SLC25A13, solute carrier family 25 member 13, 10165

N. diseases: 109; N. variants: 23
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0011206
Disease: Delirium
Delirium
0.110 GeneticVariation disease BEFREE Here, we report SLC25A13 c.1610_1612delinsAT mutation from India in a 13-year old boy who presented with recurrent episodes of delirium and hyperammonemia. 29787821 2018
CUI: C0011206
Disease: Delirium
Delirium
0.110 Biomarker disease HPO