49762007: déficience congénitale héréditaire en facteur de coagulation XI (trouble)

SNOMED CT Concept\constatation clinique\...

\constatation fonctionnelle\Disorder of haemostatic system\Blood coagulation disorder\...

\Contact factor deficiency\Hereditary factor XI deficiency disease (disorder)

\Coagulation factor deficiency syndrome\Factor XI deficiency\Hereditary factor XI deficiency disease (disorder)
\Coagulation factor deficiency syndrome\Hemophilia\Hereditary factor XI deficiency disease (disorder)

\Disease\Genetic disease\maladie héréditaire\Autosomal hereditary disorder\Autosomal recessive hereditary disorder\Hereditary factor XI deficiency disease (disorder)
\Disease\Disorder of haemostatic system\Blood coagulation disorder\Contact factor deficiency\Hereditary factor XI deficiency disease (disorder)
\Disease\Disorder of haemostatic system\Blood coagulation disorder\Coagulation factor deficiency syndrome\Factor XI deficiency\Hereditary factor XI deficiency disease (disorder)
\Disease\Disorder of haemostatic system\Blood coagulation disorder\Coagulation factor deficiency syndrome\Hemophilia\Hereditary factor XI deficiency disease (disorder)
\Disease\Congenital disease\Hereditary factor XI deficiency disease (disorder)

Status: current, Sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2018. Module: SNOMED CT core

Descriptions:

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
Hereditary factor XI deficiency disease (disorder)	a pour interprétation (attribut)	anormal	true	Inferred relationship	Some	2
Hereditary factor XI deficiency disease (disorder)	interprète (attribut)	Hemostatic function (observable entity)	true	Inferred relationship	Some	2
Hereditary factor XI deficiency disease (disorder)	est un(e) (attribut)	Hereditary coagulation factor deficiency	false	Inferred relationship	Some
Hereditary factor XI deficiency disease (disorder)	est un(e) (attribut)	Autosomal recessive hereditary disorder	true	Inferred relationship	Some
Hereditary factor XI deficiency disease (disorder)	est un(e) (attribut)	Contact factor deficiency	true	Inferred relationship	Some
Hereditary factor XI deficiency disease (disorder)	est un(e) (attribut)	Hemophilia	true	Inferred relationship	Some
Hereditary factor XI deficiency disease (disorder)	localisation d'une constatation (attribut)	structure d'un système corporel	false	Inferred relationship	Some
Hereditary factor XI deficiency disease (disorder)	est défini par la manifestation de (attribut)	constatation sur le système hémostatique	false	Inferred relationship	Some
Hereditary factor XI deficiency disease (disorder)	localisation d'une constatation (attribut)	Entire hematological system (body structure)	false	Inferred relationship	Some
Hereditary factor XI deficiency disease (disorder)	survenue (attribut)	congénital	true	Inferred relationship	Some	1
Hereditary factor XI deficiency disease (disorder)	est un(e) (attribut)	Congenital disease	true	Inferred relationship	Some
Hereditary factor XI deficiency disease (disorder)	est un(e) (attribut)	Factor XI deficiency	true	Inferred relationship	Some

Inbound Relationships	Type	Active	Source	Characteristic	Refinability	Group
Factor XI deficiency, type II	est un(e) (attribut)	True	Hereditary factor XI deficiency disease (disorder)	Inferred relationship	Some
Factor XI deficiency, type III	est un(e) (attribut)	True	Hereditary factor XI deficiency disease (disorder)	Inferred relationship	Some
Factor XI deficiency, type I	est un(e) (attribut)	True	Hereditary factor XI deficiency disease (disorder)	Inferred relationship	Some

Reference Sets

Client's clinical problems, conditions, diagnoses, symptoms, findings, complaints reference set (foundation metadata concept)

Most commonly used clinical problems, conditions, diagnoses, symptoms, findings and complaints, as interpreted by the provider reference set (foundation metadata concept)

GB English

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Id	Description	Lang	Type	Status	Case?	Module
1230778013	Thromboplastin antecedent deficiency	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
495497019	Haemophilia C	en	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
787476012	Hereditary factor XI deficiency disease (disorder)	en	Fully specified name	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
814301000241111	déficience congénitale héréditaire en facteur de coagulation XI	fr	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT Common French translation module (core metadata concept)
814311000241113	déficience congénitale héréditaire en facteur de coagulation XI (trouble)	fr	Fully specified name	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT Common French translation module (core metadata concept)
82886016	Hereditary factor XI deficiency disease	en	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
82887013	Hemophilia C	en	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
82888015	Congenital factor XI deficiency disease	en	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
82889011	Plasma thromboplastin antecedent deficiency	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
82890019	PTA deficiency	en	Synonym (core metadata concept)	Active	Entire term case sensitive (core metadata concept)	SNOMED CT core
82891015	Rosenthal's disease	en	Synonym (core metadata concept)	Active	Entire term case sensitive (core metadata concept)	SNOMED CT core
842551000241115	déficit congénital héréditaire en facteur XI	fr	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT Common French translation module (core metadata concept)