von Willebrand disease (vWD2)

Acral Mutilation Syndrome (AMS)

Adult-onset Neuropathy (AON)

Alaskan Malamute Polyneuropathy (AMPN)

Amelogenesis imperfecta/familial enamel hypoplasia (AI/FEH)

Breathing Testing (BOAS)

Breathing Testing (for brachycephalic obstructive airway syndrome (BOAS))

Canine Leukocyte Adhesion Deficiency (CLAD)

Centronuclear Myopathy (CNM)

Cerebellar Ataxia (CA)

Ceroid Lipofuscinosis (CL)

Chiari-Like Malformation (CM)

Chondrodysplasia (CDSL)

Choroidal Hypoplasia (CH)

CM - Chiari-like Malformation

Collie Eye Anomaly (CEA)

Collie Eye Anomaly/choroidal hypoplasia (CEA/CH)

Cone Degeneration (CD)

Congenital Hypothyroidism with Goitre (CHG)

Congenital Sensory Night Blindness (CSNB)

Copper Toxicosis (COMMD1)

Curly coat / Dry eye (CC/DE)

Cystinuria (CU)

Degenerative Encephalopathy (DE)

Degenerative Myelopathy (DM)

Degenerative Myleopathy (DM)

Dilated Cardiomyopathy (DCM)

DINGS2

Dyserythropoietic Anemia and Myopathy Syndrome (DAMS)

Elbow Testing

Episodic falling (EF)

Episodic falling (EF)

Exercise Induced Collapse (EIC)

Eye Testing

Eye Testing Gonioscopy (PLA)

Eye Testing minimum of once prior to being used for breeding

Eye Testing minimum of once prior to being used for breeding (for PHPV)

Factor 7 Deficiency (FVIID)

Familial nephropathy (FN)

Fucosidosis (fuco)

Gangliosidosis (GM1)

Glanzmanns Thrombasthenia

Glycogen Storage Disease (GSDII)

Glycogen Storage Disease (GSDII)

Gonioscopy (PLA)

Greyhound Neuropathy (GN)

Hearing Testing (BAER)

Heart Screening for mitral valve disease (MVD)

Hereditary Cataracts (HC-HSF4-2)

Hereditary Cataracts (HC-HSF4)

Hereditary Cerebellar Ataxia (HCA)

Hereditary Footpad Hyperkeratosis (HFH)

Hereditary Nasal Parakeratosis (HNPK)

Hereditary Necrotising Myelopathy (ENM)

Hip Testing

Hyperuricosuria (HUU)

Ichthyosis (ICT-A)

Imerslund-Grasbeck Syndrome (IGS)

Imerslund-Grasbeck Syndrome(IGS-2)

Inherited Myopathy of Great Danes (IMGD)

Juvenile Addisons Disease (JADD)

Juvenile Dilated Cardiomyopathy (JDCM)

Juvenile Dilated Cardiomyopathy (JDCM)

Juvenile Epilepsy (JE)

Juvenile Laryngeal Paralysis and Polyneuropathy (JLPP)

Juvenile Myoclonic Epilepsy (JME)

L-2-Hydroxyglutarate Dehydrogenase (L-2-HGA)

Laforas

Laryngeal Paralysis and Polyneuropathy (LPPN3)

Late Onset Ataxia (LOA)

Leonberger Polyneuropathy (LPN1)

Leonberger Polyneuropathy (LPN2)

Leukoencephalomyelopathy (LEMP-2) 

Leukoencephalomyelopathy (LEMP) 

Lysosomal Storage Disease (LSD)

Macular Corneal Dystrophy (MCD)

Mucopolysaccharidosis (MPSIIIB)

Multi Drug Resistance (MDR-1)

Multi Drug Resistance (MDR1)

Multi-drug Resistance (MDR1)

Musladin-Lueke Syndrome (MLS)

Mycobacterium Avium (MAC)

Neonatal Cerebellar Cortical Degenration (NCCD)

Neuroaxonal Dystrophy (NAD-TECPR2)

Neuronal Axonal Deficiency (NAD-PLA2G6)

Neuronal Ceroid Lipofuscinosis (NCL12) 

Neuronal Ceroid Lipofuscinosis (NCL8)

Neuronal Ceroid Lipofuscinosis (Sal-NCL)

Osteochondrodysplasia (OC)

Phosphofructokinase Deficiency (PFK)

Pituitary Dwarfism (DP-LXH3).

PLA (Gonioscopy)

Primary Ciliary Dyskinesia (PCD)

Primary Hyperparathyroidism (PHPT)

Primary Lens Luxation (PLL)

Primary Lens Luxation (PLL)

Primary Lense Luxation (PLL)

Primary Open Angle Glaucoma (POAG-2)

Primary Open Angle Glaucoma (POAG-3)

Primary Open Angle Glaucoma (POAG-5)

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