Source: CLINGEN

Gene Disease Score gda Association Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 5605
Gene Symbol: MAP2K2
MAP2K2
CUI: C0028326
Disease: Noonan Syndrome
Noonan Syndrome 		0.640 Biomarker CLINGEN External ear anomalies and hearing impairment in Noonan Syndrome. 25862627

2015
Entrez Id: 5605
Gene Symbol: MAP2K2
MAP2K2
CUI: C0028326
Disease: Noonan Syndrome
Noonan Syndrome 		0.640 Biomarker CLINGEN Multiple café au lait spots in familial patients with MAP2K2 mutation. 24311457

2014
Entrez Id: 5605
Gene Symbol: MAP2K2
MAP2K2
CUI: C0028326
Disease: Noonan Syndrome
Noonan Syndrome 		0.640 Biomarker CLINGEN The RASopathies. 23875798

2013