RAC3, Rac family small GTPase 3, 5881

N. diseases: 44; N. variants: 3
Disease: Neurodevelopmental delay ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C4022738
Disease: Neurodevelopmental delay
Neurodevelopmental delay 		0.300 Biomarker phenotype GENOMICS_ENGLAND De novo missense variants in RAC3 cause a novel neurodevelopmental syndrome. 30293988 2019