Gene Disease Score gda Association Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 57545
Gene Symbol: CC2D2A
CC2D2A
CUI: C0265215
Disease: Meckel-Gruber syndrome
Meckel-Gruber syndrome
0.430 GermlineCausalMutation ORPHANET Molecular genetics and pathogenic mechanisms for the severe ciliopathies: insights into neurodevelopment and pathogenesis of neural tube defects. 21110233

2011

Entrez Id: 57545
Gene Symbol: CC2D2A
CC2D2A
CUI: C0265215
Disease: Meckel-Gruber syndrome
Meckel-Gruber syndrome
0.430 GermlineCausalMutation ORPHANET Mutation spectrum of Meckel syndrome genes: one group of syndromes or several distinct groups? 19466712

2009