LABOGenetics XXL – DOG

Комплексний генетичний скринінг для вашого собаки! Цього року доступний в LABOGEN.

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Хочете знати, який генетичний тип вашого собаки? Новий комплексний пакет LABOGenetics XXL Dog буде містити понад 300 генетичних варіантів. Ви отримаєте інформацію про спадкові захворювання, генетичні фактори ризику, окрасу та характеристики шерсті.

Цей новий пакет цікавий для всіх, хто тримає собак, займається їх розведенням або є ветеринаром.

  • Для розплідників: приймайте обґрунтовані рішення щодо розведення, покращуйте генетичне здоров’я вашої породи та отримуйте здорове потомство.

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Test (click for more detail) number gene
Acatalasemia 8552 CAT
Achromatopsia (day blindness) (ACHM) – German Shepherd 8166 CNGA3
Achromatopsia (day blindness) (ACHM) – Labrador Retriever 8166 CNGA3
Acral mutilation syndrome (AMS) 8038 GDNF
Acute respiratory distress syndrome (ARDS) 8595 ANLN
Adipositas 8602 POMC
Afibrinogenemia (AFG) 8737 FGA
Alaskan Husky enzephalopathy (AHE) 8313 SLC19A3
Alaskan Malamute polyneuropathy (AMPN) 8479 NDRG1
Alexander disease (AxD) 8601 GFAP
A-Locus (Agouti) ASIP Analysis 8144 ASIP
Amelogenesis imperfecta (AI)(Familial enamel hypoplasia) – Akita 8303 ACP4
Amelogenesis imperfecta (AI)(Familial enamel hypoplasia) – Italian Greyhound 8303 ENAM
Amelogenesis imperfecta (AI)(Familial enamel hypoplasia) – Parson Russell Terrier 8303 ENAM
Amelogenesis imperfecta (AI)(Familial enamel hypoplasia) – Samoyed 8303 SLC24A4
Anhidrotic ectodermal dysplasia – German Shepherd EDA
B-locus (rare variants) (b4) – Australian Shepherd, Miniature American Shepherd 8639 TYRP1
B-locus (rare variants) (be) – Lancashire Heeler 8639 TYRP1
B-locus (rare variants) (bh) – Husky 8639 TYRP1
B-locus bc 8023 TYRP1
B-locus bd 8023 TYRP1
B-locus bs 8023 TYRP1
Brachyuria (stumpy tail) 8219 TBXT
Bunny Hopping Syndrome (BHS1) 8878 EFNB3
C3 deficiency (C3) 8184 C3
Canine leucocyte adhesion deficiency (CLAD) 8012 ITGB2
Canine multi-focal retinopathy (CMR1) 8330 BEST1
Canine multi-focal retinopathy (CMR2) 8330 BEST1
Canine multi-focal retinopathy (CMR3) 8330 BEST1
Canine multiple system degeneration (CMSD) – Chinese Crested 8575 SERAC1
Canine multiple system degeneration (CMSD) – Kerry Blue Terrier 8575 SERAC1
Cardiomyopathy with juvenile mortality (CJM) 8543 YARS2
Cerebellar ataxia (CA1) – Belgian Shepherd Dog 8860 RALGAPA1
Cerebellar ataxia (CA1) – Pyrenean Mountain Dog 8860 SACS
Cerebellar degeneration and myositis complex (CDMC) 8788 SLC25A12
Cerebellar hypoplasia (CH) 8868 RELN
Cerebral dysfunction (CDFS) 8314 SLC6A3
Charcot-Marie-Tooth Neuropathy (CMT) 8538 SBF2
Chondrodysplasia (dwarfism) – Norwegian Elkhound 8316 ITGA10
Chondrodysplasia and -dystrophy (IVDD risk) CDDY 8294 FGF4/CFA12
Chondrodysplasia and -dystrophy (IVDD risk) CDPA 8294 FGF4/CFA18
C-locus (albino) caL 8644 SLC45A2
C-locus (albino) OCA2 8644 OCA2
C-Lokus (OCA4) – Bullmastif 8613 SLC45A2
CNS atrophy with cerebellar ataxia (CACA) 8697 SELENOP
Coat colour, albinism, oculocutaneous type IV – Dobermann Pinscher SLC45A2
Coat length I (long or short hair) HL1 8124 FGF5
Coat length II (long or short hair) HL2 8397 FGF5
Coat length II (long or short hair) HL3 8397 FGF5
Coat length II (long or short hair) HL4 8397 FGF5
Coat length II (long or short hair) HL5 8397 FGF5
Cocoa (brown, dark chocolate) 8526 HPS3
Collie eye anomaly (CEA) (Partnerlab) 8304 NHEJ1
Color dilution and neurological defects (CDN) 8758 MYO5A
Cone Degeneration (CD) 8780 CNGB3
Congenital Hypothyroidism with goiter (CHG) – Fox, Rat Terrier 8434 TPO
Congenital Hypothyroidism with goiter (CHG) – French Bulldog 8434 TPO
Congenital Hypothyroidism with goiter (CHG) – Tenterfield Terrier 8434 TPO
Congenital myasthenic syndrome (CMS) – Golden Retriever 8206 LOC608697
Congenital myasthenic syndrome (CMS) – Labrador Retriever 8206 LOC608697
Congenital myasthenic syndrome (CMS) – Old Danish Pointing Dog 8206 CHAT
Congenital myasthenic syndrome (CMS) – Russell Terrier 8206 CHRNE
Congenital stationary night blindness (CSNB) 8011 RPE65
Copper storage disease – Copper toxicosis 1 (Partnerlab) – Doberman, Labrador Retriever 8388 ATP7B
Copper storage disease – Copper toxicosis 2 (Partnerlab) – Doberman, Labrador Retriever 8388 ATP7A
Craniomandibular osteopathy (CMO) 8348 SLC37A2
Curly (curled hair: C1, C2) 8196 KRT71
Cystinuria – Australian Cattle Dog 8013 SLC3A1
Cystinuria – Bulldog Mastiff 8013 SLC3A1
Cystinuria – Labrador Retriever 8013 SLC3A1
Cystinuria – Miniature Pinscher 8013 SLC7A9
Cystinuria – Newfoundland 8013 SLC3A1
Degenerative myelopathy exon 2 (DM exon 2) 8158 SOD1
Degenerative myelopathy risk modifier 8939 SP110
Delayed postoperative hemorrhage (DEPOH) – Deerhound 8862 SERPINF2
Dental-skeletal-retinal anomaly (DSRA) 8698 MIA3
Dermatosparaxis Ehlers-Danlos syndrome (dEDS) – Catahoula Leopard Dog ADAMTS2
Dermatosparaxis Ehlers-Danlos syndrome (dEDS) – Dobermann Pinscher ADAMTS2
Digital Hyperkeratosis (DH) – Dogue de Bordeaux 8472 KRT16
Digital Hyperkeratosis (DH) – Irish Terrier, Kromfohrländer 8472 FAM83G
Dilated cardiomyopathy (DCM) – Manchester Terrier 8764 ABCC9
Dilated cardiomyopathy (DCM) – Nova Scotia Duck Tolling Retriever 8764 LMNA
Dilated cardiomyopathy (DCM) – Schnauzer 8363 RBM20
Dilated cardiomyopathy (DCM) – Welsh Springer Spaniel 8764 PLN
Dilated cardiomyopathy (DCM1) – Doberman 8872 PKD4
Dilated cardiomyopathy (DCM2) – Doberman 8872 TTN
Dilated cardiomyopathy (DCM3) – Doberman 8872 LOC102156622 (DCM3)
Dilated cardiomyopathy (DCM4) – Doberman 8872
Disproportionate dwarfism – Dogo Argentino 8753 PRKG2
Disproportionate dwarfism – Magyar Vizsla 8753 PCYT1A
D-locus (rare variants, alleles: d2, d3) 8636 MLPH
D-locus d1 (dilution) 8136 MLPH
Double Coat (double vs single, associated snp 1) 8523 LOC106557950
Double Coat (double vs single, associated snp 2) 8523 LOC106557950
Dyserythropoietic anaemia and myopathy (DAMS) 8805 EHBP1L1
Dystrophic epidermolysis bullosa – Golden Retriever COL7A1
Dystrophic epidermolysis bullosa (DEB) – Central Asian Shepherd 8643 COL7A1
E-locus (special colours) eA 8682 MC1R
E-locus (special colours) eg 8682 MC1R
E-locus (special colours) eh 8682 MC1R
E-locus e1 (apricot, cream, lemon, red, yellow) 8018 MC1R
E-locus e3 – Alaskan Husky, Siberian Husky MC1R
EM-locus (melanistic mask) 8146 MC1R
Epidermolytic hyperkeratosis (EHK) 8311 KRT10
Episodic falling (EF) 8202 BCAN
Exercise induced collapse (EIC) 8152 DNM1
Exfoliative cutaneous lupus erythematosus (ECLE) 8688 UNC93B1
Factor VII deficiency (F7) 8151 F7
Familial Nephropathy (FN) – English Cocker Spaniel (Partnerlab) 8131 COL4A4
Familial Nephropathy (FN) – English Springer Spaniel 8192 COL4A4
Familial Nephropathy (FN) – Samoyed 8192 COL4A5
Familial thyroid follicular cell carcinoma (FTFC1) 8871 TPO
Familial thyroid follicular cell carcinoma (FTFC2) 8871 TPO
Fanconi syndrome 8272 FAN1
Finnish Hound ataxia (FHA) 8467 SEL1L
Furnishing (wire hair) 8195 RSPO2
Gallbladder mucoceles (GBM) 8323 ABCB4
Glanzmann thrombasthenia (GT) 8077 ITGA2B
Glaucoma and goniodysgenesis (GG) 8635 OLFML3
Globoid cell leukodystrophy (Krabbe-disease) 8007 GALC
Glycogen storage disease (GSD Ia) 8322 G6PC
Glycogen storage disease (GSD II) (Pompe disease) 8513 GAA
Glycogen storage disease (GSD IIIa) 8156 AGL
GM1-Gangliosidosis – Husky 8066 GLB1
GM1-Gangliosidosis – Portuguese Water Dog 8066 GLB1
GM1-Gangliosidosis – Shiba Inu 8066 GLB1
GM2-Gangliosidosis – Japanese Chin 8208 HEXA
GM2-Gangliosidosis – Poodle 8208 HEXB
GM2-Gangliosidosis – Shiba Inu 8208 HEXB
Growth-hormone deficiency Dwarfism – Chihuahua GH1
Haemophilia A (factor VIII deficiency) – Boxer 8689 F8
Haemophilia A (factor VIII deficiency) – German Shepherd 8689 F8
Haemophilia A (factor VIII deficiency) – Labrador Retriever 8689 F8
Haemophilia A (factor VIII deficiency) – Old English Sheepdog 8689 F8
Haemophilia B (factor IX deficiency) – American Akita 8221 F9
Haemophilia B (factor IX deficiency) – Hovawart 8221 F9
Haemophilia B (factor IX deficiency) – Lhasa Apso 8221 F9
Haemophilia B (factor IX deficiency) – Rhodesian Ridgeback 8221 F9
Haemorrhagic diathesis (Scott syndrome) 8319 ANO6
Hairlessness – Scottish Deerhound 8599 SGK3
Hereditary Ataxia (HA) – Australian Shepherd 8449 PNPLA8
Hereditary Ataxia (HA) – Gordon Setter 8449 RAB24
Hereditary Ataxia (HA) – Norwegian Buhund 8449 KCNIP4
Hereditary Ataxia (HA) – Norwegian Elkhound 8449 HACE1
Hereditary Cataract – Wire-Haired Pointing Griffon Korthals 8157 FYCO1
Hereditary deafness 1 (DINGS1) – Doberman 8875 PTPRQ
Hereditary deafness 2 (DINGS2) – Doberman 8875 MYO7A
Hereditary Deafness/Hearing Loss (EOAD) – Beauceron 8269 CDH23
Hereditary Deafness/Hearing Loss (EOAD) – Rhodesian Ridgeback 8269 EPS8L2
Hereditary Deafness/Hearing Loss (EOAD) – Rottweiler 8269 LOXHD1
Hereditary myopathy (CNM) – German Hunting Terrier 8073 ACADVL
Hereditary myopathy (CNM) – Great Dane 8073 BIN1
Hereditary nasal parakeratosis (HNPK) – Greyhound 8672 SUV39H2
Hereditary nasal parakeratosis (HNPK) – Labrador Retriever 8421 SUV39H2
Hereditary neuropathy (GHN) 8179 NDRG1
H-locus (harlequin) 8254 PSMB7
Hyperuricosuria (HUU/SLC) 8154 SLC2A9
Hypomyelination (Shaking Puppy Syndrome) – English Springer Spaniel 8443 PLP1
Hypomyelination (Shaking Puppy Syndrome) – Weimaraner 8443 FNIP2
Hypophosphatasia (HPP) 8389 ALPL
Ichthyosis – American Bulldog 8555 NIPAL4
Ichthyosis – German Sheperd ASPRV1
Ichthyosis (non-epidermolytic) – Chihuahua SDR9C7
Ichthyosis (Partnerlab) – Golden Retriever 8481 PNPLA1
Ichthyosis type 2 – Golden Retriever 8738 ABHD5
I-locus (pheomelanin intensity) 8366 MFSD12
Imerslund-Gräsbeck-Syndrome (IGS) – Beagle 8475 CUBN
Imerslund-Gräsbeck-Syndrome (IGS) – Border Collie 8475 CUBN
Imerslund-Gräsbeck-Syndrome (IGS) – Komondor 8475 CUBN
Improper coat 8405 RSPO2
Inflammatory myopathy (IM) 8612 SLC25A12
Inflammatory pulmonary disease (IPD) 8373 AKNA
Junctional epidermolysis bullosa (JEB) 8198 LAMA3
Juvenile brain disease (JBD) – Parson Russell Terrier 8284 PITRM1
Juvenile epilepsy (JE) – Lagotto Romagnolo 8459 LGI2
Juvenile laryngeal paralysis & polyneuropathy (JLPP) 8271 RAB3GAP1
Juvenile myoclonic epilepsy (JME) – Rhodesian Ridgeback 8557 DIRAS1
K-locus (alleles KB and ky) 8145 CBD103
L-2-Hydroxyglutaric Aciduria (L2HGA) – Staffordshire Bull Terrier 8125 L2HGDH
L-2-Hydroxyglutaric Aciduria (L2HGA) – Yorkshire Terrier 8125 L2HGDH
Lagotto storage disease (LSD) 8270 ATG4D
Larynxparalysis with polyneuropathy type 3 (LPPN3) 8685 CNTNAP1
Late onset ataxia (LOA) 8493 CAPN1
Leonberger polyneuropathy 1 (LPN1) 8487 ARHGEF10
Leonberger polyneuropathy 2 (LPN2) 8494 GJA9
Lethal acrodermatitis (LAD) – Bullterrier 8273 MKLN1
Lethal Lung diesase (LAMP3) 8598 LAMP3
Leukocyte adhesion deficiency type III (LAD3) – German Shepherd 8327 FERMT3
Leukoencephalomyelopathy (LEMP) – Leonberger 8283 NAPEPLD
Leukoencephalopathy (LEP) – Schnauzer 8364 TSEN54
Limb-Girdle Muscular Dystrophy (LGMD) 8863 SGCA
Lundehund syndrome (LHS) 8579 P3H2
Lysosomal storage disease (LSD) – Doberman 8932 MAN2B1
Macrothrombocytopenia (MTC) – Cavalier King Charles Spaniel 8217 TUBB1
Macrothrombocytopenia (MTC) – Norfolk Cairn Terrier 8217 TUBB1
Macular corneal dystrophy (MCD) – Labrador Retriever 8736 LOC489707
Malignant hyperthermia (MH) 8062 RYR1
Maxillary canine tooth mesioversion (MCM) 8819 FTSJ3
May-Hegglin anomaly (MHA) 8312 MYH9
MCAD deficiency 8288 ACADM
MDR1 gene variant (Ivermectin hypersensitivity) 8032 ABCB1
Methemoglobinemia (MetHg) 8870 CYB5R3
Microphthalmia (RBP4) – Irish Soft Coated Wheaten Terrier 8508 RBP4
Mitochondrial fission encephalopathy (MFE) 8521 MFF
Mucopolysaccharidosis type IIIa (MPS3a) – Dachshund 8306 SGSH
Mucopolysaccharidosis type IIIa (MPS3a) – New Zealand Huntaway Dog 8306 SGSH
Mucopolysaccharidosis type VI (MPS 6) – Great Dane ARSB
Mucopolysaccharidosis type VI (MPS 6) – Miniature Pinscher 8693 ARSB
Mucopolysaccharidosis type VII (MPS 7) – Brazilian Terrier 8069 GUSB
Mucopolysaccharidosis type VII (MPS 7) – German Shepherd 8069 GUSB
Muscular Dystrophy (Duchenne type) – Cavalier King Charles Spaniel DMD
Muscular Dystrophy (MD) – American Staffordshire Terrier 8068 COL6A3
Muscular Dystrophy (MD) – Cavalier King Charles Spaniel 8068 DMD
Muscular Dystrophy (MD) – Golden Retriever 8068 DMD
Muscular Dystrophy (MD) – Landseer 8068 COL6A1
Muscular Dystrophy (MD) – Norfolk Terrier 8068 DMD
Musladin-Lueke syndrome (MLS) – Beagle 8411 ADAMTSL2
Mycobacterium avium complex sensitivity (MAC) 8360 CARD9
Myostation mutation (“bully”-gene) 8220 MSTN
Myotonia congenita – Labrador Retriever 8022 CLCN1
Myotonia congenita – Miniature Schnauzer 8022 CLCN1
Myxomatous mitral valve disease (MMVD) 8831 NEBL
Narcolepsy – Dachshund (Dackel) 8067 HCRTR2
Narcolepsy – Labrador Retriever 8067 HCRTR2
Necrotizing meningoencephalitis (NME/PDE) 8429 DLA-DPB1
Necrotizing myelopathy (ENM) – Kooikerhondje 8869 IBA57
Nemalin myopathy (NM) – American Bulldog 8172 NEB
Neonatal cortical cerebellar abiotrophy (NCCD) – Beagle 8457 SPTBN2
Neonatal cortical cerebellar abiotrophy (NCCD) – Magyar Viszla 8457 SNX14
Neonatal encephalopathy with seizures (NEWS) 8155 ATF2
Neuroaxonal Dystrophy (NAD) – Lagotto Romagnolo 8308 TECPR2
Neuroaxonal Dystrophy (NAD) – Miniature American Shepherd 8308 RNF170
Neuroaxonal Dystrophy (NAD) – Papillon 8308 PLA2G6
Neuroaxonal Dystrophy (NAD) – Rottweiler 8308 VPS11
Neuroaxonal Dystrophy (NAD) – Spanish Water Dog 8308 TECPR2
Neuronal ceroid lipifuscinosis (NCL) (Partnerlab) – American Staffordshire Terrier 8396 NCL4A (ARSG)
Neuronal ceroid lipofuscinosis (NCL) – American Bulldog 8075 CLN10(CTSD)
Neuronal ceroid lipofuscinosis (NCL) – Australian Cattle Dog 8133 CLN12 (ATP13A2)
Neuronal ceroid lipofuscinosis (NCL) – Australian Shepherd 8133 CLN6
Neuronal ceroid lipofuscinosis (NCL) – Australian Shepherd 2 8133 CLN8
Neuronal ceroid lipofuscinosis (NCL) – Border Collie 8075 CLN5
Neuronal ceroid lipofuscinosis (NCL) – Cane Corso 8075 CLN1 (PPT1)
Neuronal ceroid lipofuscinosis (NCL) – Chinese Crested 8075 CLN7 (MFSD8)
Neuronal ceroid lipofuscinosis (NCL) – Dachshund 1 8133 CLN1 (PPT1)
Neuronal ceroid lipofuscinosis (NCL) – Dachshund 2 8133 CLN2 (TPP1)
Neuronal ceroid lipofuscinosis (NCL) – English Setter 8075 CLN8
Neuronal ceroid lipofuscinosis (NCL) – Golden Retriever 8075 CLN5
Neuronal ceroid lipofuscinosis (NCL) – Tibet Terrier 8075 CLN12 (ATP13A2)
Osteochondrodysplasia (OCD) 8877 SLC13A1
Osteogenesis imperfecta (brittle bone disease) – Beagle 8215 COL1A2
Osteogenesis imperfecta (brittle bone disease) – Dachshund 8215 SERPINH1
Osteogenesis imperfecta (brittle bone disease) – Golden Retriever 8215 COL1A1
Panda white spotting 8578 KIT
Paradoxical pseudomyotonia (PP) 8933 SLC7A10
Paroxysmal Exercise-Induced Dyskinesia (PED) – Shetland Sheepdog (Sheltie) 8690 PCK2
Paroxysmal Exercise-Induced Dyskinesia (PED) – Weimaraner 8690 TNR
Paroxysomal dyskinesia (PxD) 8630 PIGN
Persistent Müllerian duct syndrome (PMDS) 8462 AMHR2
Phosphofructokinase Deficiency (PFKD) – English Springer Spaniel 8017 PFKM
Phosphofructokinase Deficiency (PFKD) – German Spaniel 8017 PFKM
Pituitary Dwarfism – Karelian Bear Dog 8142 POU1F1
Polycystic kidney disease (PKD) 8476 PKD1
Polydactyly SHH
Postoperative hemorrhage (P2Y12) – Great Swiss Mountain Dog 8053 P2RY12
Prekallikrein deficiency (KLK) 8141 KLKB1
Primary Ciliary Dyskinesia (PCD) – Alaskan Malamute 8483 NME5
Primary Ciliary Dyskinesia (PCD) – Old English Sheepdog 8483 CCDC39
Primary lens luxation (PLL) 8226 ADAMTS17
Primary Open Angle Glaucoma (POAG) – Basset Fauve de Bretagne 8452 ADAMTS17
Primary Open Angle Glaucoma (POAG) – Basset Hound 8452 ADAMTS17
Primary Open Angle Glaucoma (POAG) – Beagle 8452 ADAMTS10
Primary Open Angle Glaucoma (POAG) – Norwegian Elkhound 8452 ADAMTS10
Primary open angle glaucoma and lens luxation (POAG/PLL) – Shar Pei 8641 ADAMTS17
Progressive retinal atrophy (Bas-PRA1) – Basenji 8574 SAG
Progressive retinal atrophy (BBS2-PRA) – Shetland Sheepdog 8773 BBS2
Progressive retinal atrophy (BBS4-PRA) 8207 BBS4
Progressive retinal atrophy (CNGA1-PRA) 8375 CNGA1
Progressive retinal atrophy (crd1-PRA) – American Staffordshire Terrier 8332 PDE6B
Progressive retinal atrophy (crd2-PRA) – American Pitbull Terrier 8333 IQCB1
Progressive retinal atrophy (crd3-PRA) (associated SNP) – Glen of Imaal Terrier ADAM18
Progressive retinal atrophy (crd-PRA) 8135 NPHP4
Progressive retinal atrophy (dominant PRA) – English Mastiff 8355 RHO
Progressive retinal atrophy (eo-PRA) – Portuguese Water Dog 8617 CCDC66
Progressive retinal atrophy (eo-PRA) – Spanish Water Dog 8617 PDE6B
Progressive retinal atrophy (g-PRA) – Shapendoes 8451 CCDC66
Progressive retinal atrophy (GR-PRA1) – Golden Retriever 8200 SLC4A3
Progressive retinal atrophy (GR-PRA2) – Golden Retriever 8520 TTC8
Progressive retinal atrophy (GUCY2D-PRA) – German Spitz 8894 GUCY2D
Progressive retinal atrophy (ITF122-PRA) – Lapponian Herder 8746 IFT122
Progressive retinal atrophy (JHP2-PRA) – Shih Tzu 8752 JPH2
Progressive retinal atrophy (MERTK-PRA) – Swedish Vallhund (Västgötaspets) 8861 MERTK
Progressive retinal atrophy (NECAP1-PRA) – Giant Schnauzer 8374 NECAP1
Progressive retinal atrophy (PAP-PRA) – Papillon 8573 CNGB1
Progressive retinal atrophy (Prcd-PRA) (Partnerlab) 8127 PRCD
Progressive retinal atrophy (rcd1) – Irish Setter 8042 PDE6B
Progressive retinal atrophy (rcd1a) – Sloughi 8353 PDE6B
Progressive retinal atrophy (rcd3) – Welsh Corgi 8354 PDE6A
Progressive retinal atrophy (type B1-PRA, HIVEP3) – Miniature Schnauzer 8546 HIVEP3
Protein losing nephropathy (PLN) 8492 KIRREL2, NPHS1
Pyruvate dehydrogenase phosphatase 1 deficiency (PDP1) 8104 PDP1
Pyruvatkinase-Deficiency (PK) – Basenji 8015 PKLR
Pyruvatkinase-Deficiency (PK) – Beagle 8015 PKLR
Pyruvatkinase-Deficiency (PK) – Labrador Retriever 8015 PKLR
Pyruvatkinase-Deficiency (PK) – Pug 8015 PKLR
Raine syndrome 8394 FAM20C
Renal cystadenocarcinoma and nodular fibrosis (RCND) 8301 FLCN
Renal dysplasia and hepatic fibrosis (RDHN) 8345 INPP5E
Retinal dysplasia (OSD) – Northern Inuit, Tamaskan 8677 COL9A3
Robinow-like syndrome (DVL2) 8747 DVL2
Saddle-tan 8307 RALY
Sensory neuropathy (SN) 8596 FAM134B
Severe Combined Immunodeficiency (SCID) – Frisian Water Dog 8328 RAG1
Severe Combined Immunodeficiency (SCID) – Russell Terrier 8328 PRKDC
Shar Pei autoinflammatory disease (SPAID) 8642 MTBP
Skeletal dysplasia 2 (Dwarfism) (SD2) – Labrador Retriever 8456 COL11A2
S-locus (piebald, white spotting) 8438 MITF
Spinal dysraphism (NTD) 8605 NKX2-8
Spinocerebellar Ataxia – Belgian Shepherd Mallinois SLC12A6
Spinocerebellar Ataxia (SCA) – Alpine Dachsbracke 8537 SCN8A
Spinocerebellar Ataxia (SCA) – Terrier 8537 KCNJ10
Spondylocostal dysostosis (Comma defect) 8335 HES7
Spongy degeneration with cerebellar ataxia type 1 (SDCA1) 8610 KCNJ10
Stargardt disease (retinal degeneration) (STGD) 8387 ABCA4
Startle disease – Galgo Espagnol 8191 SLC6A5
Succinic semialdehyde dehydrogenase deficiency (SSADHD) 8615 ALDH5A1
Thrombopathia – Basset Hound 8486 RASGRP2
Ticking (Roan, Mottle, Spotted) 8765 USH2A
Trapped neutrophil syndrome (TNS) 8143 VPS13B
Upper airway syndrome (UAS) 8391 ADAMTS3
van den Ende-Gupta syndrome (VDEGS) 8393 SCARF2
Ventricular arrhythmia (IVA) 8739 MICOS13
Vitamin D dependent rickets (VDR) 8302 VDR
von-Willebrand disease type I (vWD1) 8119 VWF
von-Willebrand disease type II (vWD 2) 8014 VWF
von-Willebrand disease type III (vWD3) – Kooikerhondje 8233 VWF
von-Willebrand disease type III (vWD3) – Scottish Terrier 8233 VWF
von-Willebrand disease type III (vWD3) – Shetland Sheepdog (Sheltie) 8233 VWF
Xanthinuria type II – Cavalier King Charles Spaniel 8779 MOCOS
Xanthinuria type II – Dachshund (Dackel) 8779 MOCOS
Xanthinuria type II – Manchester Terrier 8779 MOCOS
X-chromosomal severe immuno defiziency (X-SCID) – Basset Hound 8063 IL2RG
X-chromosomal severe immuno defiziency (X-SCID) – Welsh Corgi 8063 IL2RG
X-linked myopathy (XL-MTM) – Labrador Retriever 8305 MTM1
X-linked myopathy (XL-MTM) – Rottweiler 8305 MTM1