Source: ALL
Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
Isolated somatotropin deficiency
CUI: C3714796
Disease: Isolated somatotropin deficiency
0.010 GeneticVariation BEFREE Since the GH deficiency was not total, additional binding and signaling studies were performed, which revealed that the GH-P59L variant displays some of the common features of bioinactive GH syndrome. 21546299 2011