234383000: Homozygous alpha thalassemia (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\Homozygous alpha thalassemia
\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\Homozygous alpha thalassemia
\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\Homozygous alpha thalassemia
\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\Homozygous alpha thalassemia
\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\Homozygous alpha thalassemia

\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\Homozygous alpha thalassemia

\Anemia\Anemia due to disturbance of hemoglobin synthesis\Thalassemia\Alpha thalassemia\Homozygous alpha thalassemia

\Red blood cell disorder\Hereditary red blood cell disorder\Hereditary hemoglobinopathy\Thalassemia\Alpha thalassemia\Homozygous alpha thalassemia
\Red blood cell disorder\Hemoglobinopathy\Hereditary hemoglobinopathy\Thalassemia\Alpha thalassemia\Homozygous alpha thalassemia

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

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

351149014 Homozygous alpha thalassemia en Synonym Active Entire term case insensitive SNOMED CT core module

351150014 Homozygous alpha thalassaemia en Synonym Active Entire term case insensitive SNOMED CT core module

622694013 Homozygous alpha thalassemia (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
Homozygous alpha thalassemia	Is a	Alpha thalassemia	true	Inferred relationship	Existential restriction modifier
Homozygous alpha thalassemia	Finding site	Erythrocyte	false	Inferred relationship	Existential restriction modifier
Homozygous alpha thalassemia	Finding site	Hematopoietic system structure	false	Inferred relationship	Existential restriction modifier
Homozygous alpha thalassemia	Has definitional manifestation	Erythropenia	false	Inferred relationship	Existential restriction modifier
Homozygous alpha thalassemia	Finding site	Hematopoietic system structure	false	Inferred relationship	Existential restriction modifier
Homozygous alpha thalassemia	Finding site	Body system structure	false	Inferred relationship	Existential restriction modifier
Homozygous alpha thalassemia	Has interpretation	Below reference range	false	Inferred relationship	Existential restriction modifier	1
Homozygous alpha thalassemia	Interprets	Measurement of total hemoglobin concentration	false	Inferred relationship	Existential restriction modifier	1
Homozygous alpha thalassemia	Has interpretation	Below reference range	true	Inferred relationship	Existential restriction modifier	2
Homozygous alpha thalassemia	Interprets	Red blood cell count	false	Inferred relationship	Existential restriction modifier	2
Homozygous alpha thalassemia	Occurrence	Congenital	true	Inferred relationship	Existential restriction modifier	3
Homozygous alpha thalassemia	Finding site	Erythrocyte	true	Inferred relationship	Existential restriction modifier	3
Homozygous alpha thalassemia	Interprets	Measurement of total hemoglobin concentration	true	Inferred relationship	Existential restriction modifier	2

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
351149014	Homozygous alpha thalassemia	en	Synonym	Active	Entire term case insensitive	SNOMED CT core module
351150014	Homozygous alpha thalassaemia	en	Synonym	Active	Entire term case insensitive	SNOMED CT core module
622694013	Homozygous alpha thalassemia (disorder)	en	Fully specified name	Active	Entire term case insensitive	SNOMED CT core module