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- Congenital Abnormalities of The Kidney and Urinary Tract (CAKUT)
- Alport Syndrome
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- Primary Hyperoxaluria
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- Fraser Syndrome
- HDR Syndrome
- Kallmann Syndrome (KS)
- Perlman Syndrome
- Renal Coloboma Syndrome (RCS)
- Renal Cysts and Diabetes Syndrome (RCAD Syndrome)
- 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)
- Vesicoureteral Reflux (VUR)
- Renal Ciliopathies
- Alström Syndrome
- APOL1 Nephropathy
- 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)
- Nephronophthisis
- Oral-Facial-Digital Syndrome Type 1
- Renal-Hepatic-Pancreatic Dysplasia
- Sensenbrenner Syndrome
- Glomerular Diseases
- Focal Segmental Glomerulosclerosis (FSGS)
- Immunoglobulin A Nephropathy (IgAN)
- Membranous Nephropathy
- Steroid-Resistant Nephrotic Syndrome
- Benign Familial Hematuria
- Denys-Drash Syndrome
- Fabry Disease
- Familial Amyloidosis
- Familial Hypertension
- Fechtner Syndrome
- Hypokalemia
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- Nail-Patella Syndrome
- Pierson Syndrome
- Schimke Immuno-Osseous Dysplasia
- WAGR Syndrome
- Renal Tubular Diseases
- Renal Tubular Acidosis
- Andersen-Tawil Syndrome (ATS)
- Bartter Syndrome
- Dent Disease
- Dicarboxylic Aminoaciduria
- Familial Hypocalciuric Hypercalcaemia (FHH)
- Familial Juvenile Hyperuricaemic Nephropathy (FJHN)
- Fanconi-Bickel Syndrome
- Gitelman Syndrome
- Gordon Syndrome
- Hereditary Renal Hypouricemia
- Hypophosphataemic Rickets
- Liddle Syndrome
- Lowe Oculocerebrorenal Syndrome (OCRL)
- Lysinuric Protein Intolerance
- Nephrogenic Diabetes Insipidus
- Nephrogenic Syndrome of Inappropriate Antidiuresis (NSIAD)
- Pseudohypoaldosteronism Type 1 (PHA-1)
- Familial Renal Glucosuria
- SeSAME Syndrome
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- Congenital Abnormalities of The Kidney and Urinary Tract (CAKUT)
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