47047009: Thalassemia with other hemoglobinopathy (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
\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
\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
\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
\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

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

\Hereditary disorder of cellular element of blood\Hereditary red blood cell disorder\Hereditary haemoglobinopathy\Thalassaemia\Thalassaemia with other haemoglobinopathy

\Anaemia\Anaemia due to disturbance of haemoglobin synthesis\Thalassaemia\Thalassaemia with other haemoglobinopathy

\Red blood cell disorder\Hereditary red blood cell disorder\Hereditary haemoglobinopathy\Thalassaemia\Thalassaemia with other haemoglobinopathy
\Red blood cell disorder\Haemoglobinopathy\Hereditary haemoglobinopathy\Thalassaemia\Thalassaemia with other haemoglobinopathy

\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
\Disease\Blood disease\Hereditary disorder of cellular element of blood\Hereditary red blood cell disorder\Hereditary haemoglobinopathy\Thalassaemia\Thalassaemia with other haemoglobinopathy
\Disease\Blood disease\Anaemia\Anaemia due to disturbance of haemoglobin synthesis\Thalassaemia\Thalassaemia with other haemoglobinopathy
\Disease\Blood disease\Red blood cell disorder\Hereditary red blood cell disorder\Hereditary haemoglobinopathy\Thalassaemia\Thalassaemia with other haemoglobinopathy
\Disease\Blood disease\Red blood cell disorder\Haemoglobinopathy\Hereditary haemoglobinopathy\Thalassaemia\Thalassaemia with other haemoglobinopathy
\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
\Disease\Disorder of body system\Red blood cell disorder\Hereditary red blood cell disorder\Hereditary haemoglobinopathy\Thalassaemia\Thalassaemia with other haemoglobinopathy
\Disease\Disorder of body system\Red blood cell disorder\Haemoglobinopathy\Hereditary haemoglobinopathy\Thalassaemia\Thalassaemia with other haemoglobinopathy
\Disease\Congenital disease\Hereditary haemoglobinopathy\Thalassaemia\Thalassaemia with other haemoglobinopathy

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

Descriptions:

Id Description Lang Type Status Case? Module

494734018 Thalassaemia with other haemoglobinopathy en Synonym Active Case insensitive SNOMED CT core
78417011 Thalassemia with other hemoglobinopathy en Synonym Active Case insensitive SNOMED CT core
78418018 Thalassemia with other hemoglobinopathy, NOS en Synonym Inactive Initial character case insensitive SNOMED CT core
784462017 Thalassemia with other hemoglobinopathy (disorder) en Fully specified name Active Case insensitive SNOMED CT core

Expanded Value Set

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

Inbound Relationships	Type	Active	Source	Characteristic	Refinability	Group
Sickle cell-thalassaemia disease	Is a	True	Thalassaemia with other haemoglobinopathy	Inferred relationship	Some
Thalassaemia-haemoglobin C disease	Is a	True	Thalassaemia with other haemoglobinopathy	Inferred relationship	Some

Reference Sets

Australian emergency department reference set

Clinical finding foundation reference set

Australian dialect reference set

Problem/Diagnosis reference set

Back to Start

Id	Description	Lang	Type	Status	Case?	Module
494734018	Thalassaemia with other haemoglobinopathy	en	Synonym	Active	Case insensitive	SNOMED CT core
78417011	Thalassemia with other hemoglobinopathy	en	Synonym	Active	Case insensitive	SNOMED CT core
78418018	Thalassemia with other hemoglobinopathy, NOS	en	Synonym	Inactive	Initial character case insensitive	SNOMED CT core
784462017	Thalassemia with other hemoglobinopathy (disorder)	en	Fully specified name	Active	Case insensitive	SNOMED CT core