307343001: Acquired hemoglobin H 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\Acquired hemoglobin H 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\Acquired hemoglobin H 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\Acquired hemoglobin H 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\Acquired hemoglobin H 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\Acquired hemoglobin H 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\Acquired hemoglobin H disease

\Anemia\Anemia due to disturbance of hemoglobin synthesis\Thalassemia\Acquired hemoglobin H disease

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

450587018 Acquired hemoglobin H disease en Synonym Active Only initial character case insensitive SNOMED CT core module

450588011 Acquired haemoglobin H disease en Synonym Active Only initial character case insensitive SNOMED CT core module

703856012 Acquired hemoglobin H 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
Acquired hemoglobin H disease	Is a	Thalassemia	true	Inferred relationship	Existential restriction modifier
Acquired hemoglobin H disease	Finding site	Erythrocyte	false	Inferred relationship	Existential restriction modifier
Acquired hemoglobin H disease	Finding site	Hematopoietic system structure	false	Inferred relationship	Existential restriction modifier
Acquired hemoglobin H disease	Finding site	Hematopoietic system structure	false	Inferred relationship	Existential restriction modifier
Acquired hemoglobin H disease	Has definitional manifestation	Erythropenia	false	Inferred relationship	Existential restriction modifier
Acquired hemoglobin H disease	Finding site	Body system structure	false	Inferred relationship	Existential restriction modifier
Acquired hemoglobin H disease	Has interpretation	Below reference range	false	Inferred relationship	Existential restriction modifier	1
Acquired hemoglobin H disease	Interprets	Measurement of total hemoglobin concentration	false	Inferred relationship	Existential restriction modifier	1
Acquired hemoglobin H disease	Has interpretation	Below reference range	true	Inferred relationship	Existential restriction modifier	2
Acquired hemoglobin H disease	Interprets	Red blood cell count	false	Inferred relationship	Existential restriction modifier	2
Acquired hemoglobin H disease	Occurrence	Congenital	true	Inferred relationship	Existential restriction modifier	3
Acquired hemoglobin H disease	Finding site	Erythrocyte	true	Inferred relationship	Existential restriction modifier	3
Acquired hemoglobin H disease	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

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Id	Description	Lang	Type	Status	Case?	Module
450587018	Acquired hemoglobin H disease	en	Synonym	Active	Only initial character case insensitive	SNOMED CT core module
450588011	Acquired haemoglobin H disease	en	Synonym	Active	Only initial character case insensitive	SNOMED CT core module
703856012	Acquired hemoglobin H disease (disorder)	en	Fully specified name	Active	Only initial character case insensitive	SNOMED CT core module