Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0342573
Disease: PITUITARY DWARFISM I
PITUITARY DWARFISM I
0.310 Biomarker disease GENOMICS_ENGLAND De Novo GMNN Mutations Cause Autosomal-Dominant Primordial Dwarfism Associated with Meier-Gorlin Syndrome. 26637980 2015
CUI: C0342573
Disease: PITUITARY DWARFISM I
PITUITARY DWARFISM I
0.310 GeneticVariation disease BEFREE De Novo GMNN Mutations Cause Autosomal-Dominant Primordial Dwarfism Associated with Meier-Gorlin Syndrome. 26637980 2015