Health Traits



These reports provide information about inherited conditions affecting health.

NAME GENE
Androgen Insensitivity Syndrome AR
Cerebellar Abiotrophy (CA) MUTYH
Congenital Hepatic Fibrosis PKHD1
Congenital Stationary Night Blindness (CSNB) TRPM1
Foal Immunodeficiency Syndrome (FIS) SLC5A3
Glycogen Branching Enzyme Deficiency (GBED) GBE1
Hereditary Equine Regional Dermal Asthenia (HERDA) PPIB
Hoof Wall Separation Disease (HWSD) SERPINB11
Hydrocephalus in Friesian Horses B3GALNT2
Hyperkalemic Periodic Paralysis (HYPP) SCN4A
Immune-Mediated Myositis MYH1
Incontinentia Pigmenti IKPKG
Junctional Epidermolysis Bullosa (JEB1 and JEB2) LAMA3, LAMC2
Lavender Foal Syndrome (LFS) MYO5A
Lethal White Overo (LWO) EDNRB
Malignant Hyperthermia (MH) RYR1
Multiple Congenital Ocular Anomalies (MCOA) PMEL17
Myofibrillar Myopathy (MFM) FLNC, MYOZ3, PYROXD1
Myotonia CLCN1
Naked Foal Syndrome (NFS) ST1
Ovotesticular Disorder of Sexual Development SRY
Polysaccharide Storage Myopathy (PSSM) COL6A3, FLNC, GYS1, MYOT, MYOZ3, PYROXD1
Recurrent Exertional Rhabdomyolysis (RER) CACNA2D3
Severe Combined Immune Deficiency (SCID), Autosomal DNAPK
Splashed White Overo (SWO) MITF, PAX3
Thrombasthenia ITGA2B
Vacuolar Myopathy (VM) unknown
Warmblood Fragile Foal Syndrome (WFFS) PLOD1

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