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These terms define your current search. Click the × to remove a term. C16. Congenital, Hereditary, and Neonatal Diseases and Abnormalities: Congenital, Hereditary, and Neonatal Diseases and Abnormalities [MESH:D009358] > Genetic Diseases, Inborn [MESH:D030342] > Polycystic Kidney, Autosomal Recessive [MESH:D017044] × 462 items, grouped by C16. Congenital, Hereditary, and Neonatal Diseases and Abnormalities (view ungrouped items) Polycystic Kidney Disease, Potter Type I, with Microbrachycephaly, Hypertelorism , and Brachymelia [MESH:C564881] (1)    MESH:C564881   Polycystic Kidney Disease, Potter Type I, with Microbrachycephaly, Hypertelorism , and Brachymelia C564881               Polycystic kidneys, severe infantile with tuberous sclerosis [MESH:C536328] (1)    MESH:C536328   Polycystic kidneys, severe infantile with tuberous sclerosis C536328               Renal dysplasia diffuse cystic [MESH:C537755] (1)    MESH:C537755   Renal dysplasia diffuse cystic C537755                (others) (459)    MESH:C001277   geldanamycin C001277               MESH:C002070   betulinic acid C002070               MESH:C002202   4-oxoretinoic acid C002202               MESH:C002415   cholesterol alpha-oxide C002415               MESH:C002701   neocuproine C002701               MESH:C002950   methylformamide C002950               all 459 items...