48553001: Hemoglobin H 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\Alpha thalassaemia\Haemoglobin H 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\Alpha thalassaemia\Haemoglobin H 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\Alpha thalassaemia\Haemoglobin H 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\Alpha thalassaemia\Haemoglobin H disease
\Evaluation finding\Haematopoietic system finding\Haemoglobin finding\Haemoglobin level outside reference range\Haemoglobin low\Anaemia due to disturbance of haemoglobin synthesis\Thalassaemia\Alpha thalassaemia\Haemoglobin H disease

\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\Haemoglobin H disease

\Anaemia\Anaemia due to disturbance of haemoglobin synthesis\Thalassaemia\Alpha thalassaemia\Haemoglobin H disease

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

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

Descriptions:

Id Description Lang Type Status Case? Module

495133013 Haemoglobin H disease en Synonym Active Case sensitive SNOMED CT core

786134018 Hemoglobin H disease (disorder) en Fully specified name Active Case sensitive SNOMED CT core

80911013 Hemoglobin H disease en Synonym Active Case sensitive SNOMED CT core

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
Haemoglobin H disease	Interprets	Measurement of total haemoglobin concentration	true	Inferred relationship	Some	2
Haemoglobin H disease	Finding site	Haematopoietic system structure	false	Inferred relationship	Some
Haemoglobin H disease	Has definitional manifestation	Erythropenia	false	Inferred relationship	Some
Haemoglobin H disease	Is a	Alpha thalassaemia	true	Inferred relationship	Some
Haemoglobin H disease	Finding site	Body system structure	false	Inferred relationship	Some
Haemoglobin H disease	Has interpretation	Below reference range	false	Inferred relationship	Some	1
Haemoglobin H disease	Interprets	Measurement of total haemoglobin concentration	false	Inferred relationship	Some	1
Haemoglobin H disease	Has interpretation	Below reference range	true	Inferred relationship	Some	2
Haemoglobin H disease	Interprets	Red blood cell count	false	Inferred relationship	Some	2
Haemoglobin H disease	Occurrence	Congenital	true	Inferred relationship	Some	3
Haemoglobin H disease	Finding site	Erythrocyte	true	Inferred relationship	Some	3
Haemoglobin H disease	Finding site	Haematopoietic system structure	false	Inferred relationship	Some
Haemoglobin H disease	Finding site	Erythrocyte	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
495133013	Haemoglobin H disease	en	Synonym	Active	Case sensitive	SNOMED CT core
786134018	Hemoglobin H disease (disorder)	en	Fully specified name	Active	Case sensitive	SNOMED CT core
80911013	Hemoglobin H disease	en	Synonym	Active	Case sensitive	SNOMED CT core