725035001: Familial partial lipodystrophy Kobberling type (disorder)

• SNOMED CT Concept\Clinical finding\...
• \Finding of limb structure\Disorder of extremity\Familial partial lipodystrophy\Familial partial lipodystrophy Kobberling type
• \Finding of trunk structure\Disorder of trunk\Familial partial lipodystrophy\Familial partial lipodystrophy Kobberling type
• \General finding of soft tissue\Subcutaneous tissue finding\Disorder of subcutaneous tissue\Subcutaneous fat disorder\Lipodystrophy\Genetic lipodystrophy\Familial partial lipodystrophy\Familial partial lipodystrophy Kobberling type
• \General finding of soft tissue\Disorder of soft tissue\Disorder of skin and/or subcutaneous tissue\Disorder of subcutaneous tissue\Subcutaneous fat disorder\Lipodystrophy\Genetic lipodystrophy\Familial partial lipodystrophy\Familial partial lipodystrophy Kobberling type
• \Integumentary system finding\Subcutaneous tissue finding\Disorder of subcutaneous tissue\Subcutaneous fat disorder\Lipodystrophy\Genetic lipodystrophy\Familial partial lipodystrophy\Familial partial lipodystrophy Kobberling type
• \Integumentary system finding\Disorder of integument\Hereditary disorder of the integument\Familial partial lipodystrophy Kobberling type
• \Integumentary system finding\Disorder of integument\Disorder of skin and/or subcutaneous tissue\Disorder of subcutaneous tissue\Subcutaneous fat disorder\Lipodystrophy\Genetic lipodystrophy\Familial partial lipodystrophy\Familial partial lipodystrophy Kobberling type
• \Disease\Genetic disease\Genetic lipodystrophy\Familial partial lipodystrophy\Familial partial lipodystrophy Kobberling type
• \Disease\Genetic disease\Hereditary disease\Hereditary disorder by system\Hereditary disorder of the integument\Familial partial lipodystrophy Kobberling type
• \Disease\Genetic disease\Hereditary disease\Inherited disorder of connective tissue\Familial partial lipodystrophy Kobberling type
• \Disease\Genetic disease\Hereditary disease\Autosomal hereditary disorder\Autosomal dominant hereditary disorder\Familial partial lipodystrophy Kobberling type
• \Disease\Degenerative disorder\Lipodystrophy\Genetic lipodystrophy\Familial partial lipodystrophy\Familial partial lipodystrophy Kobberling type
• \Disease\Disorder of body system\Hereditary disorder by system\Hereditary disorder of the integument\Familial partial lipodystrophy Kobberling type
• \Disease\Disorder of body system\Disorder of integument\Hereditary disorder of the integument\Familial partial lipodystrophy Kobberling type
• \Disease\Disorder of body system\Disorder of integument\Disorder of skin and/or subcutaneous tissue\Disorder of subcutaneous tissue\Subcutaneous fat disorder\Lipodystrophy\Genetic lipodystrophy\Familial partial lipodystrophy\Familial partial lipodystrophy Kobberling type
• \Disease\Disorder of extremity\Familial partial lipodystrophy\Familial partial lipodystrophy Kobberling type
• \Disease\Disorder of trunk\Familial partial lipodystrophy\Familial partial lipodystrophy Kobberling type
• \Disease\Disorder of connective tissue\Inherited disorder of connective tissue\Familial partial lipodystrophy Kobberling type
• \Disease\Disorder of connective tissue\Subcutaneous fat disorder\Lipodystrophy\Genetic lipodystrophy\Familial partial lipodystrophy\Familial partial lipodystrophy Kobberling type
• \Disease\Disorder of soft tissue\Disorder of skin and/or subcutaneous tissue\Disorder of subcutaneous tissue\Subcutaneous fat disorder\Lipodystrophy\Genetic lipodystrophy\Familial partial lipodystrophy\Familial partial lipodystrophy Kobberling type

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

Descriptions:

Id	Description	Lang	Type	Status	Case?	Module
3437152010	Familial partial lipodystrophy Kobberling type (disorder)	en	Fully specified name	Active	Initial character case insensitive	SNOMED CT core
3437153017	Familial partial lipodystrophy Kobberling type	en	Synonym	Active	Initial character case insensitive	SNOMED CT core
3437154011	Familial partial lipodystrophy type 1	en	Synonym	Active	Case insensitive	SNOMED CT core
3437155012	A very rare form of familial partial lipodystrophy of unknown etiology characterized by loss of adipose tissue that is confined to the limbs and a normal or increased fat distribution of the face, neck, and trunk. Arterial hypertension and diabetes have also been associated	en	Definition	Active	Case sensitive	SNOMED CT core
3437156013	A very rare form of familial partial lipodystrophy of unknown aetiology characterised by loss of adipose tissue that is confined to the limbs and a normal or increased fat distribution of the face, neck, and trunk. Arterial hypertension and diabetes have also been associated	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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