400040008: Hereditary lymphedema type II (disorder)

SNOMED CT Concept\Clinical finding\...

\Finding of limb structure\Edema of extremity\Lymphedema of limb\Primary lymphedema\Hereditary lymphedema\Hereditary lymphedema type II
\Finding of limb structure\Disorder of extremity\Lymphedema of limb\Primary lymphedema\Hereditary lymphedema\Hereditary lymphedema type II

\Edema\Edema of extremity\Lymphedema of limb\Primary lymphedema\Hereditary lymphedema\Hereditary lymphedema type II
\Edema\Disorder characterized by edema\Lymphedema\Lymphedema of limb\Primary lymphedema\Hereditary lymphedema\Hereditary lymphedema type II

\Disease\Genetic disease\Hereditary disease\Developmental hereditary disorder\Hereditary lymphedema\Hereditary lymphedema type II
\Disease\Genetic disease\Hereditary disease\Autosomal hereditary disorder\Autosomal dominant hereditary disorder\Hereditary lymphedema type II
\Disease\Disorder of extremity\Lymphedema of limb\Primary lymphedema\Hereditary lymphedema\Hereditary lymphedema type II
\Disease\Disorder characterized by edema\Lymphedema\Lymphedema of limb\Primary lymphedema\Hereditary lymphedema\Hereditary lymphedema type II
\Disease\Developmental disorder\Primary lymphedema\Hereditary lymphedema\Hereditary lymphedema type II
\Disease\Developmental disorder\Developmental hereditary disorder\Hereditary lymphedema\Hereditary lymphedema type II

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

Descriptions:

Id Description Lang Type Status Case? Module

1767960013 Hereditary lymphedema type II (disorder) en Fully specified name Active Only initial character case insensitive SNOMED CT core module

1773487016 Hereditary lymphoedema type II en Synonym Active Only initial character case insensitive SNOMED CT core module

1774773012 Hereditary lymphedema type II en Synonym Active Only initial character case insensitive SNOMED CT core module

1783734014 Meige lymphoedema en Synonym Active Entire term case sensitive SNOMED CT core module

1784120010 Meige lymphedema en Synonym Active Entire term case sensitive SNOMED CT core module

3658941015 Meige disease en Synonym Active Entire term case sensitive SNOMED CT core module

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
Hereditary lymphedema type II	Is a	Hereditary lymphedema	true	Inferred relationship	Existential restriction modifier
Hereditary lymphedema type II	Finding site	Structure of soft tissue	false	Inferred relationship	Existential restriction modifier
Hereditary lymphedema type II	Associated morphology	Lymphatic edema	false	Inferred relationship	Existential restriction modifier
Hereditary lymphedema type II	Finding site	Structure of peripheral lymphatic vessel	false	Inferred relationship	Existential restriction modifier	1
Hereditary lymphedema type II	Finding site	Structure of lymphatic system	false	Inferred relationship	Existential restriction modifier	1
Hereditary lymphedema type II	Associated morphology	Obstruction	false	Inferred relationship	Existential restriction modifier	1
Hereditary lymphedema type II	Associated morphology	Lymphatic edema	false	Inferred relationship	Existential restriction modifier	1
Hereditary lymphedema type II	Associated morphology	Lymphatic edema	true	Inferred relationship	Existential restriction modifier	1
Hereditary lymphedema type II	Is a	Autosomal dominant hereditary disorder	true	Inferred relationship	Existential restriction modifier
Hereditary lymphedema type II	Finding site	Limb structure	true	Inferred relationship	Existential restriction modifier	1
Hereditary lymphedema type II	Pathological process	Pathological developmental process	true	Inferred relationship	Existential restriction modifier	1

Inbound Relationships

Type

Active

Source

Characteristic

Refinability

Group

This concept is not in any reference sets