rs398122394, ALG13

N. diseases: 17
Disease: Hypophosphatemia ×
Source: ALL
Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
Hypophosphatemia
CUI: C0085682
Disease: Hypophosphatemia
0.700 CausalMutation CLINVAR De novo mutations in epileptic encephalopathies. 23934111 2013