783202008: Autosomal dominant secondary polycythemia (disorder)

• SNOMED CT Concept\Clinical finding (finding)\...
• \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 (disorder)\Autosomal dominant secondary polycythemia
• \Red blood cell disorder\Hereditary red blood cell disorder (disorder)\Autosomal dominant secondary polycythemia
• \Red blood cell disorder\Erythrocytosis\Secondary polycythemia\Autosomal dominant secondary polycythemia
• \Procedure related finding\Evaluation finding\...
• \Finding of cellular component of blood (finding)\Red blood cell finding (finding)\Erythrocytosis\Secondary polycythemia\Autosomal dominant secondary polycythemia
• \Measurement finding\Measurement finding outside reference range\Blood cell count outside reference range\Red blood cell count outside reference range\Red blood cell count above reference range\Erythrocytosis\Secondary polycythemia\Autosomal dominant secondary polycythemia
• \Measurement finding\Measurement finding outside reference range\Measurement finding above reference range (finding)\Red blood cell count above reference range\Erythrocytosis\Secondary polycythemia\Autosomal dominant secondary polycythemia
• \Measurement finding\Red blood cell count - finding\Red blood cell count outside reference range\Red blood cell count above reference range\Erythrocytosis\Secondary polycythemia\Autosomal dominant secondary polycythemia
• \Haematopoietic system finding\Red blood cell finding (finding)\Erythrocytosis\Secondary polycythemia\Autosomal dominant secondary polycythemia
• \Disease\Genetic disease\Hereditary disease\Hereditary disorder by system (disorder)\Hereditary disorder of cellular element of blood\Hereditary red blood cell disorder (disorder)\Autosomal dominant secondary polycythemia
• \Disease\Genetic disease\Hereditary disease\Autosomal hereditary disorder\Autosomal dominant hereditary disorder\Autosomal dominant secondary polycythemia
• \Disease\Disorder of foetus and/or newborn\Congenital disease\Autosomal dominant secondary polycythemia
• \Disease\Disorder of cellular component of blood\Hereditary disorder of cellular element of blood\Hereditary red blood cell disorder (disorder)\Autosomal dominant secondary polycythemia
• \Disease\Disorder of cellular component of blood\Red blood cell disorder\Hereditary red blood cell disorder (disorder)\Autosomal dominant secondary polycythemia
• \Disease\Disorder of cellular component of blood\Red blood cell disorder\Erythrocytosis\Secondary polycythemia\Autosomal dominant secondary polycythemia
• \Disease\Disorder of body system\Hereditary disorder by system (disorder)\Hereditary disorder of cellular element of blood\Hereditary red blood cell disorder (disorder)\Autosomal dominant secondary polycythemia
• \Disease\Disorder of body system\Red blood cell disorder\Hereditary red blood cell disorder (disorder)\Autosomal dominant secondary polycythemia
• \Disease\Disorder of body system\Red blood cell disorder\Erythrocytosis\Secondary polycythemia\Autosomal dominant secondary polycythemia

Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). 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	Entire term case insensitive (core metadata concept)	SNOMED CT core
3758076019	Autosomal dominant secondary polycythemia	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
3758077011	Autosomal dominant secondary polycythaemia	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
3758078018	Autosomal dominant secondary erythrocytosis	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	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	Entire term case sensitive (core metadata concept)	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	Entire term case sensitive (core metadata concept)	SNOMED CT core
3758075015	Autosomal dominant secondary polycythemia (disorder)	en	Fully specified name	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
3758076019	Autosomal dominant secondary polycythemia	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
3758077011	Autosomal dominant secondary polycythaemia	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
3758078018	Autosomal dominant secondary erythrocytosis	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	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	Entire term case sensitive (core metadata concept)	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	Entire term case sensitive (core metadata concept)	SNOMED CT core
3413031001000114	Polyzythämie, sekundäre, autosomal-dominante	de	Synonym (core metadata concept)	Active	Entire term case sensitive (core metadata concept)	SNOMED CT Switzerland NRC maintained Module
5797151000241118	érythrocytose secondaire autosomique dominante	fr	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT Switzerland NRC maintained Module
5797161000241115	polycythémie secondaire autosomique dominante	fr	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT Switzerland NRC maintained Module
5797151000241118	érythrocytose secondaire autosomique dominante	fr	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT Switzerland NRC maintained Module
5797161000241115	polycythémie secondaire autosomique dominante	fr	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT Switzerland NRC maintained Module
3413031001000114	Polyzythämie, sekundäre, autosomal-dominante	de	Synonym (core metadata concept)	Active	Entire term case sensitive (core metadata concept)	SNOMED CT Switzerland NRC maintained Module

Expanded Value Set

This concept is not in any reference sets

Back to Start