Source: CURATED

Gene Disease Score gda Association Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 3952
Gene Symbol: LEP
LEP
CUI: C3554224
Disease: LEPTIN DEFICIENCY OR DYSFUNCTION
LEPTIN DEFICIENCY OR DYSFUNCTION 		0.800 GeneticVariation UNIPROT Biologically inactive leptin and early-onset extreme obesity. 25551525

2015
Entrez Id: 3952
Gene Symbol: LEP
LEP
CUI: C3554224
Disease: LEPTIN DEFICIENCY OR DYSFUNCTION
LEPTIN DEFICIENCY OR DYSFUNCTION 		0.800 GermlineCausalMutation ORPHANET Monogenic forms of childhood obesity due to mutations in the leptin gene. 26567097

2014
Entrez Id: 3952
Gene Symbol: LEP
LEP
CUI: C3554224
Disease: LEPTIN DEFICIENCY OR DYSFUNCTION
LEPTIN DEFICIENCY OR DYSFUNCTION 		0.800 GeneticVariation UNIPROT A leptin missense mutation associated with hypogonadism and morbid obesity. 9500540

1998
Entrez Id: 3952
Gene Symbol: LEP
LEP
CUI: C3554224
Disease: LEPTIN DEFICIENCY OR DYSFUNCTION
LEPTIN DEFICIENCY OR DYSFUNCTION 		0.800 Biomarker GENOMICS_ENGLAND

Entrez Id: 3952
Gene Symbol: LEP
LEP
CUI: C3554224
Disease: LEPTIN DEFICIENCY OR DYSFUNCTION
LEPTIN DEFICIENCY OR DYSFUNCTION 		0.800 Biomarker CTD_human