40855001: Hereditary factor VII deficiency disease (disorder)

SNOMED CT Concept\constatation clinique\...

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

\Prothrombin complex deficiency\Factor VII deficiency\Hereditary factor VII deficiency disease (disorder)

\Coagulation factor deficiency syndrome\Factor VII deficiency\Hereditary factor VII deficiency disease (disorder)
\Coagulation factor deficiency syndrome\Hereditary coagulation factor deficiency\Hereditary factor VII deficiency disease (disorder)

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

2789802015 Hereditary factor VII deficiency disease (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core

2794698010 Hereditary factor VII deficiency disease en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core

492809012 Hereditary hypoproconvertinaemia en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core

68137016 Hereditary factor VII deficiency syndrome en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core

68138014 Hereditary hypoproconvertinemia en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core

Expanded Value Set

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

This concept is not in any reference sets