Disease: Turner Syndrome, Male ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0041409
Disease: Turner Syndrome, Male
Turner Syndrome, Male 		0.500 Biomarker disease CTD_human Germline gain-of-function mutations in RAF1 cause Noonan syndrome. 17603482 2007
CUI: C0041409
Disease: Turner Syndrome, Male
Turner Syndrome, Male 		0.500 Biomarker disease CTD_human Cardiofaciocutaneous (CFC) syndrome associated with muscular coenzyme Q10 deficiency. 17703371 2007
CUI: C0041409
Disease: Turner Syndrome, Male
Turner Syndrome, Male 		0.500 Biomarker disease CTD_human Gain-of-function RAF1 mutations cause Noonan and LEOPARD syndromes with hypertrophic cardiomyopathy. 17603483 2007
CUI: C0041409
Disease: Turner Syndrome, Male
Turner Syndrome, Male 		0.500 Biomarker disease CTD_human Mouse model of Noonan syndrome reveals cell type- and gene dosage-dependent effects of Ptpn11 mutation. 15273746 2004
CUI: C0041409
Disease: Turner Syndrome, Male
Turner Syndrome, Male 		0.500 Biomarker disease MGD Mouse model of Noonan syndrome reveals cell type- and gene dosage-dependent effects of Ptpn11 mutation. 15273746 2004