\Hereditary red blood cell disorder\Hereditary hemoglobinopathy\Hereditary hemoglobinopathy due to globin chain mutation\Congenital methemoglobinemia with abnormal methemoglobins
\Disease\Disorder of cellular component of blood\Red blood cell disorder\Hemoglobinopathy\Hereditary hemoglobinopathy\Hereditary hemoglobinopathy due to globin chain mutation\Congenital methemoglobinemia with abnormal methemoglobins
\Disease\Disorder of cellular component of blood\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\Hereditary red blood cell disorder\Hereditary hemoglobinopathy\Hereditary hemoglobinopathy due to globin chain mutation\Congenital methemoglobinemia with abnormal methemoglobins
\Disease\Disorder of body system\Red blood cell disorder\Hereditary red blood cell disorder\Hereditary hemoglobinopathy\Hereditary hemoglobinopathy due to globin chain mutation\Congenital methemoglobinemia with abnormal methemoglobins
\Disease\Disorder of body system\Red blood cell disorder\Hemoglobinopathy\Hereditary hemoglobinopathy\Hereditary hemoglobinopathy due to globin chain mutation\Congenital methemoglobinemia with abnormal methemoglobins
\Disease\Disorder of body system\Red blood cell disorder\Hemoglobinopathy\Methemoglobinemia\Congenital methemoglobinemia\Congenital methemoglobinemia with abnormal methemoglobins
\Disease\Congenital disease\Hereditary hemoglobinopathy\Hereditary hemoglobinopathy due to globin chain mutation\Congenital methemoglobinemia with abnormal methemoglobins
\Disease\Congenital disease\Congenital methemoglobinemia\Congenital methemoglobinemia with abnormal methemoglobins

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

Descriptions:

Id Description Lang Type Status Case? Module

351177017 Congenital methemoglobinemia with abnormal methemoglobins en Synonym Active Entire term case insensitive SNOMED CT core module

351178010 Congenital methaemoglobinaemia with abnormal methaemoglobins en Synonym Active Entire term case insensitive SNOMED CT core module

622708014 Congenital methemoglobinemia with abnormal methemoglobins (disorder) en Fully specified name Active Entire term case insensitive SNOMED CT core module

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
Congenital methemoglobinemia with abnormal methemoglobins	Is a	Congenital methemoglobinemia	true	Inferred relationship	Existential restriction modifier
Congenital methemoglobinemia with abnormal methemoglobins	Finding site	Hematopoietic system structure	false	Inferred relationship	Existential restriction modifier
Congenital methemoglobinemia with abnormal methemoglobins	Finding site	Erythrocyte	false	Inferred relationship	Existential restriction modifier
Congenital methemoglobinemia with abnormal methemoglobins	Finding site	Hematopoietic system structure	false	Inferred relationship	Existential restriction modifier
Congenital methemoglobinemia with abnormal methemoglobins	Occurrence	Congenital	false	Inferred relationship	Existential restriction modifier
Congenital methemoglobinemia with abnormal methemoglobins	Has definitional manifestation	Red blood cell finding	false	Inferred relationship	Existential restriction modifier
Congenital methemoglobinemia with abnormal methemoglobins	Is a	Hereditary hemoglobinopathy due to globin chain mutation	true	Inferred relationship	Existential restriction modifier
Congenital methemoglobinemia with abnormal methemoglobins	Finding site	Body system structure	false	Inferred relationship	Existential restriction modifier
Congenital methemoglobinemia with abnormal methemoglobins	Occurrence	Congenital	true	Inferred relationship	Existential restriction modifier	1
Congenital methemoglobinemia with abnormal methemoglobins	Finding site	Erythrocyte	true	Inferred relationship	Existential restriction modifier	1

Inbound Relationships

Type

Active

Source

Characteristic

Refinability

Group

This concept is not in any reference sets

Back to Start

Id	Description	Lang	Type	Status	Case?	Module
351177017	Congenital methemoglobinemia with abnormal methemoglobins	en	Synonym	Active	Entire term case insensitive	SNOMED CT core module
351178010	Congenital methaemoglobinaemia with abnormal methaemoglobins	en	Synonym	Active	Entire term case insensitive	SNOMED CT core module
622708014	Congenital methemoglobinemia with abnormal methemoglobins (disorder)	en	Fully specified name	Active	Entire term case insensitive	SNOMED CT core module