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- Alport Syndrome
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- Renal Hypoplasia or Aplasia (RHDA)
- Renal Tubular Dysgenesis (RTD)
- Simpson-Golabi-Behmel Syndrome (SGBS)
- Split-Hand/Split-Foot Malformation (SHFM)
- Townes-Brocks syndrome (TBS)
- Urofacial Syndrome (UFS)
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- Alström Syndrome
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- Atypical Hemolytic Uremic Syndrome (aHUS)
- Autosomal Dominant Polycystic Kidney Disease (ADPKD)
- Autosomal Recessive Polycystic Kidney Disease (ARPKD)
- Bardet-Biedl Syndrome (BBS)
- C3 Glomerulonephritis (C3GN)
- C3 Glomerulopathy (C3G)
- Cranioectodermal Dysplasia (CED)
- Jeune Syndrome
- Joubert Syndrome (JS)
- Meckel–Gruber Syndrome (MKS)
- Medullary Cystic Kidney Disease
- Membranoproliferative Glomerulonephritis (MPGN)
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- Oral-Facial-Digital Syndrome Type 1
- Renal-Hepatic-Pancreatic Dysplasia
- Sensenbrenner Syndrome
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- Andersen-Tawil Syndrome (ATS)
- Bartter Syndrome
- Dent Disease
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- Familial Juvenile Hyperuricaemic Nephropathy (FJHN)
- Fanconi-Bickel Syndrome
- Gitelman Syndrome
- Gordon Syndrome
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- Hypophosphataemic Rickets
- Liddle Syndrome
- Lowe Oculocerebrorenal Syndrome (OCRL)
- Lysinuric Protein Intolerance
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- Nephrogenic Syndrome of Inappropriate Antidiuresis (NSIAD)
- Pseudohypoaldosteronism Type 1 (PHA-1)
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- Congenital Abnormalities of The Kidney and Urinary Tract (CAKUT)
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