Genetic analyses for kidney diseases

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
  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)
  Cystic kidney disease
  Cobalamin deficiency
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
  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
  Proximal tubulopathy
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

Our service portfolio for kidney diseases can be downloaded here.

You can find our request form for molecular genetic diagnostics here.

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