23269001: Double heterozygous sickling disorder (disorder)

SNOMED CT Concept\Clinical finding\...

\Finding of blood, lymphatics and immune system\Blood disease\...

\Hereditary disorder of cellular element of blood\Hereditary red blood cell disorder\Hereditary haemoglobinopathy\Hereditary haemoglobinopathy due to globin chain mutation\Hereditary haemoglobin S\Sickling disorder due to haemoglobin S\Double heterozygous sickling disorder

\Red blood cell disorder\Hereditary red blood cell disorder\Hereditary haemoglobinopathy\Hereditary haemoglobinopathy due to globin chain mutation\Hereditary haemoglobin S\Sickling disorder due to haemoglobin S\Double heterozygous sickling disorder
\Red blood cell disorder\Haemoglobinopathy\Hereditary haemoglobinopathy\Hereditary haemoglobinopathy due to globin chain mutation\Hereditary haemoglobin S\Sickling disorder due to haemoglobin S\Double heterozygous sickling disorder

\Disease\Genetic disease\Hereditary disease\Hereditary disorder by system\Hereditary disorder of cellular element of blood\Hereditary red blood cell disorder\Hereditary haemoglobinopathy\Hereditary haemoglobinopathy due to globin chain mutation\Hereditary haemoglobin S\Sickling disorder due to haemoglobin S\Double heterozygous sickling disorder
\Disease\Blood disease\Hereditary disorder of cellular element of blood\Hereditary red blood cell disorder\Hereditary haemoglobinopathy\Hereditary haemoglobinopathy due to globin chain mutation\Hereditary haemoglobin S\Sickling disorder due to haemoglobin S\Double heterozygous sickling disorder
\Disease\Blood disease\Red blood cell disorder\Hereditary red blood cell disorder\Hereditary haemoglobinopathy\Hereditary haemoglobinopathy due to globin chain mutation\Hereditary haemoglobin S\Sickling disorder due to haemoglobin S\Double heterozygous sickling disorder
\Disease\Blood disease\Red blood cell disorder\Haemoglobinopathy\Hereditary haemoglobinopathy\Hereditary haemoglobinopathy due to globin chain mutation\Hereditary haemoglobin S\Sickling disorder due to haemoglobin S\Double heterozygous sickling disorder
\Disease\Disorder of body system\Hereditary disorder by system\Hereditary disorder of cellular element of blood\Hereditary red blood cell disorder\Hereditary haemoglobinopathy\Hereditary haemoglobinopathy due to globin chain mutation\Hereditary haemoglobin S\Sickling disorder due to haemoglobin S\Double heterozygous sickling disorder
\Disease\Disorder of body system\Red blood cell disorder\Hereditary red blood cell disorder\Hereditary haemoglobinopathy\Hereditary haemoglobinopathy due to globin chain mutation\Hereditary haemoglobin S\Sickling disorder due to haemoglobin S\Double heterozygous sickling disorder
\Disease\Disorder of body system\Red blood cell disorder\Haemoglobinopathy\Hereditary haemoglobinopathy\Hereditary haemoglobinopathy due to globin chain mutation\Hereditary haemoglobin S\Sickling disorder due to haemoglobin S\Double heterozygous sickling disorder
\Disease\Congenital disease\Hereditary haemoglobinopathy\Hereditary haemoglobinopathy due to globin chain mutation\Hereditary haemoglobin S\Sickling disorder due to haemoglobin S\Double heterozygous sickling disorder

Status: current, Primitive. Date: 31-Jan 2002. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module

39059017 Double heterozygous sickling disorder en Synonym Active Case insensitive SNOMED CT core

752769019 Double heterozygous sickling disorder (disorder) en Fully specified name Active Case insensitive SNOMED CT core

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
Double heterozygous sickling disorder	Is a	Haemoglobinopathy	false	Inferred relationship	Some
Double heterozygous sickling disorder	Finding site	Haematopoietic system structure	false	Inferred relationship	Some
Double heterozygous sickling disorder	Has definitional manifestation	Red blood cell finding	false	Inferred relationship	Some
Double heterozygous sickling disorder	Is a	Sickling disorder due to haemoglobin S	true	Inferred relationship	Some
Double heterozygous sickling disorder	Finding site	Body system structure	false	Inferred relationship	Some
Double heterozygous sickling disorder	Occurrence	Congenital	true	Inferred relationship	Some	1
Double heterozygous sickling disorder	Finding site	Erythrocyte	true	Inferred relationship	Some	1
Double heterozygous sickling disorder	Finding site	Haematopoietic system structure	false	Inferred relationship	Some
Double heterozygous sickling disorder	Finding site	Erythrocyte	false	Inferred relationship	Some

Inbound Relationships	Type	Active	Source	Characteristic	Refinability	Group
Glomerular disease due to double heterozygous sickling disorder	Due to	True	Double heterozygous sickling disorder	Inferred relationship	Some	2
Gouty arthropathy due to double heterozygous sickling disorder	Due to	True	Double heterozygous sickling disorder	Inferred relationship	Some	3
Sickle cell-beta-thalassaemia	Is a	True	Double heterozygous sickling disorder	Inferred relationship	Some
Sickle cell-haemoglobin Lepore disease	Is a	True	Double heterozygous sickling disorder	Inferred relationship	Some
Sickle cell-Haemoglobin O Arab disease	Is a	True	Double heterozygous sickling disorder	Inferred relationship	Some
Sickle cell-haemoglobin D disease	Is a	True	Double heterozygous sickling disorder	Inferred relationship	Some
Sickle cell-haemoglobin C disease	Is a	True	Double heterozygous sickling disorder	Inferred relationship	Some
Sickle cell-haemoglobin E disease	Is a	True	Double heterozygous sickling disorder	Inferred relationship	Some

Reference Sets

Australian emergency department reference set

Clinical finding foundation reference set

Problem/Diagnosis reference set

Back to Start

Id	Description	Lang	Type	Status	Case?	Module
39059017	Double heterozygous sickling disorder	en	Synonym	Active	Case insensitive	SNOMED CT core
752769019	Double heterozygous sickling disorder (disorder)	en	Fully specified name	Active	Case insensitive	SNOMED CT core