Disease: NOONAN SYNDROME 9 ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C4225282
Disease: NOONAN SYNDROME 9
NOONAN SYNDROME 9 		0.700 GeneticVariation disease CLINVAR Rare variants in SOS2 and LZTR1 are associated with Noonan syndrome. 25795793 2015
CUI: C4225282
Disease: NOONAN SYNDROME 9
NOONAN SYNDROME 9 		0.700 Biomarker disease GENOMICS_ENGLAND Activating Mutations Affecting the Dbl Homology Domain of SOS2 Cause Noonan Syndrome. 26173643 2015
CUI: C4225282
Disease: NOONAN SYNDROME 9
NOONAN SYNDROME 9 		0.700 GeneticVariation disease CLINVAR Activating Mutations Affecting the Dbl Homology Domain of SOS2 Cause Noonan Syndrome. 26173643 2015
CUI: C4225282
Disease: NOONAN SYNDROME 9
NOONAN SYNDROME 9 		0.700 GeneticVariation disease UNIPROT Rare variants in SOS2 and LZTR1 are associated with Noonan syndrome. 25795793 2015
CUI: C4225282
Disease: NOONAN SYNDROME 9
NOONAN SYNDROME 9 		0.700 Biomarker disease GENOMICS_ENGLAND Rare variants in SOS2 and LZTR1 are associated with Noonan syndrome. 25795793 2015
CUI: C4225282
Disease: NOONAN SYNDROME 9
NOONAN SYNDROME 9 		0.700 Biomarker disease CTD_human
CUI: C4225282
Disease: NOONAN SYNDROME 9
NOONAN SYNDROME 9 		0.700 Biomarker disease GENOMICS_ENGLAND
CUI: C4225282
Disease: NOONAN SYNDROME 9
NOONAN SYNDROME 9 		0.700 CausalMutation disease CLINVAR