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
Muscle Integrity Myopathy (MIM)	MYOT, FLNC, MYOZ3, PYROXD1, COL6A3
Myofibrillar Myopathy (MFM)	FLNC, MYOZ3, PYROXD1
Myotonia	CLCN1
Naked Foal Syndrome (NFS)	ST1
Ovotesticular Disorder of Sexual Development	SRY
Polysaccharide Storage Myopathy (PSSM 1)	GYS1
Polysaccharide Storage Myopathy (PSSM 2)	unknown
Recurrent Exertional Rhabdomyolysis (RER)	CACNA2D3
Severe Combined Immune Deficiency (SCID), Autosomal	DNAPK
Splashed White Overo (SWO)	MITF, PAX3
Thrombasthenia	ITGA2B
Warmblood Fragile Foal Syndrome (WFFS)	PLOD1

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