https://www.askep3s.org/049d1b7949/artikel/N07.9
Artikel Klinis
ICD-10: N07.9
N07.9: Nefropati Herediter yang Tidak Dikelompokkan di Tempat Lain, Tidak Spesifik
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Terverifikasi: 2026-08-05
📚 Daftar Pustaka (APA 7)
[1]
KDIGO Clinical Practice Guideline for Glomerulonephritis. Kidney International Supplements. 2021;11(2):1-274.
[2]
Alport Syndrome. GeneReviews® [Internet]. University of Washington, Seattle; 1993-2024.
[3]
Autosomal Dominant Polycystic Kidney Disease. GeneReviews® [Internet]. University of Washington, Seattle; 1993-2024.
[4]
Kashtan CE, Ding J, Gregory M, et al. Clinical practice recommendations for the treatment of Alport syndrome. Am J Kidney Dis. 2020;76(5):641-654.
[5]
Chebib FT, Torres VE. Autosomal dominant polycystic kidney disease: core curriculum 2016. Am J Kidney Dis. 2016;68(2):318-336.
[6]
Devuyst O, Knoers NV, Remuzzi G, et al. Rare inherited kidney diseases: challenges, opportunities, and perspectives. Lancet. 2023;383(9931):2004-2019.
[7]
World Health Organization. ICD-10: International Statistical Classification of Diseases and Related Health Problems. 10th Revision. Geneva: WHO; 2019.
[8]
Eckardt KU, Kasiske BL. Kidney disease: improving global outcomes. Nat Rev Nephrol. 2020;16(4):193-194.