TPX2, TPX2 microtubule nucleation factor, 22974

N. diseases: 122; N. variants: 2
Disease: Color vision defect ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0009398
Disease: Color vision defect
Color vision defect 		0.010 Biomarker phenotype BEFREE Central or paracentral scotomata, color vision defects and delayed P100 latencies in the VEP were seen. 10447644 1999