Genetic diseases Horse
Please select your animal species. You will then get an overview of the hereditary diseases offered by LABOGEN for the selected animal species. The listed hereditary diseases are presented individually, providing information about the type of disease, an overview of the breeds available, the inheritance and the test duration as estimated by the laboratory.
Genetic diseases Horse
- 0-9
- 4-Panel-Test
- 5-Panel-Test
- A
- Androgen insensitivity syndrom (AIS)
- Androgen insensitivity syndrome (AR2, AR3, AR4, AR5)***
- C
- Cerebellar abiotrophy (CA)
- Combination Arabian
- Combination Paint Horse
- Combination Quarab
- Combination Quarter Horse / Appaloosa
- Combination Warmblood
- Congenital myotonia
- Congenital Stationary Night Blindness (CSNB2)***
- Connemara Pony hoof wall separation disease
- D
- Distichiasis**
- Dwarfism
- Dwarfism (ACAN, Chrondrodyslasie)
- E
- Equine malignant hyperthermia (EMH)
- F
- Foal immunodeficiency syndrome (FIS)
- G
- Glycogen branching enzym deficienzy (GBED)
- H
- Hereditary equine reginal dermal asthenia
- Hydrocephalus
- Hyperkalemic periodic paralysis (HYPP)
- I
- Idiopathic hypocalcemia
- Immune Mediated Myositis & MYH1 Myopathy (MYHM)
- J
- Junctional epidermolysis bullosa (JEB)
- Junctional Epidermolysis Bullosa (JEB2)**
- L
- Lavender foal syndrome (LFS)
- Lethal white foal syndrome (LWO)
- N
- Naked Foal Syndrome (NFS) - PCR
- O
- Occipitoatlantoaxial Malformation (OAAM)**
- Ocular Squamous Cell Carcinoma (SCC)
- P
- Polysaccharid storage myopathy type 1 (PSSM)
- Predictive Height test
- S
- Severe combined immuno deficienzy (SCID)
- Skeletal Atavism***
- Speed gene***
- SynchroGait (DMRT3)**
- T
- Tractability
- W
- Warmblood fragile foal syndrome (WFFS)
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