Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C1855514
Disease: Severe failure to thrive
Severe failure to thrive
0.100 CausalMutation phenotype CLINVAR De Novo GMNN Mutations Cause Autosomal-Dominant Primordial Dwarfism Associated with Meier-Gorlin Syndrome. 26637980 2015