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ACTH-independent macronodular adrenal hyperplasia

Alport syndrome

Alstrom syndrome

Amelogenesis imperfecta

Arthrogryposis renal dysfuntion and cholestasis

Atypical Hemolytic Uremic Syndrome (aHUS)

Bardet-Biedl syndrome

Bartter syndrome

BOR syndrome (Branchio-Oto-Renal dysplasia)

Ciliopathies (WES)

Combined oxidative phosphorylation deficiency

Cong. anomalies of kidney/urinary tract (CAKUT)

Congenital dominant spinal muscular atrophy

Corticosterone methyloxidase deficiency

Cysteinuria/Cystinuria

Dent's Disease (nephrolithiasis type 1)

Denys-Drash syndrome

Diabetes insipidus

Diabetes mellitus

Donnai-Barrow syndrome

Duane-radial ray syndrome

Familial hyperphosphatemic tumoral calcinosis

Familial Hypocalciuric Hypercalcemia

Familial juvenile hyperuricemic nephropathy

Fanconi renotubular syndrome

Fanconi-Bickel syndrome

Frasier syndrome

Fumarase deficiency

Gitelman syndrome

Glomerulopathy with fibronectin deposits

Glucocorticoid receptor deficiency

Glucocorticoid Remediabel Aldosteronism

Glutathione synthetase deficiency

Hypocalcemia

Hypomagnesemia, renal

Hypoparathyroidism, sensorineural deafness and renal dysplasia

Hypophosphatemic rickets

Leiomymatosis + kidney cancer

Liddle syndrome

Lowe oculocerebrorenal syndrome

Meckel syndrome

Medullary Cystic Kidney disease

Nail Patella syndrome

Neonatal hyperparathyroidism

Nephrogenic syndrome

Nephrolithiasis/osteoporosis, hypophosphatemic

Nephronophthisis

Nephropathic cystinosis

Nephrotic syndrome

Osteopetrose with renal tubular acidosis

Paraganglioma and pheochromocytoma, Hereditary

Polycystic kidney disease

Pseudohypoaldosteronism

Pseudohypoaldosteronism type 1

Renal cancer, hereditary

Renal cell carcinoma

Renal cysts and diabetes syndrome

Renal disorders (WES)

Renal glucosuria (GLYS1)

Renal tubular acidosis with deafness

Renal tubular acidosis, autosomal dominant

Renal Tubular Dysgenesis

Ritscher-Schinzel syndrome

Senior-Loken syndrome

SeSAME syndrome

Von Hippel-Lindau syndrome

Wilms tumor

Xanthinuria