For some breeds, we also offer breed-specific genetic test combinations to test for several hereditary diseases. Please contact us, we will be happy to advise you.

Diagnostic spectrum

  • Androgen insensitivity syndrome (AR1)
  • Androgen insensitivity syndrome (AR2, AR3, AR4, AR5)*
  • Cerebellar abiotrophy (CA)
  • Congenital stationary night blindness (CSNB2)*
  • Distichiasis*
  • Dwarfism
  • Dwarfism (ACAN, Chondrodysplasia)
  • Equine juvenile spinocerebellar ataxia (EJSCA)*
  • Equine malignant hyperthermia (EMH)
  • Foal immunodeficiency syndrome (FIS)
  • Glycogen branching enzyme deficiency (GBED)
  • Hereditary equine regional dermal asthenia (HERDA)
  • Junctional epidermolysis bullosa (JEB1)
  • Junctional epidermolysis bullosa (JEB2)*
  • Hereditary myotonia
  • Hoof wall separation disease (HWSD)
  • Hydrocephalus
  • Hyperkalemic periodic paralysis (HYPP)
  • Hypertriglyceridemia-induced pancreatitis (HIP)
  • Idiopathic hypocalcaemia
  • Immune mediated myositis & MYH1 myopathy (MYHM)
  • Lavender foal syndrome (LFS)
  • Lethal white foal syndrome (OLWS)
  • Naked foal syndrome (NFS)
  • Occipitoatlantoaxial malformation (OAAM)*
  • Ocular squamous cell carcinoma (SCC)
  • Polysaccharid storage myopathy type 1 (PSSM)
  • Severe combined immuno deficiency (SCID)
  • Skeletal atavism (SA)*
  • Warmblood fragile foal syndrome (WFFS)

    • * partner laboratory