has material basis in germline mutation in LMNA familial partial lipodystrophy, Dunnigan type https://github.com/monarch-initiative/mondo/issues/1567 FPLD2 SCTID:715439000 lipodystrophy, familial, of limbs and Lower trunk OMIM:151660 lipodystrophy, familial partial, type 2 lipodystrophy, familial partial, Dunnigan type icd11.foundation:2068585355 Familial Partial lipodystrophy, Dunnigan type (FPLD2) is a rare form of 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. GARD:0003126 Dunnigan syndrome UMLS:C1720860 DOID:0070202 Orphanet:2348 familial partial lipodystrophy type 2 MEDGEN:354526 MONDO:0007906 FPL2 lipodystrophy, reverse partial progeroid syndrome familial partial lipodystrophy disorder of development or morphogenesis