Knowledge of genetic causes of kidney diseases has evolved rapidly in recent years. Today we know that genetics play a significant role in the prognosis, clinical care and therapy of many kidney diseases. Therefore, upcoming interventions (e.g. kidney transplants) can be better planned and the risk of recurrence can be reliably determined, also for other family members. Our gene panels are designed with great care and in close cooperation by medical experts and specialists in human genetics.
| A | Agenesis, renal |
| Alagille syndrome | |
| Alport syndrome | |
| Alström syndrome | |
| Aminoaciduria | |
| ARC (Arthrogryposis-Renal Dysfunction-Cholestasis) syndrome | |
| Atypical hemolytic-uremic syndrome (aHUS) | |
| B | Bardet-Biedl syndrome (BBS) |
| Bartter syndrome | |
| Birt-Hogg-Dubé syndrome | |
| BOR (branchiootorenal) syndrome | |
| C | C1q deficiency |
| CAKUT (Congenital Anomalies of the Kidney and Urinary Tract) | |
| Ciliopathy | |
| Cystic kidney disease | |
| Cobalamin deficiency | |
| Cystinosis | |
| Cystinuria | |
| D | Dent disease |
| Denys-Drash syndrome | |
| Diabetes insipidus | |
| Dysplasia, renal | |
| E | Ellis-van-Creveld syndrome (EVC) |
| F | Fabry disease |
| Focal segmental glomerulosclerosis (FSGS) | |
| Frasier syndrome | |
| G | Gitelman syndrome |
| H | Hematuria |
| Heterotaxy | |
| Hypercalcemia | |
| Hyperoxaluria | |
| Hypomagnesaemia | |
| Hypophosphatemic rickets / phosphate diabetes | |
| Hypoplasia, renal | |
| I | Imerslund-Gräsbeck syndrome |
| J | Jeune syndrome |
| Joubert syndrome | |
| L | Liddle syndrome |
| M | Mainzer-Saldino syndrome |
| Meckel-Gruber syndrome | |
| MUC1 nephropathy | |
| N | Nephronophthisis (NPHP) |
| Nephrotic syndrome | |
| Nephrolithiasis (Kidney stone disease) | |
| O | Orofaciodigital syndrome (OFD) |
| P | Peroxisome biogenesis disorders |
| Polycystic liver disease (PCLD) | |
| Polycystic kidney disease, autosomal dominant (ADPKD) | |
| Polycystic kidney disease, autosomal recessive (ARPKD) | |
| Primary ciliary dyskinesia (PCD) | |
| Primary aldosteronism | |
| Proteinuria | |
| Proximal tubulopathy | |
| Pseudohypoaldosteronism | |
| R | Renal tubular dysgenesis (RTD) |
| Renal Fanconi syndrome | |
| Renal tubular acidosis (RTA) | |
| S | Senior-Loken syndrome |
| Sensenbrenner syndrome | |
| T | Thin basement membrane type nephropathy (TBMN) |
| Tuberous sclerosis (TSC) | |
| Tubulo-interstitial kidney disease, autosomal dominant (ADTKD) | |
| U | Urolithiasis |
| V | VACTERL association |
| Von Hippel-Lindau disease (VHL) | |
| W | Wilms tumor |
| X | Xanthinuria |
| Z | Zellweger syndrome |