783766005: Autosomal recessive secondary polycythemia not associated with Von Hippel Lindau gene (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)\Familial erythrocytosis\Autosomal recessive secondary polycythaemia not associated with VHL (Von Hippel Lindau) gene
• \Red blood cell disorder\Hereditary red blood cell disorder (disorder)\Familial erythrocytosis\Autosomal recessive secondary polycythaemia not associated with VHL (Von Hippel Lindau) gene
• \Red blood cell disorder\Erythrocytosis\Familial erythrocytosis\Autosomal recessive secondary polycythaemia not associated with VHL (Von Hippel Lindau) gene
• \Procedure related finding\Evaluation finding\...
• \Finding of cellular component of blood (finding)\Red blood cell finding (finding)\Erythrocytosis\Familial erythrocytosis\Autosomal recessive secondary polycythaemia not associated with VHL (Von Hippel Lindau) gene
• \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\Familial erythrocytosis\Autosomal recessive secondary polycythaemia not associated with VHL (Von Hippel Lindau) gene
• \Measurement finding\Measurement finding outside reference range\Measurement finding above reference range (finding)\Red blood cell count above reference range\Erythrocytosis\Familial erythrocytosis\Autosomal recessive secondary polycythaemia not associated with VHL (Von Hippel Lindau) gene
• \Measurement finding\Red blood cell count - finding\Red blood cell count outside reference range\Red blood cell count above reference range\Erythrocytosis\Familial erythrocytosis\Autosomal recessive secondary polycythaemia not associated with VHL (Von Hippel Lindau) gene
• \Haematopoietic system finding\Red blood cell finding (finding)\Erythrocytosis\Familial erythrocytosis\Autosomal recessive secondary polycythaemia not associated with VHL (Von Hippel Lindau) gene
• \Disease\Genetic disease\Hereditary disease\Hereditary disorder by system (disorder)\Hereditary disorder of cellular element of blood\Hereditary red blood cell disorder (disorder)\Familial erythrocytosis\Autosomal recessive secondary polycythaemia not associated with VHL (Von Hippel Lindau) gene
• \Disease\Genetic disease\Hereditary disease\Autosomal hereditary disorder\Autosomal recessive hereditary disorder\Autosomal recessive secondary polycythaemia not associated with VHL (Von Hippel Lindau) gene
• \Disease\Disorder of foetus and/or newborn\Congenital disease\Autosomal recessive secondary polycythaemia not associated with VHL (Von Hippel Lindau) gene
• \Disease\Disorder of cellular component of blood\Hereditary disorder of cellular element of blood\Hereditary red blood cell disorder (disorder)\Familial erythrocytosis\Autosomal recessive secondary polycythaemia not associated with VHL (Von Hippel Lindau) gene
• \Disease\Disorder of cellular component of blood\Red blood cell disorder\Hereditary red blood cell disorder (disorder)\Familial erythrocytosis\Autosomal recessive secondary polycythaemia not associated with VHL (Von Hippel Lindau) gene
• \Disease\Disorder of cellular component of blood\Red blood cell disorder\Erythrocytosis\Familial erythrocytosis\Autosomal recessive secondary polycythaemia not associated with VHL (Von Hippel Lindau) gene
• \Disease\Disorder of body system\Hereditary disorder by system (disorder)\Hereditary disorder of cellular element of blood\Hereditary red blood cell disorder (disorder)\Familial erythrocytosis\Autosomal recessive secondary polycythaemia not associated with VHL (Von Hippel Lindau) gene
• \Disease\Disorder of body system\Red blood cell disorder\Hereditary red blood cell disorder (disorder)\Familial erythrocytosis\Autosomal recessive secondary polycythaemia not associated with VHL (Von Hippel Lindau) gene
• \Disease\Disorder of body system\Red blood cell disorder\Erythrocytosis\Familial erythrocytosis\Autosomal recessive secondary polycythaemia not associated with VHL (Von Hippel Lindau) gene

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
3760268014	Autosomal recessive secondary polycythaemia not associated with Von Hippel Lindau gene	en	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
3760269018	Autosomal recessive secondary polycythemia not associated with Von Hippel Lindau gene (disorder)	en	Fully specified name	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
3760270017	Autosomal recessive secondary polycythemia not associated with Von Hippel Lindau gene	en	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
3760271018	Autosomal recessive secondary polycythaemia not associated with VHL (Von Hippel Lindau) gene	en	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
3760272013	Autosomal recessive secondary polycythemia not associated with VHL (Von Hippel Lindau) gene	en	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
3760276011	Autosomal recessive secondary polycythemia non-Chuvash type	en	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
3760277019	Autosomal recessive secondary erythrocytosis non-Chuvash type	en	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
3760278012	Autosomal recessive secondary polycythaemia non-Chuvash type	en	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
3760279016	A rare hereditary haematologic disease characterised by an increase in haemoglobin, haematocrit and erythrocyte mass resulting in plethora or ruddy complexion, headache, dizziness, tinnitus and exertional dyspnoea. In some cases, thrombophlebitis and arthralgia have also been reported.	en	Definition	Active	Entire term case sensitive (core metadata concept)	SNOMED CT core
3760280018	A rare hereditary hematologic disease characterized by an increase in hemoglobin, hematocrit and erythrocyte mass resulting in plethora or ruddy complexion, headache, dizziness, tinnitus and exertional dyspnea. In some cases, thrombophlebitis and arthralgia have also been reported.	en	Definition	Active	Entire term case sensitive (core metadata concept)	SNOMED CT core
3760268014	Autosomal recessive secondary polycythaemia not associated with Von Hippel Lindau gene	en	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
3760269018	Autosomal recessive secondary polycythemia not associated with Von Hippel Lindau gene (disorder)	en	Fully specified name	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
3760270017	Autosomal recessive secondary polycythemia not associated with Von Hippel Lindau gene	en	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
3760271018	Autosomal recessive secondary polycythaemia not associated with VHL (Von Hippel Lindau) gene	en	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
3760272013	Autosomal recessive secondary polycythemia not associated with VHL (Von Hippel Lindau) gene	en	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
3760276011	Autosomal recessive secondary polycythemia non-Chuvash type	en	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
3760277019	Autosomal recessive secondary erythrocytosis non-Chuvash type	en	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
3760278012	Autosomal recessive secondary polycythaemia non-Chuvash type	en	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
3760279016	A rare hereditary haematologic disease characterised by an increase in haemoglobin, haematocrit and erythrocyte mass resulting in plethora or ruddy complexion, headache, dizziness, tinnitus and exertional dyspnoea. In some cases, thrombophlebitis and arthralgia have also been reported.	en	Definition	Active	Entire term case sensitive (core metadata concept)	SNOMED CT core
3760280018	A rare hereditary hematologic disease characterized by an increase in hemoglobin, hematocrit and erythrocyte mass resulting in plethora or ruddy complexion, headache, dizziness, tinnitus and exertional dyspnea. In some cases, thrombophlebitis and arthralgia have also been reported.	en	Definition	Active	Entire term case sensitive (core metadata concept)	SNOMED CT core
3384221001000111	Polyzythämie, sekundäre, autosomal-rezessive, nicht VHL-Gen-assoziierte	de	Synonym (core metadata concept)	Active	Entire term case sensitive (core metadata concept)	SNOMED CT Switzerland NRC maintained Module
5750831000241112	polycythémie secondaire autosomique récessive non associée au gène de Von Hippel Lindau	fr	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT Switzerland NRC maintained Module
5750831000241112	polycythémie secondaire autosomique récessive non associée au gène de Von Hippel Lindau	fr	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT Switzerland NRC maintained Module
3384221001000111	Polyzythämie, sekundäre, autosomal-rezessive, nicht VHL-Gen-assoziierte	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

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