783202008: Autosomal dominant secondary polycythemia (disorder)

• SNOMED CT Concept\Clinical finding\...
• \Evaluation finding\Finding of cellular component of blood\Red blood cell finding\Erythrocytosis\Secondary polycythaemia\Autosomal dominant secondary polycythaemia
• \Evaluation finding\Measurement finding\Measurement finding outside reference range\Abnormal blood cell count\Red blood cell count outside reference range\RBC count raised\Erythrocytosis\Secondary polycythaemia\Autosomal dominant secondary polycythaemia
• \Evaluation finding\Measurement finding\Measurement finding outside reference range\Measurement finding above reference range\RBC count raised\Erythrocytosis\Secondary polycythaemia\Autosomal dominant secondary polycythaemia
• \Evaluation finding\Measurement finding\Red blood cell count - finding\Red blood cell count outside reference range\RBC count raised\Erythrocytosis\Secondary polycythaemia\Autosomal dominant secondary polycythaemia
• \Evaluation finding\Haematopoietic system finding\Red blood cell finding\Erythrocytosis\Secondary polycythaemia\Autosomal dominant secondary polycythaemia
• \Finding of blood, lymphatics and immune system\Blood disease\...
• \Hereditary disorder of cellular element of blood\Hereditary red blood cell disorder\Autosomal dominant secondary polycythaemia
• \Red blood cell disorder\Hereditary red blood cell disorder\Autosomal dominant secondary polycythaemia
• \Red blood cell disorder\Erythrocytosis\Secondary polycythaemia\Autosomal dominant secondary polycythaemia
• \Disease\Genetic disease\Hereditary disease\Hereditary disorder by system\Hereditary disorder of cellular element of blood\Hereditary red blood cell disorder\Autosomal dominant secondary polycythaemia
• \Disease\Genetic disease\Hereditary disease\Autosomal hereditary disorder\Autosomal dominant hereditary disorder\Autosomal dominant secondary polycythaemia
• \Disease\Blood disease\Hereditary disorder of cellular element of blood\Hereditary red blood cell disorder\Autosomal dominant secondary polycythaemia
• \Disease\Blood disease\Red blood cell disorder\Hereditary red blood cell disorder\Autosomal dominant secondary polycythaemia
• \Disease\Blood disease\Red blood cell disorder\Erythrocytosis\Secondary polycythaemia\Autosomal dominant secondary polycythaemia
• \Disease\Disorder of body system\Hereditary disorder by system\Hereditary disorder of cellular element of blood\Hereditary red blood cell disorder\Autosomal dominant secondary polycythaemia
• \Disease\Disorder of body system\Red blood cell disorder\Hereditary red blood cell disorder\Autosomal dominant secondary polycythaemia
• \Disease\Disorder of body system\Red blood cell disorder\Erythrocytosis\Secondary polycythaemia\Autosomal dominant secondary polycythaemia
• \Disease\Congenital disease\Autosomal dominant secondary polycythaemia

Status: current, Primitive. Date: 31-Jul 2019. Module: SNOMED CT core

Descriptions:

Id	Description	Lang	Type	Status	Case?	Module
3758075015	Autosomal dominant secondary polycythemia (disorder)	en	Fully specified name	Active	Case insensitive	SNOMED CT core
3758076019	Autosomal dominant secondary polycythemia	en	Synonym	Active	Case insensitive	SNOMED CT core
3758077011	Autosomal dominant secondary polycythaemia	en	Synonym	Active	Case insensitive	SNOMED CT core
3758078018	Autosomal dominant secondary erythrocytosis	en	Synonym	Active	Case insensitive	SNOMED CT core
3758079014	A rare genetic hematologic disease characterized by increased levels of serum hemoglobin, hematocrit and erythrocyte mass, associated with elevated or inappropriately normal erythropoietin serum levels, occurring in various members of a family and with autosomal dominant inheritance.	en	Definition	Active	Case sensitive	SNOMED CT core
3758080012	A rare genetic haematologic disease characterised by increased levels of serum haemoglobin, haematocrit and erythrocyte mass, associated with elevated or inappropriately normal erythropoietin serum levels, occurring in various members of a family and with autosomal dominant inheritance.	en	Definition	Active	Case sensitive	SNOMED CT core

Expanded Value Set

Reference Sets

Australian emergency department reference set

Clinical finding foundation reference set

Problem/Diagnosis reference set

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