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 acquired cyst of kidney (N28.1)
 * Potter's syndrome (Q60.6)
 * Q61.0 Congenital renal cyst
 * Q61.00 Congenital renal cyst, unspecified
 * Cyst of kidney NOS (congenital)
 * Q61.01 Congenital single renal cyst
 * Q61.02 Congenital multiple renal cysts
 * Q61.1 Polycystic kidney, infantile type
 * Polycystic kidney, autosomal recessive
 * Q61.11 Cystic dilatation of collecting ducts
 * Q61.19 Other polycystic kidney, infantile type
 * Q61.2 Polycystic kidney, adult type
 * Polycystic kidney, autosomal dominant
 * Q61.3 Polycystic kidney, unspecified
 * Q61.4 Renal dysplasia
 * Multicystic dysplastic kidney
 * Multicystic kidney (development)
 * Multicystic kidney disease
 * Multicystic renal dysplasia
 * Excludes1: polycystic kidney disease (Q61.11-Q61.3)
 * Q61.5 Medullary cystic kidney
 * Nephronopthisis
 * Sponge kidney NOS
 * Q61.8 Other cystic kidney diseases
 * Fibrocystic kidney
 * Fibrocystic renal degeneration or disease
 * Q61.9 Cystic kidney disease, unspecified
 * Meckel-Gruber syndrome

Q62 Congenital obstructive defects of renal pelvis and congenital malformations of ureter

 * Q62.0 Congenital hydronephrosis
 * Q62.1 Congenital occlusion of ureter
 * Atresia and stenosis of ureter
 * Q62.10 Congenital occlusion of ureter, unspecified
 * Q62.11 Congenital occlusion of ureteropelvic junction
 * Q62.12 Congenital occlusion of ureterovesical orifice
 * Q62.2 Congenital megaureter
 * Congenital dilatation of ureter
 * Q62.3 Other obstructive defects of renal pelvis and ureter
 * Q62.31 Congenital ureterocele, orthotopic
 * Q62.32 Cecoureterocele
 * Ectopic ureterocele
 * Q62.39 Other obstructive defects of renal pelvis and ureter
 * Ureteropelvic junction obstruction NOS
 * Q62.4 Agenesis of ureter
 * Congenital