Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0020505
Disease: Hyperphagia
Hyperphagia
0.400 Biomarker phenotype CTD_human A de novo mutation affecting human TrkB associated with severe obesity and developmental delay. 15494731 2004
CUI: C0020505
Disease: Hyperphagia
Hyperphagia
0.400 Biomarker phenotype HPO