399889006: Hereditary lymphedema type I (disorder)

SNOMED CT Concept\constatation clinique\...

\constatation à propos de la structure d'un membre\œdème d'une extrémité\Lymphedema of limb (disorder)\Primary lymphedema\lymphœdème héréditaire\Hereditary lymphedema type I (disorder)
\constatation à propos de la structure d'un membre\affection d'une extrémité\Lymphedema of limb (disorder)\Primary lymphedema\lymphœdème héréditaire\Hereditary lymphedema type I (disorder)

\Oedema\œdème d'une extrémité\Lymphedema of limb (disorder)\Primary lymphedema\lymphœdème héréditaire\Hereditary lymphedema type I (disorder)
\Oedema\Disorder characterized by edema\Lymphoedema\Lymphedema of limb (disorder)\Primary lymphedema\lymphœdème héréditaire\Hereditary lymphedema type I (disorder)

\Disease\Genetic disease\maladie héréditaire\Developmental hereditary disorder\lymphœdème héréditaire\Hereditary lymphedema type I (disorder)
\Disease\Genetic disease\maladie héréditaire\Autosomal hereditary disorder\Autosomal dominant hereditary disorder\Hereditary lymphedema type I (disorder)
\Disease\affection d'une extrémité\Lymphedema of limb (disorder)\Primary lymphedema\lymphœdème héréditaire\Hereditary lymphedema type I (disorder)
\Disease\Disorder characterized by edema\Lymphoedema\Lymphedema of limb (disorder)\Primary lymphedema\lymphœdème héréditaire\Hereditary lymphedema type I (disorder)
\Disease\trouble du développement\Primary lymphedema\lymphœdème héréditaire\Hereditary lymphedema type I (disorder)
\Disease\trouble du développement\Developmental hereditary disorder\lymphœdème héréditaire\Hereditary lymphedema type I (disorder)

Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2003. Module: SNOMED CT core

Descriptions:

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
Hereditary lymphedema type I (disorder)	est un(e) (attribut)	Autosomal dominant hereditary disorder	true	Inferred relationship	Some
Hereditary lymphedema type I (disorder)	localisation d'une constatation (attribut)	structure d'un membre	true	Inferred relationship	Some	1
Hereditary lymphedema type I (disorder)	Pathological process (attribute)	Pathological developmental process	true	Inferred relationship	Some	1
Hereditary lymphedema type I (disorder)	est un(e) (attribut)	lymphœdème héréditaire	true	Inferred relationship	Some
Hereditary lymphedema type I (disorder)	localisation d'une constatation (attribut)	structure d'un tissu mou (structure corporelle)	false	Inferred relationship	Some
Hereditary lymphedema type I (disorder)	morphologie associée (attribut)	Lymphatic oedema	false	Inferred relationship	Some
Hereditary lymphedema type I (disorder)	localisation d'une constatation (attribut)	Structure of peripheral lymphatic vessel (body structure)	false	Inferred relationship	Some	1
Hereditary lymphedema type I (disorder)	morphologie associée (attribut)	obstruction	false	Inferred relationship	Some	1
Hereditary lymphedema type I (disorder)	localisation d'une constatation (attribut)	Structure of lymphatic system (body structure)	false	Inferred relationship	Some	1
Hereditary lymphedema type I (disorder)	morphologie associée (attribut)	Lymphatic oedema	false	Inferred relationship	Some	1
Hereditary lymphedema type I (disorder)	morphologie associée (attribut)	Lymphatic oedema	true	Inferred relationship	Some	1

Inbound Relationships

Type

Active

Source

Characteristic

Refinability

Group

Reference Sets

Canada English language reference set (foundation metadata concept)

Client's clinical problems, conditions, diagnoses, symptoms, findings, complaints reference set (foundation metadata concept)

Most commonly used clinical problems, conditions, diagnoses, symptoms, findings and complaints, as interpreted by the provider reference set (foundation metadata concept)

Description inactivation indicator reference set

GB English

US English

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Id	Description	Lang	Type	Status	Case?	Module
1767809013	Hereditary lymphedema type I (disorder)	en	Fully specified name	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
1773470018	Hereditary lymphoedema type I	en	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
1774756010	Hereditary lymphedema type I	en	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
1783719015	Nonne-Milroy lymphoedema	en	Synonym (core metadata concept)	Active	Entire term case sensitive (core metadata concept)	SNOMED CT core
1783720014	Primary congenital lymphoedema	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
1783721013	Milroy lymphoedema	en	Synonym (core metadata concept)	Active	Entire term case sensitive (core metadata concept)	SNOMED CT core
1784105016	Nonne-Milroy lymphedema	en	Synonym (core metadata concept)	Active	Entire term case sensitive (core metadata concept)	SNOMED CT core
1784106015	Milroy lymphedema	en	Synonym (core metadata concept)	Active	Entire term case sensitive (core metadata concept)	SNOMED CT core
1784107012	Primary congenital lymphedema	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core