Genetic Disease Testing:

(Embark)

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Degenerative Myelopathy (DM)

Exercise-Induced Collapse 

Hereditary Nasal Parakeratosis

Neonatal Encephalopathy with Seizures 

Progressive Retinal Atrophy, Cone-Rod Dystrophy 4 

Progressive Retinal Atrophy, PRCD 

Von Willebrand Disease I 

Centronuclear Myopathy (CNM)

Copper Toxicosis (Attenuating) RETN (LabR Type)

Copper Toxicosis (Accumulating) ATP7B 1 Copy

Copper Toxicosis (Attenuating) ATP7A 2 Copies (GOOD)

Familial Nephropathy (Cocker Spaniel Type) 

Glycogen Storage Disease VII, PFK Deficiency 

Myotonia Congenita (Labrador Retriever)

Narcolepsy (Labrador Retriever Type) 

Day Blindness (Labrador Retriever Type)

Skeletal Dysplasia 2 

Stargardt Disease (Labrador Retriever Type)

Ullrich-Like Congentical Muscular Dystrophy

Urate Kidney & Bladder Stones

X-Linked Myotubular Myopathy

Macular Corneal Dystrophy (MCD)

Ehlers-Danlos Syndrome (EDS)

Canine Elliptocytosis

Bernard-Soulier Syndrome (BSS)

Alexander Disease

Acral Mutilation Syndrome

Additional Disease Panel:

Congenital Myasthenic Syndrome (LabR Type) 

Elliptocytosis 

GM2 Gangliosidosis (Poodle Type) 

Hyperuricosuria 

Osteochondrodysplasia 

Progressive Retinal Atrophy, Golden Retriever 2 

Pyruvate Kinase Deficiency (Labrador Retriever Type)

IVDD- CDDY 2 Copies Cdpa (Clear)