Riboflavin transporter deficiency

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Pathways column key: KEGG Reactome
Disease Term Disease ID Gene Symbol Classification References Source Pathways
RFVT2-RELATED RIBOFLAVIN TRANSPORTER DEFICIENCY
572543
SLC52A2 Unknown
26973221 30793323
Orphanet
RFVT3-RELATED RIBOFLAVIN TRANSPORTER DEFICIENCY
572550
SLC52A3 Unknown
26973221 30793323
Orphanet
RIBOFLAVIN TRANSPORTER DEFICIENCY, TYPE 1
C5779638
SLC52A1 Unknown — Disgenet
All3 Causal0 Unknown3
Related Diseases Diseases that share the most curated genes with Riboflavin transporter deficiency.
5 View disease cluster →
Brown-vialetto-van laere syndrome 2 shared genesSLC52A3, SLC52A2 Related via 2 shared genes including SLC52A3, SLC52A2. Riboflavin deficiency 1 shared geneSLC52A1 Related via 1 shared gene including SLC52A1. maternal riboflavin deficiency 1 shared geneSLC52A1 Related via 1 shared gene including SLC52A1. Bulbar palsy 1 shared geneSLC52A3 Related via 1 shared gene including SLC52A3. Auditory neuropathy 2 shared genesSLC52A3, SLC52A2 Related via 2 shared genes including SLC52A3, SLC52A2.