rs786205134, ALG9

N. diseases: 3
Source: ALL
Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
Mesatipellic pelvis
CUI: C0265729
Disease: Mesatipellic pelvis
0.700 CausalMutation CLINVAR A novel phenotype in N-glycosylation disorders: Gillessen-Kaesbach-Nishimura skeletal dysplasia due to pathogenic variants in ALG9. 25966638 2016