45366001: Hereditary dysfibrinogenemia (disorder)

SNOMED CT Concept\constatation clinique\...

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

\Fibrinogen abnormality\anomalie congénitale du fibrinogène\...

\Dysfibrinogenemia\Hereditary dysfibrinogenemia (disorder)

\Hereditary factor I deficiency disease\Hereditary dysfibrinogenemia (disorder)

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

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

2786838014 Hereditary dysfibrinogenemia (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core

2792832010 Hereditary dysfibrinogenaemia en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core

2795322018 Hereditary dysfibrinogenemia en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core

494185015 Congenital dysfibrinogenaemia en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core

75627010 Congenital dysfibrinogenemia en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core

Expanded Value Set

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

Inbound Relationships	Type	Active	Source	Characteristic	Refinability	Group
Hereditary thrombophilic dysfibrinogenemia (disorder)	est un(e) (attribut)	True	Hereditary dysfibrinogenemia (disorder)	Inferred relationship	Some

Reference Sets

Canada English language reference set (foundation metadata concept)

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)