123772008: Homozygous hemoglobinopathy (disorder)

SNOMED CT Concept\Clinical finding (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 (disorder)\Hereditary hemoglobinopathy (disorder)\Homozygous haemoglobinopathy

\Red blood cell disorder\Hereditary red blood cell disorder (disorder)\Hereditary hemoglobinopathy (disorder)\Homozygous haemoglobinopathy
\Red blood cell disorder\Haemoglobinopathy\Hereditary hemoglobinopathy (disorder)\Homozygous haemoglobinopathy

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

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 haemoglobinopathy	Is a	Haemoglobinopathy	false	Inferred relationship	Existential restriction modifier (core metadata concept)
Homozygous haemoglobinopathy	Finding site	Hematopoietic system structure	false	Inferred relationship	Existential restriction modifier (core metadata concept)
Homozygous haemoglobinopathy	Finding site	Erythrocyte	false	Inferred relationship	Existential restriction modifier (core metadata concept)
Homozygous haemoglobinopathy	Finding site	Hematopoietic system structure	false	Inferred relationship	Existential restriction modifier (core metadata concept)
Homozygous haemoglobinopathy	Has definitional manifestation	Red blood cell finding (finding)	false	Inferred relationship	Existential restriction modifier (core metadata concept)
Homozygous haemoglobinopathy	Is a	Hereditary hemoglobinopathy (disorder)	true	Inferred relationship	Existential restriction modifier (core metadata concept)
Homozygous haemoglobinopathy	Finding site	Body system structure	false	Inferred relationship	Existential restriction modifier (core metadata concept)
Homozygous haemoglobinopathy	Occurrence	Congenital	true	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Homozygous haemoglobinopathy	Finding site	Erythrocyte	true	Inferred relationship	Existential restriction modifier (core metadata concept)	1

Inbound Relationships	Type	Active	Source	Characteristic	Refinability	Group
Hb S disease	Is a	True	Homozygous haemoglobinopathy	Inferred relationship	Existential restriction modifier (core metadata concept)
Vaso-occlusive pain co-occurrent and due to sickle cell disease (disorder)	Due to	True	Homozygous haemoglobinopathy	Inferred relationship	Existential restriction modifier (core metadata concept)	2
Vaso-occlusive pain co-occurrent and due to sickle cell disease (disorder)	Is a	True	Homozygous haemoglobinopathy	Inferred relationship	Existential restriction modifier (core metadata concept)

This concept is not in any reference sets

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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
192261019	Homozygous hemoglobinopathy	en	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
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	Only initial character 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	Only initial character 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
4768281000241113	hémoglobinopathie homozygote	fr	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT Switzerland NRC maintained Module
4768281000241113	hémoglobinopathie homozygote	fr	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT Switzerland NRC maintained Module