Gene Disease Score gda Association Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 27077
Gene Symbol: B9D1
B9D1
CUI: C0265215
Disease: Meckel-Gruber syndrome
Meckel-Gruber syndrome
0.410 GermlineCausalMutation ORPHANET B9D1 is revealed as a novel Meckel syndrome (MKS) gene by targeted exon-enriched next-generation sequencing and deletion analysis. 21493627

2011