43217004: Hereditary factor XII deficiency disease (disorder)

SNOMED CT Concept\constatation clinique\...

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

\Contact factor deficiency\Factor XII deficiency disease\Hereditary factor XII deficiency disease

\Coagulation factor deficiency syndrome\Factor XII deficiency disease\Hereditary factor XII deficiency disease
\Coagulation factor deficiency syndrome\Hereditary coagulation factor deficiency\Hereditary factor XII deficiency disease

\Disease\Genetic disease\maladie héréditaire\Hereditary coagulation factor deficiency\Hereditary factor XII deficiency disease
\Disease\Genetic disease\maladie héréditaire\Autosomal hereditary disorder\Autosomal recessive hereditary disorder\Hereditary factor XII deficiency disease
\Disease\Disorder of haemostatic system\Blood coagulation disorder\Contact factor deficiency\Factor XII deficiency disease\Hereditary factor XII deficiency disease
\Disease\Disorder of haemostatic system\Blood coagulation disorder\Coagulation factor deficiency syndrome\Factor XII deficiency disease\Hereditary factor XII deficiency disease
\Disease\Disorder of haemostatic system\Blood coagulation disorder\Coagulation factor deficiency syndrome\Hereditary coagulation factor deficiency\Hereditary factor XII deficiency disease

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

72102014 Hereditary factor XII deficiency disease en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core

72103016 Hereditary Hageman factor deficiency disease en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core

780203015 Hereditary factor XII 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
Hereditary factor XII deficiency disease	interprète (attribut)	Hemostatic function (observable entity)	true	Inferred relationship	Some	1
Hereditary factor XII deficiency disease	a pour interprétation (attribut)	anormal	true	Inferred relationship	Some	1
Hereditary factor XII deficiency disease	est un(e) (attribut)	Autosomal recessive hereditary disorder	true	Inferred relationship	Some
Hereditary factor XII deficiency disease	est un(e) (attribut)	Hereditary coagulation factor deficiency	true	Inferred relationship	Some
Hereditary factor XII deficiency disease	est un(e) (attribut)	Factor XII deficiency disease	true	Inferred relationship	Some
Hereditary factor XII deficiency disease	localisation d'une constatation (attribut)	structure d'un système corporel	false	Inferred relationship	Some
Hereditary factor XII deficiency disease	est défini par la manifestation de (attribut)	constatation sur le système hémostatique	false	Inferred relationship	Some
Hereditary factor XII deficiency disease	localisation d'une constatation (attribut)	Entire hematological system (body structure)	false	Inferred relationship	Some

Inbound Relationships

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This concept is not in any reference sets