MC4R, melanocortin 4 receptor, 4160

N. diseases: 149; N. variants: 58
Disease: Congenital leptin deficiency ×
Source: ALL
Disease Type Disease Class Semantic Type N. genes d N. SNPs d Score gda EL gda EI gda N. PMIDs N. SNPs gda First Ref. Last Ref.
CUI: C3838754
Disease: Congenital leptin deficiency
Congenital leptin deficiency 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities Disease or Syndrome; Congenital Abnormality 3 0.020 None 1.000 2 2000 2018