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Cystic or dysplastic kidney disease

International Classification of Diseases for Mortality and Morbidity Statistics, 11th Revision, v2024-01

Any disease of the kidney, caused by determinants arising during the antenatal period or after birth. These diseases are characterised by pathological changes to one or both kidneys, and may manifest in other anatomical tissues.

code elsewhere

• Tuberous sclerosis  (LD2D.2)
• Noonan syndrome  (LD2F.15)
• Meckel-Gruber syndrome  (LD2F.13)
• Asphyxiating thoracic dystrophy  (LD24.B1)
• Multicystic renal dysplasia  (LB30.9)

sections/codes in this section (GB80-GB8Z)

• Nonfamilial nongenetic cystic kidney disease  (GB80)
• Autosomal dominant polycystic kidney disease  (GB81)
• Autosomal dominant tubulointerstitial disease  (GB82)
• Nephronophthisis  (GB83)
• Other specified cystic or dysplastic kidney disease  (GB8Y)
• Cystic or dysplastic kidney disease, unspecified  (GB8Z)

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