ERKNet

The European Rare Kidney Disease Reference Network

  

Patient Information Materials

Glomerulopathies

AA amyloidosis  - [IT]
Behçet disease  - [EN]
C3 glomerulopathy  - [EN]
Collagenopathy (incl. Alport syndrome)  - [DE] - [EN] - [ES] - [FR] - [IT] - [PL] - [PT]
Familial Mediterranean fever and other autoinflammatory diseases  - [IT]
Granulomatosis with polyangiitis (Wegener)  - [EN]
Immunoglobulin A vasculitis  - [EN] - [FR]
Membranoproliferative glomerulonephritis  - [DE] - [EN] - [ES] - [IT] - [LT] - [NL]
Membranous nephropathy  - [DE] - [EN] - [ES] - [FR] - [IT] - [LT] - [NL] - [PT] - [SE]
Nail-patella syndrome  - [DE] - [EN] - [ES] - [FR] - [IT] - [NL] - [PL] - [PT]
Nephrotic syndrome, congenital and genetic  - [DE] - [EN] - [ES] - [FR] - [IT] - [LT] - [NL] - [PT]
Nephrotic syndrome, idiopathic  - [DE] - [EN] - [ES] - [FR] - [IT] - [NL] - [PT]
Pediatric systemic lupus erythematosus  - [FR] - [IT]
Primary IgA nephropathy (Berger disease)  - [EN] - [ES] - [FR] - [IT] - [NL]
Takayasu arteritis  - [EN]

Hereditary cystic renal diseases (ciliopathies)

Hereditary cystic renal diseases (ciliopathies) (general)  - [EN]
Alström Syndrome  - [DE] - [EN] - [ES] - [FR] - [IT] - [NL] - [PT]
Autosomal dominant polycystic kidney disease  - [DE] - [EN] - [ES] - [FR] - [IT] - [LT] - [NL] - [PL] - [PT] - [SE]
Autosomal dominant tubulointerstitial kidney disease  - [DE] - [EN] - [ES] - [FR] - [IT] - [PT]
Autosomal recessive polycystic kidney disease  - [DE] - [EN] - [ES] - [FR] - [IT]
Bardet-Biedl syndrome (ciliopathies)  - [EN] - [ES] - [FR] - [PL] - [PT]
HNF1B nephropathy  - [EN] - [ES] - [FR] - [NL] - [PL]
Jeune syndrome (ciliopathies)  - [DE] - [EN] - [ES] - [IT] - [NL] - [PL] - [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  - [DE] - [EN] - [ES] - [FR] - [IT] - [NL] - [SE]
Von Hippel-Lindau disease  - [DE] - [EN] - [ES] - [FR] - [IT] - [LT] - [NL] - [PL] - [PT] - [SE]

Metabolic nephropathies

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

Paediatric Chronic Kidney Disease

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

Paediatric Dialysis

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

Paediatric Transplantation

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

Renal or urinary tract malformations

Congenital hydronephrosis  - [DE] - [EN] - [FR] - [IT] - [NL] - [PT]
Congenital primary megaureter  - [IT]
Fetal lower urinary tract obstruction  - [EN]
Multicystic dysplastic kidney  - [DE] - [EN] - [ES] - [FR] - [IT] - [PT] - [SE]
Neurogenic bladder, congenital or acquired  - [DE] - [EN] - [ES] - [FR] - [IT] - [NL] - [PL] - [PT] - [SE]
Renal agenesis  - [DE] - [EN] - [ES] - [FR] - [IT] - [PL]
Renal dysplasia  - [EN] - [ES] - [FR]
Renal hypoplasia  - [DE] - [EN] - [ES] - [FR] - [IT]
Vesicoureteric reflux, familial  - [EN] - [IT]

Thrombotic microangiopathies

Thrombotic microangiopathies (general)  - [DE] - [EN]
Atypical HUS  - [DE] - [EN] - [ES] - [FR] - [LT] - [NL] - [PL]
Thrombotic thrombocytopenic purpura  - [DE] - [EN] - [ES] - [FR] - [IT] - [LT] - [NL] - [PT]
Typical HUS  - [DE] - [EN] - [ES] - [FR] - [IT] - [LT] - [NL] - [PT]

Tubulopathies

Bartter syndrome  - [DE] - [EN] - [ES] - [FR] - [IT] - [NL] - [PT] - [SE]
Familial renal glucosuria  - [EN]
Fanconi syndrome, primary  - [DE] - [EN] - [ES] - [FR] - [IT] - [PL] - [PT]
Gitelman syndrome  - [DE] - [EN] - [ES] - [FR] - [IT] - [NL] - [PL] - [SE]
Hereditary renal hypouricemia  - [EN] - [ES]
Hypercalciuria, idiopathic  - [EN] - [IT]
Hypomagnesemia, primary familial  - [DE] - [EN] - [ES] - [FR] - [IT] - [NL] - [PL]
Hypophosphatemic rickets  - [DE] - [EN] - [ES] - [FR] - [IT] - [NL] - [SE]
Nephrogenic diabetes insipidus  - [DE] - [EN] - [ES] - [FR] - [IT] - [NL] - [PL] - [PT]
Nephrogenic syndrome of inappropriate antidiuresis  - [DE] - [EN] - [ES] - [FR] - [IT] - [PT]
Primary renal tubular acidosis  - [DE] - [EN] - [ES] - [FR] - [IT] - [LT] - [NL] - [PL] - [PT]

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