NIEUW! Vanaf 1 januari 2025
Wilt u meer weten over de genetische eigenschappen van uw hond? Voor alle hondenrassen en kruisingen bieden wij nu een uitgebreid pakket aan met meer dan 300 genetische varianten. LABOGenetics XXL Dog geeft u informatie over genetische ziektes en risicofactoren, vachtkleuren en vachteigenschappen.
De test is interessant voor zowel hondenfokkers, eigenaren en dierenartsen.
- Voor fokkers: Neem weloverwogen fokbeslissingen, verbeter de genetische gezondheid van uw ras en zorg ervoor dat er gezondere pups geboren worden.
- Voor eigenaren: Krijg inzicht in de genetica van uw hond en leer over mogelijke genetische gezondheidsrisico’s.
- Voor dierenartsen: Verbeter uw diagnose en behandelopties door waardevolle genetische informatie te gebruiken om de beste zorg voor uw patiënten te bepalen.
- Voor rasverenigingen: Bied uw clubleden geavanceerde genetische tests en steun verantwoorde fokpraktijken.
Vanwege het grote aantal testen, is voor de LABOGenetics XXL Dog EDTA-bloed het voorkeursmateriaal. In bloed zit tot 100x meer DNA-materiaal dan op swabs. Alternatief kan een speciale swab worden gebruikt. Bij correcte afname van deze swab kunnen we ook hier voldoende DNA uit isoleren. Deze swab kunt u HIER bestellen. Gewone swabs kunnen we helaas niet gebruiken.
In zeldzame gevallen staat er bij één of enkele test(en) ‘Not evaluable’ als resultaat. Dit betekent dat de hoeveelheid of kwaliteit van het DNA onvoldoende was voor een betrouwbaar resultaat voor deze test. Met de Next Generation Sequencing (NGS) techniek – welke gebruikt wordt voor LABOGenetics XXL Dog – is het helaas niet mogelijk om individuele testen opnieuw kosteloos uit te laten voeren. Ontbrekende testen kunnen eventueel wel tegen een gereduceerde prijs worden hertest. Neem in deze gevallen contact met ons op voor de details.
Welke testen zijn inclusief in het LABOGenetics XXL Dog pakket?
| Testnaam | Afkorting | Gen | Testnummer |
|---|---|---|---|
| Achromatopsia (day blindness) - ACHM (Duitse Herder) | ACHM | CNGA3 | 8166 |
| Achromatopsia (day blindness) - ACHM (Labrador) | ACHM | CNGA3 | 8166 |
| Obesity | ADI | POMC | 8602 |
| Afibrinogenemia | FGA | 8737 | |
| Acatalasemia (Beagle) | CAT | 8552 | |
| Acral mutilation syndrome - AMS | AMS | GDNF | 8038 |
| Acute respiratory distress syndrome - ARDS | ARDS | ANLN | 8595 |
| Alaskan Husky encephalopathy - AHE | AHE | SLC19A3 | 8313 |
| Alaskan Malamute polyneuropathy - AMPN | AMPN | NDRG1 | 8479 |
| Alexander disease | AxD | GFAP | 8601 |
| Amelogenesis imperfecta - AI/FEH (Akita) | AI/FEH | ACP4 | 8303 |
| Amelogenesis imperfecta - AI/FEH (Parson Russell Terrier) | AI/FEH | ENAM | 8303 |
| Amelogenesis imperfecta - AI/FEH (Italiaanse Windhond) | AI/FEH | ENAM | 8303 |
| Amelogenesis imperfecta - AI/FEH (Samoyed) | AI/FEH | SLC24A4 | 8303 |
| Anhidrotic ectodermal dysplasia (Duitse Herder) | EDA | ||
| Ataxia, spinocerebellar (Belgische/Mechelse Herder) | SLC12A6 | ||
| B-locus (rare variants) - be (Lancashire Heeler) | TYRP1 | 8639 | |
| B-locus (rare variants) - bh (Husky) | TYRP1 | 8639 | |
| B-locus (rare variants) - b4 (Australian Shepherd, Miniature American Shepherd) | TYRP1 | 8639 | |
| B-locus - bc | TYRP1 | 8023 | |
| B-locus - bd | TYRP1 | 8023 | |
| B-locus - bs | TYRP1 | 8023 | |
| Progressive retinal atrophy (BBS4-PRA) | BBS4-PRA | BBS4 | 8207 |
| Brachyuria – stumpy tail | TBXT | 8219 | |
| Bunny Hopping Syndrome | BHS1 | EFNB3 | 8878 |
| C-locus (albino) (Bullmastif) | SLC45A2 | 8613 | |
| C-locus (albino) - caL | SLC45A2 | 8644 | |
| C-locus (albino) - OCAs | OCA2 | 8644 | |
| C3-deficiency | C3 | C3 | 8184 |
| Canine multi-focal retinopathy - CMR1 | CMR1 | BEST1 | 8330 |
| Canine multi-focal retinopathy - CMR2 | CMR2 | BEST1 | 8330 |
| Canine multi-focal retinopathy - CMR3 | CMR3 | BEST1 | 8330 |
| Canine multiple system degeneration - CMSD (Chinese Crested) | CMSD | SERAC1 | 8575 |
| Canine multiple system degeneration - CMSD (Kerry Blue Terrier) | CMSD | SERAC1 | 8575 |
| Cardiomyopathy with juvenile mortality | CJM | YARS2 | 8543 |
| Centronuclear myopathy (Duitse Jachtterrier) | CNM | ACADVL | 8073 |
| Centronuclear myopathy (Duitse Dog) | CNM | BIN1 | 8073 |
| Cerebellar ataxia (Belgische Herder) | CA | RALGAPA1 | 8860 |
| Cerebellar ataxia (Pyrenese Berghond) | CA | SACS | 8860 |
| Cerebellar degeneration and myositis complex - CDMC (Nova Scotia Duck Tolling Retriever) | CDMC | SLC25A12 | 8788 |
| Cerebellar hypoplasia - CH | CH | RELN | 8868 |
| Cerebral dysfunktion - CDFS | CDFS | SLC6A3 | 8314 |
| Charcot-Marie-Tooth Neuropathy (CMT) | CMT | SBF2 | 8538 |
| Chondrodysplasia and -dystrophy (IVDD risk) CDDY | CDDY | FGF4 retrogene CFA18 (CDDY) | 8294 |
| Chondrodysplasia and -dystrophy (IVDD risk) CDPA | CDPA | FGF4 (CDPA) | 8294 |
| Chondrodysplasia (dwarfism) (Noorse Elandhond) | ITGA10 | 8316 | |
| Canine leukocyte adhesion deficiency - CLAD (Ierse Setter) | CLAD | ITGB2 | 8012 |
| Progressive retinal atrophy (CNGA1-PRA) | CNGA1-PRA | CNGA1 | 8375 |
| Coat colour, albinism, oculocutaneous type IV (Dobermann Pinscher) | SLC45A2 | ||
| Coat, double vs single, associated snp 1 | LOC106557950 | 8523 | |
| Coat, double vs single, associated snp 2 | LOC106557950 | 8523 | |
| Cocoa (dark brown, dark chocolate) | HPS3 | 8526 | |
| Collie eye anomaly CEA (Partnerlab) | CEA | NHEJ1 | 8304 |
| Cone Degeneration (Duitse Staande Hond) | CD | CNGB3 | 8780 |
| Progressive retinal atrophy (crd3-PRA) Cone-rod dystrophy 9 (Glen of Imaal Terrier) | crd3-PRA | ADAM18 | 8691 |
| Congenital hypothyroidism with goiter (Franse Bulldog) | CHG | TPO | 8434 |
| Congenital hypothyroidism with goiter (Tenterfield Terrier) | CHG | TPO | 8434 |
| Congenital hypothyroidism with goiter (Toy Fox Rat Terrier) | CHG | TPO | 8434 |
| Congenital myasthenic syndrome - CMS (Gammel dansk hønsehund) | CMS | CHAT | 8206 |
| Congenital myasthenic syndrome - CMS (Golden Retriever) | CMS | LOC608697 | 8206 |
| Congenital myasthenic syndrome - CMS (Labrador) | CMS | LOC608697 | 8206 |
| Congenital myasthenic syndrome - CMS (Jack Russel Terrier) | CMS | CHRNE | 8206 |
| Craniomandibular osteopathy | CMO | SLC37A2 | 8348 |
| Curly (curled hair) | KRT71 | 8196 | |
| Cystinuria (Australian Cattle Dog) | SLC3A1 | 8013 | |
| Cystinuria (Bulldog Mastiff) | SLC3A1 | 8013 | |
| Cystinuria (Labrador) | SLC3A1 | 8013 | |
| Cystinuria (Newfoundland) | SLC3A1 | 8013 | |
| Cystinuria (Miniature Pinscher) | SLC7A9 | 8013 | |
| Degenerative myelopathy (exon 2) | DM exon 2 | SOD1 | 8158 |
| Degenerative myelopathy risk modifier SP110 | SP110 | 8939 | |
| Dental-skeletal-retinal anomaly - DSRA | DSRA | MIA3 | 8698 |
| Dermatosparaxis Ehlers-Danlos syndrome (dEDS) (Catahoula Leopard Dog) | dEDS | ADAMTS2 | |
| Dermatosparaxis Ehlers-Danlos syndrome (dEDS) (Dobermann Pinscher) | dEDS | ADAMTS2 | |
| Digital hyperkeratosis (Bordeaux Dog) | DH/HFH | KRT16 | 8472 |
| Digital hyperkeratosis (Ierse Terrier, Kromfohrländer) | DH/HFH | FAM83G | 8472 |
| Dilated cardiomyopathy - DCM1 (Doberman) | DCM1 | PKD4 | 8872 |
| Dilated cardiomyopathy - DCM2 (Doberman) | DCM2 | TTN | 8872 |
| Dilated cardiomyopathy - DCM3 (Doberman) | DCM3 | LOC102156622 (DCM3) | 8872 |
| Dilated cardiomyopathy - DCM4 (Doberman) | DCM4 | 8872 | |
| Dilated cardiomyopathy (Manchester Terrier) | DCM | ABCC9 | 8764 |
| Dilated cardiomyopathy (Nova Scotia Duck Tolling Retriever) | DCM | LMNA | 8764 |
| Dilated cardiomyopathy (Welsh Springer Spaniel) | DCM | PLN | 8764 |
| Dilated cardiomyopathy (Schnauzer) | DCM | RBM20 | 8363 |
| D-locus d1 (dilution) | MLPH | 8136 | |
| D-locus (rare variants) d2 and d3 | MLPH | 8636 | |
| Disproportionate dwarfism (Dogo Argentino) | PCYT1A | 8753 | |
| Disproportionate dwarfism (Magyar Vizsla) | PRKG2 | 8753 | |
| Dwarfism, growth-hormone deficiency (Chihuahua) | GH1 | ||
| Dyserythropoietic anemia and myopathy - DAMS | DAMS | EHBP1L1 | 8805 |
| Dystrophic epidermolysis bullosa - DEB | DEB | COL7A1 | 8643 |
| E-locus e3 (Alaskan Husky, Siberian Husky) | MC1R | ||
| E-locus e1 (abrikoos, creme, lemon, rood, geel) | MC1R | 8018 | |
| E-locus (special colours) - eg | MC1R | 8682 | |
| E-locus (special colours) - eh | MC1R | 8682 | |
| EM-locus (melanistic mask) | MC1R | 8146 | |
| Inflammatory pulmonary disease - IPD | IPD | AKNA | 8373 |
| Inflammatory myopathy - IM | IM | SLC25A12 | 8612 |
| Epidermolysis bullosa, dystrophic (Golden Retriever) | COL7A1 | ||
| Epidermolytic hyperkeratosis | EHK | KRT10 | 8311 |
| Episodic falling | EF | BCAN | 8202 |
| Hereditary deafness (Beauceron) | EOAD | CDH23 | 8269 |
| Hereditary deafness 1 (Doberman) | DINGS1 | PTPRQ | 8875 |
| Hereditary deafness (Rhodesian Ridgeback) | EOAD | EPS8L2 | 8269 |
| Hereditary deafness (Rottweiler) | EOAD | LOXHD1 | 8269 |
| Hereditary deafness 2 Doberman | DINGS2 | MYO7A | 8875 |
| Exercise induced collapse | EIC | DNM1 | 8152 |
| Exfoliative cutaneous lupus erythematosus | ECLE | UNC93B1 | 8688 |
| Faktor VII deficiency | F7 | F7 | 8151 |
| Familial nephropathy (English Cocker Spaniel) (Partnerlab) | FN | COL4A4 | 8131 |
| Familial nephropathy (Samoyed) | FN | COL4A5 | 8192 |
| Familial nephropathy (English Springer Spaniel) | FN | COL4A4 | 8192 |
| Familial thyroid follicular cell carcinoma | FTFC1 | TPO | 8871 |
| Familial thyroid follicular cell carcinoma | FTFC2 | TPO | 8871 |
| Fanconi syndrome | FAN1 | 8272 | |
| Color dilution and neurological defects | MYO5A | 8758 | |
| Finnish Hound ataxia | FHA | SEL1L | 8467 |
| Furnishing (wire hair) | RSPO2 | 8195 | |
| Gallbladder mucoceles | ABCB4 | 8323 | |
| Glanzmann Thrombastenia | GT | ITGA2B | 8077 |
| Osteogenesis imperfecta (brittle bone disease) (Dachshund) | SERPINH1 | 8215 | |
| Osteogenesis imperfecta (brittle bone disease) (Beagle) | COL1A2 | 8215 | |
| Osteogenesis imperfecta (brittle bone disease) (Golden Retriever) | COL1A1 | 8215 | |
| Glaucoma and goniodysgenesis | GG | OLFML3 | 8635 |
| Limb-Girdle Muscular Dystrophy | SGCA | 8863 | |
| Globoid cell leukodystrophy – Krabbe disease | GALC | 8007 | |
| Glycogen storage disease type IIIa | GSDIIIa | AGL | 8156 |
| Glycogen storage disease type II (Pompe disease) | GSDII | GAA | 8513 |
| Glycogen storage disease type Ia | GSDIa | G6PC | 8322 |
| GM1-Gangliosidosis (Husky) | GM1 | GLB1 | 8066 |
| GM1-Gangliosidosis (Portuguese Waterdog) | GM1 | GLB1 | 8066 |
| GM1-Gangliosidosis (Shiba Inu) | GM1 | GLB1 | 8066 |
| GM2-Gangliosidosis (Japanse Spaniel) | GM2 | HEXA | 8208 |
| GM2-Gangliosidosis (Poedel) | GM2 | HEXB | 8208 |
| GM2-Gangliosidosis (Shiba Inu) | GM2 | HEXB | 8208 |
| Progressive retinal atrophy (GR-PRA2) (Golden Retriever) | GR-PRA2 | TTC8 | 8520 |
| H-locus (harlequin) | PSMB7 | 8254 | |
| Coat length I (long or short hair) | HL1 | FGF5 | 8124 |
| Coat length II (long or short hair) | HL2 | FGF5 | 8397 |
| Coat length II (long or short hair) | HL3 | FGF5 | 8397 |
| Coat length II (long or short hair) | HL4 | FGF5 | 8397 |
| Coat length II (long or short hair) | HL5 | FGF5 | 8397 |
| Hairlessness (Scottish Deerhound) | SGK3 | 8599 | |
| Haemophilia A (factor VIII deficiency) (Old English Sheepdog) | F8 | 8689 | |
| Haemophilia A (factor VIII deficiency) (Boxer) | F8 | 8689 | |
| Haemophilia A (factor VIII deficiency) (Duitse Herder) | F8 | 8689 | |
| Haemophilia B (factor IX deficiency) (Hovawart) | F9 | 8221 | |
| Haemophilia B (factor IX deficiency) (Lhasa Apso) | F9 | 8221 | |
| Haemophilia B (factor IX deficiency) (Rhodesian Ridgeback) | F9 | 8221 | |
| Haemorrhagic diathesis (Scott syndrome) | ANO6 | 8319 | |
| Haemophilia A (factor VIII deficiency) (Labrador) | F8 | 8689 | |
| Haemophilia B (factor IX deficiency) (American Akita) | F9 | 8221 | |
| Hereditary ataxia (Gordon Setter) | RAB24 | 8449 | |
| Hereditary nasal parakeratosis (Greyhound) | HNPK | SUV39H2 | 8672 |
| Hereditary nasal parakeratosis (Labrador) | HNPK | SUV39H2 | 8421 |
| Hereditary neuropathy (Greyhound) | GHN | NDRG1 | 8179 |
| Hereditary ataxia (Australian Shepherd) | HSF4 | PNPLA8 | 8449 |
| Hereditary ataxia (Norwegian Buhund) | KCNIP4 | 8449 | |
| Hereditary ataxia (Noorse Elandhond) | HACE1 | 8449 | |
| Hereditary cataract (Griffon Korthals) | HSF4 | FYCO1 | 8157 |
| Hyperurikosuria | SLC | SLC2A9 | 8154 |
| Hypomyelination (Shaking Puppy Syndrome) (English Springer Spaniel) | SPS | PLP1 | 8443 |
| Hypomyelination (Shaking Puppy Syndrome) (Weimaraner) | SPS | FNIP2 | 8443 |
| Hypophosphatasia | HPP | ALPL | 8389 |
| I-locus (pheomelanin intensity) | MFSD12 | 8366 | |
| Ichthyosis (American Bulldog) | NIPAL4 | 8555 | |
| Ichthyosis (Golden Retriever) | PNPLA1 | 8481 | |
| Ichthyosis type 2 (Golden Retriever) | ABHD5 | 8738 | |
| Ichthyosis (Duitse Herder) | ASPRV1 | ||
| Ichthyosis, non-epidermolytic (Chihuahua) | SDR9C7 | ||
| Imerslund-Gräsbeck syndrome (Beagle) | IGS | CUBN | 8475 |
| Imerslund-Gräsbeck syndrome (Border Collie) | IGS | CUBN | 8475 |
| Imerslund-Gräsbeck syndrome (Komondor) | IGS | CUBN | 8475 |
| Improper coat | IC | RSPO2 | 8405 |
| Junctional epidermolysis bullosa (Duitse Staande Hond) | JEB | LAMA3 | 8198 |
| Juvenile brain disease (Parson Russell Terrier) | JBD | PITRM1 | 8284 |
| Juvenile epilepsy (Lagotto Romagnolo) | JE | LGI2 | 8459 |
| Juvenile laryngeal paralysis & polyneuropathy | JLPP | RAB3GAP1 | 8271 |
| Juvenile myoclonic epilepsy (Rhodesian Ridgeback) | JME | DIRAS1 | 8557 |
| K-locus (alleles KB and ky) | CBD103 | 8145 | |
| Copper storage disease – Copper toxicosis 1 (Doberman, Labrador) (partnerlab) | CT | ATP7B | 8388 |
| Copper storage disease – Copper toxicosis 2 (Doberman, Labrador) (partnerlab) | CT | ATP7A | 8388 |
| L-2-hydroxyglutaric aciduria (Yorkshire Terrier) | L-2-HGA | L2HGDH | 8125 |
| L-2-hydroxyglutaric aciduria (Staffordshire Bull Terrier) | L-2-HGA | L2HGDH | 8125 |
| Lagotto storage disease | LSD | ATG4D | 8270 |
| Laryngeal paralysis with polyneuropathy type 3 | LPPN3 | CNTNAP1 | 8685 |
| Late onset ataxia | LOA | CAPN1 | 8493 |
| Leonberger polyneuropathy | LPN2 | GJA9 | 8494 |
| Leonberger polyneuropathy | LPN1 | ARHGEF10 | 8487 |
| Lethal acrodermatitis (Bullterrier) | LAD | MKLN1 | 8273 |
| Lethal lung disease | LAMP3 | LAMP3 | 8598 |
| Leukoencephalomyelopathy (Leonberger) | LEMP | NAPEPLD | 8283 |
| Leukoencephalopathy (Schnauzer) | LEP | TSEN54 | 8364 |
| Leukocyte adhesion deficiency type III (Duitse Herder) | LAD3 | FERMT3 | 8327 |
| Lundehund syndrome | LHS | P3H2 | 8579 |
| Lysosomal storage disease (Doberman) | LSD | MAN2B1 | 8932 |
| Macrothrombocytopenia (Cavalier King Charles Spaniel) | MTC | TUBB1 | 8217 |
| Macrothrombocytopenia (Norfolk Terrier, Cairn Terrier) | MTC | TUBB1 | 8217 |
| Macular corneal dystrophy (Labrador) | MCD | LOC489707 | 8736 |
| Malignant hyperthermia | MH | RYR1 | 8062 |
| Maxillary canine tooth mesioversion | MCM | FTSJ3 | 8819 |
| May-Hegglin anomaly | MHA | MYH9 | 8312 |
| MCAD deficiency | ACADM | 8288 | |
| MDR1 gene variant – Ivermectin hypersensitivity | ABCB1 | 8032 | |
| Methaemoglobinaemia | MetHg | CYB5R3 | 8870 |
| Microphthalmia RBP4 (Irish Soft Coated Wheaten Terrier) | RBP4 | RBP4 | 8508 |
| Mitochondrial fission encephalopathy | MFE | MFF | 8521 |
| Myxomatous mitral valve disease | MMVD | NEBL | 8831 |
| Mucopolysaccharidosis type IIIa (Dachshund) | MPS3a | SGSH | 8306 |
| Mucopolysaccharidosis type IIIa (New Zealand Huntaway Dog) | MPS3a | SGSH | 8306 |
| Mucopolysaccharidosis type VII (Brazilian Terrier) | MPS7 | GUSB | 8069 |
| Mucopolysaccharidosis type VI (Duitse Dog) | ARSB | ||
| Mucopolysaccharidosis type VII (Duitse Herder) | MPS7 | GUSB | 8069 |
| Persistent Müllerian duct syndrome | PMDS | AMHR2 | 8462 |
| Mucopolysaccharidosis type VI (Miniature Pinscher) | MPS6 | ARSB | 8693 |
| Muscular dystrophy, Duchenne type (Cavalier King Charles Spaniel) | MD | DMD | |
| Muscular dystrophy (American Staffordshire Terrier) | MD | DMD | 8068 |
| Muscular dystrophy (Cavalier King Charles Spaniel) | MD | DMD | 8068 |
| Muscular dystrophy (Norfolk Terrier) | MD | COL6A3 | 8068 |
| Muscular dystrophy (Golden Retriever) | MD | DMD | 8068 |
| Muscular dystrophy (Landseer) | MD | COL6A1 | 8068 |
| Musladin-Lueke syndrome (Beagle) | MLS | ADAMTSL2 | 8411 |
| Mycobacterium avium complex sensitivity | MAC | CARD9 | 8360 |
| Myostatin mutation – bully gene | MSTN | 8220 | |
| Myotonia congenita (Labrador) | CLCN1 | 8022 | |
| Myotonia congenita (Dwergschnauzer) | CLCN1 | 8022 | |
| Congenital stationary night blindness | CSNB | RPE65 | 8011 |
| Narcolepsy (Labrador Retriever) | HCRTR2 | 8067 | |
| Narcolepsy (Dachshund) | HCRTR2 | 8067 | |
| Necrotizing meningoencephalitis | NME/PDE | DLA-DPB1 | 8429 |
| necrotizing myelopathy (Kooikerhondje) | ENM | IBA57 | 8869 |
| Nemalin myopathy (American Bulldog) | NM | NEB | 8172 |
| Neonatal cortical cerebellar abiotrophy (Beagle) | NCCD | SPTBN2 | 8457 |
| Neonatal cortical cerebellar abiotrophy (Magyar Viszla) | NCCD | SNX14 | 8457 |
| Neonatal encephalopathy with seizures | NEWS | ATF2 | 8155 |
| Spinal dysraphism | NTD | NKX2-8 | 8605 |
| Neuroaxonal dystophy (Lagotto Romagnolo) | NAD | TECPR2 | 8308 |
| Neuroaxonal dystrophy (Miniature Australian Shepherd) | NAD | RNF170 | 8308 |
| Neuroaxonal dystrophy (Papillon) | NAD | PLA2G6 | 8308 |
| Neuroaxonal dystrophy (Rottweiler) | NAD | VPS11 | 8308 |
| Neuroaxonal dystrophy (Spaanse Waterhond) | NAD | TECPR2 | 8308 |
| Neuronal ceroid lipofuscinosis (American Bulldog) | NCL | CLN10(CTSD) | 8075 |
| Neuronal ceroid lipofuscinosis (Border Collie) | NCL | CLN5 | 8075 |
| Neuronal ceroid lipofuscinosis (Tibetaanse Terrier) | NCL | CLN12 (ATP13A2) | 8075 |
| Neuronal ceroid lipofuscinosis (Australian Shepherd) | NCL | CLN8 | 8133 |
| Neuronal ceroid lipofuscinosis (Cane Corso) | NCL | CLN1 (PPT1) | 8075 |
| Neuronal ceroid lipofuscinosis (American Staffordshire Terrier) (Partnerlab) | NCL | NCL4A (ARSG) | 8396 |
| Neuronal ceroid lipofuscinosis (Australian Cattle Dog) | NCL | CLN12 (ATP13A2) | 8133 |
| Neuronal ceroid lipofuscinosis (Australian Shepherd 2) | NCL | CLN6 | 8133 |
| Neuronal ceroid lipofuscinosis (Chinese Crested) | NCL | CLN7 (MFSD8) | 8075 |
| Neuronal ceroid lipofuscinosis (Dachshund 1) | NCL | CLN1 (PPT1) | 8133 |
| Neuronal ceroid lipofuscinosis (Dachshund 2) | NCL | CLN2 (TPP1) | 8133 |
| Neuronal ceroid lipofuscinosis (English Setter) | NCL | CLN8 | 8075 |
| Neuronal ceroid lipofuscinosis (Golden Retriever) | NCL | CLN5 | 8075 |
| Renal dysplasia and hepatic fibrosis | RDHN | INPP5E | 8345 |
| Renal cystadenocarcinoma and nodular dermatofibrosis | RCND | FLCN | 8301 |
| Upper airway syndrome | UAS | ADAMTS3 | 8391 |
| Osteochondrodysplasia | OCD | SLC13A1 | 8877 |
| Panda white spotting | KIT | 8578 | |
| Paradoxical pseudomyotonia | PP | SLC7A10 | 8933 |
| Paroxysmal exercise-induced dyskinesia (Shetland Sheepdog) | PED | PCK2 | 8690 |
| Paroxysmal exercise-induced dyskinesia (Weimaraner) | PED | TNR | 8690 |
| Paroxysmal dyskinesia | PxD | PIGN | 8630 |
| Pyruvate dehydrogenase phosphatase 1 deficiency | PDP1 | PDP1 | 8104 |
| Phosphofructokinase deficiency (English Springer Spaniel) | PFKD | PFKM | 8017 |
| Phosphofructokinase deficiency (Duitse Spaniel) | PFKD | PFKM | 8017 |
| Pyruvate kinase deficiency (Basenji) | PK | PKLR | 8015 |
| Polydactyly | SHH | ||
| Polycystic kidney disease | PKD | PKD1 | 8476 |
| Postoperative haemorrhage (Grote Zwitserse sennenhond) | P2Y12 | P2RY12 | 8053 |
| Delayed postoperative haemorrhage (Deerhound) | DEPOH | SERPINF2 | 8862 |
| Progressive retinal atrophy (dominant Form) (English Mastiff) | RHO | 8355 | |
| Progressive retinal atrophy (Ierse Setter) | rcd1-PRA | PDE6B | 8042 |
| Progressive retinal atrophy (Sloughi) | rcd1a-PRA | PDE6B | 8353 |
| Progressive retinal atrophy (Welsh Corgi) | rcd3-PRA | PDE6A | 8354 |
| Prekallikrein deficiency | KLK | KLKB1 | 8141 |
| Progressive retinal atrophy (Prcd-PRA) (Partnerlab) | Prcd-PRA | PRCD | 8127 |
| Primary ciliary dyskinesia (Old English Sheepdog) | PCD | CCDC39 | 8483 |
| Primary ciliary dyskinesia (Alaskan Malamute) | PCD | NME5 | 8483 |
| Primary lens luxation | PLL | ADAMTS17 | 8226 |
| Primary open angle glaucoma (Beagle) | POAG | ADAMTS10 | 8452 |
| Primary open angle glaucoma and lens luxation (Shar Pei) | POAG/PLL | ADAMTS17 | 8641 |
| Primary open angle glaucoma (Noorse Elandhond) | POAG | ADAMTS10 | 8452 |
| Primary open angle glaucoma (Basset Fauve de Bretagne) | POAG | ADAMTS17 | 8452 |
| Primary open angle glaucoma (Basset Hound) | POAG | ADAMTS17 | 8452 |
| Progressive retinal atrophy (crd-PRA) | crd-PRA | NPHP4 | 8135 |
| Progressive retinal atrophy (Keeshond) | GUCY2D-PRA | GUCY2D | 8894 |
| Progressive retinal atrophy (Lapponian Herder) | ITF122-PRA | IFT122 | 8746 |
| Progressive retinal atrophy (Portugese Waterhond) | eo-PRA | CCDC66 | 8617 |
| Progressive retinal atrophy (Riesenschnauzer) | NECAP1-PRA | NECAP1 | 8374 |
| Progressive retinal atrophy (Swedish Vallhund (Västgötaspets)) | MERTK-PRA | MERTK | 8861 |
| Progressive retinal atrophy (Shetland Sheepdog) | BBS2-PRA | BBS2 | 8773 |
| Progressive retinal atrophy (Shih Tzu) | JHP2-PRA | JPH2 | 8752 |
| Progressive retinal atrophy (Spaanse Waterhond) | eo-PRA | PDE6B | 8617 |
| Progressive retinal atrophy (Dwergschnauzer) | type B1-PRA, HIVEP3 | HIVEP3 | 8546 |
| Progressive retinal atrophy (American Staffordshire Terrier) | crd1-PRA | PDE6B | 8332 |
| Progressive retinal atrophy (American Pitbull Terrier) | crd2-PRA | IQCB1 | 8333 |
| Progressive retinal atrophy (Golden Retriever) | GR-PRA1 | SLC4A3 | 8200 |
| Progressive retinal atrophy (Basenji) | Bas-PRA1 | SAG | 8574 |
| Progressive retinal atrophy (Papillon) | PAP-PRA | CNGB1 | 8573 |
| Progressive retinal atrophy (Shapendoes) | g-PRA | CCDC66 | 8451 |
| Protein losing nephropathy | PLN | KIRREL2, NPHS1 | 8492 |
| Pyruvate kinase deficiency (Beagle) | PK | PKLR | 8015 |
| Pyruvate kinase deficiency (Labrador) | PK | PKLR | 8015 |
| Pyruvate kinase deficiency (Mopshond) | PK | PKLR | 8015 |
| Raine syndrome | FAM20C | 8394 | |
| Retinal dysplasia (Northern Inuit, Tamaskan) | OSD | COL9A3 | 8677 |
| Robinow-like syndrome | DVL2 | DVL2 | 8747 |
| Saddle-tan | RALY | 8307 | |
| Spinocerebellar ataxia | SCA | KCNJ10 | 8537 |
| Severe combined immuno deficiency (Wetterhoun) | SCID | RAG1 | 8328 |
| Severe combined immuno deficiency (Jack Russell Terrier) | SCID | PRKDC | 8328 |
| Sensory neuropathy | SN | FAM134B | 8596 |
| Shar Pei autoinflammatory disease | SPAID | MTBP | 8642 |
| Spinocerebellar ataxia (Alpine Dachsbracke) | SCA | SCN8A | 8537 |
| Spondylocostal dysostosis (Comma defect) | HES7 | 8335 | |
| Spongy degeneration with cerebellar ataxia type 1 | SDCA1 | KCNJ10 | 8610 |
| Stargardt disease (retinal degeneration) | STGD | ABCA4 | 8387 |
| Startle disease (Galgo Espagnol) | SLC6A5 | 8191 | |
| Succinic semialdehyde dehydrogenase deficiency (Saluki) | SSADHD | ALDH5A1 | 8615 |
| Thrombopathia (Basset Hound) | RASGRP2 | 8486 | |
| Ticking (Roan, Mottle, Spotted) | USH2A | 8765 | |
| Trapped neutrophil syndrome | TNS | VPS13B | 8143 |
| van den Ende-Gupta syndrome | VDEGS | SCARF2 | 8393 |
| Ventricular Arrhythmia | IVA | MICOS13 | 8739 |
| Vitamin-D dependent rickets | VDR | VDR | 8302 |
| von-Willebrand disease type III (Kooiker) | vWD3 | VWF | 8233 |
| von-Willebrand disease type III (Schotse Terrier) | vWD3 | VWF | 8233 |
| von-Willebrand disease type III (Sheltie) | vWD3 | VWF | 8233 |
| von-Willebrand disease type I | vWD1 | VWF | 8119 |
| von-Willebrand disease type II | vWD2 | VWF | 8014 |
| X-chromosomal severe immuno deficiency (Basset Hound) | XSCID | IL2RG | 8063 |
| X-chromosomal severe immuno deficiency (Welsh Corgi) | XSCID | IL2RG | 8063 |
| X-linked myopathy (Labrador) | XL-MTM | MTM1 | 8305 |
| X-linked myopathy (Rottweiler) | XL-MTM | MTM1 | 8305 |
| Xanthinuria type II (Cavalier King Charles Spaniel) | MOCOS | 8779 | |
| Xanthinuria type II (Dachshund) | MOCOS | 8779 | |
| Xanthinuria type II (Manchester Terrier) | MOCOS | 8779 | |
| CNS atrophy with cerebellar ataxia | SELENOP | 8697 | |
| Pituitary dwarfism (Karelische Berenhond) | POU1F1 | 8142 | |
| Skeletal dysplasia 2 – dwarfism (Labrador) | SD2 | COL11A2 | 8456 |
| A-locus ASIP analysis AAA | AAA | ASIP | 8144 |
| A-locus ASIP analysis AAY | AAY | ASIP | 8144 |
| A-locus ASIP analysis AWF | AWF | ASIP | 8144 |
| A-locus ASIP analysis AHCP1 | AHCP1 | ASIP | 8144 |
| A-locus ASIP analysis AHCP4 | AHCP4 | ASIP | 8144 |
| A-locus ASIP analysis AVP2 | AVP2 | ASIP | 8144 |
| E-locus (special colours) eA | eA | MC1R | 8682 |
| S-locus (piebald, white spotting) | MITF | 8438 |
