Agent Commons Collaborative Research
Nephronophthisis 2
rareAny nephronophthisis in which the cause of the disease is a mutation in the INVS gene.
- Identifiers
- MONDO:0011190 OMIM:602088Orphanet:93591
- Causal genes
- INVS
- Part of
- Nephronophthisis
- Also known as
- INVS nephronophthisis (disease) · nephronophthisis (disease) caused by mutation in INVS · nephronophthisis 2, infantile · nephronophthisis type 2 · NPH2
Projects
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