Genetic testing for dogs
Hereditary diseases
Coat colors and types
Coat colors and types
Prices
Owners
Breeders, Partners
*Price per test, VAT is included.
Prices
Owners
Breeders, Partners
*Price per test, VAT is included.
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Coat colors
Locus A, alleles Ay, at, a*
allele Ay - dominant red (ASIP: c.246G>T and c.250G>A)
allele a - recessive black (ASIP: c.288C>T)
allele at - tan points (ASIP, SINE insertion)
RALY - saddle vs tan points**
Locus A, extended: alleles Ay, Ays, aw, asa, at, a***
allele Ay - dominant red (ASIP, VP1+HCP1)
allele Ays - shaded red (ASIP, VP2+HCP1)
allele aw - wolf-like (ASIP, VP2+HCP2)
allele asa - saddle (ASIP, VP1+HCP4)
allele at - tan points (ASIP, VP2+HCP3-5)
allele a - recessive black (ASIP: c.288C>T)
Locus B, brown: alleles bc, bd, bs, bAS
Locus C, albinism
Locus D, dark pidment dilution: alleles d1 and d2
Locus E, allele e1 - recessive red
Locus E, allele Em - facial mask
Locus E, allele Eg - grizzle
Locus E, allele eA - domino
Locus H - harlequin
Locus I, red pigment dilution
Locus K, allele Kb - dominant black
Locus S, allele sp - piebald
Cocoa - cocoa color in French bulldogs
* Linked markers of alleles Ay and at; causal mutation for allele a. Allele aw determined by exclusion.
** Linked marker discriminating alleles asa and at in some breeds
*** Causal promoter combinations for alleles Ay, Ays, aw, asa, and at; causal mutation for allele a.
** Linked marker discriminating alleles asa and at in some breeds
*** Causal promoter combinations for alleles Ay, Ays, aw, asa, and at; causal mutation for allele a.
Coat types
Curly hair
Long hair, allele L1 (many breeds)
Long hair, allele L2
Long hair, allele L4
Furnishing
Breed;Test name
Afghan Hound;ᴥ Degenerative Myelopathy, DM (gene SOD1)<br>ᴥ Hyperuricosuria, HUU (gene SLC2A9)<br>
Airedale Terrier;ᴥ Degenerative Myelopathy, DM (gene SOD1)<br>ᴥ Factor VII Deficiency, FVII (gene F7)<br>ᴥ Hyperuricosuria, HUU (gene SLC2A9)<br>
Akita Inu;ᴥ Amelogenesis Imperfecta, Akita type, AI-A (gene ACPT)<br>ᴥ Degenerative Myelopathy, DM (gene SOD1)<br>ᴥ Hyperuricosuria, HUU (gene SLC2A9)<br>
Alaskan Malamute;ᴥ Alaskan Malamute polyneuropathy, AMPN (gene NDRG1)<br>ᴥ Primary Ciliary Dyskinesia, Alaskan Malamute type, PCD-AM (gene NME5)<br>ᴥ Degenerative Myelopathy, DM (gene SOD1)<br>ᴥ Hyperuricosuria, HUU (gene SLC2A9)<br>
American Akita;ᴥ Amelogenesis Imperfecta, Akita type, AI-A (gene ACPT)<br>ᴥ Degenerative Myelopathy, DM (gene SOD1)<br>ᴥ Hyperuricosuria, HUU (gene SLC2A9)<br>
American Bulldog;ᴥ Ichthyosis, NIPAL4-related, C-ICT (gene NIPAL4)<br>ᴥ Multifocal retinopathy 1, CMR1 (gene BEST1)<br>ᴥ Degenerative Myelopathy, DM (gene SOD1)<br>ᴥ Hyperuricosuria, HUU (gene SLC2A9)<br>ᴥ screw tail, screw (gene DVL2)<br>
American Bully;ᴥ Progressive Retinal Atrophy crd4 / cord1-PRA, cord1-PRA (gene RPGRIP1)<br>ᴥ Progressive Retinal Atrophy crd1-PRA, crd1-PRA (gene PDE6B)<br>ᴥ Multifocal retinopathy 1, CMR1 (gene BEST1)<br>ᴥ Neuronal ceroid lipofuscinosis 4A, NCL4A (gene ARSG)<br>ᴥ Degenerative Myelopathy, DM (gene SOD1)<br>ᴥ Hyperuricosuria, HUU (gene SLC2A9)<br>ᴥ Ichthyosis, NIPAL4-related, C-ICT (gene NIPAL4)<br>
American Cocker Spaniel;ᴥ Dwarfism / Skeletal Dysplasia 2, SD2 (gene COL11A2)<br>ᴥ Exercise induced collapse, EIC (gene DNM1)<br>ᴥ Glycogen storage disease VII / Phosphofructokinase Deficiency, PFKD (gene PFKM)<br>ᴥ Degenerative Myelopathy, DM (gene SOD1)<br>ᴥ Hyperuricosuria, HUU (gene SLC2A9)<br>ᴥ Progressive Retinal Atrophy prcd-PRA, prcd-PRA (gene PRCD)<br>
American hairless terrier;ᴥ Primary Lens Luxation, PLL (gene ADAMTS17)<br>ᴥ Degenerative Myelopathy, DM (gene SOD1)<br>ᴥ Hyperuricosuria, HUU (gene SLC2A9)<br>ᴥ Progressive Retinal Atrophy prcd-PRA, prcd-PRA (gene PRCD)<br>
American Pit Bull Terrier;ᴥ Neuronal ceroid lipofuscinosis 4A, NCL4A (gene ARSG)<br>ᴥ Degenerative Myelopathy, DM (gene SOD1)<br>ᴥ Hyperuricosuria, HUU (gene SLC2A9)<br>ᴥ Progressive Retinal Atrophy crd1-PRA, crd1-PRA (gene PDE6B)<br>ᴥ Multifocal retinopathy 1, CMR1 (gene BEST1)<br>
American Staffordshire Terrier;ᴥ Progressive Retinal Atrophy crd1-PRA, crd1-PRA (gene PDE6B)<br>ᴥ Neuronal ceroid lipofuscinosis 4A, NCL4A (gene ARSG)<br>ᴥ Degenerative Myelopathy, DM (gene SOD1)<br>ᴥ Hyperuricosuria, HUU (gene SLC2A9)<br>ᴥ screw tail, screw (gene DVL2)<br>
Appenzeller Sennenhund;ᴥ Degenerative Myelopathy, DM (gene SOD1)<br>ᴥ Hyperuricosuria, HUU (gene SLC2A9)<br>
Australian Cattle Dog;ᴥ Multidrug resistance 1, MDR1 (gene ABCB1)<br>ᴥ Neuronal ceroid lipofuscinosis, NCL5 (gene CLN5)<br>ᴥ Primary Lens Luxation, PLL (gene ADAMTS17)<br>ᴥ Degenerative Myelopathy, DM (gene SOD1)<br>ᴥ Brachyury / bob-tail / stumpy tail, BRCH (gene TBXT)<br>ᴥ Progressive Retinal Atrophy rcd4-PRA, rcd4-PRA (gene C2orf71)<br>ᴥ Hyperuricosuria, HUU (gene SLC2A9)<br>ᴥ Progressive Retinal Atrophy prcd-PRA, prcd-PRA (gene PRCD)<br>
Australian kelpie;ᴥ Collie Eye Anomaly, CEA (gene NHEJ1)<br>ᴥ Multidrug resistance 1, MDR1 (gene ABCB1)<br>ᴥ Degenerative Myelopathy, DM (gene SOD1)<br>ᴥ Progressive Retinal Atrophy prcd-PRA, prcd-PRA (gene PRCD)<br>
Australian Shepherd;ᴥ Collie Eye Anomaly, CEA (gene NHEJ1)<br>ᴥ Hereditary Cataract, HSF4d (gene HSF4)<br>ᴥ Multidrug resistance 1, MDR1 (gene ABCB1)<br>ᴥ Multifocal retinopathy 1, CMR1 (gene BEST1)<br>ᴥ Degenerative Myelopathy, DM (gene SOD1)<br>ᴥ Hyperuricosuria, HUU (gene SLC2A9)<br>ᴥ Progressive Retinal Atrophy prcd-PRA, prcd-PRA (gene PRCD)<br>ᴥ von Willebrand disease type I, vWD1 (gene VWF)<br>ᴥ Brachyury / bob-tail / stumpy tail, BRCH (gene TBXT)<br>ᴥ Craniomandibular osteopathy, CMO (gene SLC37A2)<br>ᴥ Neuronal ceroid lipofuscinosis, type 6, NCL6-AS (gene CLN6)<br>ᴥ Neuronal ceroid lipofuscinosis, type 8, NCL8 (gene CLN8)<br>
Australian silky terrier;ᴥ von Willebrand disease type I, vWD1 (gene VWF)<br>ᴥ Degenerative Myelopathy, DM (gene SOD1)<br>ᴥ Hyperuricosuria, HUU (gene SLC2A9)<br>
Basenji;ᴥ Degenerative Myelopathy, DM (gene SOD1)<br>ᴥ Hyperuricosuria, HUU (gene SLC2A9)<br>
Basset Hound;ᴥ Factor VII Deficiency, FVII (gene F7)<br>ᴥ Degenerative Myelopathy, DM (gene SOD1)<br>ᴥ Hyperuricosuria, HUU (gene SLC2A9)<br>
Beagle;ᴥ Progressive Retinal Atrophy crd4 / cord1-PRA, cord1-PRA (gene RPGRIP1)<br>ᴥ Factor VII Deficiency, FVII (gene F7)<br>ᴥ Musladin-Lueke Syndrome, MLS (gene ADAMTSL2)<br>ᴥ Neonatal cerebellar cortical degeneration, NCCD (gene SPTBN2)<br>ᴥ Primary open angle glaucoma, POAG-BG (gene ADAMTS10)<br>ᴥ Hypocatalasia / Аcatalasemia, ACAT (gene CAT)<br>ᴥ Osteogenesis imperfecta, Beagle type, OI-B (gene COL1A2)<br>ᴥ Pyruvate kinase deficiency, PK-BG (gene PKLR)<br>ᴥ Degenerative Myelopathy, DM (gene SOD1)<br>ᴥ Hyperuricosuria, HUU (gene SLC2A9)<br>
Beauceron;ᴥ Degenerative Myelopathy, DM (gene SOD1)<br>ᴥ Hyperuricosuria, HUU (gene SLC2A9)<br>
Bedlington Terrier;ᴥ Hereditary Footpad Hyperkeratosis, HFH (gene FAM83G)<br>ᴥ Degenerative Myelopathy, DM (gene SOD1)<br>ᴥ Hyperuricosuria, HUU (gene SLC2A9)<br>
Bernese Mountain Dog;ᴥ Degenerative Myelopathy, exon 1, DM1 (gene SOD1)<br>ᴥ Degenerative Myelopathy, exon 2, DM (gene SOD1)<br>ᴥ Hyperuricosuria, HUU (gene SLC2A9)<br>ᴥ von Willebrand disease type I, vWD1 (gene VWF)<br>
Bichon Frise;ᴥ Degenerative Myelopathy, DM (gene SOD1)<br>ᴥ Hyperuricosuria, HUU (gene SLC2A9)<br>ᴥ Progressive Retinal Atrophy prcd-PRA, prcd-PRA (gene PRCD)<br>
Biewer Terrier;ᴥ Primary Lens Luxation, PLL (gene ADAMTS17)<br>ᴥ Degenerative Myelopathy, DM (gene SOD1)<br>ᴥ Hyperuricosuria, HUU (gene SLC2A9)<br>ᴥ Progressive Retinal Atrophy prcd-PRA, prcd-PRA (gene PRCD)<br>
Black Russian Terrier;ᴥ Juvenile laryngeal paralysis & polyneuropathy, JLPP (gene RAB3GAP1)<br>ᴥ Hyperuricosuria, HUU (gene SLC2A9)<br>ᴥ Progressive Retinal Atrophy prcd-PRA, prcd-PRA (gene PRCD)<br>ᴥ Degenerative Myelopathy, DM (gene SOD1)<br>
Bloodhound;ᴥ Degenerative Myelopathy, DM (gene SOD1)<br>ᴥ Hyperuricosuria, HUU (gene SLC2A9)<br>
Boerboel;ᴥ Multifocal retinopathy 1, CMR1 (gene BEST1)<br>ᴥ Hyperuricosuria, HUU (gene SLC2A9)<br>ᴥ Degenerative Myelopathy, DM (gene SOD1)<br>
Bolonka;ᴥ Progressive Retinal Atrophy prcd-PRA, prcd-PRA (gene PRCD)<br>ᴥ Degenerative Myelopathy, DM (gene SOD1)<br>ᴥ Hyperuricosuria, HUU (gene SLC2A9)<br>
Border Collie;ᴥ Collie Eye Anomaly, CEA (gene NHEJ1)<br>ᴥ Dental hypomineralization / Raine Syndrome, DH (gene FAM20C)<br>ᴥ Early adult onset deafness, EAOD (gene USP31)<br>ᴥ Glaucoma and Goniodysgenesis, GGD (gene OLFML3)<br>ᴥ Multidrug resistance 1, MDR1 (gene ABCB1)<br>ᴥ Neuronal ceroid lipofuscinosis, NCL5 (gene CLN5)<br>ᴥ Phenobarbital resistance, MDR2 (gene ABCB1)<br>ᴥ Trapped Neutrophil Syndrome, TNS (gene VPS13B)<br>ᴥ Primary Lens Luxation, PLL (gene ADAMTS17)<br>ᴥ Degenerative Myelopathy, DM (gene SOD1)<br>ᴥ Hyperuricosuria, HUU (gene SLC2A9)<br>
Borzoi;ᴥ Degenerative Myelopathy, DM (gene SOD1)<br>ᴥ Hyperuricosuria, HUU (gene SLC2A9)<br>
Boston Terrier;ᴥ Hereditary Cataract, HSF4r (gene HSF4)<br>ᴥ Degenerative Myelopathy, DM (gene SOD1)<br>ᴥ Hyperuricosuria, HUU (gene SLC2A9)<br>
Bouvier des Flandres;ᴥ Exercise induced collapse, EIC (gene DNM1)<br>ᴥ Degenerative Myelopathy, DM (gene SOD1)<br>ᴥ Hyperuricosuria, HUU (gene SLC2A9)<br>
Boxer;ᴥ Degenerative Myelopathy, DM (gene SOD1)<br>ᴥ Hyperuricosuria, HUU (gene SLC2A9)<br>
Boykin Spaniel;ᴥ Collie Eye Anomaly, CEA (gene NHEJ1)<br>ᴥ Exercise induced collapse, EIC (gene DNM1)<br>ᴥ Degenerative Myelopathy, DM (gene SOD1)<br>ᴥ Progressive Retinal Atrophy crd4 / cord1-PRA, cord1-PRA (gene RPGRIP1)<br>ᴥ Hyperuricosuria, HUU (gene SLC2A9)<br>ᴥ Progressive Retinal Atrophy prcd-PRA, prcd-PRA (gene PRCD)<br>
Bull Terrier;ᴥ Lethal acrodermatitis, LAD (gene MKLN1)<br>ᴥ Laryngeal paralysis, LP (gene RAPGEF6)<br>ᴥ Hereditary Cataract, HSF4r (gene HSF4)<br>ᴥ Polycystic kidney disease, PKD (gene PKD1)<br>ᴥ Degenerative Myelopathy, DM (gene SOD1)<br>ᴥ Hyperuricosuria, HUU (gene SLC2A9)<br>
Bulldog;ᴥ Multifocal retinopathy 1, CMR1 (gene BEST1)<br>ᴥ Degenerative Myelopathy, DM (gene SOD1)<br>ᴥ Hyperuricosuria, HUU (gene SLC2A9)<br>ᴥ Cystinuria, CYS-BD (gene SLC3A1)<br>
Bullmastiff;ᴥ Multifocal retinopathy 1, CMR1 (gene BEST1)<br>ᴥ Degenerative Myelopathy, DM (gene SOD1)<br>ᴥ Hyperuricosuria, HUU (gene SLC2A9)<br>
Ca de Bou;ᴥ Degenerative Myelopathy, DM (gene SOD1)<br>ᴥ Hyperuricosuria, HUU (gene SLC2A9)<br>
Cairn Terrier;ᴥ Craniomandibular osteopathy, CMO (gene SLC37A2)<br>ᴥ Macrothrombocytopenia, recessive, Cairn Terrier type, MTC-r (gene TUBB1)<br>ᴥ Degenerative Myelopathy, DM (gene SOD1)<br>ᴥ von Willebrand disease type I, vWD1 (gene VWF)<br>ᴥ Hyperuricosuria, HUU (gene SLC2A9)<br>
Cane Corso;ᴥ Dental-skeletal-retinal anomaly, DSRA (gene MIA3)<br>ᴥ Multifocal retinopathy 1, CMR1 (gene BEST1)<br>ᴥ Multidrug resistance 1, MDR1 (gene ABCB1)<br>ᴥ Degenerative Myelopathy, DM (gene SOD1)<br>ᴥ Hyperuricosuria, HUU (gene SLC2A9)<br>
Caucasian Shepherd Dog;ᴥ Degenerative Myelopathy, DM (gene SOD1)<br>ᴥ Hyperuricosuria, HUU (gene SLC2A9)<br>
Cavalier King Charles Spaniel;ᴥ Dry eye curly coat syndrome, CKCSID (gene FAM83H)<br>ᴥ Episodic falling syndrome, EFS (gene BCAN)<br>ᴥ Dwarfism / Skeletal Dysplasia 2, SD2 (gene COL11A2)<br>ᴥ Degenerative Myelopathy, DM (gene SOD1)<br>ᴥ Hyperuricosuria, HUU (gene SLC2A9)<br>
Central Asian Shepherd Dog;ᴥ Dystrophic Epidermolysis Bullosa, DEB (gene COL7A1)<br>ᴥ Degenerative Myelopathy, DM (gene SOD1)<br>ᴥ Hyperuricosuria, HUU (gene SLC2A9)<br>
Chesapeake Bay Retriever;ᴥ Exercise induced collapse, EIC (gene DNM1)<br>ᴥ Degenerative Myelopathy, DM (gene SOD1)<br>ᴥ Progressive Retinal Atrophy prcd-PRA, prcd-PRA (gene PRCD)<br>ᴥ Multidrug resistance 1, MDR1 (gene ABCB1)<br>ᴥ Hyperuricosuria, HUU (gene SLC2A9)<br>
Chihuahua;ᴥ Macrothrombocytopenia, recessive, Cairn Terrier type, MTC-r (gene TUBB1)<br>ᴥ Progressive Retinal Atrophy prcd-PRA, prcd-PRA (gene PRCD)<br>ᴥ Progressive Retinal Atrophy crd4 / cord1-PRA, cord1-PRA (gene RPGRIP1)<br>ᴥ Degenerative Myelopathy, DM (gene SOD1)<br>ᴥ Hyperuricosuria, HUU (gene SLC2A9)<br>
Chinese Crested Dog;ᴥ Primary Lens Luxation, PLL (gene ADAMTS17)<br>ᴥ Degenerative Myelopathy, DM (gene SOD1)<br>ᴥ Progressive Retinal Atrophy prcd-PRA, prcd-PRA (gene PRCD)<br>ᴥ Hyperuricosuria, HUU (gene SLC2A9)<br>
Chongqing dog;ᴥ Degenerative Myelopathy, DM (gene SOD1)<br>ᴥ Hyperuricosuria, HUU (gene SLC2A9)<br>
Chow Chow;ᴥ Degenerative Myelopathy, DM (gene SOD1)<br>ᴥ Hyperuricosuria, HUU (gene SLC2A9)<br>
Clumber Spaniel;ᴥ Exercise induced collapse, EIC (gene DNM1)<br>ᴥ Pyruvate dehydrogenase deficiency, PDP1 (gene PDP1)<br>ᴥ Degenerative Myelopathy, DM (gene SOD1)<br>ᴥ Hyperuricosuria, HUU (gene SLC2A9)<br>
Collie;ᴥ Collie Eye Anomaly, CEA (gene NHEJ1)<br>ᴥ Multidrug resistance 1, MDR1 (gene ABCB1)<br>ᴥ Degenerative Myelopathy, DM (gene SOD1)<br>ᴥ Cyclic Neutropenia, GCS (gene AP3B1)<br>ᴥ Dermatomyositis, DMS (genes PAN2, MAP3K7CL, DLA-DRB1)<br>ᴥ Recurrent inflammatory pulmonary disease, IPD (gene AKNA)<br>ᴥ Hyperuricosuria, HUU (gene SLC2A9)<br>
Coton de Tulear;ᴥ Multifocal retinopathy 2, CMR2 (gene BEST1)<br>ᴥ Primary hyperoxaluria, PH (gene AGXT)<br>ᴥ Degenerative Myelopathy, DM (gene SOD1)<br>ᴥ Progressive Retinal Atrophy prcd-PRA, prcd-PRA (gene PRCD)<br>ᴥ von Willebrand disease type I, vWD1 (gene VWF)<br>ᴥ Exercise induced collapse, EIC (gene DNM1)<br>ᴥ Hyperuricosuria, HUU (gene SLC2A9)<br>
Curly Coated Retriever;ᴥ Progressive Retinal Atrophy crd4 / cord1-PRA, cord1-PRA (gene RPGRIP1)<br>ᴥ Exercise induced collapse, EIC (gene DNM1)<br>ᴥ Glycogen Storage Disease, GSDIIIa (gene AGL)<br>ᴥ Degenerative Myelopathy, DM (gene SOD1)<br>ᴥ Hyperuricosuria, HUU (gene SLC2A9)<br>
Dachshund - longhaired;ᴥ Mucopolysaccharidosis type IIIa, MPSIIIA (gene SGSH)<br>ᴥ Osteogenesis imperfecta, OI (gene SERPINH1)<br>ᴥ Progressive Retinal Atrophy crd4 / cord1-PRA, cord1-PRA (gene RPGRIP1)<br>ᴥ Narcolepsy, NRCL-DS (gene HCRTR2)<br>ᴥ Neuronal ceroid lipofuscinosis, NCL2 (gene TPP1)<br>ᴥ Degenerative Myelopathy, DM (gene SOD1)<br>ᴥ Hyperuricosuria, HUU (gene SLC2A9)<br>
Dachshund - miniature longhaired;ᴥ Progressive Retinal Atrophy crd4 / cord1-PRA, cord1-PRA (gene RPGRIP1)<br>ᴥ Osteogenesis imperfecta, OI (gene SERPINH1)<br>ᴥ Degenerative Myelopathy, DM (gene SOD1)<br>ᴥ Mucopolysaccharidosis type IIIa, MPSIIIA (gene SGSH)<br>ᴥ Narcolepsy, NRCL-DS (gene HCRTR2)<br>ᴥ Neuronal ceroid lipofuscinosis, NCL2 (gene TPP1)<br>ᴥ Hyperuricosuria, HUU (gene SLC2A9)<br>
Dachshund - miniature smooth-haired;ᴥ Osteogenesis imperfecta, OI (gene SERPINH1)<br>ᴥ Progressive Retinal Atrophy crd4 / cord1-PRA, cord1-PRA (gene RPGRIP1)<br>ᴥ Factor VII Deficiency, FVII (gene F7)<br>ᴥ Mucopolysaccharidosis type IIIa, MPSIIIA (gene SGSH)<br>ᴥ Narcolepsy, NRCL-DS (gene HCRTR2)<br>ᴥ Neuronal ceroid lipofuscinosis, NCL2 (gene TPP1)<br>ᴥ Degenerative Myelopathy, DM (gene SOD1)<br>ᴥ Hyperuricosuria, HUU (gene SLC2A9)<br>
Dachshund - miniature wirehaired;ᴥ Osteogenesis imperfecta, OI (gene SERPINH1)<br>ᴥ Degenerative Myelopathy, DM (gene SOD1)<br>ᴥ Progressive Retinal Atrophy crd4 / cord1-PRA, cord1-PRA (gene RPGRIP1)<br>ᴥ Mucopolysaccharidosis type IIIa, MPSIIIA (gene SGSH)<br>ᴥ Narcolepsy, NRCL-DS (gene HCRTR2)<br>ᴥ Neuronal ceroid lipofuscinosis, NCL2 (gene TPP1)<br>ᴥ Hyperuricosuria, HUU (gene SLC2A9)<br>
Dachshund - shorthaired;ᴥ Mucopolysaccharidosis type IIIa, MPSIIIA (gene SGSH)<br>ᴥ Osteogenesis imperfecta, OI (gene SERPINH1)<br>ᴥ Progressive Retinal Atrophy crd4 / cord1-PRA, cord1-PRA (gene RPGRIP1)<br>ᴥ Narcolepsy, NRCL-DS (gene HCRTR2)<br>ᴥ Neuronal ceroid lipofuscinosis, NCL2 (gene TPP1)<br>ᴥ Degenerative Myelopathy, DM (gene SOD1)<br>ᴥ Hyperuricosuria, HUU (gene SLC2A9)<br>
Dachshund - wirehaired;ᴥ Mucopolysaccharidosis type IIIa, MPSIIIA (gene SGSH)<br>ᴥ Osteogenesis imperfecta, OI (gene SERPINH1)<br>ᴥ Progressive Retinal Atrophy crd4 / cord1-PRA, cord1-PRA (gene RPGRIP1)<br>ᴥ Narcolepsy, NRCL-DS (gene HCRTR2)<br>ᴥ Neuronal ceroid lipofuscinosis, NCL2 (gene TPP1)<br>ᴥ Degenerative Myelopathy, DM (gene SOD1)<br>ᴥ Hyperuricosuria, HUU (gene SLC2A9)<br>
Dalmatian;ᴥ Degenerative Myelopathy, DM (gene SOD1)<br>ᴥ Hyperuricosuria, HUU (gene SLC2A9)<br>
Dobermann;ᴥ Hereditary deafness/Deafness, bilateral, and vestibular dysfunction, HD (gene MYO7A)<br>ᴥ von Willebrand disease type I, vWD1 (gene VWF)<br>ᴥ Degenerative Myelopathy, DM (gene SOD1)<br>ᴥ Hyperuricosuria, HUU (gene SLC2A9)<br>
Dogue de Bordeaux;ᴥ screw tail, screw (gene DVL2)<br>ᴥ Hereditary Footpad Hyperkeratosis Dogue de Bordeaux type, HFH-B (gene KRT16)<br>ᴥ Multifocal retinopathy 1, CMR1 (gene BEST1)<br>ᴥ Degenerative Myelopathy, DM (gene SOD1)<br>ᴥ Hyperuricosuria, HUU (gene SLC2A9)<br>
East Siberian Laika;ᴥ Primary open angle glaucoma, POAG-BG (gene ADAMTS10)<br>ᴥ Degenerative Myelopathy, DM (gene SOD1)<br>ᴥ Hyperuricosuria, HUU (gene SLC2A9)<br>
East-European Shepherd;ᴥ Multidrug resistance 1, MDR1 (gene ABCB1)<br>ᴥ Degenerative Myelopathy, DM (gene SOD1)<br>ᴥ Hyperuricosuria, HUU (gene SLC2A9)<br>
English Cocker Spaniel;ᴥ Familial Nephropathy, FN-ECS (gene COL4A4)<br>ᴥ Progressive Retinal Atrophy prcd-PRA, prcd-PRA (gene PRCD)<br>ᴥ Acral Mutilation Syndrome, AMS (gene GDNF)<br>ᴥ Exercise induced collapse, EIC (gene DNM1)<br>ᴥ Glycogen storage disease VII / Phosphofructokinase Deficiency, PFKD (gene PFKM)<br>ᴥ Degenerative Myelopathy, DM (gene SOD1)<br>ᴥ Hyperuricosuria, HUU (gene SLC2A9)<br>
English Mastiff;ᴥ Multifocal retinopathy 1, CMR1 (gene BEST1)<br>ᴥ Degenerative Myelopathy, DM (gene SOD1)<br>ᴥ Hyperuricosuria, HUU (gene SLC2A9)<br>
English setter;ᴥ Progressive Retinal Atrophy rcd4-PRA, rcd4-PRA (gene C2orf71)<br>ᴥ Hyperuricosuria, HUU (gene SLC2A9)<br>ᴥ Degenerative Myelopathy, DM (gene SOD1)<br>
English Springer Spaniel;ᴥ Degenerative Myelopathy, DM (gene SOD1)<br>ᴥ Acral Mutilation Syndrome, AMS (gene GDNF)<br>ᴥ Progressive Retinal Atrophy crd4 / cord1-PRA, cord1-PRA (gene RPGRIP1)<br>ᴥ Glycogen storage disease VII / Phosphofructokinase Deficiency, PFKD (gene PFKM)<br>ᴥ Hyperuricosuria, HUU (gene SLC2A9)<br>
Entlebucher Mountain Dog;ᴥ Degenerative Myelopathy, DM (gene SOD1)<br>ᴥ Hyperuricosuria, HUU (gene SLC2A9)<br>ᴥ Progressive Retinal Atrophy prcd-PRA, prcd-PRA (gene PRCD)<br>
Field Spaniel;ᴥ Progressive Retinal Atrophy crd4 / cord1-PRA, cord1-PRA (gene RPGRIP1)<br>ᴥ Progressive Retinal Atrophy prcd-PRA, prcd-PRA (gene PRCD)<br>ᴥ Degenerative Myelopathy, DM (gene SOD1)<br>ᴥ Hyperuricosuria, HUU (gene SLC2A9)<br>
Flat-coated Retriever;ᴥ Exercise induced collapse, EIC (gene DNM1)<br>ᴥ Degenerative Myelopathy, DM (gene SOD1)<br>ᴥ Hyperuricosuria, HUU (gene SLC2A9)<br>
French Bulldog;ᴥ Congenital hypothyroidism with goiter, CHG (gene TPO)<br>ᴥ Cystinuria, CYS-BD (gene SLC3A1)<br>ᴥ Multifocal retinopathy 1, CMR1 (gene BEST1)<br>ᴥ Hereditary Cataract, HSF4r (gene HSF4)<br>ᴥ Degenerative Myelopathy, DM (gene SOD1)<br>ᴥ Hyperuricosuria, HUU (gene SLC2A9)<br>ᴥ Progressive Retinal Atrophy crd4 / cord1-PRA, cord1-PRA (gene RPGRIP1)<br>ᴥ Multidrug resistance 1, MDR1 (gene ABCB1)<br>
German Pinscher;ᴥ Degenerative Myelopathy, DM (gene SOD1)<br>ᴥ von Willebrand disease type I, vWD1 (gene VWF)<br>ᴥ Hyperuricosuria, HUU (gene SLC2A9)<br>
German Shepherd;ᴥ Multidrug resistance 1, MDR1 (gene ABCB1)<br>ᴥ Degenerative Myelopathy, DM (gene SOD1)<br>ᴥ Achromatopsia, ACHM-GSD (gene CNGA3)<br>ᴥ Hyperuricosuria, HUU (gene SLC2A9)<br>
German Shorthaired Pointer;ᴥ Acral Mutilation Syndrome, AMS (gene GDNF)<br>ᴥ Degenerative Myelopathy, DM (gene SOD1)<br>ᴥ Factor VII Deficiency, FVII (gene F7)<br>ᴥ Neuronal ceroid lipofuscinosis, type 8, NCL8 (gene CLN8)<br>ᴥ Hyperuricosuria, HUU (gene SLC2A9)<br>
German Spitz;ᴥ Progressive Retinal Atrophy prcd-PRA, prcd-PRA (gene PRCD)<br>ᴥ von Willebrand disease type I, vWD1 (gene VWF)<br>ᴥ Degenerative Myelopathy, DM (gene SOD1)<br>ᴥ Hyperuricosuria, HUU (gene SLC2A9)<br>
German Wirehaired Pointer;ᴥ Exercise induced collapse, EIC (gene DNM1)<br>ᴥ Factor VII Deficiency, FVII (gene F7)<br>ᴥ Degenerative Myelopathy, DM (gene SOD1)<br>ᴥ Hyperuricosuria, HUU (gene SLC2A9)<br>
Giant Schnauzer;ᴥ Hyperuricosuria, HUU (gene SLC2A9)<br>ᴥ Factor VII Deficiency, FVII (gene F7)<br>ᴥ Degenerative Myelopathy, DM (gene SOD1)<br>ᴥ Progressive Retinal Atrophy prcd-PRA, prcd-PRA (gene PRCD)<br>
Golden Retriever;ᴥ Golden Retriever Progressive Retinal Atrophy 1, GR-PRA1 (gene SLC4A3)<br>ᴥ Golden Retriever Progressive Retinal Atrophy 2, GR-PRA2 (gene TTC8)<br>ᴥ Ichthyosis, PNPLA1-related, ICT (gene PNPLA1)<br>ᴥ Progressive Retinal Atrophy prcd-PRA, prcd-PRA (gene PRCD)<br>ᴥ Golden Retriever Muscular Dystrophy, GRMD (gene DMD)<br>ᴥ Degenerative Myelopathy, DM (gene SOD1)<br>ᴥ Hyperuricosuria, HUU (gene SLC2A9)<br>
Gordon Setter;ᴥ Hereditary Ataxia or Cerebellar Ataxia, HA (gene RAB24)<br>ᴥ Progressive Retinal Atrophy rcd4-PRA, rcd4-PRA (gene C2orf71)<br>ᴥ Degenerative Myelopathy, DM (gene SOD1)<br>ᴥ Hyperuricosuria, HUU (gene SLC2A9)<br>
Great Dane;ᴥ Leukoencephalomyelopathy, LEMP (gene NAPEPLD)<br>ᴥ Degenerative Myelopathy, DM (gene SOD1)<br>ᴥ Hyperuricosuria, HUU (gene SLC2A9)<br>ᴥ von Willebrand disease type I, vWD1 (gene VWF)<br>
Greater Swiss Mountain Dog;ᴥ Hyperuricosuria, HUU (gene SLC2A9)<br>ᴥ Degenerative Myelopathy, DM (gene SOD1)<br>
Greek Harehound;ᴥ Degenerative Myelopathy, DM (gene SOD1)<br>ᴥ Hyperuricosuria, HUU (gene SLC2A9)<br>
Greyhound;ᴥ Degenerative Myelopathy, DM (gene SOD1)<br>ᴥ Hyperuricosuria, HUU (gene SLC2A9)<br>
Griffon, Brussells Griffon/Belgian Griffon/Brabancon Griffon);ᴥ Degenerative Myelopathy, DM (gene SOD1)<br>ᴥ Hyperuricosuria, HUU (gene SLC2A9)<br>
Groenendael, Belgian Shepherd Dog);ᴥ Degenerative Myelopathy, DM (gene SOD1)<br>ᴥ Hyperuricosuria, HUU (gene SLC2A9)<br>
Irish Setter;ᴥ Degenerative Myelopathy, DM (gene SOD1)<br>ᴥ Progressive Retinal Atrophy rcd4-PRA, rcd4-PRA (gene C2orf71)<br>ᴥ Hyperuricosuria, HUU (gene SLC2A9)<br>
Irish Terrier;ᴥ Hereditary Footpad Hyperkeratosis, HFH (gene FAM83G)<br>ᴥ Degenerative Myelopathy, DM (gene SOD1)<br>ᴥ Hyperuricosuria, HUU (gene SLC2A9)<br>
Irish Wolfhound;ᴥ Degenerative Myelopathy, DM (gene SOD1)<br>ᴥ Hyperuricosuria, HUU (gene SLC2A9)<br>
Italian Greyhound;ᴥ Amelogenesis Imperfecta, Italian Greyhound type, AI-IG (gene ENAM)<br>ᴥ Degenerative Myelopathy, DM (gene SOD1)<br>ᴥ Hyperuricosuria, HUU (gene SLC2A9)<br>
Jack Russell Terrier;ᴥ Primary Lens Luxation, PLL (gene ADAMTS17)<br>ᴥ Spinocerebellar Ataxia / Late-Onset Ataxia, LOA (gene CAPN1)<br>ᴥ Spinocerebellar Ataxia with Myokymia and/or Seizures, SCA-J (gene KCNJ10)<br>ᴥ Degenerative Myelopathy, DM (gene SOD1)<br>ᴥ Hyperuricosuria, HUU (gene SLC2A9)<br>ᴥ Brachyury / bob-tail / stumpy tail, BRCH (gene TBXT)<br>ᴥ Congenital myasthenic syndrome, Jack Russell terrier type, CMS-JRT (gene CHRNE)<br>ᴥ Progressive Retinal Atrophy prcd-PRA, prcd-PRA (gene PRCD)<br>
Jagdterrier;ᴥ Primary Lens Luxation, PLL (gene ADAMTS17)<br>ᴥ Degenerative Myelopathy, DM (gene SOD1)<br>ᴥ Hereditary Footpad Hyperkeratosis, HFH (gene FAM83G)<br>ᴥ Hyperuricosuria, HUU (gene SLC2A9)<br>
Kangal Shepherd Dog;ᴥ Hyperuricosuria, HUU (gene SLC2A9)<br>ᴥ Degenerative Myelopathy, DM (gene SOD1)<br>
Keeshond;ᴥ Degenerative Myelopathy, DM (gene SOD1)<br>ᴥ Hyperuricosuria, HUU (gene SLC2A9)<br>
Kerry Blue Terrier;ᴥ Macrothrombocytopenia, recessive, Cairn Terrier type, MTC-r (gene TUBB1)<br>ᴥ Degenerative Myelopathy, DM (gene SOD1)<br>ᴥ von Willebrand disease type I, vWD1 (gene VWF)<br>ᴥ Hyperuricosuria, HUU (gene SLC2A9)<br>
Komondor;ᴥ Degenerative Myelopathy, DM (gene SOD1)<br>ᴥ Hyperuricosuria, HUU (gene SLC2A9)<br>
Labrador Retriever;ᴥ Dwarfism / Skeletal Dysplasia 2, SD2 (gene COL11A2)<br>ᴥ Exercise induced collapse, EIC (gene DNM1)<br>ᴥ Progressive Retinal Atrophy prcd-PRA, prcd-PRA (gene PRCD)<br>ᴥ Achromatopsia / Day blindness, ACHM-LR (gene CNGA3)<br>ᴥ Progressive Retinal Atrophy crd4 / cord1-PRA, cord1-PRA (gene RPGRIP1)<br>ᴥ Cystinuria, Labrador Retriever type, L-CYS (gene SLC3A1)<br>ᴥ Myotubular myopathy 1 / X-linked myotubular myopathy, Labrador retriever type, XLMTM (gene MTM1)<br>ᴥ Narcolepsy Labrador Type, NRCL-LR (gene HCRTR2)<br>ᴥ Degenerative Myelopathy, DM (gene SOD1)<br>ᴥ Hyperuricosuria, HUU (gene SLC2A9)<br>ᴥ von Willebrand disease type I, vWD1 (gene VWF)<br>
Lagotto Romagnolo;ᴥ Progressive Retinal Atrophy prcd-PRA, prcd-PRA (gene PRCD)<br>ᴥ Degenerative Myelopathy, DM (gene SOD1)<br>ᴥ Hyperuricosuria, HUU (gene SLC2A9)<br>
Lancashire Heeler;ᴥ Collie Eye Anomaly, CEA (gene NHEJ1)<br>ᴥ Primary Lens Luxation, PLL (gene ADAMTS17)<br>ᴥ Degenerative Myelopathy, DM (gene SOD1)<br>ᴥ Progressive Retinal Atrophy prcd-PRA, prcd-PRA (gene PRCD)<br>ᴥ Craniomandibular osteopathy, CMO (gene SLC37A2)<br>ᴥ Hyperuricosuria, HUU (gene SLC2A9)<br>
Landseer;ᴥ Degenerative Myelopathy, DM (gene SOD1)<br>ᴥ Hyperuricosuria, HUU (gene SLC2A9)<br>
Lhasa Apso;ᴥ Degenerative Myelopathy, DM (gene SOD1)<br>ᴥ Hyperuricosuria, HUU (gene SLC2A9)<br>
Malinois, Belgian Shepherd);ᴥ Spinocerebellar Ataxia with Myokymia and/or Seizures, Malinois type, SCA-M (gene KCNJ10)<br>ᴥ Degenerative Myelopathy, DM (gene SOD1)<br>ᴥ Hyperuricosuria, HUU (gene SLC2A9)<br>
Maltese;ᴥ Hyperuricosuria, HUU (gene SLC2A9)<br>ᴥ Degenerative Myelopathy, DM (gene SOD1)<br>
Maltipoo;ᴥ Degenerative Myelopathy, DM (gene SOD1)<br>ᴥ Hyperuricosuria, HUU (gene SLC2A9)<br>ᴥ von Willebrand disease type I, vWD1 (gene VWF)<br>
Maremmano-Abruzzese Sheepdog;ᴥ Macrothrombocytopenia, recessive, Cairn Terrier type, MTC-r (gene TUBB1)<br>ᴥ Degenerative Myelopathy, DM (gene SOD1)<br>ᴥ Hyperuricosuria, HUU (gene SLC2A9)<br>
Miniature American Shepherd;ᴥ Neuroaxonal dystrophy, MAS type, NAD-MAS (gene RNF170)<br>ᴥ Collie Eye Anomaly, CEA (gene NHEJ1)<br>ᴥ Multidrug resistance 1, MDR1 (gene ABCB1)<br>ᴥ Progressive Retinal Atrophy prcd-PRA, prcd-PRA (gene PRCD)<br>ᴥ Degenerative Myelopathy, DM (gene SOD1)<br>ᴥ Bardet–Biedl syndrome 2, BBS2 (gene BBS2)<br>ᴥ Hyperuricosuria, HUU (gene SLC2A9)<br>
Miniature Bull Terrier;ᴥ Lethal acrodermatitis, LAD (gene MKLN1)<br>ᴥ Laryngeal paralysis, LP (gene RAPGEF6)<br>ᴥ Primary Lens Luxation, PLL (gene ADAMTS17)<br>ᴥ Degenerative Myelopathy, DM (gene SOD1)<br>ᴥ Hyperuricosuria, HUU (gene SLC2A9)<br>
Miniature Pinscher;ᴥ Hereditary Cataract, HSF4d (gene HSF4)<br>ᴥ Primary Lens Luxation, PLL (gene ADAMTS17)<br>ᴥ Degenerative Myelopathy, DM (gene SOD1)<br>ᴥ Hyperuricosuria, HUU (gene SLC2A9)<br>
Miniature Schnauzer;ᴥ Spondylocostal Dysostosis / Comma defect, SCD (gene HES7)<br>ᴥ Charcot-Marie-Tooth disease type 4B2, CMT-MS (gene SBF2)<br>ᴥ Mycobacterium Avium Complex, MAC (gene CARD9)<br>ᴥ Myotonia Congenita, MC (gene CLCN1)<br>ᴥ Persistent Mullerian duct syndrome, PMDS (gene AMHR2)<br>ᴥ Progressive Retinal Atrophy - PRA-B / Type 1 / Type B1, PRA-B1 (gene HIVEP3)<br>ᴥ Factor VII Deficiency, FVII (gene F7)<br>ᴥ Degenerative Myelopathy, DM (gene SOD1)<br>ᴥ Hyperuricosuria, HUU (gene SLC2A9)<br>
Moscow Watchdog;ᴥ Degenerative Myelopathy, DM (gene SOD1)<br>ᴥ Hyperuricosuria, HUU (gene SLC2A9)<br>
Mudi;ᴥ Brachyury / bob-tail / stumpy tail, BRCH (gene TBXT)<br>ᴥ Degenerative Myelopathy, DM (gene SOD1)<br>ᴥ Hyperuricosuria, HUU (gene SLC2A9)<br>
Neapolitan Mastiff;ᴥ Degenerative Myelopathy, DM (gene SOD1)<br>ᴥ Hyperuricosuria, HUU (gene SLC2A9)<br>
Newfoundland;ᴥ Degenerative Myelopathy, DM (gene SOD1)<br>ᴥ Hyperuricosuria, HUU (gene SLC2A9)<br>
Norfolk Terrier;ᴥ Macrothrombocytopenia, recessive, Cairn Terrier type, MTC-r (gene TUBB1)<br>ᴥ Degenerative Myelopathy, DM (gene SOD1)<br>ᴥ Primary Lens Luxation, PLL (gene ADAMTS17)<br>ᴥ Hyperuricosuria, HUU (gene SLC2A9)<br>
Norwegian Buhund;ᴥ Degenerative Myelopathy, DM (gene SOD1)<br>ᴥ Hyperuricosuria, HUU (gene SLC2A9)<br>
Norwegian Elkhound;ᴥ Primary open angle glaucoma, POAG-NE (gene ADAMTS10)<br>ᴥ Degenerative Myelopathy, DM (gene SOD1)<br>ᴥ Hyperuricosuria, HUU (gene SLC2A9)<br>ᴥ Progressive Retinal Atrophy prcd-PRA, prcd-PRA (gene PRCD)<br>
Norwich Terrier;ᴥ Brachycephalic Obstructive Airway Syndrome, BOAS (gene ADAMTS3)<br>ᴥ Degenerative Myelopathy, DM (gene SOD1)<br>ᴥ Primary Lens Luxation, PLL (gene ADAMTS17)<br>ᴥ Hyperuricosuria, HUU (gene SLC2A9)<br>ᴥ Cystic Renal Dysplasia and Hepatic Fibrosis, CRDHF (gene INPP5E)<br>
Nova Scotia Duck Tolling Retriever;ᴥ Cleft Palate and Syndactyly, CLPS (gene ADAMTS20)<br>ᴥ Collie Eye Anomaly, CEA (gene NHEJ1)<br>ᴥ Degenerative Myelopathy, DM (gene SOD1)<br>ᴥ Hyperuricosuria, HUU (gene SLC2A9)<br>ᴥ Progressive Retinal Atrophy prcd-PRA, prcd-PRA (gene PRCD)<br>
Old English Sheepdog;ᴥ Exercise induced collapse, EIC (gene DNM1)<br>ᴥ Hereditary Ataxia or Cerebellar Ataxia, HA (gene RAB24)<br>ᴥ Multidrug resistance 1, MDR1 (gene ABCB1)<br>ᴥ Primary Ciliary Dyskinesia, Old English Sheepdog type, PCD (gene CCDC39)<br>ᴥ Haemophilia A, Bobtail type, F8-OES (gene F8)<br>ᴥ Degenerative Myelopathy, DM (gene SOD1)<br>ᴥ Hyperuricosuria, HUU (gene SLC2A9)<br>
Papillon;ᴥ Neuroaxonal dystrophy, NAD (gene PLA2G6)<br>ᴥ Progressive Retinal Atrophy PAP1, PAP1-PRA (gene CNGB1)<br>ᴥ von Willebrand disease type I, vWD1 (gene VWF)<br>ᴥ Progressive Retinal Atrophy crd4 / cord1-PRA, cord1-PRA (gene RPGRIP1)<br>ᴥ Factor VII Deficiency, FVII (gene F7)<br>ᴥ Degenerative Myelopathy, DM (gene SOD1)<br>ᴥ Hyperuricosuria, HUU (gene SLC2A9)<br>
Pekingese;ᴥ Degenerative Myelopathy, DM (gene SOD1)<br>ᴥ Hyperuricosuria, HUU (gene SLC2A9)<br>
Phalène;ᴥ Neuroaxonal dystrophy, NAD (gene PLA2G6)<br>ᴥ Progressive Retinal Atrophy PAP1, PAP1-PRA (gene CNGB1)<br>ᴥ Degenerative Myelopathy, DM (gene SOD1)<br>ᴥ von Willebrand disease type I, vWD1 (gene VWF)<br>ᴥ Progressive Retinal Atrophy crd4 / cord1-PRA, cord1-PRA (gene RPGRIP1)<br>ᴥ Factor VII Deficiency, FVII (gene F7)<br>ᴥ Hyperuricosuria, HUU (gene SLC2A9)<br>
Pomeranian;ᴥ Degenerative Myelopathy, DM (gene SOD1)<br>ᴥ Progressive Retinal Atrophy prcd-PRA, prcd-PRA (gene PRCD)<br>ᴥ von Willebrand disease type I, vWD1 (gene VWF)<br>ᴥ Hyperuricosuria, HUU (gene SLC2A9)<br>
Pomsky;ᴥ Degenerative Myelopathy, DM (gene SOD1)<br>ᴥ Hyperuricosuria, HUU (gene SLC2A9)<br>ᴥ Progressive Retinal Atrophy prcd-PRA, prcd-PRA (gene PRCD)<br>ᴥ von Willebrand disease type I, vWD1 (gene VWF)<br>
Poodle, Miniature Poodle, Toy Poodle);ᴥ Degenerative Myelopathy, DM (gene SOD1)<br>ᴥ Hyperuricosuria, HUU (gene SLC2A9)<br>ᴥ Progressive Retinal Atrophy prcd-PRA, prcd-PRA (gene PRCD)<br>ᴥ Neonatal encephalopathy with seizures, NEWS (gene ATF2)<br>ᴥ Progressive Retinal Atrophy rcd4-PRA, rcd4-PRA (gene C2orf71)<br>ᴥ von Willebrand disease type I, vWD1 (gene VWF)<br>
Poodle, Standard Poodle);ᴥ Neonatal encephalopathy with seizures, NEWS (gene ATF2)<br>ᴥ Degenerative Myelopathy, DM (gene SOD1)<br>ᴥ Progressive Retinal Atrophy prcd-PRA, prcd-PRA (gene PRCD)<br>ᴥ Progressive Retinal Atrophy rcd4-PRA, rcd4-PRA (gene C2orf71)<br>ᴥ Hyperuricosuria, HUU (gene SLC2A9)<br>ᴥ von Willebrand disease type I, vWD1 (gene VWF)<br>
Portuguese Water Dog;ᴥ Progressive Retinal Atrophy prcd-PRA, prcd-PRA (gene PRCD)<br>ᴥ Degenerative Myelopathy, DM (gene SOD1)<br>ᴥ Hyperuricosuria, HUU (gene SLC2A9)<br>
Pug;ᴥ Necrotizing meningoencephalitis, NME / PDE, variant DQB1*01501)<br> ᴥ Degenerative Myelopathy, DM (gene SOD1)<br>ᴥ von Willebrand disease type I, vWD1 (gene VWF)<br>ᴥ Primary Lens Luxation, PLL (gene ADAMTS17)<br>ᴥ Pyruvate kinase deficiency, PK-P (gene PKLR)<br>ᴥ Hyperuricosuria, HUU (gene SLC2A9)<br>
Puli;ᴥ Progressive Retinal Atrophy prcd-PRA, prcd-PRA (gene PRCD)<br>ᴥ von Willebrand disease type I, vWD1 (gene VWF)<br>ᴥ Primary Lens Luxation, PLL (gene ADAMTS17)<br>ᴥ Degenerative Myelopathy, DM (gene SOD1)<br>ᴥ Hyperuricosuria, HUU (gene SLC2A9)<br>
Rat Terrier;ᴥ Primary Lens Luxation, PLL (gene ADAMTS17)<br>ᴥ Degenerative Myelopathy, DM (gene SOD1)<br>ᴥ Hyperuricosuria, HUU (gene SLC2A9)<br>ᴥ Progressive Retinal Atrophy prcd-PRA, prcd-PRA (gene PRCD)<br>
Rhodesian Ridgeback;ᴥ Juvenile Myoclonic Epilepsy, JME (gene DIRAS1)<br>ᴥ Degenerative Myelopathy, DM (gene SOD1)<br>ᴥ Exercise induced collapse, EIC (gene DNM1)<br>ᴥ Hyperuricosuria, HUU (gene SLC2A9)<br>
Rottweiler;ᴥ Juvenile laryngeal paralysis & polyneuropathy, JLPP (gene RAB3GAP1)<br>ᴥ Leukoencephalomyelopathy, LEMP (gene NAPEPLD)<br>ᴥ Degenerative Myelopathy, DM (gene SOD1)<br>ᴥ Hyperuricosuria, HUU (gene SLC2A9)<br>ᴥ von Willebrand disease type I, vWD1 (gene VWF)<br>
Russian Spaniel;ᴥ Degenerative Myelopathy, DM (gene SOD1)<br>ᴥ Hyperuricosuria, HUU (gene SLC2A9)<br>
Russkiy Toy;ᴥ Primary Lens Luxation, PLL (gene ADAMTS17)<br>ᴥ Degenerative Myelopathy, DM (gene SOD1)<br>ᴥ Hyperuricosuria, HUU (gene SLC2A9)<br>ᴥ Progressive Retinal Atrophy prcd-PRA, prcd-PRA (gene PRCD)<br>
Saluki;ᴥ Degenerative Myelopathy, DM (gene SOD1)<br>ᴥ Hyperuricosuria, HUU (gene SLC2A9)<br>
Samoyed;ᴥ Progressive Retinal Atrophy X-linked 1, PRA-XL1 (gene RPGR)<br>ᴥ X-Linked Hereditary Nephropathy/Nephritis, X-linked, HN (gene COL4A5)<br>ᴥ Degenerative Myelopathy, DM (gene SOD1)<br>ᴥ Hyperuricosuria, HUU (gene SLC2A9)<br>
Schipperke;ᴥ Mucopolysaccharidosis type IIIB, MPSIIIB (gene NAGLU)<br>ᴥ von Willebrand disease type I, vWD1 (gene VWF)<br>ᴥ Brachyury / bob-tail / stumpy tail, BRCH (gene TBXT)<br>ᴥ Degenerative Myelopathy, DM (gene SOD1)<br>ᴥ Hyperuricosuria, HUU (gene SLC2A9)<br>ᴥ Progressive Retinal Atrophy prcd-PRA, prcd-PRA (gene PRCD)<br>
Scottish Terrier;ᴥ Craniomandibular osteopathy, CMO (gene SLC37A2)<br>ᴥ von Willebrand disease type III, vWD3 (gene VWF)<br>ᴥ Degenerative Myelopathy, DM (gene SOD1)<br>ᴥ Hyperuricosuria, HUU (gene SLC2A9)<br>
Sealyham Terrier;ᴥ Primary Lens Luxation, PLL (gene ADAMTS17)<br>ᴥ Degenerative Myelopathy, DM (gene SOD1)<br>ᴥ Hyperuricosuria, HUU (gene SLC2A9)<br>
Shar Pei;ᴥ Familial Shar-Pei fever, SPAID (gene MTBP)<br>ᴥ Primary open angle glaucoma, POAG-SH (gene ADAMTS17)<br>ᴥ Degenerative Myelopathy, DM (gene SOD1)<br>ᴥ Hyperuricosuria, HUU (gene SLC2A9)<br>
Shetland Sheepdog;ᴥ Collie Eye Anomaly, CEA (gene NHEJ1)<br>ᴥ Bardet–Biedl syndrome 2, BBS2 (gene BBS2)<br>ᴥ Dermatomyositis, DMS (genes PAN2, MAP3K7CL, DLA-DRB1)<br>ᴥ Multidrug resistance 1, MDR1 (gene ABCB1)<br>ᴥ Degenerative Myelopathy, DM (gene SOD1)<br>ᴥ Hyperuricosuria, HUU (gene SLC2A9)<br>
Shiba Inu;ᴥ GM1 Gangliosidosis, GM1-S (gene GLB1)<br>ᴥ GM2 Gangliosidosis, GM2-S (gene HEXB)<br>ᴥ Degenerative Myelopathy, DM (gene SOD1)<br>ᴥ Hyperuricosuria, HUU (gene SLC2A9)<br>
Shih Tzu;ᴥ Degenerative Myelopathy, DM (gene SOD1)<br>ᴥ screw tail, screw (gene DVL2)<br>ᴥ Prekallikrein Deficiency, KLK (gene KLKB1)<br>ᴥ Hyperuricosuria, HUU (gene SLC2A9)<br>
Shikoku;ᴥ Degenerative Myelopathy, DM (gene SOD1)<br>ᴥ Hyperuricosuria, HUU (gene SLC2A9)<br>
Siberian Husky;ᴥ Progressive Retinal Atrophy X-linked 1, PRA-XL1 (gene RPGR)<br>ᴥ Degenerative Myelopathy, DM (gene SOD1)<br>ᴥ Hyperuricosuria, HUU (gene SLC2A9)<br>
Smooth Fox Terrier;ᴥ Primary Lens Luxation, PLL (gene ADAMTS17)<br>ᴥ Spinocerebellar Ataxia with Myokymia and/or Seizures, SCA-J (gene KCNJ10)<br>ᴥ Degenerative Myelopathy, DM (gene SOD1)<br>ᴥ Hyperuricosuria, HUU (gene SLC2A9)<br>
Soft-coated Wheaten Terrier;ᴥ Degenerative Myelopathy, DM (gene SOD1)<br>ᴥ Paroxysmal Dyskinesia, PxD (gene PIGN)<br>ᴥ Hyperuricosuria, HUU (gene SLC2A9)<br>
South Russian Shepherd;ᴥ Degenerative Myelopathy, DM (gene SOD1)<br>ᴥ Hyperuricosuria, HUU (gene SLC2A9)<br>
Spanish Water Dog;ᴥ Hyperuricosuria, HUU (gene SLC2A9)<br>ᴥ Progressive Retinal Atrophy prcd-PRA, prcd-PRA (gene PRCD)<br>ᴥ Brachyury / bob-tail / stumpy tail, BRCH (gene TBXT)<br>ᴥ Degenerative Myelopathy, DM (gene SOD1)<br>
St. Bernard;ᴥ Degenerative Myelopathy, DM (gene SOD1)<br>ᴥ Hyperuricosuria, HUU (gene SLC2A9)<br>
Staffordshire Bull Terrier;ᴥ L-2-hydroxyglutaricacidemia, HGA-S (gene L2HGDH)<br>ᴥ Hereditary Cataract, HSF4r (gene HSF4)<br>ᴥ screw tail, screw (gene DVL2)<br>ᴥ Degenerative Myelopathy, DM (gene SOD1)<br>ᴥ Hyperuricosuria, HUU (gene SLC2A9)<br>
Standard Schnauzer;ᴥ Degenerative Myelopathy, DM (gene SOD1)<br>ᴥ Hyperuricosuria, HUU (gene SLC2A9)<br>
Sussex Spaniel;ᴥ Dwarfism / Skeletal Dysplasia 2, SD2 (gene COL11A2)<br>ᴥ Pyruvate dehydrogenase deficiency, PDP1 (gene PDP1)<br>ᴥ Degenerative Myelopathy, DM (gene SOD1)<br>ᴥ Hyperuricosuria, HUU (gene SLC2A9)<br>
Tervuren, Belgian Shepherd);ᴥ Hyperuricosuria, HUU (gene SLC2A9)<br>ᴥ Degenerative Myelopathy, DM (gene SOD1)<br>
Thai Ridgeback;ᴥ Degenerative Myelopathy, DM (gene SOD1)<br>ᴥ Hyperuricosuria, HUU (gene SLC2A9)<br>
Tibetan spaniel;ᴥ Degenerative Myelopathy, DM (gene SOD1)<br>ᴥ Hyperuricosuria, HUU (gene SLC2A9)<br>
Tibetan Terrier;ᴥ Primary Lens Luxation, PLL (gene ADAMTS17)<br>ᴥ Degenerative Myelopathy, DM (gene SOD1)<br>ᴥ Progressive Retinal Atrophy rcd4-PRA, rcd4-PRA (gene C2orf71)<br>ᴥ Hyperuricosuria, HUU (gene SLC2A9)<br>ᴥ Progressive Retinal Atrophy prcd-PRA, prcd-PRA (gene PRCD)<br>
Toy Fox Terrier;ᴥ Primary Lens Luxation, PLL (gene ADAMTS17)<br>ᴥ Spinocerebellar Ataxia with Myokymia and/or Seizures, SCA-J (gene KCNJ10)<br>ᴥ Degenerative Myelopathy, DM (gene SOD1)<br>ᴥ Hyperuricosuria, HUU (gene SLC2A9)<br>
Vizsla, short-haired);ᴥ Exercise induced collapse, EIC (gene DNM1)<br>ᴥ Degenerative Myelopathy, DM (gene SOD1)<br>ᴥ Hyperuricosuria, HUU (gene SLC2A9)<br>ᴥ Progressive Retinal Atrophy prcd-PRA, prcd-PRA (gene PRCD)<br>
Weimaraner;ᴥ Hyperuricosuria, HUU (gene SLC2A9)<br>ᴥ Degenerative Myelopathy, DM (gene SOD1)<br>
Welsh Corgi Cardigan;ᴥ Severe combined immunodeficiency disease, X-linked, XSCID (gene IL2RG)<br>ᴥ Degenerative Myelopathy, DM (gene SOD1)<br>ᴥ Hyperuricosuria, HUU (gene SLC2A9)<br>ᴥ von Willebrand disease type I, vWD1 (gene VWF)<br>
Welsh Corgi Pembroke;ᴥ Degenerative Myelopathy Risk Modifier, DMRM (gene SP110)<br>ᴥ Exercise induced collapse, EIC (gene DNM1)<br>ᴥ Degenerative Myelopathy, DM (gene SOD1)<br>ᴥ von Willebrand disease type I, vWD1 (gene VWF)<br>ᴥ Brachyury / bob-tail / stumpy tail, BRCH (gene TBXT)<br>ᴥ Severe combined immunodeficiency disease, X-linked, XSCID (gene IL2RG)<br>ᴥ Hyperuricosuria, HUU (gene SLC2A9)<br>
West Highland White Terrier;ᴥ Craniomandibular osteopathy, CMO (gene SLC37A2)<br>ᴥ Degenerative Myelopathy, DM (gene SOD1)<br>ᴥ Hyperuricosuria, HUU (gene SLC2A9)<br>ᴥ von Willebrand disease type I, vWD1 (gene VWF)<br>
West Siberian Laika;ᴥ Degenerative Myelopathy, DM (gene SOD1)<br>ᴥ Hyperuricosuria, HUU (gene SLC2A9)<br>
Whippet;ᴥ Multidrug resistance 1, MDR1 (gene ABCB1)<br>ᴥ Collie Eye Anomaly, CEA (gene NHEJ1)<br>ᴥ Factor VII Deficiency, FVII (gene F7)<br>ᴥ Glycogen storage disease VII / Phosphofructokinase Deficiency, PFKD (gene PFKM)<br>ᴥ Myostatin Mutation, bully (gene MSTN)<br>ᴥ Degenerative Myelopathy, DM (gene SOD1)<br>ᴥ Hyperuricosuria, HUU (gene SLC2A9)<br>
White Swiss Shepherd Dog;ᴥ Multidrug resistance 1, MDR1 (gene ABCB1)<br>ᴥ Degenerative Myelopathy, DM (gene SOD1)<br>ᴥ Hyperuricosuria, HUU (gene SLC2A9)<br>
Wire Fox Terrier;ᴥ Van den Ende-Gupta syndrome, VDEGS (gene SCARF2)<br>ᴥ Primary Lens Luxation, PLL (gene ADAMTS17)<br>ᴥ Degenerative Myelopathy, DM (gene SOD1)<br>ᴥ Hyperuricosuria, HUU (gene SLC2A9)<br>
Wolfdog;ᴥ Degenerative Myelopathy, DM (gene SOD1)<br>ᴥ Hyperuricosuria, HUU (gene SLC2A9)<br>
Xoloitzcuintle;ᴥ Progressive Retinal Atrophy prcd-PRA, prcd-PRA (gene PRCD)<br>ᴥ Degenerative Myelopathy, DM (gene SOD1)<br>ᴥ Hyperuricosuria, HUU (gene SLC2A9)<br>
Yakutian Laika;ᴥ Progressive Retinal Atrophy X-linked 1, PRA-XL1 (gene RPGR)<br>ᴥ Degenerative Myelopathy, DM (gene SOD1)<br>ᴥ Hyperuricosuria, HUU (gene SLC2A9)<br>
Yorkshire Terrier;ᴥ Primary Lens Luxation, PLL (gene ADAMTS17)<br>ᴥ Degenerative Myelopathy, DM (gene SOD1)<br>ᴥ Hyperuricosuria, HUU (gene SLC2A9)<br>ᴥ Progressive Retinal Atrophy prcd-PRA, prcd-PRA (gene PRCD)<br>
