INSR, insulin receptor, 3643

N. diseases: 452; N. variants: 109
Disease: Learning Disabilities ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0751265
Disease: Learning Disabilities
Learning Disabilities 		0.010 GeneticVariation disease BEFREE De novo 19p13.2 microdeletion encompassing the insulin receptor and resistin genes in a patient with obesity and learning disability. 23637016 2013