# Genetic kidney diseases – from discovery to precision care

**Authors:** Matias Simons, Julia Hoefele

PMC · DOI: 10.1515/medgen-2025-2049 · Medizinische Genetik · 2026-02-18

## Full-text entities

- **Diseases:** Genetic kidney diseases (MESH:D007674), renal cysts (MESH:D003560), ADTKD (OMIM:162000), cystic and ciliopathic diseases (MESH:C563237), ADPKD (MESH:D016891), primary hyperoxaluria type 1 (MESH:C536414), complement (MESH:D007153), CAKUT (MESH:C566906), Alport syndrome (MESH:D009394), chronic glomerulonephritis (MESH:D005921), tubular transport disorders (MESH:D015499), cystinosis (MESH:D003554), hemolytic uremic syndrome (MESH:D006463), cardiovascular complications (MESH:D002318), mediated nephropathies (MESH:C567355), interstitial nephritis (MESH:D009395), structural malformations (MESH:D020914), dominantly inherited disorders (MESH:D030342), metabolic and stone-forming diseases (MESH:D008659), proteinuria (MESH:D011507), hereditary disorders (MESH:D009386), hematuria (MESH:D006417), aHUS (MESH:D065766), hypertensive nephrosclerosis (MESH:D009400), C3 glomerulopathy (MESH:C562875), Morphological abnormalities (MESH:D000013), CKD (MESH:D051436), kidney failure (MESH:D051437)
- **Species:** Homo sapiens (human, species) [taxon 9606]

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Source: https://tomesphere.com/paper/PMC12910340