LB30.8ICD-11 MMS 2026-01
Medullary sponge kidney
Description
A condition characterised by cystic or saccular dilatations of the medullary collecting ducts seen with radiocontrast filling. A predisposition to stones and associated often with renal tubular acidosis. There is no clear genetic predisposition.
Index terms
- Medullary sponge kidney
- Cacchi-Ricci disease
- MSK - [medullary sponge kidney]
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- sponge kidney NOS
- Medullary sponge kidney, unilateral
- Medullary sponge kidney, bilateral
Exclusions from above levels
- http://id.who.int/icd/entity/733825440 – Inborn errors of metabolism
Sibling codes
LB30.0– Renal agenesis or other reduction defects of kidneyLB30.1– Renal dysplasiaLB30.2– Congenital single renal cystLB30.3– Renal tubular dysgenesisLB30.4– OligomeganephroniaLB30.5– Accessory kidneyLB30.6– Fusion anomaly of kidneysLB30.7– Ectopic or pelvic kidneyLB30.9– Multicystic renal dysplasiaLB30.Y– Other specified structural developmental anomalies of kidneysLB30.Z– Structural developmental anomalies of kidneys, unspecified
Foundation entity
Medullary sponge kidney – http://id.who.int/icd/entity/1723148250
Allowed postcoordination axes
Part of: LB30: Structural developmental anomalies of kidneys › 20: Developmental anomalies