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obesity due to leptin receptor gene deficiency

Disease Summary
Associated Targets (1)
Tclin

1


Uniprot Description A rare disease characterized by normal levels of serum leptin, hyperphagia and severe obesity from an early age. Additional features include alterations in immune function, and delayed puberty due to hypogonadotropic hypogonadism.
Mondo Term and Equivalent IDs
MONDO:0013992:  obesity due to leptin receptor gene deficiency
NCIT:C120386: 
Orphanet:179494: 
UMLS:C3554225: