Familial partial lipodystrophy, Dunnigan type

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A rare, genetic lipodystrophy characterized by a 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, diabetes mellitus, dyslipidemia and liver steatosis.

Synonyms: Familial partial lipodystrophy type 2 Dunnigan syndrome FPLD2

This is just here as a test because I lose it

Term information

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ICD-10:E88.1
UMLS:C1720860
OMIM:151660

notation

ORPHA:2348