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Summary Literature (0)
MIM:269700 - LIPODYSTROPHY, CONGENITAL GENERALIZED, TYPE 2; CGL2

Xenbase Genes: bscl2

Human Disease Resource: MIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0010020 - tubotympanic recess epithelium
MONDO:0018883 - Berardinelli-Seip congenital lipodystrophy

Disease Ontology (DO):
DOID:0111136 - congenital generalized lipodystrophy type 2