ICD-11 MMS

21 Symptoms, signs or clinical findings, not elsewhere classified

Symptoms, signs or clinical findings of the genitourinary system  (MF30-MG0Y)

Clinical findings in specimens from the urinary system  (MF80-MF8Z)

MF81 Fibronectin glomerulopathy

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


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-stage renal failure in the second to sixth decade of life. This disease may be associated with mutations in the FN1 gene.

synonyms

demo
request yours today
 subscribe
start today
 newsletter
free subscription

Thank you for choosing Find-A-Code, please Sign In to remove ads.