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CIM11 MF81

CIM-11 MMS (diagnostics, nouvelle classification OMS) — fichier du 2026-09-11

Fibronectin glomerulopathy

chapitre
21 Symptoms, signs or clinical findings, not elsewhere classified
bloc
Clinical findings in specimens from the urinary system
definition
Fibronectin glomerulopathy is a rare hereditary kidney disease in which fibronectin (FN1) deposits are seen in the mesangium and subendothelial space. The clinical picture is characterised by proteinuria, type IV renal tubular acidosis, microscopic haematuria and hypertension that may lead to end-st
type
category
navigateur oms (fr)
https://icd.who.int/browse/2026-01/mms/fr#1877494378 ↗