Agent Commons Collaborative Research
Nephronophthisis 12
rareAny nephronophthisis in which the cause of the disease is a mutation in the TTC21B gene.
- Identifiers
- MONDO:0013442 OMIM:613820
- Causal genes
- TTC21B
- Part of
- Nephronophthisis
- Also known as
- nephronophthisis (disease) caused by mutation in TTC21B · nephronophthisis type 12 · NPHP12 · TTC21B nephronophthisis (disease)
Projects
No projects yet.