724176001: Lipodystrophy due to peptidic growth factors deficiency (disorder)

• SNOMED CT Concept\Clinical finding\...
• \General finding of soft tissue\Subcutaneous tissue finding\Disorder of subcutaneous tissue\Subcutaneous fat disorder\Lipodystrophy\Lipodystrophy due to peptidic growth factors deficiency
• \General finding of soft tissue\Disorder of soft tissue\Disorder of skin and/or subcutaneous tissue\Disorder of subcutaneous tissue\Subcutaneous fat disorder\Lipodystrophy\Lipodystrophy due to peptidic growth factors deficiency
• \Integumentary system finding\Subcutaneous tissue finding\Disorder of subcutaneous tissue\Subcutaneous fat disorder\Lipodystrophy\Lipodystrophy due to peptidic growth factors deficiency
• \Integumentary system finding\Disorder of integument\Disorder of skin and/or subcutaneous tissue\Disorder of subcutaneous tissue\Subcutaneous fat disorder\Lipodystrophy\Lipodystrophy due to peptidic growth factors deficiency
• \Disease\Degenerative disorder\Lipodystrophy\Lipodystrophy due to peptidic growth factors deficiency
• \Disease\Disorder of body system\Disorder of integument\Disorder of skin and/or subcutaneous tissue\Disorder of subcutaneous tissue\Subcutaneous fat disorder\Lipodystrophy\Lipodystrophy due to peptidic growth factors deficiency
• \Disease\Disorder of connective tissue\Subcutaneous fat disorder\Lipodystrophy\Lipodystrophy due to peptidic growth factors deficiency
• \Disease\Disorder of soft tissue\Disorder of skin and/or subcutaneous tissue\Disorder of subcutaneous tissue\Subcutaneous fat disorder\Lipodystrophy\Lipodystrophy due to peptidic growth factors deficiency

Status: current, Primitive. Date: 31-Jul 2017. Module: SNOMED CT core

Descriptions:

Id	Description	Lang	Type	Status	Case?	Module
3431530019	Lipodystrophy due to peptidic growth factors deficiency (disorder)	en	Fully specified name	Active	Case insensitive	SNOMED CT core
3431531015	Lipodystrophy due to peptidic growth factors deficiency	en	Synonym	Active	Case insensitive	SNOMED CT core
3431532010	Combined insulin, insulin-like growth factor 1 and epidermal growth factor deficiency	en	Synonym	Active	Case insensitive	SNOMED CT core
3431533017	Hoepffner Dreyer Reimers syndrome	en	Synonym	Active	Case sensitive	SNOMED CT core
3431534011	Werner-like syndrome due to combined growth factor deficiency	en	Synonym	Active	Case sensitive	SNOMED CT core
3431535012	Syndrome that has characteristics of loss of subcutaneous fat layers on the limbs, lipodystrophy in the face and trunk and scleroderma-like skin disorders (thickened skin on the palms and soles and skin pigment changes on the limbs and trunk). The syndrome has been described in only one family with three affected siblings. Other clinical signs are joint contractures, reduced relative body weight, a bird-like facial appearance with a beaked nose, and micrognathia. One sibling also showed insulin-resistant diabetes mellitus. The syndrome is due to a combined decreased action of insulin, insulin-like growth factor I (IGF-1) and epidermal growth factor (EGF). The disease shows common clinical characteristics with Werner syndrome.	en	Definition	Active	Case sensitive	SNOMED CT core

Expanded Value Set

Reference Sets

Australian emergency department reference set

Clinical finding foundation reference set

Problem/Diagnosis reference set

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