48553001: 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\Alpha thalassemia\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\Alpha thalassemia\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\Alpha thalassemia\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\Alpha thalassemia\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\Alpha thalassemia\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\Alpha thalassemia\Hemoglobin H disease

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

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

80911013 Hemoglobin H disease en Synonym Active Entire term case sensitive SNOMED CT core module

495133013 Haemoglobin H disease en Synonym Active Entire term case sensitive SNOMED CT core module

786134018 Hemoglobin H disease (disorder) en Fully specified name Active Entire term case sensitive SNOMED CT core module

Expanded Value Set

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

Inbound Relationships	Type	Active	Source	Characteristic	Refinability	Group
National Health Service Sickle Cell and Thalassaemia Screening Programme result consistent with haemoglobin H disease (situation)	Associated finding	True	Hemoglobin H disease	Inferred relationship	Existential restriction modifier	1

This concept is not in any reference sets

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Id	Description	Lang	Type	Status	Case?	Module
80911013	Hemoglobin H disease	en	Synonym	Active	Entire term case sensitive	SNOMED CT core module
495133013	Haemoglobin H disease	en	Synonym	Active	Entire term case sensitive	SNOMED CT core module
786134018	Hemoglobin H disease (disorder)	en	Fully specified name	Active	Entire term case sensitive	SNOMED CT core module