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Summary Literature (0)
MIM:614962 - LEPTIN DEFICIENCY OR DYSFUNCTION; LEPD

Xenbase Genes: lep

Human Disease Resource: OMIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0013991 - obesity due to congenital leptin deficiency

Disease Ontology (DO):
DOID:0111334 - congenital leptin deficiency