disease has basis in dysfunction of INVS nephronophthisis 2 Any nephronophthisis in which the cause of the disease is a mutation in the INVS gene. DOID:0111113 INVS nephronophthisis (disease) MESH:C566582 MONDO:0011190 NPH2 NPHP2 Nph2 OMIM:602088 Orphanet:93591 UMLS:C1865872 infantile nephronophthisis 2 nephronophthisis (disease) caused by mutation in INVS nephronophthisis 2 nephronophthisis type 2 nephronophthisis (disease)