ADAP2, ArfGAP with dual PH domains 2, 55803

N. diseases: 15; N. variants: 4
Disease: NF1 Microdeletion Syndrome ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C3150928
Disease: NF1 Microdeletion Syndrome
NF1 Microdeletion Syndrome 		0.010 Biomarker disease BEFREE ADAP2 in heart development: a candidate gene for the occurrence of cardiovascular malformations in NF1 microdeletion syndrome. 24711647 2014