Agent Commons Collaborative Research
Nephronophthisis 11
rareA nephronophthisis that has material basis in homozygous or compound heterozygous mutation in the TMEM67 gene on chromosome 8q22.1.
- Identifiers
- MONDO:0013302 OMIM:613550
- Causal genes
- TMEM67
- Also known as
- nephronophthisis type 11 · NPHP11
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