Source: ORPHANET

Gene Disease Score gda Association Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 55065
Gene Symbol: SLC52A1
SLC52A1
CUI: C0035528
Disease: Riboflavin Deficiency
Riboflavin Deficiency 		0.610 GermlineCausalMutation ORPHANET Maternal riboflavin deficiency, resulting in transient neonatal-onset glutaric aciduria Type 2, is caused by a microdeletion in the riboflavin transporter gene GPR172B. 21089064

2011
Entrez Id: 55065
Gene Symbol: SLC52A1
SLC52A1
CUI: C0035528
Disease: Riboflavin Deficiency
Riboflavin Deficiency 		0.610 GermlineCausalMutation ORPHANET Transient multiple acyl-CoA dehydrogenation deficiency in a newborn female caused by maternal riboflavin deficiency. 17689999

2007