33297000: Hereditary factor II deficiency disease (disorder)

SNOMED CT Concept\constatation clinique\...

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

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

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

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

485473013 Hereditary hypoprothrombinaemia en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core

55565011 Hereditary factor II deficiency disease en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core

55566012 Hereditary hypoprothrombinemia en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core

764682017 Hereditary factor II 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 II deficiency disease	interprète (attribut)	Hemostatic function (observable entity)	true	Inferred relationship	Some	1
Hereditary factor II deficiency disease	a pour interprétation (attribut)	anormal	true	Inferred relationship	Some	1
Hereditary factor II deficiency disease	est un(e) (attribut)	Hereditary coagulation factor deficiency	true	Inferred relationship	Some
Hereditary factor II deficiency disease	est un(e) (attribut)	Factor II deficiency	true	Inferred relationship	Some
Hereditary factor II deficiency disease	localisation d'une constatation (attribut)	structure d'un système corporel	false	Inferred relationship	Some
Hereditary factor II deficiency disease	est défini par la manifestation de (attribut)	constatation sur le système hémostatique	false	Inferred relationship	Some
Hereditary factor II deficiency disease	localisation d'une constatation (attribut)	Entire hematological system (body structure)	false	Inferred relationship	Some

Inbound Relationships

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Characteristic

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This concept is not in any reference sets