770407006: erythrocytose de Tchouvachie (trouble)

SNOMED CT Concept\constatation clinique\...

\Evaluation finding\Finding of cellular component of blood (finding)\constatation à propos de la lignée rouge\Erythrocytosis\Familial erythrocytosis\Chuvash erythrocytosis
\Evaluation finding\Measurement finding\Measurement finding outside reference range\Abnormal blood cell count\RBC count abnormal\Red blood cell count raised (finding)\Erythrocytosis\Familial erythrocytosis\Chuvash erythrocytosis
\Evaluation finding\Measurement finding\Measurement finding outside reference range\Measurement finding above reference range\Red blood cell count raised (finding)\Erythrocytosis\Familial erythrocytosis\Chuvash erythrocytosis
\Evaluation finding\Measurement finding\Red blood cell count - finding\RBC count abnormal\Red blood cell count raised (finding)\Erythrocytosis\Familial erythrocytosis\Chuvash erythrocytosis
\Evaluation finding\Hematopoietic system finding\constatation à propos de la lignée rouge\Erythrocytosis\Familial erythrocytosis\Chuvash erythrocytosis

\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)\Familial erythrocytosis\Chuvash erythrocytosis

\anomalie de la lignée rouge\Hereditary red blood cell disorder (disorder)\Familial erythrocytosis\Chuvash erythrocytosis
\anomalie de la lignée rouge\Erythrocytosis\Familial erythrocytosis\Chuvash erythrocytosis

\Disease\Genetic disease\maladie héréditaire\Hereditary disorder by system\troubles héréditaires des éléments figurés du sang\Hereditary red blood cell disorder (disorder)\Familial erythrocytosis\Chuvash erythrocytosis
\Disease\Genetic disease\maladie héréditaire\Autosomal hereditary disorder\Autosomal recessive hereditary disorder\Chuvash erythrocytosis
\Disease\anomalie des éléments figurés du sang (trouble)\troubles héréditaires des éléments figurés du sang\Hereditary red blood cell disorder (disorder)\Familial erythrocytosis\Chuvash erythrocytosis
\Disease\anomalie des éléments figurés du sang (trouble)\anomalie de la lignée rouge\Hereditary red blood cell disorder (disorder)\Familial erythrocytosis\Chuvash erythrocytosis
\Disease\anomalie des éléments figurés du sang (trouble)\anomalie de la lignée rouge\Erythrocytosis\Familial erythrocytosis\Chuvash erythrocytosis
\Disease\affection d'un système corporel\Hereditary disorder by system\troubles héréditaires des éléments figurés du sang\Hereditary red blood cell disorder (disorder)\Familial erythrocytosis\Chuvash erythrocytosis
\Disease\affection d'un système corporel\anomalie de la lignée rouge\Hereditary red blood cell disorder (disorder)\Familial erythrocytosis\Chuvash erythrocytosis
\Disease\affection d'un système corporel\anomalie de la lignée rouge\Erythrocytosis\Familial erythrocytosis\Chuvash erythrocytosis
\Disease\Congenital disease\Chuvash erythrocytosis

Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2019. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module

3700721010 Chuvash polycythemia en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core

3700722015 Chuvash polycythaemia en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core

3700723013 Chuvash erythrocytosis en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core

3700724019 Von Hippel Lindau dependent polycythaemia en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core

3700725018 Von Hippel Lindau dependent polycythemia en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core

3700726017 Chuvash erythrocytosis (disorder) en Fully specified name Active Entire term case sensitive (core metadata concept) SNOMED CT core

769251000241117 erythrocytose de Tchouvachie (trouble) fr Fully specified name Active Entire term case sensitive (core metadata concept) SNOMED CT Common French translation module (core metadata concept)

925481000172116 erythrocytose de Tchouvachie fr Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Common French translation module (core metadata concept)

965871000172113 erythrocytose tchouvache fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Common French translation module (core metadata concept)

3700727014 A rare genetic congenital secondary polycythaemia disorder characterised by increased haemoglobin, haematocrit and erythropoietin serum levels and normal oxygen affinity, which usually manifests with headache, dizziness, dyspnoea and/or plethora. Patients present an increased risk of haemorrhage, thrombosis and early death. There is evidence this disease is caused by homozygous or compound heterozygous mutation in the VHL gene on chromosome 3p25. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core

3700728016 A rare genetic congenital secondary polycythemia disorder characterized by increased hemoglobin, hematocrit and erythropoietin serum levels and normal oxygen affinity, which usually manifests with headache, dizziness, dyspnea and/or plethora. Patients present an increased risk of hemorrhage, thrombosis and early death. There is evidence this disease is caused by homozygous or compound heterozygous mutation in the VHL gene on chromosome 3p25. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
Chuvash erythrocytosis	interprète (attribut)	Haematology procedure	true	Inferred relationship	Some	3
Chuvash erythrocytosis	est un(e) (attribut)	Congenital disease	true	Inferred relationship	Some
Chuvash erythrocytosis	est un(e) (attribut)	Autosomal recessive hereditary disorder	true	Inferred relationship	Some
Chuvash erythrocytosis	est un(e) (attribut)	Familial erythrocytosis	true	Inferred relationship	Some
Chuvash erythrocytosis	interprète (attribut)	Red blood cell count	true	Inferred relationship	Some	1
Chuvash erythrocytosis	survenue (attribut)	congénital	true	Inferred relationship	Some	2
Chuvash erythrocytosis	localisation d'une constatation (attribut)	Erythrocyte	true	Inferred relationship	Some	2
Chuvash erythrocytosis	a pour interprétation (attribut)	au-dessus de l'étendue de référence	true	Inferred relationship	Some	1

Inbound Relationships

Type

Active

Source

Characteristic

Refinability

Group

This concept is not in any reference sets

Back to Start

Id	Description	Lang	Type	Status	Case?	Module
3700721010	Chuvash polycythemia	en	Synonym (core metadata concept)	Active	Entire term case sensitive (core metadata concept)	SNOMED CT core
3700722015	Chuvash polycythaemia	en	Synonym (core metadata concept)	Active	Entire term case sensitive (core metadata concept)	SNOMED CT core
3700723013	Chuvash erythrocytosis	en	Synonym (core metadata concept)	Active	Entire term case sensitive (core metadata concept)	SNOMED CT core
3700724019	Von Hippel Lindau dependent polycythaemia	en	Synonym (core metadata concept)	Active	Entire term case sensitive (core metadata concept)	SNOMED CT core
3700725018	Von Hippel Lindau dependent polycythemia	en	Synonym (core metadata concept)	Active	Entire term case sensitive (core metadata concept)	SNOMED CT core
3700726017	Chuvash erythrocytosis (disorder)	en	Fully specified name	Active	Entire term case sensitive (core metadata concept)	SNOMED CT core
769251000241117	erythrocytose de Tchouvachie (trouble)	fr	Fully specified name	Active	Entire term case sensitive (core metadata concept)	SNOMED CT Common French translation module (core metadata concept)
925481000172116	erythrocytose de Tchouvachie	fr	Synonym (core metadata concept)	Active	Entire term case sensitive (core metadata concept)	SNOMED CT Common French translation module (core metadata concept)
965871000172113	erythrocytose tchouvache	fr	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT Common French translation module (core metadata concept)
3700727014	A rare genetic congenital secondary polycythaemia disorder characterised by increased haemoglobin, haematocrit and erythropoietin serum levels and normal oxygen affinity, which usually manifests with headache, dizziness, dyspnoea and/or plethora. Patients present an increased risk of haemorrhage, thrombosis and early death. There is evidence this disease is caused by homozygous or compound heterozygous mutation in the VHL gene on chromosome 3p25.	en	Definition	Active	Entire term case sensitive (core metadata concept)	SNOMED CT core
3700728016	A rare genetic congenital secondary polycythemia disorder characterized by increased hemoglobin, hematocrit and erythropoietin serum levels and normal oxygen affinity, which usually manifests with headache, dizziness, dyspnea and/or plethora. Patients present an increased risk of hemorrhage, thrombosis and early death. There is evidence this disease is caused by homozygous or compound heterozygous mutation in the VHL gene on chromosome 3p25.	en	Definition	Active	Entire term case sensitive (core metadata concept)	SNOMED CT core