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128096008: Hereditary platelet function disorder (disorder)

SNOMED CT Concept\constatation clinique\...

\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\Hereditary platelet function disorder

\Platelet disorder\Qualitative platelet disorder (disorder)\Hereditary platelet function disorder
\Platelet disorder\anomalie plaquettaire héréditaire\Hereditary platelet function disorder

\constatation fonctionnelle\Disorder of haemostatic system\Platelet disorder\...

\Qualitative platelet disorder (disorder)\Hereditary platelet function disorder

\anomalie plaquettaire héréditaire\Hereditary platelet function disorder

\Disease\Genetic disease\maladie héréditaire\Hereditary disorder by system\troubles héréditaires des éléments figurés du sang\anomalie plaquettaire héréditaire\Hereditary platelet function disorder
\Disease\anomalie des éléments figurés du sang (trouble)\troubles héréditaires des éléments figurés du sang\anomalie plaquettaire héréditaire\Hereditary platelet function disorder
\Disease\anomalie des éléments figurés du sang (trouble)\Platelet disorder\Qualitative platelet disorder (disorder)\Hereditary platelet function disorder
\Disease\anomalie des éléments figurés du sang (trouble)\Platelet disorder\anomalie plaquettaire héréditaire\Hereditary platelet function disorder
\Disease\Disorder of haemostatic system\Platelet disorder\Qualitative platelet disorder (disorder)\Hereditary platelet function disorder
\Disease\Disorder of haemostatic system\Platelet disorder\anomalie plaquettaire héréditaire\Hereditary platelet function disorder
\Disease\affection d'un système corporel\Hereditary disorder by system\troubles héréditaires des éléments figurés du sang\anomalie plaquettaire héréditaire\Hereditary platelet function disorder

Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2002. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module

194690019 Hereditary platelet function disorder en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core

732056019 Hereditary platelet function disorder (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
Hereditary platelet function disorder	interprète (attribut)	Hemostatic function (observable entity)	true	Inferred relationship	Some	1
Hereditary platelet function disorder	a pour interprétation (attribut)	anormal	true	Inferred relationship	Some	1
Hereditary platelet function disorder	est un(e) (attribut)	anomalie plaquettaire héréditaire	true	Inferred relationship	Some
Hereditary platelet function disorder	est un(e) (attribut)	Hereditary disorder of hematologic system	false	Inferred relationship	Some
Hereditary platelet function disorder	est un(e) (attribut)	Qualitative platelet disorder	false	Inferred relationship	Some
Hereditary platelet function disorder	localisation d'une constatation (attribut)	structure du système hématopoïétique	false	Inferred relationship	Some
Hereditary platelet function disorder	est défini par la manifestation de (attribut)	constatation à propos des plaquettes	false	Inferred relationship	Some
Hereditary platelet function disorder	est défini par la manifestation de (attribut)	constatation sur le système hémostatique	false	Inferred relationship	Some
Hereditary platelet function disorder	est un(e) (attribut)	Qualitative platelet disorder (disorder)	true	Inferred relationship	Some
Hereditary platelet function disorder	localisation d'une constatation (attribut)	structure d'un système corporel	true	Inferred relationship	Some	2
Hereditary platelet function disorder	localisation d'une constatation (attribut)	structure du système hématopoïétique	false	Inferred relationship	Some
Hereditary platelet function disorder	localisation d'une constatation (attribut)	Platelet (cell structure)	false	Inferred relationship	Some

Inbound Relationships	Type	Active	Source	Characteristic	Refinability	Group
Bleeding diathesis due to collagen receptor defect	est un(e) (attribut)	True	Hereditary platelet function disorder	Inferred relationship	Some
Cytosolic phospholipase-A2 alpha deficiency associated bleeding disorder (disorder)	est un(e) (attribut)	True	Hereditary platelet function disorder	Inferred relationship	Some
Severe autosomal recessive macrothrombocytopenia (disorder)	est un(e) (attribut)	True	Hereditary platelet function disorder	Inferred relationship	Some
Scott syndrome	est un(e) (attribut)	True	Hereditary platelet function disorder	Inferred relationship	Some
Platelet storage pool defect	est un(e) (attribut)	True	Hereditary platelet function disorder	Inferred relationship	Some
Familial alpha>2< adrenergic receptor defect in platelets	est un(e) (attribut)	True	Hereditary platelet function disorder	Inferred relationship	Some
Isolated collagen aggregation defect	est un(e) (attribut)	True	Hereditary platelet function disorder	Inferred relationship	Some
Glanzmann's thrombasthenia	est un(e) (attribut)	True	Hereditary platelet function disorder	Inferred relationship	Some
Platelet procoagulant activity deficiency	est un(e) (attribut)	True	Hereditary platelet function disorder	Inferred relationship	Some
Platelet secretory disorder (disorder)	est un(e) (attribut)	True	Hereditary platelet function disorder	Inferred relationship	Some
syndrome de Bernard-Soulier (trouble)	est un(e) (attribut)	True	Hereditary platelet function disorder	Inferred relationship	Some
Bleeding disorder due to deficiency of calcium and diacylglycerol-regulated guanine nucleotide exchange factor I (disorder)	est un(e) (attribut)	True	Hereditary platelet function disorder	Inferred relationship	Some
Defect of purinergic receptor p2y G protein-coupled 12 (disorder)	est un(e) (attribut)	True	Hereditary platelet function disorder	Inferred relationship	Some
Platelet type pseudo-von Willebrand disease	est un(e) (attribut)	True	Hereditary platelet function disorder	Inferred relationship	Some

This concept is not in any reference sets

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Id	Description	Lang	Type	Status	Case?	Module
194690019	Hereditary platelet function disorder	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
732056019	Hereditary platelet function disorder (disorder)	en	Fully specified name	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core