417048006: Sickle cell-thalassemia disease without crisis (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\Sickle cell-thalassaemia disease without crisis
\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\Sickle cell-thalassaemia disease without crisis
\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\Sickle cell-thalassaemia disease without crisis
\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\Sickle cell-thalassaemia disease without crisis
\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\Sickle cell-thalassaemia disease without crisis

\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\Sickle cell-thalassaemia disease without crisis

\Thalassaemia\Thalassaemia with other haemoglobinopathy\Sickle cell-thalassaemia disease\Sickle cell-thalassaemia disease without crisis

\Anaemia\Anaemia due to disturbance of haemoglobin synthesis\Thalassaemia\Thalassaemia with other haemoglobinopathy\Sickle cell-thalassaemia disease\Sickle cell-thalassaemia disease without crisis

\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\Sickle cell-thalassaemia disease without crisis
\Red blood cell disorder\Hereditary red blood cell disorder\Hereditary haemoglobinopathy\Thalassaemia\Thalassaemia with other haemoglobinopathy\Sickle cell-thalassaemia disease\Sickle cell-thalassaemia disease without crisis
\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\Sickle cell-thalassaemia disease without crisis
\Red blood cell disorder\Haemoglobinopathy\Hereditary haemoglobinopathy\Thalassaemia\Thalassaemia with other haemoglobinopathy\Sickle cell-thalassaemia disease\Sickle cell-thalassaemia disease without crisis

\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\Sickle cell-thalassaemia disease without crisis
\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\Sickle cell-thalassaemia disease without crisis
\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\Sickle cell-thalassaemia disease without crisis
\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\Sickle cell-thalassaemia disease without crisis
\Disease\Blood disease\Anaemia\Anaemia due to disturbance of haemoglobin synthesis\Thalassaemia\Thalassaemia with other haemoglobinopathy\Sickle cell-thalassaemia disease\Sickle cell-thalassaemia disease without crisis
\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\Sickle cell-thalassaemia disease without crisis
\Disease\Blood disease\Red blood cell disorder\Hereditary red blood cell disorder\Hereditary haemoglobinopathy\Thalassaemia\Thalassaemia with other haemoglobinopathy\Sickle cell-thalassaemia disease\Sickle cell-thalassaemia disease without crisis
\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\Sickle cell-thalassaemia disease without crisis
\Disease\Blood disease\Red blood cell disorder\Haemoglobinopathy\Hereditary haemoglobinopathy\Thalassaemia\Thalassaemia with other haemoglobinopathy\Sickle cell-thalassaemia disease\Sickle cell-thalassaemia disease without crisis
\Disease\Disorder of body system\Disorder of haematopoietic structure\Sickle cell-thalassaemia disease\Sickle cell-thalassaemia disease without crisis
\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\Sickle cell-thalassaemia disease without crisis
\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\Sickle cell-thalassaemia disease without crisis
\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\Sickle cell-thalassaemia disease without crisis
\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\Sickle cell-thalassaemia disease without crisis
\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\Sickle cell-thalassaemia disease without crisis
\Disease\Disorder of body system\Red blood cell disorder\Haemoglobinopathy\Hereditary haemoglobinopathy\Thalassaemia\Thalassaemia with other haemoglobinopathy\Sickle cell-thalassaemia disease\Sickle cell-thalassaemia disease without crisis
\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\Sickle cell-thalassaemia disease without crisis
\Disease\Congenital disease\Hereditary haemoglobinopathy\Thalassaemia\Thalassaemia with other haemoglobinopathy\Sickle cell-thalassaemia disease\Sickle cell-thalassaemia disease without crisis

Status: current, Primitive. Date: 31-Jul 2005. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module

2547258013 Sickle cell-thalassemia disease without crisis (disorder) en Fully specified name Active Case insensitive SNOMED CT core

2549593012 Sickle cell-thalassemia disease without crisis en Synonym Active Case insensitive SNOMED CT core

2549594018 Sickle cell-thalassaemia disease without crisis en Synonym Active Case insensitive SNOMED CT core

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
Sickle cell-thalassaemia disease without crisis	Is a	Sickle cell-thalassaemia disease	true	Inferred relationship	Some
Sickle cell-thalassaemia disease without crisis	Finding site	Haematopoietic system structure	false	Inferred relationship	Some	1
Sickle cell-thalassaemia disease without crisis	Has definitional manifestation	Erythropenia	false	Inferred relationship	Some
Sickle cell-thalassaemia disease without crisis	Associated morphology	Drepanocyte	false	Inferred relationship	Some	1
Sickle cell-thalassaemia disease without crisis	Associated morphology	Drepanocyte	true	Inferred relationship	Some	1
Sickle cell-thalassaemia disease without crisis	Finding site	Haematopoietic system structure	true	Inferred relationship	Some	1
Sickle cell-thalassaemia disease without crisis	Finding site	Erythrocyte	false	Inferred relationship	Some
Sickle cell-thalassaemia disease without crisis	Has interpretation	Below reference range	true	Inferred relationship	Some	2
Sickle cell-thalassaemia disease without crisis	Has interpretation	Below reference range	false	Inferred relationship	Some	3
Sickle cell-thalassaemia disease without crisis	Interprets	Measurement of total haemoglobin concentration	true	Inferred relationship	Some	2
Sickle cell-thalassaemia disease without crisis	Interprets	Red blood cell count	false	Inferred relationship	Some	3
Sickle cell-thalassaemia disease without crisis	Occurrence	Congenital	true	Inferred relationship	Some	4
Sickle cell-thalassaemia disease without crisis	Finding site	Erythrocyte	true	Inferred relationship	Some	4

Inbound Relationships

Type

Active

Source

Characteristic

Refinability

Group

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
2547258013	Sickle cell-thalassemia disease without crisis (disorder)	en	Fully specified name	Active	Case insensitive	SNOMED CT core
2549593012	Sickle cell-thalassemia disease without crisis	en	Synonym	Active	Case insensitive	SNOMED CT core
2549594018	Sickle cell-thalassaemia disease without crisis	en	Synonym	Active	Case insensitive	SNOMED CT core