CEP55, centrosomal protein 55, 55165

N. diseases: 134; N. variants: 4
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0235831
Disease: Renal Cell Dysplasia
Renal Cell Dysplasia
0.110 Biomarker disease BEFREE An Amish founder variant consolidates disruption of CEP55 as a cause of hydranencephaly and renal dysplasia. 30622327 2019
CUI: C0235831
Disease: Renal Cell Dysplasia
Renal Cell Dysplasia
0.110 Biomarker disease HPO