715439000: Familial partial lipodystrophy type 2 (disorder)

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

Status: current, Primitive. Date: 31-Jul 2016. Module: SNOMED CT core

Descriptions:

Id	Description	Lang	Type	Status	Case?	Module
3302634017	Familial partial lipodystrophy type 2 (disorder)	en	Fully specified name	Active	Case insensitive	SNOMED CT core
3302635016	Familial partial lipodystrophy type 2	en	Synonym	Active	Case insensitive	SNOMED CT core
3302636015	Familial partial lipodystrophy Dunnigan type	en	Synonym	Active	Initial character case insensitive	SNOMED CT core
3302637012	Dunnigan syndrome	en	Synonym	Active	Case sensitive	SNOMED CT core
3302638019	A rare form of genetic lipodystrophy with loss of subcutaneous adipose tissue from the trunk, buttocks and limbs; fat accumulation in the neck, face, axillary and pelvic regions; muscular hypertrophy; and usually associated with metabolic complications such as insulin resistance. Inherited in an autosomal dominant manner.	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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