ERKNet

The European Rare Kidney Disease Reference Network
  

Patient Information Materials

Glomerulopathies

AA amyloidosis  - [EN] - [IT] - [NL]
Alport syndrome  - [DE] - [EN] - [ES] - [FR] - [IT] - [PL] - [PT] - [SE] - [SL]
Anti-glomerular basement membrane disease  - [EN] - [IT] - [NL]
Behçet disease  - [EN] - [IT] - [NL]
Buerger disease  - [IT]
C3 glomerulonephritis  - [EN] - [IT] - [NL]
Cryoglobulinemic vasculitis  - [EN] - [IT] - [NL]
Eosinophilic granulomatosis with polyangiitis  - [IT] - [NL]
Familial Mediterranean fever  - [EN] - [IT] - [NL]
Granulomatosis with polyangiitis (Wegener)  - [EN] - [IT] - [NL]
IgA nephropathy  - [DE] - [EN] - [ES] - [FR] - [IT] - [NL]
Immunoglobulin A vasculitis (Henoch Schonlein nephritis, PSH)  - [EN] - [FR] - [IT]
Membranous glomerulonephritis  - [DE] - [EN] - [ES] - [FR] - [IT] - [LT] - [NL] - [PT] - [SE]
Microscopic polyangiitis  - [EN] - [IT] - [NL]
Monoclonal gammopathy of renal significance (MGRS)  - [EN] - [IT]
Nail-patella syndrome  - [DE] - [EN] - [ES] - [FR] - [IT] - [NL] - [PL] - [PT]
Nephrotic syndrome without extrarenal manifestations  - [DE] - [EN] - [ES] - [FR] - [IT] - [NL] - [PT] - [SL]
Nephrotic syndrome, genetic  - [DE] - [EN] - [ES] - [FR] - [IT] - [NL] - [PT]
Nephrotic syndrome, idiopathic  - [DE] - [EN] - [ES] - [FR] - [IT] - [NL] - [PT] - [SL]
Pediatric systemic lupus erythematosus (SLE)  - [EN] - [FR] - [IT]
Primary membranoproliferative glomerulonephritis (MPGN)  - [DE] - [EN] - [ES] - [IT] - [LT] - [NL]
Sarcoidosis  - [IT]
Systemic vasculitis associated with glomerulopathy  - [DE] - [EN]
Takayasu arteritis  - [EN] - [IT] - [NL]

Hereditary cystic renal diseases (ciliopathies)

Hereditary cystic renal diseases (ciliopathies) (general)  - [EN] - [IT]
Alström Syndrome  - [DE] - [EN] - [ES] - [FR] - [IT] - [NL] - [PT] - [SE]
Autosomal dominant tubulointerstitial kidney disease (ADTKD)  - [DE] - [EN] - [ES] - [FR] - [IT] - [PT]
Autosomal recessive polycystic kidney disease (ARPKD)  - [DE] - [EN] - [ES] - [FR] - [IT] - [NL] - [SE]
Autosomal  dominant polycystic kidney disease (ADPKD)  - [DE] - [EN] - [ES] - [FR] - [IT] - [NL] - [PT] - [SE] - [SL]
Bardet-Biedl syndrome  - [DE] - [EN] - [ES] - [FR] - [IT] - [NL] - [PT] - [SE]
Jeune syndrome (ciliopathies)  - [DE] - [EN] - [ES] - [IT] - [NL] - [PT]
Joubert syndrome with renal defect  - [DE] - [EN] - [ES] - [FR] - [IT] - [LT] - [NL] - [PL] - [PT] - [SE]
Meckel syndrome (ciliopathies)  - [DE] - [EN] - [ES] - [FR] - [IT] - [NL] - [PL]
Nephronophthisis  - [DE] - [EN] - [ES] - [FR] - [IT] - [NL] - [PT]
Senior-Loken syndrome  - [DE] - [EN] - [ES] - [FR] - [NL] - [PL] - [PT]
Tuberous sclerosis complex (TSC)  - [DE] - [EN] - [ES] - [FR] - [IT] - [NL] - [SE] - [SL]
Von Hippel-Lindau disease (vHL)  - [DE] - [EN] - [ES] - [FR] - [IT] - [LT] - [NL] - [PL] - [PT] - [SE]

Metabolic nephropathies

Dent disease  - [EN] - [ES] - [FR] - [NL]
Fabry disease  - [DE] - [EN] - [ES] - [FR] - [IT] - [NL] - [PL] - [PT] - [SE]
LCAT deficiency  - [DE] - [EN] - [ES] - [FR] - [IT] - [PT]
Lowe syndrome  - [DE] - [EN] - [ES] - [FR] - [IT] - [NL] - [SE]
Nephropathic cystinosis  - [DE] - [EN] - [ES] - [FR] - [IT] - [NL] - [PT]
Primary hyperoxaluria  - [DE] - [EN] - [ES] - [FR] - [IT] - [NL] - [PL]

Paediatric Chronic Kidney Disease

Paediatric Chronic Kidney Disease (general)  - [DE] - [EN] - [ES] - [FR] - [IT] - [NL] - [SL]

Paediatric Dialysis

Paediatric Dialysis (general)  - [DE] - [EN] - [ES] - [IT] - [NL]

Paediatric Transplantation

Paediatric Transplantation (general)  - [DE] - [EN] - [IT] - [NL]

Renal or urinary tract malformations

Congenital hydronephrosis  - [DE] - [EN] - [FR] - [IT] - [NL] - [PT]
Congenital primary megaureter  - [EN] - [IT]
Fetal lower urinary tract obstruction (LUTO)  - [DE] - [EN] - [NL]
Multicystic dysplastic kidney  - [DE] - [EN] - [ES] - [FR] - [IT] - [PT] - [SE]
Neurogenic bladder, congenital or acquired  - [DE] - [EN] - [ES] - [FR] - [IT] - [NL] - [PL] - [PT] - [SE]
Posterior urethral valve (PUV)  - [IT]
Prune belly syndrome  - [SE]
RCAD (Renal cysts and diabetes) syndrome  - [EN] - [ES] - [FR] - [IT] - [NL]
Renal agenesis  - [DE] - [EN] - [ES] - [FR] - [IT] - [NL] - [PL]
Renal dysplasia  - [EN] - [ES] - [FR] - [IT] - [NL]
Renal hypoplasia  - [DE] - [EN] - [ES] - [FR] - [IT]
Vesicoureteric reflux (VUR), familial  - [EN] - [IT] - [NL]
Vesicoureteric reflux (VUR), high-grade  - [IT] - [NL]

Thrombotic microangiopathies

Thrombotic microangiopathies (general)  - [DE] - [EN]
Atypical hemolytic uremic syndrome (aHUS)  - [DE] - [EN] - [ES] - [FR] - [IT] - [LT] - [NL] - [SE]
Shiga toxin-associated hemolytic uremic syndrome (STEC-HUS)  - [DE] - [EN] - [ES] - [FR] - [IT] - [LT] - [NL] - [PT]
Thrombotic thrombocytopenic purpura (TTP)  - [DE] - [EN] - [ES] - [FR] - [IT] - [LT] - [NL] - [PT]

Tubulopathies

Bartter syndrome  - [DE] - [EN] - [ES] - [FR] - [IT] - [NL] - [PT] - [SE]
Cystinuria  - [DE] - [EN] - [ES] - [FR] - [IT] - [PT]
Familial renal glucosuria  - [EN] - [IT]
Fanconi syndrome, primary  - [DE] - [EN] - [ES] - [FR] - [IT] - [PT]
Genetic primary hypomagnesemia  - [DE] - [EN] - [ES] - [FR] - [IT] - [NL]
Gitelman syndrome  - [DE] - [EN] - [ES] - [FR] - [IT] - [NL] - [SE]
Hereditary renal hypouricemia  - [EN] - [ES]
Hypercalciuria, idiopathic  - [EN] - [IT]
Hypophosphatemic rickets  - [DE] - [EN] - [ES] - [FR] - [IT] - [NL] - [SE]
Nephrogenic diabetes insipidus  - [DE] - [EN] - [ES] - [FR] - [IT] - [NL] - [PT]
Nephrogenic syndrome of inappropriate antidiuresis  - [DE] - [EN] - [ES] - [FR] - [IT]
Primary renal tubular acidosis  - [DE] - [EN] - [ES] - [FR] - [IT] - [LT] - [NL] - [PL] - [PT]
Tubulointerstitial nephritis and uveitis syndrome  - [EN]
« Back to disease information startpage
European Reference Networks
ERKNet is one of the 24 European Reference Networks (ERNs) approved by the ERN Board of Member States. The ERNs are co-funded by the European Commission.
For more information about the ERNs and the EU health strategy, please visit http://ec.europa.eu/health/ern