1. Q61 Cystic kidney disease

    1. Q61.0 Congenital renal cyst

      1. Q61.00 Congenital renal cyst, unspecified

        Inclusion term(s):

        • Cyst of kidney NOS (congenital)
      2. Q61.01 Congenital single renal cyst

      3. Q61.02 Congenital multiple renal cysts

    2. Q61.1 Polycystic kidney, infantile type

      Inclusion term(s):

      • Polycystic kidney, autosomal recessive
      1. Q61.11 Cystic dilatation of collecting ducts

      2. Q61.19 Other polycystic kidney, infantile type

    3. Q61.2 Polycystic kidney, adult type

      Inclusion term(s):

      • Polycystic kidney, autosomal dominant
    4. Q61.3 Polycystic kidney, unspecified

    5. Q61.4 Renal dysplasia

      Inclusion term(s):

      • Multicystic dysplastic kidney
      • Multicystic kidney (development)
      • Multicystic kidney disease
      • Multicystic renal dysplasia
    6. Q61.5 Medullary cystic kidney

      Inclusion term(s):

      • Nephronophthisis
      • Sponge kidney NOS
    7. Q61.8 Other cystic kidney diseases

      Inclusion term(s):

      • Fibrocystic kidney
      • Fibrocystic renal degeneration or disease
    8. Q61.9 Cystic kidney disease, unspecified

      Inclusion term(s):

      • Meckel-Gruber syndrome
Abbreviations used here:

NEC Not elsewhere classifiable
This abbreviation in the Tabular List represents “other specified”. When a specific code is not available for a condition, the Tabular List includes an NEC entry under a code to identify the code as the “other specified” code.

NOS Not otherwise specified
This abbreviation is the equivalent of unspecified.