33169001: Factor XI deficiency, type II (disorder)

SNOMED CT Concept\constatation clinique\...

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

\Contact factor deficiency\Hereditary factor XI deficiency disease (disorder)\Factor XI deficiency, type II

\Coagulation factor deficiency syndrome\Factor XI deficiency\Hereditary factor XI deficiency disease (disorder)\Factor XI deficiency, type II
\Coagulation factor deficiency syndrome\Hemophilia\Hereditary factor XI deficiency disease (disorder)\Factor XI deficiency, type II

\Disease\Genetic disease\maladie héréditaire\Autosomal hereditary disorder\Autosomal recessive hereditary disorder\Hereditary factor XI deficiency disease (disorder)\Factor XI deficiency, type II
\Disease\Disorder of haemostatic system\Blood coagulation disorder\Contact factor deficiency\Hereditary factor XI deficiency disease (disorder)\Factor XI deficiency, type II
\Disease\Disorder of haemostatic system\Blood coagulation disorder\Coagulation factor deficiency syndrome\Factor XI deficiency\Hereditary factor XI deficiency disease (disorder)\Factor XI deficiency, type II
\Disease\Disorder of haemostatic system\Blood coagulation disorder\Coagulation factor deficiency syndrome\Hemophilia\Hereditary factor XI deficiency disease (disorder)\Factor XI deficiency, type II
\Disease\Congenital disease\Hereditary factor XI deficiency disease (disorder)\Factor XI deficiency, type II

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

55354017 Factor XI deficiency, type II en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core

764538019 Factor XI deficiency, type II (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
Factor XI deficiency, type II	interprète (attribut)	Hemostatic function (observable entity)	true	Inferred relationship	Some	1
Factor XI deficiency, type II	a pour interprétation (attribut)	anormal	true	Inferred relationship	Some	1
Factor XI deficiency, type II	est un(e) (attribut)	Hereditary factor XI deficiency disease (disorder)	true	Inferred relationship	Some
Factor XI deficiency, type II	localisation d'une constatation (attribut)	structure d'un système corporel	false	Inferred relationship	Some
Factor XI deficiency, type II	est défini par la manifestation de (attribut)	constatation sur le système hémostatique	false	Inferred relationship	Some
Factor XI deficiency, type II	localisation d'une constatation (attribut)	Entire hematological system (body structure)	false	Inferred relationship	Some
Factor XI deficiency, type II	survenue (attribut)	congénital	true	Inferred relationship	Some	2

Inbound Relationships

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This concept is not in any reference sets