CEP152, centrosomal protein 152, 22995

N. diseases: 66; N. variants: 32
Disease: SECKEL SYNDROME 5 ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C3151187
Disease: SECKEL SYNDROME 5
SECKEL SYNDROME 5 		0.600 Biomarker disease GENOMICS_ENGLAND CEP152 is a genome maintenance protein disrupted in Seckel syndrome. 21131973 2011
CUI: C3151187
Disease: SECKEL SYNDROME 5
SECKEL SYNDROME 5 		0.600 Biomarker disease GENOMICS_ENGLAND CEP152 is a genome maintenance protein disrupted in Seckel syndrome. 21131973 2011
CUI: C3151187
Disease: SECKEL SYNDROME 5
SECKEL SYNDROME 5 		0.600 CausalMutation disease CLINVAR CEP152 is a genome maintenance protein disrupted in Seckel syndrome. 21131973 2011
CUI: C3151187
Disease: SECKEL SYNDROME 5
SECKEL SYNDROME 5 		0.600 GeneticVariation disease UNIPROT CEP152 is a genome maintenance protein disrupted in Seckel syndrome. 21131973 2011