18604004: Factor XIII deficiency disease (disorder)

SNOMED CT Concept\constatation clinique\...

\constatation fonctionnelle\Disorder of haemostatic system\Blood coagulation disorder\Coagulation factor deficiency syndrome\Factor XIII deficiency disease

\Disease\Disorder of haemostatic system\Blood coagulation disorder\Coagulation factor deficiency syndrome\Factor XIII deficiency disease

Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2007. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module

1222141018 Factor XIII deficiency en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core

31367019 Factor XIII deficiency disease en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core

31369016 Fibrin stabilizing factor deficiency en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core

478723018 Fibrin stabilising factor deficiency en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core

746118017 Factor XIII deficiency disease (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
Factor XIII deficiency disease	interprète (attribut)	Hemostatic function (observable entity)	true	Inferred relationship	Some	1
Factor XIII deficiency disease	a pour interprétation (attribut)	anormal	true	Inferred relationship	Some	1
Factor XIII deficiency disease	est un(e) (attribut)	Hereditary coagulation factor deficiency	false	Inferred relationship	Some
Factor XIII deficiency disease	est un(e) (attribut)	Fibrinogen abnormality	false	Inferred relationship	Some
Factor XIII deficiency disease	localisation d'une constatation (attribut)	structure d'un système corporel	false	Inferred relationship	Some
Factor XIII deficiency disease	est défini par la manifestation de (attribut)	constatation sur le système hémostatique	false	Inferred relationship	Some
Factor XIII deficiency disease	est un(e) (attribut)	Coagulation factor deficiency syndrome	true	Inferred relationship	Some
Factor XIII deficiency disease	localisation d'une constatation (attribut)	Entire hematological system (body structure)	false	Inferred relationship	Some
Factor XIII deficiency disease	interprète (attribut)	Nutritional deficiency state	false	Inferred relationship	Some

Inbound Relationships	Type	Active	Source	Characteristic	Refinability	Group
Hereditary factor I deficiency disease	est un(e) (attribut)	False	Factor XIII deficiency disease	Inferred relationship	Some
Hereditary factor XIII deficiency disease (disorder)	est un(e) (attribut)	True	Factor XIII deficiency disease	Inferred relationship	Some
Acquired factor XIII deficiency disease	est un(e) (attribut)	True	Factor XIII deficiency disease	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)