Familial cystic renal disease
MONDO:0019741An instance of cystic kidney disease that is caused by an inherited modification of the individual's genome.
Also known as: hereditary cystic kidney disease
78 clinical trials for this condition and its sub-types.
Follow this condition — get notified about new trialsSub-types
Autosomal dominant polycystic kidney disease
(55)
Polycystic kidney disease
(12)
Autosomal dominant medullary cystic kidney disease with or without hyperuricemia
(7)
Autosomal recessive polycystic kidney disease
(6)
Polycystic kidney disease 1
(1)
Adult familial nephronophthisis-spastic quadriparesia syndrome
(0)
ALG9-associated autosomal dominant polycystic kidney disease
(0)
Autosomal dominant polycystic kidney disease type 1 with tuberous sclerosis
(0)
Familial juvenile hyperuricemic nephropathy type 1
(0)
Polycystic kidney disease 2
(0)
Polycystic kidney disease 3 with or without polycystic liver disease
(0)
Polycystic kidney disease 4
(0)
Polycystic kidney disease 5
(0)
Polycystic kidney disease 6 with or without polycystic liver disease
(0)
Polycystic kidney disease 7
(0)
Polycystic kidney disease 8
(0)
Tubulointerstitial kidney disease, autosomal dominant, 2
(0)