18273004: Unstable hemoglobin disease (disorder)

SNOMED CT Concept\Clinical finding\...

\Evaluation finding\Measurement finding\Finding of substance level\Finding of protein level\Hemoglobin finding\Hemoglobin level outside reference range\Hemoglobin below reference range\Congenital anemia\Unstable hemoglobin disease
\Evaluation finding\Measurement finding\Measurement finding outside reference range\Blood cell count outside reference range\Red blood cell count outside reference range\Red blood cell count below reference range\Congenital anemia\Unstable hemoglobin disease
\Evaluation finding\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
\Evaluation finding\Measurement finding\Measurement finding outside reference range\Measurement finding below reference range\Hemoglobin below reference range\Congenital anemia\Unstable hemoglobin disease
\Evaluation finding\Measurement finding\Measurement finding outside reference range\Measurement finding below reference range\Cytopenia\Red blood cell count below reference range\Congenital anemia\Unstable hemoglobin disease
\Evaluation finding\Measurement finding\Measurement finding outside reference range\Hemoglobin level outside reference range\Hemoglobin below reference range\Congenital anemia\Unstable hemoglobin disease
\Evaluation finding\Measurement finding\Finding of red blood cell count\Red blood cell count outside reference range\Red blood cell count below reference range\Congenital anemia\Unstable hemoglobin disease
\Evaluation finding\Hematopoietic system finding\Hematology test outside reference range\Hemoglobin level outside reference range\Hemoglobin below reference range\Congenital anemia\Unstable hemoglobin disease
\Evaluation finding\Hematopoietic system finding\Hemoglobin finding\Hemoglobin level outside reference range\Hemoglobin below reference range\Congenital anemia\Unstable hemoglobin disease

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

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

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

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

Descriptions:

Id Description Lang Type Status Case? Module

30860015 Unstable hemoglobin disease en Synonym Active Entire term case insensitive SNOMED CT core module

30862011 Congenital Heinz body anemia en Synonym Active Only initial character case insensitive SNOMED CT core module

478536016 Congenital Heinz body anaemia en Synonym Active Only initial character case insensitive SNOMED CT core module

478537013 Unstable haemoglobin disease en Synonym Active Entire term case insensitive SNOMED CT core module

478538015 CHBHA - Congenital Heinz body hemolytic anemia en Synonym Active Entire term case sensitive SNOMED CT core module

478539011 Congenital Heinz body hemolytic anemia en Synonym Active Only initial character case insensitive SNOMED CT core module

478540013 CHBHA - Congenital Heinz body haemolytic anaemia en Synonym Active Entire term case sensitive SNOMED CT core module

478541012 Congenital Heinz body haemolytic anaemia en Synonym Active Only initial character case insensitive SNOMED CT core module

745671014 Unstable hemoglobin disease (disorder) en Fully specified name Active Entire term case insensitive SNOMED CT core module

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	Existential restriction modifier
Unstable hemoglobin disease	Is a	Congenital anemia	true	Inferred relationship	Existential restriction modifier
Unstable hemoglobin disease	Occurrence	Congenital	false	Inferred relationship	Existential restriction modifier
Unstable hemoglobin disease	Finding site	Erythrocyte	false	Inferred relationship	Existential restriction modifier
Unstable hemoglobin disease	Finding site	Hematopoietic system structure	false	Inferred relationship	Existential restriction modifier
Unstable hemoglobin disease	Has definitional manifestation	Erythropenia	false	Inferred relationship	Existential restriction modifier
Unstable hemoglobin disease	Finding site	Hematopoietic system structure	false	Inferred relationship	Existential restriction modifier
Unstable hemoglobin disease	Finding site	Body system structure	false	Inferred relationship	Existential restriction modifier
Unstable hemoglobin disease	Is a	Anemia	false	Inferred relationship	Existential restriction modifier
Unstable hemoglobin disease	Occurrence	Congenital	true	Inferred relationship	Existential restriction modifier	1
Unstable hemoglobin disease	Finding site	Erythrocyte	true	Inferred relationship	Existential restriction modifier	1
Unstable hemoglobin disease	Has interpretation	Below reference range	true	Inferred relationship	Existential restriction modifier	3
Unstable hemoglobin disease	Has interpretation	Below reference range	true	Inferred relationship	Existential restriction modifier	2
Unstable hemoglobin disease	Interprets	Red blood cell count	true	Inferred relationship	Existential restriction modifier	2
Unstable hemoglobin disease	Interprets	Measurement of total hemoglobin concentration	true	Inferred relationship	Existential restriction modifier	3

Inbound Relationships

Type

Active

Source

Characteristic

Refinability

Group

This concept is not in any reference sets

Back to Start

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