Absence of renal corticomedullary differentiation
Symptom Information:
All diseases associated with this symptom:
Autosomal recessive polycystic kidney disease | (Orphanet:731) |
Nephronophthisis 2 | (OMIM:602088) |
Autosomal recessive polycystic kidney disease | (Orphanet:731) |
Nephronophthisis 2 | (OMIM:602088) |