Gene Disease Score gda Association Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 55165
Gene Symbol: CEP55
CEP55
CUI: C0265215
Disease: Meckel-Gruber syndrome
Meckel-Gruber syndrome
0.300 GermlineCausalMutation ORPHANET A nonsense mutation in CEP55 defines a new locus for a Meckel-like syndrome, an autosomal recessive lethal fetal ciliopathy. 28295209

2017