18273004: Unstable hemoglobin disease (disorder)

SNOMED CT Concept\Clinical finding (finding)\...

\Finding of blood, lymphatics and immune system\Disorder of cellular component of blood (disorder)\...

\Hereditary disorder of cellular element of blood (disorder)\Hereditary red blood cell disorder (disorder)\Hereditary hemoglobinopathy (disorder)\Hereditary hemoglobinopathy due to globin chain mutation\Unstable hemoglobin disease

\Anemia\Congenital anemia\Unstable hemoglobin disease

\Red blood cell disorder\Hereditary red blood cell disorder (disorder)\Hereditary hemoglobinopathy (disorder)\Hereditary hemoglobinopathy due to globin chain mutation\Unstable hemoglobin disease
\Red blood cell disorder\Hemoglobinopathy\Hereditary hemoglobinopathy (disorder)\Hereditary hemoglobinopathy due to globin chain mutation\Unstable hemoglobin disease

\Procedure related finding\Evaluation finding\...

\Measurement finding\Finding of substance level (finding)\Protein level - finding\Hemoglobin finding\Hemoglobin level outside reference range (finding)\Hemoglobin below reference range (finding)\Congenital anemia\Unstable hemoglobin disease
\Measurement finding\Measurement finding outside reference range\Blood cell count outside reference range\Red blood cell count outside reference range (finding)\Red blood cell count below reference range\Congenital anemia\Unstable hemoglobin disease
\Measurement finding\Measurement finding outside reference range\Blood cell count outside reference range\Cytopenia\Red blood cell count below reference range\Congenital anemia\Unstable hemoglobin disease
\Measurement finding\Measurement finding outside reference range\Measurement finding below reference range (finding)\Hemoglobin below reference range (finding)\Congenital anemia\Unstable hemoglobin disease
\Measurement finding\Measurement finding outside reference range\Measurement finding below reference range (finding)\Cytopenia\Red blood cell count below reference range\Congenital anemia\Unstable hemoglobin disease
\Measurement finding\Measurement finding outside reference range\Hemoglobin level outside reference range (finding)\Hemoglobin below reference range (finding)\Congenital anemia\Unstable hemoglobin disease
\Measurement finding\Red blood cell count - finding\Red blood cell count outside reference range (finding)\Red blood cell count below reference range\Congenital anemia\Unstable hemoglobin disease

\Hematopoietic system finding\Haematology test outside reference range\Hemoglobin level outside reference range (finding)\Hemoglobin below reference range (finding)\Congenital anemia\Unstable hemoglobin disease
\Hematopoietic system finding\Hemoglobin finding\Hemoglobin level outside reference range (finding)\Hemoglobin below reference range (finding)\Congenital anemia\Unstable hemoglobin disease

\Disease\Genetic disease\Hereditary disease\Hereditary disorder by system\Hereditary disorder of cellular element of blood (disorder)\Hereditary red blood cell disorder (disorder)\Hereditary hemoglobinopathy (disorder)\Hereditary hemoglobinopathy due to globin chain mutation\Unstable hemoglobin disease
\Disease\Disorder of foetus and/or newborn\Congenital disease (disorder)\Hereditary hemoglobinopathy (disorder)\Hereditary hemoglobinopathy due to globin chain mutation\Unstable hemoglobin disease
\Disease\Disorder of foetus and/or newborn\Congenital disease (disorder)\Congenital anemia\Unstable hemoglobin disease
\Disease\Disorder of cellular component of blood (disorder)\Hereditary disorder of cellular element of blood (disorder)\Hereditary red blood cell disorder (disorder)\Hereditary hemoglobinopathy (disorder)\Hereditary hemoglobinopathy due to globin chain mutation\Unstable hemoglobin disease
\Disease\Disorder of cellular component of blood (disorder)\Anemia\Congenital anemia\Unstable hemoglobin disease
\Disease\Disorder of cellular component of blood (disorder)\Red blood cell disorder\Hereditary red blood cell disorder (disorder)\Hereditary hemoglobinopathy (disorder)\Hereditary hemoglobinopathy due to globin chain mutation\Unstable hemoglobin disease
\Disease\Disorder of cellular component of blood (disorder)\Red blood cell disorder\Hemoglobinopathy\Hereditary hemoglobinopathy (disorder)\Hereditary hemoglobinopathy due to globin chain mutation\Unstable hemoglobin disease
\Disease\Disorder of body system\Hereditary disorder by system\Hereditary disorder of cellular element of blood (disorder)\Hereditary red blood cell disorder (disorder)\Hereditary hemoglobinopathy (disorder)\Hereditary hemoglobinopathy due to globin chain mutation\Unstable hemoglobin disease
\Disease\Disorder of body system\Red blood cell disorder\Hereditary red blood cell disorder (disorder)\Hereditary hemoglobinopathy (disorder)\Hereditary hemoglobinopathy due to globin chain mutation\Unstable hemoglobin disease
\Disease\Disorder of body system\Red blood cell disorder\Hemoglobinopathy\Hereditary hemoglobinopathy (disorder)\Hereditary hemoglobinopathy due to globin chain mutation\Unstable hemoglobin disease

Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2002. Module: SNOMED CT core

Descriptions:

Expanded Value Set

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

Inbound Relationships

Type

Active

Source

Characteristic

Refinability

Group

This concept is not in any reference sets

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Id	Description	Lang	Type	Status	Case?	Module
30860015	Unstable hemoglobin disease	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
30862011	Congenital Heinz body anemia	en	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
478536016	Congenital Heinz body anaemia	en	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
478537013	Unstable haemoglobin disease	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
478538015	CHBHA - Congenital Heinz body hemolytic anemia	en	Synonym (core metadata concept)	Active	Entire term case sensitive (core metadata concept)	SNOMED CT core
478539011	Congenital Heinz body hemolytic anemia	en	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
478540013	CHBHA - Congenital Heinz body haemolytic anaemia	en	Synonym (core metadata concept)	Active	Entire term case sensitive (core metadata concept)	SNOMED CT core
478541012	Congenital Heinz body haemolytic anaemia	en	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
745671014	Unstable hemoglobin disease (disorder)	en	Fully specified name	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core