CEP152, centrosomal protein 152, 22995

N. diseases: 66; N. variants: 32
Disease: Seckel syndrome 1 ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C4551474
Disease: Seckel syndrome 1
Seckel syndrome 1 		0.300 Biomarker disease CTD_human CEP152 is a genome maintenance protein disrupted in Seckel syndrome. 21131973 2011