400040008: Hereditary lymphedema type II (disorder)

• SNOMED CT Concept\Clinical finding\...
• \Finding of limb structure\Edema of extremity\Lymphoedema of limb\Primary lymphoedema\Hereditary lymphoedema\Hereditary lymphoedema type II
• \Finding of limb structure\Disorder of extremity\Lymphoedema of limb\Primary lymphoedema\Hereditary lymphoedema\Hereditary lymphoedema type II
• \Oedema\Edema of extremity\Lymphoedema of limb\Primary lymphoedema\Hereditary lymphoedema\Hereditary lymphoedema type II
• \Oedema\Disorder characterised by oedema\Lymphoedema\Lymphoedema of limb\Primary lymphoedema\Hereditary lymphoedema\Hereditary lymphoedema type II
• \Disease\Genetic disease\Hereditary disease\Developmental hereditary disorder\Hereditary lymphoedema\Hereditary lymphoedema type II
• \Disease\Genetic disease\Hereditary disease\Autosomal hereditary disorder\Autosomal dominant hereditary disorder\Hereditary lymphoedema type II
• \Disease\Disorder of extremity\Lymphoedema of limb\Primary lymphoedema\Hereditary lymphoedema\Hereditary lymphoedema type II
• \Disease\Disorder characterised by oedema\Lymphoedema\Lymphoedema of limb\Primary lymphoedema\Hereditary lymphoedema\Hereditary lymphoedema type II
• \Disease\Developmental disorder\Primary lymphoedema\Hereditary lymphoedema\Hereditary lymphoedema type II
• \Disease\Developmental disorder\Developmental hereditary disorder\Hereditary lymphoedema\Hereditary lymphoedema type II

Status: current, Primitive. Date: 31-Jul 2003. Module: SNOMED CT core

Descriptions:

Id	Description	Lang	Type	Status	Case?	Module
1767960013	Hereditary lymphedema type II (disorder)	en	Fully specified name	Active	Initial character case insensitive	SNOMED CT core
1773487016	Hereditary lymphoedema type II	en	Synonym	Active	Initial character case insensitive	SNOMED CT core
1774773012	Hereditary lymphedema type II	en	Synonym	Active	Initial character case insensitive	SNOMED CT core
1783734014	Meige lymphoedema	en	Synonym	Active	Case sensitive	SNOMED CT core
1784120010	Meige lymphedema	en	Synonym	Active	Case sensitive	SNOMED CT core
3658941015	Meige disease	en	Synonym	Active	Case sensitive	SNOMED CT core

Expanded Value Set

Reference Sets

Australian emergency department reference set

Queensland allied health clinical finding reference set

Clinical finding foundation reference set

Problem/Diagnosis reference set

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