Glomerulopathies
Tubulopathies
Thrombotic microangiopathies
Metabolic nephropathies
Renal or urinary tract malformations
Familial cystic renal diseases
Any rare kidney disease (A-Z)
Patient Information Materials
Hereditary cystic renal diseases (ciliopathies)
Autosomal dominant tubulointerstitial kidney diseaseAutosomal dominant medullary cystic kidney disease with hyperuricemia (UMOD-related)Autosomal dominant medullary cystic kidney disease without hyperuricemia (Mucin-related)Familial juvenile hyperuricemic nephropathy type 2 (Renin-related)RCAD (Renal Cysts and Diabetes) Syndrome (HNF1b-related)Autosomal dominant polycystic kidney diseaseAutosomal dominant polycystic kidney disease type 1 with tuberous sclerosisTuberous sclerosis complexVon Hippel-Lindau diseaseAutosomal recessive polycystic kidney diseaseHNF1B nephropathyNephronophthisisInfantile nephronophthisisJuvenile nephronophthisisLate-onset nephronophthisisBardet-Biedl syndrome (ciliopathies)Jeune syndrome (ciliopathies)Joubert syndrome with oculorenal defectJoubert syndrome with renal defect Senior-Loken syndromeSenior-Boichis syndromeSaldino-Mainzer (conorenal) syndromeMeckel syndrome (ciliopathies)Cerebrorenodigital (Meckel-like) syndromeCranioectodermal dysplasia (Sensenbrenner syndrome)Ellis van Creveld syndromeAlström SyndromeRenal-hepatic-pancreatic dysplasiaRHYNS (retinitis pigmentosa, hypopituitarism, nephronophthisis, skeletal dysaplasia) syndromeNeonatal diabetes-congenital hypothyroidism-congenital glaucoma-hepatic fibrosis-polycystic kidneys syndrome Karyomegalic interstitial nephritisLethal fetal brain malformation-duodenal atresia-bilateral renal hypoplasia syndromeLethal fetal cerebrorenogenitourinary agenesis/hypoplasia syndrome
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