18273004: Unstable hemoglobin 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\Congenital anaemia\Unstable haemoglobin disease
\Evaluation finding\Measurement finding\Measurement finding outside reference range\Abnormal blood cell count\Red blood cell count outside reference range\RBC count low\Congenital anaemia\Unstable haemoglobin disease
\Evaluation finding\Measurement finding\Measurement finding outside reference range\Abnormal blood cell count\Cytopenia\RBC count low\Congenital anaemia\Unstable haemoglobin disease
\Evaluation finding\Measurement finding\Measurement finding outside reference range\Measurement finding below reference range\Haemoglobin low\Congenital anaemia\Unstable haemoglobin disease
\Evaluation finding\Measurement finding\Measurement finding outside reference range\Measurement finding below reference range\Cytopenia\RBC count low\Congenital anaemia\Unstable haemoglobin disease
\Evaluation finding\Measurement finding\Measurement finding outside reference range\Haemoglobin level outside reference range\Haemoglobin low\Congenital anaemia\Unstable haemoglobin disease
\Evaluation finding\Measurement finding\Red blood cell count - finding\Red blood cell count outside reference range\RBC count low\Congenital anaemia\Unstable haemoglobin disease
\Evaluation finding\Haematopoietic system finding\Haematology test outside reference range\Haemoglobin level outside reference range\Haemoglobin low\Congenital anaemia\Unstable haemoglobin disease
\Evaluation finding\Haematopoietic system finding\Haemoglobin finding\Haemoglobin level outside reference range\Haemoglobin low\Congenital anaemia\Unstable haemoglobin 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\Unstable haemoglobin disease

\Anaemia\Congenital anaemia\Unstable haemoglobin disease

\Red blood cell disorder\Hereditary red blood cell disorder\Hereditary haemoglobinopathy\Hereditary haemoglobinopathy due to globin chain mutation\Unstable haemoglobin disease
\Red blood cell disorder\Haemoglobinopathy\Hereditary haemoglobinopathy\Hereditary haemoglobinopathy due to globin chain mutation\Unstable haemoglobin 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\Unstable haemoglobin 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\Unstable haemoglobin disease
\Disease\Blood disease\Anaemia\Congenital anaemia\Unstable haemoglobin disease
\Disease\Blood disease\Red blood cell disorder\Hereditary red blood cell disorder\Hereditary haemoglobinopathy\Hereditary haemoglobinopathy due to globin chain mutation\Unstable haemoglobin disease
\Disease\Blood disease\Red blood cell disorder\Haemoglobinopathy\Hereditary haemoglobinopathy\Hereditary haemoglobinopathy due to globin chain mutation\Unstable haemoglobin 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\Unstable haemoglobin disease
\Disease\Disorder of body system\Red blood cell disorder\Hereditary red blood cell disorder\Hereditary haemoglobinopathy\Hereditary haemoglobinopathy due to globin chain mutation\Unstable haemoglobin disease
\Disease\Disorder of body system\Red blood cell disorder\Haemoglobinopathy\Hereditary haemoglobinopathy\Hereditary haemoglobinopathy due to globin chain mutation\Unstable haemoglobin disease
\Disease\Congenital disease\Hereditary haemoglobinopathy\Hereditary haemoglobinopathy due to globin chain mutation\Unstable haemoglobin disease
\Disease\Congenital disease\Congenital anaemia\Unstable haemoglobin disease

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

Descriptions:

Id Description Lang Type Status Case? Module

30860015 Unstable hemoglobin disease en Synonym Active Case insensitive SNOMED CT core
30861016 Unstable hemoglobin disease, NOS en Synonym Inactive Initial character case insensitive SNOMED CT core
30862011 Congenital Heinz body anemia en Synonym Active Initial character case insensitive SNOMED CT core
478536016 Congenital Heinz body anaemia en Synonym Active Initial character case insensitive SNOMED CT core
478537013 Unstable haemoglobin disease en Synonym Active Case insensitive SNOMED CT core
478538015 CHBHA - Congenital Heinz body hemolytic anemia en Synonym Active Case sensitive SNOMED CT core
478539011 Congenital Heinz body hemolytic anemia en Synonym Active Initial character case insensitive SNOMED CT core
478540013 CHBHA - Congenital Heinz body haemolytic anaemia en Synonym Active Case sensitive SNOMED CT core
478541012 Congenital Heinz body haemolytic anaemia en Synonym Active Initial character case insensitive SNOMED CT core
745671014 Unstable hemoglobin disease (disorder) en Fully specified name Active Case insensitive SNOMED CT core

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
Unstable haemoglobin disease	Is a	Hereditary haemoglobinopathy due to globin chain mutation	true	Inferred relationship	Some
Unstable haemoglobin disease	Is a	Congenital anaemia	true	Inferred relationship	Some
Unstable haemoglobin disease	Has definitional manifestation	Erythropenia	false	Inferred relationship	Some
Unstable haemoglobin disease	Finding site	Haematopoietic system structure	false	Inferred relationship	Some
Unstable haemoglobin disease	Finding site	Body system structure	false	Inferred relationship	Some
Unstable haemoglobin disease	Is a	Anaemia	false	Inferred relationship	Some
Unstable haemoglobin disease	Occurrence	Congenital	true	Inferred relationship	Some	1
Unstable haemoglobin disease	Finding site	Erythrocyte	true	Inferred relationship	Some	1
Unstable haemoglobin disease	Occurrence	Congenital	false	Inferred relationship	Some
Unstable haemoglobin disease	Finding site	Erythrocyte	false	Inferred relationship	Some
Unstable haemoglobin disease	Finding site	Haematopoietic system structure	false	Inferred relationship	Some
Unstable haemoglobin disease	Has interpretation	Below reference range	true	Inferred relationship	Some	3
Unstable haemoglobin disease	Has interpretation	Below reference range	true	Inferred relationship	Some	2
Unstable haemoglobin disease	Interprets	Red blood cell count	true	Inferred relationship	Some	2
Unstable haemoglobin disease	Interprets	Measurement of total haemoglobin concentration	true	Inferred relationship	Some	3

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
30860015	Unstable hemoglobin disease	en	Synonym	Active	Case insensitive	SNOMED CT core
30861016	Unstable hemoglobin disease, NOS	en	Synonym	Inactive	Initial character case insensitive	SNOMED CT core
30862011	Congenital Heinz body anemia	en	Synonym	Active	Initial character case insensitive	SNOMED CT core
478536016	Congenital Heinz body anaemia	en	Synonym	Active	Initial character case insensitive	SNOMED CT core
478537013	Unstable haemoglobin disease	en	Synonym	Active	Case insensitive	SNOMED CT core
478538015	CHBHA - Congenital Heinz body hemolytic anemia	en	Synonym	Active	Case sensitive	SNOMED CT core
478539011	Congenital Heinz body hemolytic anemia	en	Synonym	Active	Initial character case insensitive	SNOMED CT core
478540013	CHBHA - Congenital Heinz body haemolytic anaemia	en	Synonym	Active	Case sensitive	SNOMED CT core
478541012	Congenital Heinz body haemolytic anaemia	en	Synonym	Active	Initial character case insensitive	SNOMED CT core
745671014	Unstable hemoglobin disease (disorder)	en	Fully specified name	Active	Case insensitive	SNOMED CT core