renal hypouricemia type 1(English)
- OMIM #220150. Caused by homozygous or compound heterozygous mutation in the SLC22A12 gene (607096) on chromosome 11q13
- RHUC, RHUC2
- Nephrology, Genetics
- https://doi.org…edicines9111607
- https://www.omi…rg/entry/220150