234383000: Homozygous alpha thalassemia (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\Alpha thalassaemia\Homozygous alpha thalassaemia
\Evaluation finding\Measurement finding\Measurement finding outside reference range\Measurement finding below reference range\Haemoglobin low\Anaemia due to disturbance of haemoglobin synthesis\Thalassaemia\Alpha thalassaemia\Homozygous alpha thalassaemia
\Evaluation finding\Measurement finding\Measurement finding outside reference range\Haemoglobin level outside reference range\Haemoglobin low\Anaemia due to disturbance of haemoglobin synthesis\Thalassaemia\Alpha thalassaemia\Homozygous alpha thalassaemia
\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\Alpha thalassaemia\Homozygous alpha thalassaemia
\Evaluation finding\Haematopoietic system finding\Haemoglobin finding\Haemoglobin level outside reference range\Haemoglobin low\Anaemia due to disturbance of haemoglobin synthesis\Thalassaemia\Alpha thalassaemia\Homozygous alpha thalassaemia

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

\Hereditary disorder of cellular element of blood\Hereditary red blood cell disorder\Hereditary haemoglobinopathy\Thalassaemia\Alpha thalassaemia\Homozygous alpha thalassaemia

\Anaemia\Anaemia due to disturbance of haemoglobin synthesis\Thalassaemia\Alpha thalassaemia\Homozygous alpha thalassaemia

\Red blood cell disorder\Hereditary red blood cell disorder\Hereditary haemoglobinopathy\Thalassaemia\Alpha thalassaemia\Homozygous alpha thalassaemia
\Red blood cell disorder\Haemoglobinopathy\Hereditary haemoglobinopathy\Thalassaemia\Alpha thalassaemia\Homozygous alpha thalassaemia

\Disease\Genetic disease\Hereditary disease\Hereditary disorder by system\Hereditary disorder of cellular element of blood\Hereditary red blood cell disorder\Hereditary haemoglobinopathy\Thalassaemia\Alpha thalassaemia\Homozygous alpha thalassaemia
\Disease\Blood disease\Hereditary disorder of cellular element of blood\Hereditary red blood cell disorder\Hereditary haemoglobinopathy\Thalassaemia\Alpha thalassaemia\Homozygous alpha thalassaemia
\Disease\Blood disease\Anaemia\Anaemia due to disturbance of haemoglobin synthesis\Thalassaemia\Alpha thalassaemia\Homozygous alpha thalassaemia
\Disease\Blood disease\Red blood cell disorder\Hereditary red blood cell disorder\Hereditary haemoglobinopathy\Thalassaemia\Alpha thalassaemia\Homozygous alpha thalassaemia
\Disease\Blood disease\Red blood cell disorder\Haemoglobinopathy\Hereditary haemoglobinopathy\Thalassaemia\Alpha thalassaemia\Homozygous alpha thalassaemia
\Disease\Disorder of body system\Hereditary disorder by system\Hereditary disorder of cellular element of blood\Hereditary red blood cell disorder\Hereditary haemoglobinopathy\Thalassaemia\Alpha thalassaemia\Homozygous alpha thalassaemia
\Disease\Disorder of body system\Red blood cell disorder\Hereditary red blood cell disorder\Hereditary haemoglobinopathy\Thalassaemia\Alpha thalassaemia\Homozygous alpha thalassaemia
\Disease\Disorder of body system\Red blood cell disorder\Haemoglobinopathy\Hereditary haemoglobinopathy\Thalassaemia\Alpha thalassaemia\Homozygous alpha thalassaemia
\Disease\Congenital disease\Hereditary haemoglobinopathy\Thalassaemia\Alpha thalassaemia\Homozygous alpha thalassaemia

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

Descriptions:

Id Description Lang Type Status Case? Module

351149014 Homozygous alpha thalassemia en Synonym Active Case insensitive SNOMED CT core

351150014 Homozygous alpha thalassaemia en Synonym Active Case insensitive SNOMED CT core

622694013 Homozygous alpha thalassemia (disorder) en Fully specified name Active Case insensitive SNOMED CT core

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
Homozygous alpha thalassaemia	Interprets	Measurement of total haemoglobin concentration	true	Inferred relationship	Some	2
Homozygous alpha thalassaemia	Has definitional manifestation	Erythropenia	false	Inferred relationship	Some
Homozygous alpha thalassaemia	Finding site	Haematopoietic system structure	false	Inferred relationship	Some
Homozygous alpha thalassaemia	Finding site	Body system structure	false	Inferred relationship	Some
Homozygous alpha thalassaemia	Is a	Alpha thalassaemia	true	Inferred relationship	Some
Homozygous alpha thalassaemia	Has interpretation	Below reference range	false	Inferred relationship	Some	1
Homozygous alpha thalassaemia	Interprets	Measurement of total haemoglobin concentration	false	Inferred relationship	Some	1
Homozygous alpha thalassaemia	Has interpretation	Below reference range	true	Inferred relationship	Some	2
Homozygous alpha thalassaemia	Interprets	Red blood cell count	false	Inferred relationship	Some	2
Homozygous alpha thalassaemia	Occurrence	Congenital	true	Inferred relationship	Some	3
Homozygous alpha thalassaemia	Finding site	Erythrocyte	true	Inferred relationship	Some	3
Homozygous alpha thalassaemia	Finding site	Erythrocyte	false	Inferred relationship	Some
Homozygous alpha thalassaemia	Finding site	Haematopoietic system structure	false	Inferred relationship	Some

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
351149014	Homozygous alpha thalassemia	en	Synonym	Active	Case insensitive	SNOMED CT core
351150014	Homozygous alpha thalassaemia	en	Synonym	Active	Case insensitive	SNOMED CT core
622694013	Homozygous alpha thalassemia (disorder)	en	Fully specified name	Active	Case insensitive	SNOMED CT core