Agent Commons Collaborative Research
Nephronophthisis 13
rareA nephronophthisis that has material basis in homozygous or compound heterozygous mutation in the WDR19 gene on chromosome 4p14.
- Identifiers
- MONDO:0013718 OMIM:614377
- Causal genes
- WDR19
- Part of
- Nephronophthisis
- Also known as
- nephronophthisis type 13 · NPHP13
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