36472007: Sickle cell-thalassemia disease (disorder)

SNOMED CT Concept\Clinical finding\...

\Evaluation finding\Measurement finding\Finding of substance level\Protein level - finding\Haemoglobin finding\Haemoglobin level outside reference range\Haemoglobin low\Anaemia due to disturbance of haemoglobin synthesis\Thalassaemia\Thalassaemia with other haemoglobinopathy\Sickle cell-thalassaemia disease
\Evaluation finding\Measurement finding\Measurement finding outside reference range\Measurement finding below reference range\Haemoglobin low\Anaemia due to disturbance of haemoglobin synthesis\Thalassaemia\Thalassaemia with other haemoglobinopathy\Sickle cell-thalassaemia disease
\Evaluation finding\Measurement finding\Measurement finding outside reference range\Haemoglobin level outside reference range\Haemoglobin low\Anaemia due to disturbance of haemoglobin synthesis\Thalassaemia\Thalassaemia with other haemoglobinopathy\Sickle cell-thalassaemia disease
\Evaluation finding\Haematopoietic system finding\Haematology test outside reference range\Haemoglobin level outside reference range\Haemoglobin low\Anaemia due to disturbance of haemoglobin synthesis\Thalassaemia\Thalassaemia with other haemoglobinopathy\Sickle cell-thalassaemia disease
\Evaluation finding\Haematopoietic system finding\Haemoglobin finding\Haemoglobin level outside reference range\Haemoglobin low\Anaemia due to disturbance of haemoglobin synthesis\Thalassaemia\Thalassaemia with other haemoglobinopathy\Sickle cell-thalassaemia disease

\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\Sickle cell-thalassaemia disease

\Thalassaemia\Thalassaemia with other haemoglobinopathy\Sickle cell-thalassaemia disease

\Anaemia\Anaemia due to disturbance of haemoglobin synthesis\Thalassaemia\Thalassaemia with other haemoglobinopathy\Sickle cell-thalassaemia 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\Sickle cell-thalassaemia disease
\Red blood cell disorder\Hereditary red blood cell disorder\Hereditary haemoglobinopathy\Thalassaemia\Thalassaemia with other haemoglobinopathy\Sickle cell-thalassaemia disease
\Red blood cell disorder\Haemoglobinopathy\Hereditary haemoglobinopathy\Hereditary haemoglobinopathy due to globin chain mutation\Hereditary haemoglobin S\Sickling disorder due to haemoglobin S\Sickle cell-thalassaemia disease
\Red blood cell disorder\Haemoglobinopathy\Hereditary haemoglobinopathy\Thalassaemia\Thalassaemia with other haemoglobinopathy\Sickle cell-thalassaemia disease

\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\Sickle cell-thalassaemia disease
\Disease\Genetic disease\Hereditary disease\Hereditary disorder by system\Hereditary disorder of cellular element of blood\Hereditary red blood cell disorder\Hereditary haemoglobinopathy\Thalassaemia\Thalassaemia with other haemoglobinopathy\Sickle cell-thalassaemia disease
\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\Sickle cell-thalassaemia disease
\Disease\Blood disease\Hereditary disorder of cellular element of blood\Hereditary red blood cell disorder\Hereditary haemoglobinopathy\Thalassaemia\Thalassaemia with other haemoglobinopathy\Sickle cell-thalassaemia disease
\Disease\Blood disease\Anaemia\Anaemia due to disturbance of haemoglobin synthesis\Thalassaemia\Thalassaemia with other haemoglobinopathy\Sickle cell-thalassaemia disease
\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\Sickle cell-thalassaemia disease
\Disease\Blood disease\Red blood cell disorder\Hereditary red blood cell disorder\Hereditary haemoglobinopathy\Thalassaemia\Thalassaemia with other haemoglobinopathy\Sickle cell-thalassaemia disease
\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\Sickle cell-thalassaemia disease
\Disease\Blood disease\Red blood cell disorder\Haemoglobinopathy\Hereditary haemoglobinopathy\Thalassaemia\Thalassaemia with other haemoglobinopathy\Sickle cell-thalassaemia disease
\Disease\Disorder of body system\Disorder of haematopoietic structure\Sickle cell-thalassaemia disease
\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\Sickle cell-thalassaemia disease
\Disease\Disorder of body system\Hereditary disorder by system\Hereditary disorder of cellular element of blood\Hereditary red blood cell disorder\Hereditary haemoglobinopathy\Thalassaemia\Thalassaemia with other haemoglobinopathy\Sickle cell-thalassaemia disease
\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\Sickle cell-thalassaemia disease
\Disease\Disorder of body system\Red blood cell disorder\Hereditary red blood cell disorder\Hereditary haemoglobinopathy\Thalassaemia\Thalassaemia with other haemoglobinopathy\Sickle cell-thalassaemia disease
\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\Sickle cell-thalassaemia disease
\Disease\Disorder of body system\Red blood cell disorder\Haemoglobinopathy\Hereditary haemoglobinopathy\Thalassaemia\Thalassaemia with other haemoglobinopathy\Sickle cell-thalassaemia disease
\Disease\Congenital disease\Hereditary haemoglobinopathy\Hereditary haemoglobinopathy due to globin chain mutation\Hereditary haemoglobin S\Sickling disorder due to haemoglobin S\Sickle cell-thalassaemia disease
\Disease\Congenital disease\Hereditary haemoglobinopathy\Thalassaemia\Thalassaemia with other haemoglobinopathy\Sickle cell-thalassaemia disease

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

Descriptions:

Id Description Lang Type Status Case? Module

3035990017 Sickle cell thalassaemia disease en Synonym Active Case insensitive SNOMED CT core

3036285019 Sickle cell thalassemia disease en Synonym Active Case insensitive SNOMED CT core

486462013 Sickle cell-thalassaemia disease en Synonym Active Case insensitive SNOMED CT core

486463015 Haemoglobin S-F disease en Synonym Active Initial character case insensitive SNOMED CT core

486464014 Thalassaemia-haemoglobin S disease en Synonym Active Initial character case insensitive SNOMED CT core

60878015 Hemoglobin S-F disease en Synonym Active Case sensitive SNOMED CT core

60879011 Thalassemia-hemoglobin S disease en Synonym Active Initial character case insensitive SNOMED CT core

60880014 Sickle cell-thalassemia disease en Synonym Active Case insensitive SNOMED CT core

60881013 Microdrepanocytic disease en Synonym Active Case insensitive SNOMED CT core

60882018 Microdrepanocytosis en Synonym Active Case insensitive SNOMED CT core

768228015 Sickle cell-thalassemia disease (disorder) en Fully specified name Active Case insensitive SNOMED CT core

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
Sickle cell-thalassaemia disease	Interprets	Measurement of total haemoglobin concentration	true	Inferred relationship	Some	3
Sickle cell-thalassaemia disease	Is a	Sickle cell-haemoglobin SS disease	false	Inferred relationship	Some
Sickle cell-thalassaemia disease	Is a	Thalassaemia with other haemoglobinopathy	true	Inferred relationship	Some
Sickle cell-thalassaemia disease	Finding site	Haematopoietic system structure	false	Inferred relationship	Some	1
Sickle cell-thalassaemia disease	Has definitional manifestation	Erythropenia	false	Inferred relationship	Some
Sickle cell-thalassaemia disease	Associated morphology	Drepanocyte	false	Inferred relationship	Some	1
Sickle cell-thalassaemia disease	Associated morphology	Drepanocyte	false	Inferred relationship	Some	2
Sickle cell-thalassaemia disease	Is a	Hereditary red blood cell disorder	false	Inferred relationship	Some
Sickle cell-thalassaemia disease	Is a	Disorder of haematopoietic structure	true	Inferred relationship	Some
Sickle cell-thalassaemia disease	Finding site	Erythroid cell	false	Inferred relationship	Some	2
Sickle cell-thalassaemia disease	Is a	Sickling disorder due to haemoglobin S	true	Inferred relationship	Some
Sickle cell-thalassaemia disease	Associated morphology	Drepanocyte	true	Inferred relationship	Some	1
Sickle cell-thalassaemia disease	Finding site	Haematopoietic system structure	true	Inferred relationship	Some	1
Sickle cell-thalassaemia disease	Has interpretation	Below reference range	false	Inferred relationship	Some	2
Sickle cell-thalassaemia disease	Has interpretation	Below reference range	true	Inferred relationship	Some	3
Sickle cell-thalassaemia disease	Interprets	Measurement of total haemoglobin concentration	false	Inferred relationship	Some	2
Sickle cell-thalassaemia disease	Interprets	Red blood cell count	false	Inferred relationship	Some	3
Sickle cell-thalassaemia disease	Occurrence	Congenital	true	Inferred relationship	Some	4
Sickle cell-thalassaemia disease	Finding site	Erythrocyte	true	Inferred relationship	Some	4
Sickle cell-thalassaemia disease	Associated morphology	Drepanocyte	false	Inferred relationship	Some	1
Sickle cell-thalassaemia disease	Finding site	Erythrocyte	false	Inferred relationship	Some
Sickle cell-thalassaemia disease	Causative agent	Haemoglobin S	false	Inferred relationship	Some
Sickle cell-thalassaemia disease	Finding site	Entire haematological system	false	Inferred relationship	Some	1
Sickle cell-thalassaemia disease	Finding site	Haematopoietic system structure	false	Inferred relationship	Some

Inbound Relationships	Type	Active	Source	Characteristic	Refinability	Group
Sickle cell-beta-thalassaemia	Is a	True	Sickle cell-thalassaemia disease	Inferred relationship	Some
Sickle cell-delta beta^0^-thalassaemia	Is a	False	Sickle cell-thalassaemia disease	Inferred relationship	Some
Sickle cell anaemia with coexistent alpha-thalassaemia	Is a	True	Sickle cell-thalassaemia disease	Inferred relationship	Some
Sickle cell trait with coexistent alpha-thalassaemia	Is a	False	Sickle cell-thalassaemia disease	Inferred relationship	Some
Sickle cell-thalassaemia disease with crisis	Is a	True	Sickle cell-thalassaemia disease	Inferred relationship	Some
Sickle cell-thalassaemia disease without crisis	Is a	True	Sickle cell-thalassaemia disease	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
3035990017	Sickle cell thalassaemia disease	en	Synonym	Active	Case insensitive	SNOMED CT core
3036285019	Sickle cell thalassemia disease	en	Synonym	Active	Case insensitive	SNOMED CT core
486462013	Sickle cell-thalassaemia disease	en	Synonym	Active	Case insensitive	SNOMED CT core
486463015	Haemoglobin S-F disease	en	Synonym	Active	Initial character case insensitive	SNOMED CT core
486464014	Thalassaemia-haemoglobin S disease	en	Synonym	Active	Initial character case insensitive	SNOMED CT core
60878015	Hemoglobin S-F disease	en	Synonym	Active	Case sensitive	SNOMED CT core
60879011	Thalassemia-hemoglobin S disease	en	Synonym	Active	Initial character case insensitive	SNOMED CT core
60880014	Sickle cell-thalassemia disease	en	Synonym	Active	Case insensitive	SNOMED CT core
60881013	Microdrepanocytic disease	en	Synonym	Active	Case insensitive	SNOMED CT core
60882018	Microdrepanocytosis	en	Synonym	Active	Case insensitive	SNOMED CT core
768228015	Sickle cell-thalassemia disease (disorder)	en	Fully specified name	Active	Case insensitive	SNOMED CT core