Monarch Disease Ontology identifier MONDO_0012072 (familial partial lipodystrophy, Kobberling type), is a very rare form of familial partial lipodystrophy (FPLD) of unknown etiology characterized by lipoatrophy 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. Inheritance is thought to be autosomal dominant. Also known as: FPLD1, familial partial lipodystrophy type 1.