50189006: Hereditary 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\Hereditary factor XIII deficiency disease (disorder)

\Hereditary coagulation factor deficiency\Hereditary factor XIII deficiency disease (disorder)

\Disease\Genetic disease\maladie héréditaire\Hereditary coagulation factor deficiency\Hereditary factor XIII deficiency disease (disorder)
\Disease\Disorder of haemostatic system\Blood coagulation disorder\Coagulation factor deficiency syndrome\Factor XIII deficiency disease\Hereditary factor XIII deficiency disease (disorder)
\Disease\Disorder of haemostatic system\Blood coagulation disorder\Coagulation factor deficiency syndrome\Hereditary coagulation factor deficiency\Hereditary factor XIII deficiency disease (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

787949018 Hereditary factor XIII deficiency disease (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core

83596013 Hereditary factor XIII deficiency disease en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core

83597016 Laki-Lorand factor deficiency disease en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core

Expanded Value Set

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

Inbound Relationships	Type	Active	Source	Characteristic	Refinability	Group
Hereditary factor XIII A subunit and B subunit deficiency (disorder)	est un(e) (attribut)	True	Hereditary factor XIII deficiency disease (disorder)	Inferred relationship	Some
Hereditary factor XIII B subunit deficiency (disorder)	est un(e) (attribut)	True	Hereditary factor XIII deficiency disease (disorder)	Inferred relationship	Some
Hereditary factor XIII A subunit deficiency (disorder)	est un(e) (attribut)	True	Hereditary factor XIII deficiency disease (disorder)	Inferred relationship	Some

This concept is not in any reference sets