Brown-vialetto-van laere syndrome

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Pathways column key: KEGG Reactome
Disease Term Disease ID Gene Symbol Classification References Source Pathways
BROWN-VIALETTO-VAN LAERE SYNDROME 1
C0796274211530MONDO:0024537
SLC52A2 Causal — Disgenet
SLC52A3 Causal
21110228 16122634 20920669 20206331 27702554 22273710 22718020 22824638 22633641
ClinGen, ClinVar, Disgenet, GWAS catalog, HPO
BROWN-VIALETTO-VAN LAERE SYNDROME 2
614707C3553538MONDO:0013867
SLC52A2 Causal
22740598 24253200 27702554 23243084 22864630
ClinGen, ClinVar, Disgenet, HPO, Orphanet
All2 Causal2 Unknown2
Related Diseases Diseases that share the most curated genes with Brown-vialetto-van laere syndrome.
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Riboflavin transporter deficiency 2 shared genesSLC52A3, SLC52A2 Related via 2 shared genes including SLC52A3, SLC52A2. 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. Obstructive sleep apnea syndrome 1 shared geneSLC52A3 Related via 1 shared gene including SLC52A3. Esophageal squamous cell carcinoma 1 shared geneSLC52A3 Related via 1 shared gene including SLC52A3.