Brown-Vialetto-van Laere Syndrome 1
| Disease Aliases (7) | Brown-vialetto-van laere syndrome 1, mild Brown-vialetto-van laere syndrome caused by mutation in slc52a3 Bulbar palsy, progressive, with sensorineural deafness Rfvt2-related riboflavin transporter deficiency Riboflavin transporter deficiency 2 Riboflavin transporter deficiency, type 3 (brown-vialetto-van laere syndrome 1) Rtd2 |
Associated Genes (0) | |||||||
| Cross-references of Brown-Vialetto-van Laere syndrome 1 | OMIM | GARD | Orphanet | NCBI-GTR | NCBI-MedGen | MalaCards | MeSH | Annotations | |