1148897000: Hemoglobin Paksé 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\Anemia due to disturbance of hemoglobin synthesis\Thalassemia\Alpha thalassemia\Hemoglobin Paksé disease
\Evaluation finding\Measurement finding\Measurement finding outside reference range\Measurement finding below reference range\Hemoglobin below reference range\Anemia due to disturbance of hemoglobin synthesis\Thalassemia\Alpha thalassemia\Hemoglobin Paksé disease
\Evaluation finding\Measurement finding\Measurement finding outside reference range\Hemoglobin level outside reference range\Hemoglobin below reference range\Anemia due to disturbance of hemoglobin synthesis\Thalassemia\Alpha thalassemia\Hemoglobin Paksé disease
\Evaluation finding\Hematopoietic system finding\Hematology test outside reference range\Hemoglobin level outside reference range\Hemoglobin below reference range\Anemia due to disturbance of hemoglobin synthesis\Thalassemia\Alpha thalassemia\Hemoglobin Paksé disease
\Evaluation finding\Hematopoietic system finding\Hemoglobin finding\Hemoglobin level outside reference range\Hemoglobin below reference range\Anemia due to disturbance of hemoglobin synthesis\Thalassemia\Alpha thalassemia\Hemoglobin Paksé 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\Thalassemia\Alpha thalassemia\Hemoglobin Paksé disease

\Anemia\Anemia due to disturbance of hemoglobin synthesis\Thalassemia\Alpha thalassemia\Hemoglobin Paksé disease

\Red blood cell disorder\Hereditary red blood cell disorder\Hereditary hemoglobinopathy\Thalassemia\Alpha thalassemia\Hemoglobin Paksé disease
\Red blood cell disorder\Hemoglobinopathy\Hereditary hemoglobinopathy\Thalassemia\Alpha thalassemia\Hemoglobin Paksé disease

\Disease\Genetic disease\Hereditary disease\Hereditary disorder by system\Hereditary disorder of cellular element of blood\Hereditary red blood cell disorder\Hereditary hemoglobinopathy\Thalassemia\Alpha thalassemia\Hemoglobin Paksé disease
\Disease\Disorder of cellular component of blood\Hereditary disorder of cellular element of blood\Hereditary red blood cell disorder\Hereditary hemoglobinopathy\Thalassemia\Alpha thalassemia\Hemoglobin Paksé disease
\Disease\Disorder of cellular component of blood\Anemia\Anemia due to disturbance of hemoglobin synthesis\Thalassemia\Alpha thalassemia\Hemoglobin Paksé disease
\Disease\Disorder of cellular component of blood\Red blood cell disorder\Hereditary red blood cell disorder\Hereditary hemoglobinopathy\Thalassemia\Alpha thalassemia\Hemoglobin Paksé disease
\Disease\Disorder of cellular component of blood\Red blood cell disorder\Hemoglobinopathy\Hereditary hemoglobinopathy\Thalassemia\Alpha thalassemia\Hemoglobin Paksé disease
\Disease\Disorder of body system\Hereditary disorder by system\Hereditary disorder of cellular element of blood\Hereditary red blood cell disorder\Hereditary hemoglobinopathy\Thalassemia\Alpha thalassemia\Hemoglobin Paksé disease
\Disease\Disorder of body system\Red blood cell disorder\Hereditary red blood cell disorder\Hereditary hemoglobinopathy\Thalassemia\Alpha thalassemia\Hemoglobin Paksé disease
\Disease\Disorder of body system\Red blood cell disorder\Hemoglobinopathy\Hereditary hemoglobinopathy\Thalassemia\Alpha thalassemia\Hemoglobin Paksé disease
\Disease\Congenital disease\Hereditary hemoglobinopathy\Thalassemia\Alpha thalassemia\Hemoglobin Paksé disease

Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Jul 2021. Module: SNOMED CT core module

Descriptions:

Id Description Lang Type Status Case? Module

4553855018 Haemoglobin Paksé disease en Synonym Active Only initial character case insensitive SNOMED CT core module

4553856017 Hemoglobin Paksé disease en Synonym Active Only initial character case insensitive SNOMED CT core module

4553857014 Hemoglobin Paksé disease (disorder) en Fully specified name Active Only initial character case insensitive SNOMED CT core module

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
Hemoglobin Paksé disease	Interprets	Measurement of total hemoglobin concentration	false	Inferred relationship	Existential restriction modifier	3
Hemoglobin Paksé disease	Occurrence	Congenital	true	Inferred relationship	Existential restriction modifier	2
Hemoglobin Paksé disease	Finding site	Erythrocyte	true	Inferred relationship	Existential restriction modifier	2
Hemoglobin Paksé disease	Interprets	Red blood cell count	false	Inferred relationship	Existential restriction modifier	1
Hemoglobin Paksé disease	Has interpretation	Below reference range	false	Inferred relationship	Existential restriction modifier	3
Hemoglobin Paksé disease	Has interpretation	Below reference range	true	Inferred relationship	Existential restriction modifier	1
Hemoglobin Paksé disease	Is a	Alpha thalassemia	true	Inferred relationship	Existential restriction modifier
Hemoglobin Paksé disease	Interprets	Measurement of total hemoglobin concentration	true	Inferred relationship	Existential restriction modifier	1

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
4553855018	Haemoglobin Paksé disease	en	Synonym	Active	Only initial character case insensitive	SNOMED CT core module
4553856017	Hemoglobin Paksé disease	en	Synonym	Active	Only initial character case insensitive	SNOMED CT core module
4553857014	Hemoglobin Paksé disease (disorder)	en	Fully specified name	Active	Only initial character case insensitive	SNOMED CT core module