720950009: thrombocytose familiale (trouble)

• SNOMED CT Concept\constatation clinique\...
• \Evaluation finding\Measurement finding\Measurement finding outside reference range\Abnormal blood cell count\Platelet count abnormal\Platelet count above reference range (finding)\Thrombocytosis\Familial thrombocytosis (disorder)
• \Evaluation finding\Measurement finding\Measurement finding outside reference range\Measurement finding above reference range\Platelet count above reference range (finding)\Thrombocytosis\Familial thrombocytosis (disorder)
• \Evaluation finding\Measurement finding\Platelet count - finding\Platelet count abnormal\Platelet count above reference range (finding)\Thrombocytosis\Familial thrombocytosis (disorder)
• \Evaluation finding\Hematopoietic system finding\constatation sur le système hémostatique\Platelet count - finding\Platelet count abnormal\Platelet count above reference range (finding)\Thrombocytosis\Familial thrombocytosis (disorder)
• \Evaluation finding\Hematopoietic system finding\constatation sur le système hémostatique\constatation à propos des plaquettes\Thrombocytosis\Familial thrombocytosis (disorder)
• \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\anomalie plaquettaire héréditaire\Familial thrombocytosis (disorder)
• \Platelet disorder\anomalie plaquettaire héréditaire\Familial thrombocytosis (disorder)
• \Platelet disorder\Thrombocytosis\Familial thrombocytosis (disorder)
• \constatation fonctionnelle\Disorder of haemostatic system\Platelet disorder\...
• \anomalie plaquettaire héréditaire\Familial thrombocytosis (disorder)
• \Thrombocytosis\Familial thrombocytosis (disorder)
• \Disease\Genetic disease\maladie héréditaire\Hereditary disorder by system\troubles héréditaires des éléments figurés du sang\anomalie plaquettaire héréditaire\Familial thrombocytosis (disorder)
• \Disease\anomalie des éléments figurés du sang (trouble)\troubles héréditaires des éléments figurés du sang\anomalie plaquettaire héréditaire\Familial thrombocytosis (disorder)
• \Disease\anomalie des éléments figurés du sang (trouble)\Platelet disorder\anomalie plaquettaire héréditaire\Familial thrombocytosis (disorder)
• \Disease\anomalie des éléments figurés du sang (trouble)\Platelet disorder\Thrombocytosis\Familial thrombocytosis (disorder)
• \Disease\Disorder of haemostatic system\Platelet disorder\anomalie plaquettaire héréditaire\Familial thrombocytosis (disorder)
• \Disease\Disorder of haemostatic system\Platelet disorder\Thrombocytosis\Familial thrombocytosis (disorder)
• \Disease\affection d'un système corporel\Hereditary disorder by system\troubles héréditaires des éléments figurés du sang\anomalie plaquettaire héréditaire\Familial thrombocytosis (disorder)

Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2017. Module: SNOMED CT core

Descriptions:

Id	Description	Lang	Type	Status	Case?	Module
3322607010	Familial thrombocytosis (disorder)	en	Fully specified name	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
3322608017	Familial thrombocytosis	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
3322609013	Familial thrombocythemia	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
3322610015	Hereditary thrombocythaemia	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
3322611016	Hereditary thrombocythemia	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
3322612011	Familial thrombocythaemia	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
756691000241111	thrombocytose familiale (trouble)	fr	Fully specified name	Active	Entire term case insensitive (core metadata concept)	SNOMED CT Common French translation module (core metadata concept)
870831000172119	thrombocytémie familiale	fr	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT Common French translation module (core metadata concept)
995931000172118	thrombocytose familiale	fr	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT Common French translation module (core metadata concept)
3322613018	A type of thrombocytosis, a sustained elevation of platelet numbers, which affects the platelet/megakaryocyte lineage and may create a tendency for thrombosis and hemorrhage but does not cause myeloproliferation. The disease usually presents at birth but can be discovered at any time during life and thus can affect all ages. Familial thrombocytosis is caused by germline mutations in the THPO gene (3q26.3-q27) or in the MPL (MPL S505N) gene (1p34).	en	Definition	Active	Entire term case sensitive (core metadata concept)	SNOMED CT core
3322614012	A type of thrombocytosis, a sustained elevation of platelet numbers, which affects the platelet/megakaryocyte lineage and may create a tendency for thrombosis and haemorrhage but does not cause myeloproliferation. The disease usually presents at birth but can be discovered at any time during life and thus can affect all ages. Familial thrombocytosis is caused by germline mutations in the THPO gene (3q26.3-q27) or in the MPL (MPL S505N) gene (1p34).	en	Definition	Active	Entire term case sensitive (core metadata concept)	SNOMED CT core

Expanded Value Set

This concept is not in any reference sets

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