se-atlas

CHARGE syndrome Thrombotic microangiopathy Senior-Loken syndrome Townes-Brocks syndrome Idiopathic steroid-sensitive nephrotic syndrome Alport syndrome Renal agenesis Multicystic dysplastic kidney Primary glomerular disease Renal hypoplasia Gitelman syndrome Primary membranoproliferative glomerulonephritis Renal dysplasia BOR syndrome Nephronophthisis Bardet-Biedl syndrome Renal coloboma syndrome Bartter syndrome Beckwith-Wiedemann syndrome Renal or urinary tract malformation Glomerular disease Atypical hemolytic-uremic syndrome Cystinosis Cystinuria Autosomal dominant polycystic kidney disease Autosomal recessive polycystic kidney disease Familial primary hypomagnesemia Nephrogenic diabetes insipidus Congenital and infantile nephrotic syndrome Familial primary hypomagnesemia with hypercalciuria and nephrocalcinosis Familial primary hypomagnesemia with hypocalcuria Familial primary hypomagnesemia with normocalcuria Primary hyperoxaluria Typical hemolytic-uremic syndrome Jeune syndrome Joubert syndrome