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416417002: Hereditary hemoglobin S (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\Hereditary hemoglobin S

\Red blood cell disorder\Hereditary red blood cell disorder\Hereditary hemoglobinopathy\Hereditary hemoglobinopathy due to globin chain mutation\Hereditary hemoglobin S
\Red blood cell disorder\Hemoglobinopathy\Hereditary hemoglobinopathy\Hereditary hemoglobinopathy due to globin chain mutation\Hereditary hemoglobin S

\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\Hereditary hemoglobin S
\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\Hereditary hemoglobin S
\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\Hereditary hemoglobin S
\Disease\Disorder of cellular component of blood\Red blood cell disorder\Hemoglobinopathy\Hereditary hemoglobinopathy\Hereditary hemoglobinopathy due to globin chain mutation\Hereditary hemoglobin S
\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\Hereditary hemoglobin S
\Disease\Disorder of body system\Red blood cell disorder\Hereditary red blood cell disorder\Hereditary hemoglobinopathy\Hereditary hemoglobinopathy due to globin chain mutation\Hereditary hemoglobin S
\Disease\Disorder of body system\Red blood cell disorder\Hemoglobinopathy\Hereditary hemoglobinopathy\Hereditary hemoglobinopathy due to globin chain mutation\Hereditary hemoglobin S
\Disease\Congenital disease\Hereditary hemoglobinopathy\Hereditary hemoglobinopathy due to globin chain mutation\Hereditary hemoglobin S

Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Jul 2005. Module: SNOMED CT core module

Descriptions:

Id Description Lang Type Status Case? Module

2546627012 Hereditary hemoglobin S (disorder) en Fully specified name Active Only initial character case insensitive SNOMED CT core module

2548928011 Hereditary hemoglobin S en Synonym Active Only initial character case insensitive SNOMED CT core module

2548929015 Hereditary haemoglobin S en Synonym Active Only initial character case insensitive SNOMED CT core module

Expanded Value Set

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

Inbound Relationships	Type	Active	Source	Characteristic	Refinability	Group
Sickling disorder due to hemoglobin S	Is a	True	Hereditary hemoglobin S	Inferred relationship	Existential restriction modifier
Sickle cell trait	Is a	True	Hereditary hemoglobin S	Inferred relationship	Existential restriction modifier
Sickle cell retinopathy	Due to	True	Hereditary hemoglobin S	Inferred relationship	Existential restriction modifier	2
Sickle cell disease not suspected	Associated finding	False	Hereditary hemoglobin S	Inferred relationship	Existential restriction modifier

This concept is not in any reference sets

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Id	Description	Lang	Type	Status	Case?	Module
2546627012	Hereditary hemoglobin S (disorder)	en	Fully specified name	Active	Only initial character case insensitive	SNOMED CT core module
2548928011	Hereditary hemoglobin S	en	Synonym	Active	Only initial character case insensitive	SNOMED CT core module
2548929015	Hereditary haemoglobin S	en	Synonym	Active	Only initial character case insensitive	SNOMED CT core module