400040008: Hereditary lymphedema type II (disorder)

SNOMED CT Concept\Clinical finding (finding)\...

\Finding of limb structure (finding)\Edema of extremity (finding)\Lymphedema of limb (disorder)\Primary lymphedema\Hereditary lymphedema\Hereditary lymphedema type II (disorder)
\Finding of limb structure (finding)\Disorder of limb\Lymphedema of limb (disorder)\Primary lymphedema\Hereditary lymphedema\Hereditary lymphedema type II (disorder)

\Oedema\Edema of extremity (finding)\Lymphedema of limb (disorder)\Primary lymphedema\Hereditary lymphedema\Hereditary lymphedema type II (disorder)
\Oedema\Disorder characterized by edema\Lymphoedema\Lymphedema of limb (disorder)\Primary lymphedema\Hereditary lymphedema\Hereditary lymphedema type II (disorder)

\Disease\Genetic disease\Hereditary disease\Developmental hereditary disorder\Hereditary lymphedema\Hereditary lymphedema type II (disorder)
\Disease\Genetic disease\Hereditary disease\Autosomal hereditary disorder\Autosomal dominant hereditary disorder\Hereditary lymphedema type II (disorder)
\Disease\Disorder of limb\Lymphedema of limb (disorder)\Primary lymphedema\Hereditary lymphedema\Hereditary lymphedema type II (disorder)
\Disease\Disorder characterized by edema\Lymphoedema\Lymphedema of limb (disorder)\Primary lymphedema\Hereditary lymphedema\Hereditary lymphedema type II (disorder)
\Disease\Developmental disorder (disorder)\Primary lymphedema\Hereditary lymphedema\Hereditary lymphedema type II (disorder)
\Disease\Developmental disorder (disorder)\Developmental hereditary disorder\Hereditary lymphedema\Hereditary lymphedema type II (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 II (disorder)	Is a	Hereditary lymphedema	true	Inferred relationship	Existential restriction modifier (core metadata concept)
Hereditary lymphedema type II (disorder)	Finding site	Structure of soft tissue (body structure)	false	Inferred relationship	Existential restriction modifier (core metadata concept)
Hereditary lymphedema type II (disorder)	Associated morphology	Lymphatic edema	false	Inferred relationship	Existential restriction modifier (core metadata concept)
Hereditary lymphedema type II (disorder)	Finding site	Structure of peripheral lymphatic vessel (body structure)	false	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Hereditary lymphedema type II (disorder)	Finding site	Structure of lymphatic system	false	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Hereditary lymphedema type II (disorder)	Associated morphology	Obstruction	false	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Hereditary lymphedema type II (disorder)	Associated morphology	Lymphatic edema	false	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Hereditary lymphedema type II (disorder)	Associated morphology	Lymphatic edema	true	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Hereditary lymphedema type II (disorder)	Is a	Autosomal dominant hereditary disorder	true	Inferred relationship	Existential restriction modifier (core metadata concept)
Hereditary lymphedema type II (disorder)	Finding site	Limb structure	true	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Hereditary lymphedema type II (disorder)	Pathological process (attribute)	Pathological developmental process (qualifier value)	true	Inferred relationship	Existential restriction modifier (core metadata concept)	1

Inbound Relationships

Type

Active

Source

Characteristic

Refinability

Group

This concept is not in any reference sets

Back to Start

Id	Description	Lang	Type	Status	Case?	Module
1767960013	Hereditary lymphedema type II (disorder)	en	Fully specified name	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
1773487016	Hereditary lymphoedema type II	en	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
1774773012	Hereditary lymphedema type II	en	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
1783734014	Meige lymphoedema	en	Synonym (core metadata concept)	Active	Entire term case sensitive (core metadata concept)	SNOMED CT core
1784120010	Meige lymphedema	en	Synonym (core metadata concept)	Active	Entire term case sensitive (core metadata concept)	SNOMED CT core
3658941015	Meige disease	en	Synonym (core metadata concept)	Active	Entire term case sensitive (core metadata concept)	SNOMED CT core
1767960013	Hereditary lymphedema type II (disorder)	en	Fully specified name	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
1773487016	Hereditary lymphoedema type II	en	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
1774773012	Hereditary lymphedema type II	en	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
1783734014	Meige lymphoedema	en	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
1783734014	Meige lymphoedema	en	Synonym (core metadata concept)	Active	Entire term case sensitive (core metadata concept)	SNOMED CT core
1783735010	Lymphoedema praecox	en	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
1784120010	Meige lymphedema	en	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
1784120010	Meige lymphedema	en	Synonym (core metadata concept)	Active	Entire term case sensitive (core metadata concept)	SNOMED CT core
1784121014	Lymphedema praecox	en	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
3658941015	Meige disease	en	Synonym (core metadata concept)	Active	Entire term case sensitive (core metadata concept)	SNOMED CT core
3417371001000117	Meige-Krankheit	de	Synonym (core metadata concept)	Active	Entire term case sensitive (core metadata concept)	SNOMED CT Switzerland NRC maintained Module
6064521000241111	lymphœdème héréditaire type II	fr	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT Switzerland NRC maintained Module
6064521000241111	lymphœdème héréditaire type II	fr	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT Switzerland NRC maintained Module
3417371001000117	Meige-Krankheit	de	Synonym (core metadata concept)	Active	Entire term case sensitive (core metadata concept)	SNOMED CT Switzerland NRC maintained Module