307343001: Acquired hemoglobin H disease (disorder)

• SNOMED CT Concept\constatation clinique\...
• \Evaluation finding\Measurement finding\Finding of substance level (finding)\Protein level - finding\Hemoglobin level outside reference range (finding)\Hemoglobin low\Anemia due to disturbance of hemoglobin synthesis\thalassémie\Acquired hemoglobin H disease
• \Evaluation finding\Measurement finding\Measurement finding outside reference range\Measurement finding below reference range (finding)\Hemoglobin low\Anemia due to disturbance of hemoglobin synthesis\thalassémie\Acquired hemoglobin H disease
• \Evaluation finding\Measurement finding\Measurement finding outside reference range\Hemoglobin level outside reference range (finding)\Hemoglobin low\Anemia due to disturbance of hemoglobin synthesis\thalassémie\Acquired hemoglobin H disease
• \Evaluation finding\Hematopoietic system finding\Hemoglobin level outside reference range (finding)\Hemoglobin low\Anemia due to disturbance of hemoglobin synthesis\thalassémie\Acquired hemoglobin H disease
• \constatation à propos du sang, des lymphatiques et du système immunitaire\anomalie des éléments figurés du sang (trouble)\...
• \troubles héréditaires des éléments figurés du sang\Hereditary red blood cell disorder (disorder)\Hereditary hemoglobinopathy (disorder)\thalassémie\Acquired hemoglobin H disease
• \anémie\Anemia due to disturbance of hemoglobin synthesis\thalassémie\Acquired hemoglobin H disease
• \anomalie de la lignée rouge\Hereditary red blood cell disorder (disorder)\Hereditary hemoglobinopathy (disorder)\thalassémie\Acquired hemoglobin H disease
• \anomalie de la lignée rouge\Hemoglobinopathy\Hereditary hemoglobinopathy (disorder)\thalassémie\Acquired hemoglobin H disease
• \Disease\Genetic disease\maladie héréditaire\Hereditary disorder by system\troubles héréditaires des éléments figurés du sang\Hereditary red blood cell disorder (disorder)\Hereditary hemoglobinopathy (disorder)\thalassémie\Acquired hemoglobin H disease
• \Disease\anomalie des éléments figurés du sang (trouble)\troubles héréditaires des éléments figurés du sang\Hereditary red blood cell disorder (disorder)\Hereditary hemoglobinopathy (disorder)\thalassémie\Acquired hemoglobin H disease
• \Disease\anomalie des éléments figurés du sang (trouble)\anémie\Anemia due to disturbance of hemoglobin synthesis\thalassémie\Acquired hemoglobin H disease
• \Disease\anomalie des éléments figurés du sang (trouble)\anomalie de la lignée rouge\Hereditary red blood cell disorder (disorder)\Hereditary hemoglobinopathy (disorder)\thalassémie\Acquired hemoglobin H disease
• \Disease\anomalie des éléments figurés du sang (trouble)\anomalie de la lignée rouge\Hemoglobinopathy\Hereditary hemoglobinopathy (disorder)\thalassémie\Acquired hemoglobin H disease
• \Disease\affection d'un système corporel\Hereditary disorder by system\troubles héréditaires des éléments figurés du sang\Hereditary red blood cell disorder (disorder)\Hereditary hemoglobinopathy (disorder)\thalassémie\Acquired hemoglobin H disease
• \Disease\affection d'un système corporel\anomalie de la lignée rouge\Hereditary red blood cell disorder (disorder)\Hereditary hemoglobinopathy (disorder)\thalassémie\Acquired hemoglobin H disease
• \Disease\affection d'un système corporel\anomalie de la lignée rouge\Hemoglobinopathy\Hereditary hemoglobinopathy (disorder)\thalassémie\Acquired hemoglobin H disease
• \Disease\Congenital disease\Hereditary hemoglobinopathy (disorder)\thalassémie\Acquired hemoglobin H disease

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

Descriptions:

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

Expanded Value Set

Reference Sets

Client's clinical problems, conditions, diagnoses, symptoms, findings, complaints reference set (foundation metadata concept)

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