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 disease (ADTKD)UMOD-related autosomal dominant tubulointerstitial kidney disease (ADTKD)MUC1-related autosomal dominant tubulointerstitial kidney disease (ADTKD)REN-related autosomal dominant tubulointerstitial kidney disease (ADTKD, FJHN type 1)HNF1B-related autosomal dominant tubulointerstitial kidney disease (ADTKD)Autosomal dominant polycystic kidney disease (ADPKD)Autosomal dominant polycystic kidney disease type 1 with tuberous sclerosis (ADPKD-TSC)Tuberous sclerosis complex (TSC)Von Hippel-Lindau disease (vHL)Autosomal recessive polycystic kidney disease (ARPKD)NephronophthisisInfantile nephronophthisisJuvenile nephronophthisisLate-onset nephronophthisisBardet-Biedl syndrome 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
No matches
« Back to disease groups
