37350004: Hereditary factor X deficiency disease (disorder)

SNOMED CT Concept\constatation clinique\...

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

\Prothrombin complex deficiency\Factor X deficiency\Hereditary factor X deficiency disease

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

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

62309012 Hereditary factor X deficiency disease en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
62310019 Hereditary Stuart factor deficiency disease en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
62311015 Hereditary Stuart-Prower deficiency disease en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
769207019 Hereditary factor X 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 X deficiency disease	interprète (attribut)	Hemostatic function (observable entity)	true	Inferred relationship	Some	1
Hereditary factor X deficiency disease	a pour interprétation (attribut)	anormal	true	Inferred relationship	Some	1
Hereditary factor X deficiency disease	est un(e) (attribut)	Factor X deficiency	true	Inferred relationship	Some
Hereditary factor X deficiency disease	est un(e) (attribut)	Autosomal recessive hereditary disorder	true	Inferred relationship	Some
Hereditary factor X deficiency disease	est un(e) (attribut)	Hereditary coagulation factor deficiency	true	Inferred relationship	Some
Hereditary factor X deficiency disease	localisation d'une constatation (attribut)	structure d'un système corporel	false	Inferred relationship	Some
Hereditary factor X deficiency disease	est défini par la manifestation de (attribut)	constatation sur le système hémostatique	false	Inferred relationship	Some
Hereditary factor X 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