CEP63, centrosomal protein 63, 80254

N. diseases: 44; N. variants: 15
Disease: Severe Congenital Microcephaly ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C3853041
Disease: Severe Congenital Microcephaly
Severe Congenital Microcephaly 		0.300 Biomarker disease CTD_human A primary microcephaly protein complex forms a ring around parental centrioles. 21983783 2011