Acral Mutilation Syndrome:  WT/WT (clear)
Acute Respiratory Distress Syndrome:  WT/WT (clear)
Adult Paroxysmal Dyskinesia:  WT/WT (clear)
Afibrinogenemia:  WT/WT (clear)
Alaskan Husky Encephalopathy:  WT/WT (clear)
Alaskan Malamute Polyneuropathy :  WT/WT (clear)
Amelogenesis Imperfecta: WT/WT (clear)
Ataxia:  WT/WT (clear)
Benign Familial Juvenile Epilepsy:  WT/WT (clear)
Benard-Soulier Syndrome:  WT/WT (clear)
Canine Multiple System Degeneration:  WT/WT (clear)
Canine Scott Syndrome:  WT/WT (clear)
Cardiomyopathy and Juvenile Mortality:  WT/WT (clear)
Catalase Deficiency:  WT/WT (clear)
Centronuclear Myopathy:  WT/WT (clear)
Cerebellar Ataxia:  WT/WT (clear)
Cerebellar Ataxia 1 :  WT/WT (clear)
Cerebellar Ataxia 2 :  WT/WT (clear)
Cerebellar Cortical Degeneration:  WT/WT (clear)
Cerebellar Degeneration:  WT/WT (clear)
Charcot-Marie-Tooth Disease:  WT/WT (clear)
Chondrodysplasia:  WT/WT (clear)
Cleft Palate and Syndactyly:  WT/WT (clear)
Coagulation Factor VII Deficiency:  WT/WT (clear)
Collie Eye Anomaly:  WT/WT (clear)
Complement 3 Deficiency:  WT/WT (clear)
Cone Degeneration:  WT/WT (clear)
Congenital Hypothyroidism with Goiter:  WT/WT (clear)
Congenital Macrothrombocytopenia:  WT/WT (clear)
Congenital Methemoglobinemia:  WT/WT (clear)
Congenital Myasthenic Syndrome:  WT/WT (clear)
Congenital Stationary Night Blindness:  WT/WT (clear)
Copper Storage Disease:  WT/WT (clear)
Craniomandibular Osteopathy:  WT/WT (clear)
Cyclic Neutropenia:  WT/WT (clear)
Cystinuria:  WT/WT (clear)
Cystinuria Type 3 (Bulldog Type Risk Factor, Variant 3):  WT/WT (clear)
Cystinuria Type 3 (Bulldog Type Risk Factor, Variants 1 and 2): 1 copy carrier
Dandy-Walker-Like Malformation:  WT/WT (clear)
Darier Disease and Associated Infundibular Cyst Formation:  WT/WT (clear)
Deafness and Vestibular Dysfunction:  WT/WT (clear)
Degenerative Myelopathy WT/WT (clear)
Degenerative Myelopathy Early-Onset Risk Modifier:  WT/WT (clear)
Dental Hypomineralization:  WT/WT (clear)
Diffuse Cystic Renal Dysplasia and Hepatic Fibrosis:  WT/WT (clear)
Dilated Cardiomyopathy:  WT/WT (clear)
Dry Eye Curly Coat Syndrome:  WT/WT (clear)
Dystrophic Epidermolysis Bullosa:  WT/WT (clear)
Early Onset Adult Deafness:  WT/WT (clear)
Early Retinal Degeneration:  WT/WT (clear)
Early-Onset Epilepsy:  WT/WT (clear)
Ectodermal Dysplasia:  WT/WT (clear)
Ectodermal Dysplasia, X-Linked:  WT/WT (clear)
Ehlers-Danlos Syndrome:  WT/WT (clear)
Elliptocytosis:  WT/WT (clear)
Epidermolytic Hyperkeratosis:  WT/WT (clear)
Episodic Falling Syndrome:  WT/WT (clear)
Exercise-Induced Collapse:  WT/WT (clear)
Exfoliative Cutaneous Lupus Erythematosus (ECLE):  WT/WT (clear)
Factor XI Deficiency:  WT/WT (clear)
Familial Nephropathy:  WT/WT (clear)
Fucosidosis:  WT/WT (clear)
Gallbladder Mucoceles:  WT/WT (clear)
Glanzmann’s Thrombasthenia:  WT/WT (clear)
Glaucoma:  WT/WT (clear)
Globoid Cell Leukodystrophy:  WT/WT (clear)
Glycogen Storage Disease Ia:  WT/WT (clear)
Glycogen Storage Disease IIIa:  WT/WT (clear)
Glycogen Storage Disease VII:  WT/WT (clear)
Glycogen Storage Disease VII, PFK Deficiency:  WT/WT (clear)
GM1 Gangliosidosis:  WT/WT (clear)
GM2 Gangliosidosis:  WT/WT (clear)
Greyhound Polyneuropathy:  WT/WT (clear)
Hemophilia A:  WT/WT (clear)
Hemophilia B:  WT/WT (clear)
Hereditary Ataxia:  WT/WT (clear)
Hereditary Cataracts:  WT/WT (clear)
Hereditary Footpad Hyperkeratosis:  WT/WT (clear)
Hereditary Nasal Parakeratosis:  WT/WT (clear)
Hereditary Nephritis:  WT/WT (clear)
Hyperuricosuria:  WT/WT (clear)
Hypomyelination:  WT/WT (clear)
Ichthyosis:  WT/WT (clear)
Inflammatory Myopathy:  WT/WT (clear)
Intervertebral Disc Disease Risk Factor and Chondrodystrophy (CDDY with IVDD):  WT/WT (clear)
Intestinal Cobalamin Malabsorption:  WT/WT (clear)
Intestinal Lipid Malabsorption:  WT/WT (clear)
Junctional Epidermolysis Bullosa:  WT/WT (clear)
Juvenile Laryngeal Paralysis and Polyneuropathy (JLPP):  WT/WT (clear)
Juvenile Myoclonic Epilepsy:  WT/WT (clear)
L-2-Hydroxyglutaric Aciduria:  WT/WT (clear)
Lagotto Storage Disease:  WT/WT (clear)
Laryngeal Paralysis and Polyneuropathy:  WT/WT (clear)
Late Onset Ataxia:  WT/WT (clear)
Lethal Acrodermatitis:  WT/WT (clear)
Leukocyte Adhesion Deficiency, Type I:  WT/WT (clear)
Leukocyte Adhesion Deficiency, Type III:  WT/WT (clear)
Ligneous Membranitis:  WT/WT (clear)
Limb-Girdle Muscular Dystrophy:  WT/WT (clear)
Lundehund Syndrome:  WT/WT (clear)
Macular Corneal Dystrophy:  WT/WT (clear)
Mammary Tumors:  WT/WT (clear)
May-Hegglin Anomaly:  WT/WT (clear)
Microphthalmia:  WT/WT (clear)
Mucopolysaccharidosis I:  WT/WT (clear)
Mucopolysaccharidosis IIIA:  WT/WT (clear)
Mucopolysaccharidosis IIIB:  WT/WT (clear)
Mucopolysaccharidosis VI:  WT/WT (clear)
Mucopolysaccharidosis VII:  WT/WT (clear)
Multidrug Resistance 1:  WT/WT (clear)
Multifocal Retinopathy1:  WT/WT (clear)
Multifocal Retinopathy 2:  WT/WT (clear)
Multifocal Retinopathy 3:  WT/WT (clear)
Muscular Dystrophy:  WT/WT (clear)
Musladin-Lueke Syndrome:  WT/WT (clear)
Myostatin Deficiency:  WT/WT (clear)
Mytonia Congenita:  WT/WT (clear)
Myotubular Myopathy 1:  WT/WT (clear)
Narcolepsy:  WT/WT (clear)
Neonatal Ataxia:  WT/WT (clear)
Neonatal Cerebellar Cortical Degeneration:  WT/WT (clear)
Neonatal Encephalopathy with Seizures:  WT/WT (clear)
Neuroaxonal Dystrophy:  WT/WT (clear)
Neuronal Ceroid Lipofuscinosis 1:  WT/WT (clear)
Neuronal Ceroid Lipofuscinosis 10:  WT/WT (clear)
Neuronal Ceroid Lipofuscinosis 12:  WT/WT (clear)
Neuronal Ceroid Lipofuscinosis 2:  WT/WT (clear)
Neuronal Ceroid Lipofuscinosis 4A:  WT/WT (clear)
Neuronal Ceroid Lipofuscinosis 5:  WT/WT (clear)
Neuronal Ceroid Lipofuscinosis 6:  WT/WT (clear)
Neuronal Ceroid Lipofuscinosis 7:  WT/WT (clear)
Neuronal Ceroid Lipofuscinosis 8:  WT/WT (clear)
Nonsyndromic Hearing Loss:  WT/WT (clear)
Oculocutaneous Albinism:  WT/WT (clear)
Osteochondrodysplasia:  WT/WT (clear)
Osteogenesis Imperfecta:  WT/WT (clear)
P2RY12 Receptor Platelet Disorder:  WT/WT (clear)
Pancreatitis:  WT/WT (clear)
Pembroke Welsh Corgi Duchenne Muscular Dystrophy:  WT/WT (clear)
Persistent Mullerian Duct Syndrome:  WT/WT (clear)
Pituitary Dwarfism:  WT/WT (clear)
Polyneuropathy:  WT/WT (clear)
Polyneuropathy with Ocular Abnormalities and Neuronal Vacuolation:  WT/WT (clear)
Pompe Disease:  WT/WT (clear)
Prekallikrein Deficiency:  WT/WT (clear)
Primary Ciliary Dyskinesia:  WT/WT (clear)
Primary Hyperoxaluria:  WT/WT (clear)
Primary Lens Luxation:  WT/WT (clear)
Primary Open Angle Glaucoma:  WT/WT (clear)
Primary Open Angle Glaucoma and Primary Lens Luxation:  WT/WT (clear)
Progressive Retinal Atrophy:  WT/WT (clear)
Progressive Retinal Atrophy, Cone-Rod Dystrophy:  WT/WT (clear)
Progressive Retinal Atrophy, Cone-Rod Dystrophy 1:  WT/WT (clear)
Progressive Retinal Atrophy, Cone-Rod Dystrophy 2:  WT/WT (clear)
Progressive Retinal Atrophy, Cone-Rod Dystrophy 3:  WT/WT (clear)
Progressive Retinal Atrophy, Cone-Rod Dystrophy 4:  WT/WT (clear)
Progressive Retinal Atrophy, Early Onset:  WT/WT (clear)
Progressive Retinal Atrophy, Generalized:  WT/WT (clear)
Progressive Retinal Atrophy, Late-Onset:  WT/WT (clear)
Progressive Retinal Atrophy, PRA1:  WT/WT (clear)
Progressive Retinal Atrophy, PRA3:  WT/WT (clear)
Progressive Retinal Atrophy, Progressive Cone-Rod Degeneration (prcd):  WT/WT (clear)
Progressive Retinal Atrophy, Cone-Rod Dysplasia 3:  WT/WT (clear)
Progressive Retinal Atrophy, Cone-Rod Dysplasia 4:  WT/WT (clear)
Progressive Retinal Atrophy, Syndromic Retinal Degeneration:  WT/WT (clear)
Progressive Retinal Atrophy, X-Linked 1:  WT/WT (clear)
Progressive Retinal Atrophy, X-Linked 2:  WT/WT (clear)
Protein Losing Nephropathy:  WT/WT (clear)
Pyruvate Dehydrogenase Deficiency:  WT/WT (clear)
Pyruvate Kinase Deficiency:  WT/WT (clear)
Recurrent Inflammatory Pulmonary Disease:  WT/WT (clear)
Renal Cystadenocarcinoma and Nodular Dermatofibrosis:  WT/WT (clear)
Retinal Dysplasia/Oculoskeletal Dysplasia 1:  WT/WT (clear)
Dysplasia/Oculoskeletal Dysplasia 2:  WT/WT (clear)
Sensory Neuropathy:  WT/WT (clear)
Severe Combined Immunodeficiency Disease:  WT/WT (clear)
Severe Combined Immunodeficiency Disease, X-Linked:  WT/WT (clear)
Shar-Pei Autoinflammatory Disease:  WT/WT (clear)
Skeletal Dysplasia 2:  WT/WT (clear)
Spinal Dysraphism:  WT/WT (clear)
Spinocerebellar Ataxia:  WT/WT (clear)
Spondylocostal Dysostosis:  WT/WT (clear)
Stargardt Disease:  WT/WT (clear)
Startle Disease:  WT/WT (clear)
Subacute Necrotizing Encephalopathy:  WT/WT (clear)
Thrombopathia:  WT/WT (clear)
Trapped Neutrophil Syndrome:  WT/WT (clear)
Ullrich Congenital Muscular Dystrophy (LR Type 1):  WT/WT (clear)
Ullrich Congenital Muscular Dystrophy (LR Type 2):  WT/WT (clear)
Urolithiasis:  WT/WT (clear)
Van Den Ende-Gupta Syndrome:  WT/WT (clear)
Von Willebrand Disease 1:  WT/WT (clear)
Von Willebrand Disease II:  WT/WT (clear)
Von Willebrand Disease III:  WT/WT (clear)

Eyes:
Hereditary Cataracts: WT/WT (clear)
Hyperuricosuria: WT/WT (clear)
Multifocal Retinopathy 1: WT/WT (clear)
Oculocutaneous Albinism: WT/WT (clear)
Progressive Retinal Atrophy, Cone-Rod Dystrophy 4:  WT/WT (clear)

Coat:
A Locus:  AyAt- (Sable/fawn; carries tricolor/black & tan)
B Locos:  B/b- (Black coat, nose, foot pads; carries 1 copy brown)
Co Locos:  CO/CO-  Black coat, nose & foot pads (does not carry cocoa)
Cu Locos:  Cu/Cu-  Straight coat
D Locus:  D/d- Carries one copy dilute color
E Locus:  E/e- Carrier Melanistic Mask (face color), yellow/red
L Locus:  Sh/Sh- Does not carry Fluffy
M Locus:  m/m- Non Merle
S Locus:  S/S- No white spotting, flash, parti or piebald
SD Locus:  sd/sd- Low Shedding

Polydactyly: pd/pd- normal, likely no rear dew claws

Social Behavior:  WT/WT; WT/M- May demonstrate more social behavior

T Locus (Natural Bobtail):  t/t- Normal Frenchie Tail