We also offer genetic test combinations to test for several hereditary diseases. Please contact us, we will be happy to advise you.

Diagnostic spectrum

  • Acrodermatitis enteropathica (AE)
  • Alpha-Mannosidosis (AMD)
  • Atherosclerosis (ATH)
  • Autoimmune lymphoproliferative syndrome (ALPS)
  • Genetic blood group determination
  • Serological Blood Group Typing (dog, cat)
  • Blue eyes
  • Congenital hypothyroidism (CH)
  • Congenital myasthenic syndrome (CMS)
  • Cystinuria
  • Epileptic encephalopathy (EE)
  • Factor XI deficiency (F11)
  • Factor XII deficiency (F12)
  • Gangliosidosis (GM1)
  • Gangliosidosis (GM2)
  • Gangliosidosis (GM2)
  • Glycogen storage disease type 4 (GSD4)
  • Head defect
  • Hypertrophic cardiomyopathy (HCM1)
  • Hypertrophic cardiomyopathy (HCM3)
  • Hypertrophic cardiomyopathy (HCM4)
  • Hypokalaemia
  • Hypotrichosis and short life expectancy
  • MDR1 gene variant
  • Mucopolysaccharidosis type VI (MPS6)
  • Mucopolysaccharidosis type VII (MPS7)
  • Myotonia congenita
  • Osteochondrodysplasia (OCD)
  • Polycystic kidney disease (PKD)
  • Polycystic kidney disease (PKD2)
  • Polydactyly
  • Primary congenital glaucoma (PCG)
  • Progressive retinal atrophy (b-PRA)
  • Progressive retinal atrophy (pd-PRA)
  • Progressive retinal atrophy (rdAc-PRA)
  • Progressive retinal atrophy (rdy-PRA)
  • Pyruvate kinase deficiency (PK)
  • Skeletal dysplasia (SD)
  • Spinal muscular atrophy (SMA)