Genetic diseases Horse
choose your species
Genetic diseases Horse
- 4-Panel Test (GBED, HERDA, HYPP, EMH)
- 5-panel-test (PSSM, GBED, HERDA, HYPP, EMH)
- Androgen insensitivity syndrom (AIS)
- Cerebellar abiotrophy (CA)
- Combi: Arabian Horse (CA, LFS, SCID)
- Combi: Paint (PSSM, HERDA, GBED, HYPP, LWO)
- Combi: Quarab (PSSM, HERDA, GBED, CA, SCID)
- Combi: Quarter Horse (PSSM, HERDA, GBED, HYPP
- Combi: Warmblood (WFFS, PSSM)
- Congenital myotonia (NFP)
- Connemara Pony hoof wall separation disease
- Dwarfism
- Equine malignant hyperthermia (EMH)
- Foal immunodeficiency syndrome (FIS)
- Glycogen branching enzym deficienzy (GBED)
- Hereditary eqine reginal dermal asthenia
- Hydrocephalus
- Hyperkalemic periodic paralysis (HYPP)
- Immune Mediated Myositis & MYH1 Myopathy (MYHM)
- Junctional epidermolysis bullosa (JEB)
- Lavender foal syndrome (LFS)
- Lethal white foal syndrome (LWO)
- Naked Foal Syndrome (NFS) - PCR
- Ocular Squamous Cell Carcinoma (SCC)
- Polysaccharid storage myopathy type 1 (PSSM)
- Severe combined immuno deficienzy (SCID)
- Speed-gene***
- Warmblood fragile foal syndrome (WFFS)
