307343001: Acquired hemoglobin H disease (disorder)

SNOMED CT Concept\Clinical finding (finding)\...

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

\Hereditary disorder of cellular element of blood (disorder)\Hereditary red blood cell disorder (disorder)\Hereditary hemoglobinopathy (disorder)\Thalassemia\Acquired haemoglobin H disease

\Anemia\Anaemia due to disturbance of haemoglobin synthesis\Thalassemia\Acquired haemoglobin H disease

\Red blood cell disorder\Hereditary red blood cell disorder (disorder)\Hereditary hemoglobinopathy (disorder)\Thalassemia\Acquired haemoglobin H disease
\Red blood cell disorder\Hemoglobinopathy\Hereditary hemoglobinopathy (disorder)\Thalassemia\Acquired haemoglobin H disease

\Procedure related finding\Evaluation finding\...

\Measurement finding\Finding of substance level (finding)\Protein level - finding\Hemoglobin finding\Hemoglobin level outside reference range (finding)\Hemoglobin below reference range (finding)\Anaemia due to disturbance of haemoglobin synthesis\Thalassemia\Acquired haemoglobin H disease
\Measurement finding\Measurement finding outside reference range\Measurement finding below reference range (finding)\Hemoglobin below reference range (finding)\Anaemia due to disturbance of haemoglobin synthesis\Thalassemia\Acquired haemoglobin H disease
\Measurement finding\Measurement finding outside reference range\Hemoglobin level outside reference range (finding)\Hemoglobin below reference range (finding)\Anaemia due to disturbance of haemoglobin synthesis\Thalassemia\Acquired haemoglobin H disease

\Hematopoietic system finding\Haematology test outside reference range\Hemoglobin level outside reference range (finding)\Hemoglobin below reference range (finding)\Anaemia due to disturbance of haemoglobin synthesis\Thalassemia\Acquired haemoglobin H disease
\Hematopoietic system finding\Hemoglobin finding\Hemoglobin level outside reference range (finding)\Hemoglobin below reference range (finding)\Anaemia due to disturbance of haemoglobin synthesis\Thalassemia\Acquired haemoglobin H disease

\Disease\Genetic disease\Hereditary disease\Hereditary disorder by system\Hereditary disorder of cellular element of blood (disorder)\Hereditary red blood cell disorder (disorder)\Hereditary hemoglobinopathy (disorder)\Thalassemia\Acquired haemoglobin H disease
\Disease\Fetal and/or neonatal disorder\Congenital disease\Hereditary hemoglobinopathy (disorder)\Thalassemia\Acquired haemoglobin H disease
\Disease\Disorder of cellular component of blood (disorder)\Hereditary disorder of cellular element of blood (disorder)\Hereditary red blood cell disorder (disorder)\Hereditary hemoglobinopathy (disorder)\Thalassemia\Acquired haemoglobin H disease
\Disease\Disorder of cellular component of blood (disorder)\Anemia\Anaemia due to disturbance of haemoglobin synthesis\Thalassemia\Acquired haemoglobin H disease
\Disease\Disorder of cellular component of blood (disorder)\Red blood cell disorder\Hereditary red blood cell disorder (disorder)\Hereditary hemoglobinopathy (disorder)\Thalassemia\Acquired haemoglobin H disease
\Disease\Disorder of cellular component of blood (disorder)\Red blood cell disorder\Hemoglobinopathy\Hereditary hemoglobinopathy (disorder)\Thalassemia\Acquired haemoglobin H disease
\Disease\Disorder of body system\Hereditary disorder by system\Hereditary disorder of cellular element of blood (disorder)\Hereditary red blood cell disorder (disorder)\Hereditary hemoglobinopathy (disorder)\Thalassemia\Acquired haemoglobin H disease
\Disease\Disorder of body system\Red blood cell disorder\Hereditary red blood cell disorder (disorder)\Hereditary hemoglobinopathy (disorder)\Thalassemia\Acquired haemoglobin H disease
\Disease\Disorder of body system\Red blood cell disorder\Hemoglobinopathy\Hereditary hemoglobinopathy (disorder)\Thalassemia\Acquired haemoglobin H disease

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

Descriptions:

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
Acquired haemoglobin H disease	Is a	Thalassemia	true	Inferred relationship	Some
Acquired haemoglobin H disease	Finding site	Erythrocyte (cell)	false	Inferred relationship	Some
Acquired haemoglobin H disease	Finding site	Hematopoietic system structure	false	Inferred relationship	Some
Acquired haemoglobin H disease	Finding site	Hematopoietic system structure	false	Inferred relationship	Some
Acquired haemoglobin H disease	Has definitional manifestation	érythropénie	false	Inferred relationship	Some
Acquired haemoglobin H disease	Finding site	Body system structure	false	Inferred relationship	Some
Acquired haemoglobin H disease	Has interpretation	Below reference range	false	Inferred relationship	Some	1
Acquired haemoglobin H disease	Interprets	Measurement of total haemoglobin concentration	false	Inferred relationship	Some	1
Acquired haemoglobin H disease	Has interpretation	Below reference range	true	Inferred relationship	Some	2
Acquired haemoglobin H disease	Interprets	Red blood cell count	false	Inferred relationship	Some	2
Acquired haemoglobin H disease	Occurrence	Congenital	true	Inferred relationship	Some	3
Acquired haemoglobin H disease	Finding site	Erythrocyte (cell)	true	Inferred relationship	Some	3
Acquired haemoglobin H disease	Interprets	Measurement of total haemoglobin concentration	true	Inferred relationship	Some	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 (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
450588011	Acquired haemoglobin H disease	en	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
703856012	Acquired hemoglobin H disease (disorder)	en	Fully specified name	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
5199601000241114	maladie à hémoglobine H	fr	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT Switzerland NRC maintained Module
3427661001000111	Alpha-Thalassämie-myelodysplastisches Syndrom	de	Synonym (core metadata concept)	Active	Entire term case sensitive (core metadata concept)	SNOMED CT Switzerland NRC maintained Module