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Summary Literature (0)
MIM:151660 - LIPODYSTROPHY, FAMILIAL PARTIAL, TYPE 2; FPLD2

Xenbase Genes: pparg, lmna

Human Disease Resource: MIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0007906 - familial partial lipodystrophy, Dunnigan type

Disease Ontology (DO):
DOID:0050440 - familial partial lipodystrophy
DOID:0070202 - familial partial lipodystrophy type 2