Gene: ALG9 ×
Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 79796
Gene Symbol: ALG9
ALG9 		0.100 CausalMutation group CLINVAR A novel phenotype in N-glycosylation disorders: Gillessen-Kaesbach-Nishimura skeletal dysplasia due to pathogenic variants in ALG9. 25966638 2016
Entrez Id: 79796
Gene Symbol: ALG9
ALG9 		0.100 Biomarker group HPO