Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C3714796
Disease: Isolated somatotropin deficiency
Isolated somatotropin deficiency
0.100 GeneticVariation disease CLINVAR Mutations in two large pedigrees highlight the role of ZNF711 in X-linked intellectual disability. 27993705 2017
CUI: C3714796
Disease: Isolated somatotropin deficiency
Isolated somatotropin deficiency
0.100 GeneticVariation disease CLINVAR A systematic, large-scale resequencing screen of X-chromosome coding exons in mental retardation. 19377476 2009