111589005: dysfibrinogénémie (trouble)

SNOMED CT Concept\constatation clinique\...

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

\Fibrinogen abnormality\anomalie congénitale du fibrinogène\Dysfibrinogenemia

\Coagulation factor deficiency syndrome\Factor I deficiency disease (disorder)\Dysfibrinogenemia

\Disease\Disorder of haemostatic system\Blood coagulation disorder\Fibrinogen abnormality\anomalie congénitale du fibrinogène\Dysfibrinogenemia
\Disease\Disorder of haemostatic system\Blood coagulation disorder\Coagulation factor deficiency syndrome\Factor I deficiency disease (disorder)\Dysfibrinogenemia
\Disease\Congenital disease\anomalie congénitale du fibrinogène\Dysfibrinogenemia

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

178844010 Dysfibrinogenemia en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
189812014 Dysfibrinogenemia, NOS en Synonym (core metadata concept) Inactive Only initial character case insensitive (core metadata concept) SNOMED CT core
363901010 Dysfibrinogenaemia en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
632834017 Dysfibrinogenemia (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
817081000241112 dysfibrinogénémie fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Common French translation module (core metadata concept)
817091000241114 dysfibrinogénémie (trouble) fr Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT Common French translation module (core metadata concept)

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
Dysfibrinogenemia	interprète (attribut)	Hemostatic function (observable entity)	true	Inferred relationship	Some	1
Dysfibrinogenemia	a pour interprétation (attribut)	anormal	true	Inferred relationship	Some	1
Dysfibrinogenemia	survenue (attribut)	congénital	true	Inferred relationship	Some	2
Dysfibrinogenemia	localisation d'une constatation (attribut)	structure d'un système corporel	false	Inferred relationship	Some
Dysfibrinogenemia	est défini par la manifestation de (attribut)	constatation sur le système hémostatique	false	Inferred relationship	Some
Dysfibrinogenemia	est un(e) (attribut)	Factor I deficiency disease (disorder)	true	Inferred relationship	Some
Dysfibrinogenemia	localisation d'une constatation (attribut)	Entire hematological system (body structure)	false	Inferred relationship	Some
Dysfibrinogenemia	est un(e) (attribut)	anomalie congénitale du fibrinogène	true	Inferred relationship	Some
Dysfibrinogenemia	est un(e) (attribut)	Coagulation factor deficiency syndrome	false	Inferred relationship	Some

Inbound Relationships	Type	Active	Source	Characteristic	Refinability	Group
Hereditary dysfibrinogenemia (disorder)	est un(e) (attribut)	True	Dysfibrinogenemia	Inferred relationship	Some
Alpha chain defect dysfibrinogenemia	est un(e) (attribut)	True	Dysfibrinogenemia	Inferred relationship	Some
Beta chain defect dysfibrinogenaemia	est un(e) (attribut)	True	Dysfibrinogenemia	Inferred relationship	Some
Gamma chain defect dysfibrinogenemia	est un(e) (attribut)	True	Dysfibrinogenemia	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)