Congenital renal cystic disease

Common: Autosomal dominant polycystic kidney disease; Autosomal recessive polycystic kidney disease; Hepatic fibrosis-renal cystic disease; Potter sequence; Tuberous sclerosis
Uncommon: Apert syndrome; Aplasia cutis congenita; Asphyxiating thoracic dysplasia; Asplenia syndrome; Axial osteomalacia; Bardet-Biedl syndrome; Beckwith-Wiedemann syndrome; Brachymesomelia-renal syndrome; Branchio-oto-renal syndrome; Caroli disease; Cerebro-costo-mandibular syndrome; Cutis laxa; Darier disease; DiGeorge syndrome; Ehlers-Danlos syndrome; Eronen syndrome; Femoral hypoplasia-unusual facies syndrome; Fetal alcohol syndrome; Fetal hydantoin syndrome; Fryns syndrome; Glomerulocystic kidney disease; Goldston syndrome; Hemihypertrophy; Joubert syndrome; Kaufman-McKusick syndrome; Lissencephaly; Marden-Walker syndrome; Meckel syndrome; Nail-patella syndrome; Nephronophthisis; Noonan syndrome; Oculo-auriculo-vertebral spectrum; Opitz trigonocephaly syndrome; Orofaciodigital syndrome type 1; Polysplenia syndrome; Renal-hepatic-pancreatic dysplasia; Roberts syndrome; Short rib-polydactyly syndrome type 1; Short rib-polydactyly syndrome type 2; Trisomy 13; Trisomy 18; Trisomy 21; Turner syndrome; Von Hippel-Lindau disease; Zellweger syndrome

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