Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0271561
Disease: Somatotropin deficiency
Somatotropin deficiency
0.010 GeneticVariation disease BEFREE One novel GPR101 variant, c.589 G>T (p.V197L), was seen in the heterozygous state in a patient with isolated GHD. 26797872 2016