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123772008: Homozygous hemoglobinopathy (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)\Homozygous hemoglobinopathy

\Red blood cell disorder\Hereditary red blood cell disorder (disorder)\Hereditary hemoglobinopathy (disorder)\Homozygous hemoglobinopathy
\Red blood cell disorder\Hemoglobinopathy\Hereditary hemoglobinopathy (disorder)\Homozygous 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)\Homozygous 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)\Homozygous hemoglobinopathy
\Disease\Disorder of cellular component of blood (disorder)\Red blood cell disorder\Hereditary red blood cell disorder (disorder)\Hereditary hemoglobinopathy (disorder)\Homozygous hemoglobinopathy
\Disease\Disorder of cellular component of blood (disorder)\Red blood cell disorder\Hemoglobinopathy\Hereditary hemoglobinopathy (disorder)\Homozygous 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)\Homozygous hemoglobinopathy
\Disease\Disorder of body system\Red blood cell disorder\Hereditary red blood cell disorder (disorder)\Hereditary hemoglobinopathy (disorder)\Homozygous hemoglobinopathy
\Disease\Disorder of body system\Red blood cell disorder\Hemoglobinopathy\Hereditary hemoglobinopathy (disorder)\Homozygous hemoglobinopathy
\Disease\Congenital disease (disorder)\Hereditary hemoglobinopathy (disorder)\Homozygous 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
Homozygous hemoglobinopathy	Is a	Hemoglobinopathy	false	Inferred relationship	Some
Homozygous hemoglobinopathy	Finding site	Hematopoietic system structure	false	Inferred relationship	Some
Homozygous hemoglobinopathy	Finding site	Erythrocyte	false	Inferred relationship	Some
Homozygous hemoglobinopathy	Finding site	Hematopoietic system structure	false	Inferred relationship	Some
Homozygous hemoglobinopathy	Has definitional manifestation	Red blood cell finding	false	Inferred relationship	Some
Homozygous hemoglobinopathy	Is a	Hereditary hemoglobinopathy (disorder)	true	Inferred relationship	Some
Homozygous hemoglobinopathy	Finding site	Body system structure	false	Inferred relationship	Some
Homozygous hemoglobinopathy	Occurrence	Congenital	true	Inferred relationship	Some	1
Homozygous hemoglobinopathy	Finding site	Erythrocyte	true	Inferred relationship	Some	1

Inbound Relationships	Type	Active	Source	Characteristic	Refinability	Group
Sickle cell-hemoglobin SS disease	Is a	True	Homozygous hemoglobinopathy	Inferred relationship	Some
Vaso-occlusive pain co-occurrent and due to sickle cell disease (disorder)	Due to	True	Homozygous hemoglobinopathy	Inferred relationship	Some	2
Vaso-occlusive pain co-occurrent and due to sickle cell disease (disorder)	Is a	True	Homozygous hemoglobinopathy	Inferred relationship	Some

Reference Sets

Belgian subset for medical problems in patient health records

Back to Start

Id	Description	Lang	Type	Status	Case?	Module
192261019	Homozygous hemoglobinopathy	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
203427013	Homozygous haemoglobinopathy	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
726889010	Homozygous hemoglobinopathy (disorder)	en	Fully specified name	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
5691671000172114	hémoglobinopathie homozygote	fr	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	Belgian module (core metadata concept)
4216601000172117	homozygote hemoglobinopathie	nl	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	Belgian module (core metadata concept)