LABOGenetics XXL – Chien

Le screening génétique complet pour votre chien ! Disponible cette année encore chez LABOGEN.

Aperçu des produits

Vous voulez savoir ce qui se cache génétiquement dans votre chien ? Le nouveau pack complet LABOGenetics XXL Chien contiendra plus de 300 variantes génétiques. Vous obtiendrez des informations sur les maladies héréditaires, les facteurs à risque génétiques, les couleurs et les caractéristiques du pelage.

Ce nouveau pack est intéressant pour tous, que vous soyez propriétaire de chiens, éleveur ou vétérinaire.

  • Pour les éleveurs : prenez des décisions d’élevage éclairées, améliorez la santé génétique de votre race et élevez une progéniture plus saine.

  • Pour les propriétaires de chiens : obtenez un aperçu de la génétique de votre chien et découvrez les risques potentiels pour sa santé.

  • Pour les vétérinaires : améliorez vos plans de diagnostic et de traitement grâce à de précieuses informations génétiques et permettez ainsi une meilleure prise en charge de vos patients canins.

  • Pour les clubs d’élevage : mettez à la disposition des membres de votre club des tests génétiques avancés et soutenez ainsi des pratiques d’élevage responsables.

Commandez LABOGenetics XXL Chien maintenant!

Quels sont les tests inclus dans l'ensemble LABOGenetics XXL Dog ?

Test (click for more detail)numbergene
Acatalasemia8552CAT
Achromatopsia (day blindness) (ACHM) – German Shepherd8166CNGA3
Achromatopsia (day blindness) (ACHM) – Labrador Retriever8166CNGA3
Acral mutilation syndrome (AMS)8038GDNF
Acute respiratory distress syndrome (ARDS)8595ANLN
Adipositas8602POMC
Afibrinogenemia (AFG)8737FGA
Alaskan Husky enzephalopathy (AHE)8313SLC19A3
Alaskan Malamute polyneuropathy (AMPN)8479NDRG1
Alexander disease (AxD)8601GFAP
A-Locus (Agouti) ASIP Analysis8144ASIP
Amelogenesis imperfecta (AI)(Familial enamel hypoplasia) – Akita8303ACP4
Amelogenesis imperfecta (AI)(Familial enamel hypoplasia) – Italian Greyhound8303ENAM
Amelogenesis imperfecta (AI)(Familial enamel hypoplasia) – Parson Russell Terrier8303ENAM
Amelogenesis imperfecta (AI)(Familial enamel hypoplasia) – Samoyed8303SLC24A4
Anhidrotic ectodermal dysplasia – German Shepherd EDA
B-locus (rare variants) (b4) – Australian Shepherd, Miniature American Shepherd8639TYRP1
B-locus (rare variants) (be) – Lancashire Heeler8639TYRP1
B-locus (rare variants) (bh) – Husky8639TYRP1
B-locus bc8023TYRP1
B-locus bd8023TYRP1
B-locus bs8023TYRP1
Brachyuria (stumpy tail)8219TBXT
Bunny Hopping Syndrome (BHS1)8878EFNB3
C3 deficiency (C3)8184C3
Canine leucocyte adhesion deficiency (CLAD)8012ITGB2
Canine multi-focal retinopathy (CMR1)8330BEST1
Canine multi-focal retinopathy (CMR2)8330BEST1
Canine multi-focal retinopathy (CMR3)8330BEST1
Canine multiple system degeneration (CMSD) – Chinese Crested8575SERAC1
Canine multiple system degeneration (CMSD) – Kerry Blue Terrier8575SERAC1
Cardiomyopathy with juvenile mortality (CJM)8543YARS2
Cerebellar ataxia (CA1) – Belgian Shepherd Dog8860RALGAPA1
Cerebellar ataxia (CA1) – Pyrenean Mountain Dog8860SACS
Cerebellar degeneration and myositis complex (CDMC)8788SLC25A12
Cerebellar hypoplasia (CH)8868RELN
Cerebral dysfunction (CDFS)8314SLC6A3
Charcot-Marie-Tooth Neuropathy (CMT)8538SBF2
Chondrodysplasia (dwarfism) – Norwegian Elkhound8316ITGA10
Chondrodysplasia and -dystrophy (IVDD risk) CDDY8294FGF4/CFA12
Chondrodysplasia and -dystrophy (IVDD risk) CDPA8294FGF4/CFA18
C-locus (albino) caL8644SLC45A2
C-locus (albino) OCA28644OCA2
C-Lokus (OCA4) – Bullmastif8613SLC45A2
CNS atrophy with cerebellar ataxia (CACA)8697SELENOP
Coat colour, albinism, oculocutaneous type IV – Dobermann Pinscher SLC45A2
Coat length I (long or short hair) HL18124FGF5
Coat length II (long or short hair) HL28397FGF5
Coat length II (long or short hair) HL38397FGF5
Coat length II (long or short hair) HL48397FGF5
Coat length II (long or short hair) HL58397FGF5
Cocoa (brown, dark chocolate)8526HPS3
Collie eye anomaly (CEA) (Partnerlab)8304NHEJ1
Color dilution and neurological defects (CDN)8758MYO5A
Cone Degeneration (CD)8780CNGB3
Congenital Hypothyroidism with goiter (CHG) – Fox, Rat Terrier8434TPO
Congenital Hypothyroidism with goiter (CHG) – French Bulldog8434TPO
Congenital Hypothyroidism with goiter (CHG) – Tenterfield Terrier8434TPO
Congenital myasthenic syndrome (CMS) – Golden Retriever8206LOC608697
Congenital myasthenic syndrome (CMS) – Labrador Retriever8206LOC608697
Congenital myasthenic syndrome (CMS) – Old Danish Pointing Dog8206CHAT
Congenital myasthenic syndrome (CMS) – Russell Terrier8206CHRNE
Congenital stationary night blindness (CSNB)8011RPE65
Copper storage disease – Copper toxicosis 1 (Partnerlab) – Doberman, Labrador Retriever8388ATP7B
Copper storage disease – Copper toxicosis 2 (Partnerlab) – Doberman, Labrador Retriever8388ATP7A
Craniomandibular osteopathy (CMO)8348SLC37A2
Curly (curled hair: C1)8196KRT71
Cystinuria – Australian Cattle Dog8013SLC3A1
Cystinuria – Bulldog Mastiff8013SLC3A1
Cystinuria – Labrador Retriever8013SLC3A1
Cystinuria – Miniature Pinscher8013SLC7A9
Cystinuria – Newfoundland8013SLC3A1
Degenerative myelopathy exon 2 (DM exon 2)8158SOD1
Degenerative myelopathy risk modifier8939SP110
Delayed postoperative hemorrhage (DEPOH) – Deerhound8862SERPINF2
Dental-skeletal-retinal anomaly (DSRA)8698MIA3
Dermatosparaxis Ehlers-Danlos syndrome (dEDS) – Catahoula Leopard Dog ADAMTS2
Dermatosparaxis Ehlers-Danlos syndrome (dEDS) – Dobermann Pinscher ADAMTS2
Digital Hyperkeratosis (DH) – Dogue de Bordeaux8472KRT16
Digital Hyperkeratosis (DH) – Irish Terrier, Kromfohrländer8472FAM83G
Dilated cardiomyopathy (DCM) – Manchester Terrier8764ABCC9
Dilated cardiomyopathy (DCM) – Nova Scotia Duck Tolling Retriever8764LMNA
Dilated cardiomyopathy (DCM) – Schnauzer8363RBM20
Dilated cardiomyopathy (DCM) – Welsh Springer Spaniel8764PLN
Dilated cardiomyopathy (DCM1) – Doberman8872PKD4
Dilated cardiomyopathy (DCM2) – Doberman8872TTN
Dilated cardiomyopathy (DCM3) – Doberman8872LOC102156622 (DCM3)
Dilated cardiomyopathy (DCM4) – Doberman8872 
Disproportionate dwarfism – Dogo Argentino8753PRKG2
Disproportionate dwarfism – Magyar Vizsla8753PCYT1A
D-locus (rare variants, alleles: d2)8636MLPH
D-locus d1 (dilution)8136MLPH
Double Coat (double vs single, associated snp 1)8523LOC106557950
Double Coat (double vs single, associated snp 2)8523LOC106557950
Dyserythropoietic anaemia and myopathy (DAMS) – Labrador Retriever8805EHBP1L1
Dystrophic epidermolysis bullosa – Golden Retriever COL7A1
Dystrophic epidermolysis bullosa (DEB) – Central Asian Shepherd8643COL7A1
E-locus (special colours) eA8682MC1R
E-locus (special colours) eg8682MC1R
E-locus (special colours) eh8682MC1R
E-locus e1 (apricot, cream, lemon, red, yellow)8018MC1R
E-locus e3 – Alaskan Husky, Siberian Husky MC1R
EM-locus (melanistic mask)8146MC1R
Epidermolytic hyperkeratosis (EHK)8311KRT10
Episodic falling (EF)8202BCAN
Exercise induced collapse (EIC)8152DNM1
Exfoliative cutaneous lupus erythematosus (ECLE)8688UNC93B1
Factor VII deficiency (F7)8151F7
Familial Nephropathy (FN) – English Cocker Spaniel (Partnerlab)8131COL4A4
Familial Nephropathy (FN) – English Springer Spaniel8192COL4A4
Familial Nephropathy (FN) – Samoyed8192COL4A5
Familial thyroid follicular cell carcinoma (FTFC1)8871TPO
Familial thyroid follicular cell carcinoma (FTFC2)8871TPO
Fanconi syndrome8272FAN1
Finnish Hound ataxia (FHA)8467SEL1L
Furnishing (wire hair)8195RSPO2
Gallbladder mucoceles (GBM)8323ABCB4
Glanzmann thrombasthenia (GT)8077ITGA2B
Glaucoma and goniodysgenesis (GG)8635OLFML3
Globoid cell leukodystrophy (Krabbe-disease) – Cairn Terrier8007GALC
Globoid cell leukodystrophy (Krabbe-disease) – West Highland White Terrier8007GALC
Glycogen storage disease (GSD Ia) – Maltese8322G6PC
Glycogen storage disease (GSD II) (Pompe disease)8513GAA
Glycogen storage disease (GSD IIIa)8156AGL
GM1-Gangliosidosis – Husky8066GLB1
GM1-Gangliosidosis – Portuguese Water Dog8066GLB1
GM1-Gangliosidosis – Shiba Inu8066GLB1
GM2-Gangliosidosis – Japanese Chin8208HEXA
GM2-Gangliosidosis – Poodle8208HEXB
GM2-Gangliosidosis – Shiba Inu8208HEXB
Growth-hormone deficiency Dwarfism – Chihuahua GH1
Haemophilia A (factor VIII deficiency) – Boxer8689F8
Haemophilia A (factor VIII deficiency) – German Shepherd8689F8
Haemophilia A (factor VIII deficiency) – Labrador Retriever8689F8
Haemophilia A (factor VIII deficiency) – Old English Sheepdog8689F8
Haemophilia B (factor IX deficiency) – American Akita8221F9
Haemophilia B (factor IX deficiency) – Hovawart8221F9
Haemophilia B (factor IX deficiency) – Lhasa Apso8221F9
Haemophilia B (factor IX deficiency) – Rhodesian Ridgeback8221F9
Haemorrhagic diathesis (Scott syndrome)8319ANO6
Hairlessness – Scottish Deerhound8599SGK3
Hereditary Ataxia (HA) – Australian Shepherd8449PNPLA8
Hereditary Ataxia (HA) – Gordon Setter8449RAB24
Hereditary Ataxia (HA) – Norwegian Buhund8449KCNIP4
Hereditary Ataxia (HA) – Norwegian Elkhound8449HACE1
Hereditary Ataxia (HA) – Old English Sheepdog8449RAB24
Hereditary Cataract – Wire-Haired Pointing Griffon Korthals8157FYCO1
Hereditary deafness 1 (DINGS1) – Doberman8875PTPRQ
Hereditary deafness 2 (DINGS2) – Doberman8875MYO7A
Hereditary Deafness/Hearing Loss (EOAD) – Beauceron8269CDH23
Hereditary Deafness/Hearing Loss (EOAD) – Rhodesian Ridgeback8269EPS8L2
Hereditary Deafness/Hearing Loss (EOAD) – Rottweiler8269LOXHD1
Hereditary myopathy (CNM) – German Hunting Terrier8073ACADVL
Hereditary myopathy (CNM) – Great Dane8073BIN1
Hereditary nasal parakeratosis (HNPK) – Greyhound8672SUV39H2
Hereditary nasal parakeratosis (HNPK) – Labrador Retriever8421SUV39H2
Hereditary neuropathy (GHN)8179NDRG1
H-locus (harlequin)8254PSMB7
Hyperuricosuria (HUU/SLC)8154SLC2A9
Hypomyelination (Shaking Puppy Syndrome) – English Springer Spaniel8443PLP1
Hypomyelination (Shaking Puppy Syndrome) – Weimaraner8443FNIP2
Hypophosphatasia (HPP)8389ALPL
Ichthyosis – American Bulldog8555NIPAL4
Ichthyosis – German Sheperd ASPRV1
Ichthyosis (non-epidermolytic) – Chihuahua SDR9C7
Ichthyosis (Partnerlab) – Golden Retriever8481PNPLA1
Ichthyosis type 2 – Golden Retriever8738ABHD5
I-locus (pheomelanin intensity)8366MFSD12
Imerslund-Gräsbeck-Syndrome (IGS) – Beagle8475CUBN
Imerslund-Gräsbeck-Syndrome (IGS) – Border Collie8475CUBN
Imerslund-Gräsbeck-Syndrome (IGS) – Komondor8475CUBN
Improper coat8405RSPO2
Inflammatory myopathy (IM)8612SLC25A12
Inflammatory pulmonary disease (IPD)8373AKNA
Junctional epidermolysis bullosa (JEB)8198LAMA3
Juvenile brain disease (JBD) – Parson Russell Terrier8284PITRM1
Juvenile epilepsy (JE) – Lagotto Romagnolo8459LGI2
Juvenile laryngeal paralysis & polyneuropathy (JLPP)8271RAB3GAP1
Juvenile myoclonic epilepsy (JME) – Rhodesian Ridgeback8557DIRAS1
K-locus (alleles KB and ky)8145CBD103
L-2-Hydroxyglutaric Aciduria (L2HGA) – Staffordshire Bull Terrier8125L2HGDH
L-2-Hydroxyglutaric Aciduria (L2HGA) – Yorkshire Terrier8125L2HGDH
Lagotto storage disease (LSD)8270ATG4D
Larynxparalysis with polyneuropathy type 3 (LPPN3)8685CNTNAP1
Late onset ataxia (LOA)8493CAPN1
Leonberger polyneuropathy 1 (LPN1)8487ARHGEF10
Leonberger polyneuropathy 2 (LPN2)8494GJA9
Lethal acrodermatitis (LAD) – Bullterrier8273MKLN1
Lethal Lung diesase (LAMP3)8598LAMP3
Leukocyte adhesion deficiency type III (LAD3) – German Shepherd8327FERMT3
Leukoencephalomyelopathy (LEMP) – Leonberger8283NAPEPLD
Leukoencephalopathy (LEP) – Schnauzer8364TSEN54
Limb-Girdle Muscular Dystrophy (LGMD)8863SGCA
Lundehund syndrome (LHS)8579P3H2
Lysosomal storage disease (LSD) – Doberman8932MAN2B1
Macrothrombocytopenia (MTC) – Cavalier King Charles Spaniel8217TUBB1
Macrothrombocytopenia (MTC) – Norfolk Cairn Terrier8217TUBB1
Macular corneal dystrophy (MCD) – Labrador Retriever8736LOC489707
Malignant hyperthermia (MH)8062RYR1
Maxillary canine tooth mesioversion (MCM)8819FTSJ3
May-Hegglin anomaly (MHA)8312MYH9
MCAD deficiency8288ACADM
MDR1 gene variant (Ivermectin hypersensitivity)8032ABCB1
Methemoglobinemia (MetHg)8870CYB5R3
Microphthalmia (RBP4) – Irish Soft Coated Wheaten Terrier8508RBP4
Mitochondrial fission encephalopathy (MFE)8521MFF
Mucopolysaccharidosis type IIIa (MPS3a) – Dachshund8306SGSH
Mucopolysaccharidosis type IIIa (MPS3a) – New Zealand Huntaway Dog8306SGSH
Mucopolysaccharidosis type VI (MPS 6) – Great Dane ARSB
Mucopolysaccharidosis type VI (MPS 6) – Miniature Pinscher8693ARSB
Mucopolysaccharidosis type VII (MPS 7) – Brazilian Terrier8069GUSB
Mucopolysaccharidosis type VII (MPS 7) – German Shepherd8069GUSB
Muscular Dystrophy (Duchenne type) – Cavalier King Charles Spaniel DMD
Muscular Dystrophy (MD) – American Staffordshire Terrier8068COL6A3
Muscular Dystrophy (MD) – Cavalier King Charles Spaniel8068DMD
Muscular Dystrophy (MD) – Golden Retriever8068DMD
Muscular Dystrophy (MD) – Landseer8068COL6A1
Muscular Dystrophy (MD) – Norfolk Terrier8068DMD
Musladin-Lueke syndrome (MLS) – Beagle8411ADAMTSL2
Mycobacterium avium complex sensitivity (MAC)8360CARD9
Myostation mutation (“bully”-gene)8220MSTN
Myotonia congenita – Labrador Retriever8022CLCN1
Myotonia congenita – Miniature Schnauzer8022CLCN1
Myxomatous mitral valve disease (MMVD)8831NEBL
Narcolepsy – Dachshund (Dackel)8067HCRTR2
Narcolepsy – Labrador Retriever8067HCRTR2
Necrotizing meningoencephalitis (NME/PDE)8429DLA-DPB1
Necrotizing myelopathy (ENM) – Kooikerhondje8869IBA57
Nemalin myopathy (NM) – American Bulldog8172NEB
Neonatal cortical cerebellar abiotrophy (NCCD) – Beagle8457SPTBN2
Neonatal cortical cerebellar abiotrophy (NCCD) – Magyar Viszla8457SNX14
Neonatal encephalopathy with seizures (NEWS)8155ATF2
Neuroaxonal Dystrophy (NAD) – Lagotto Romagnolo8308TECPR2
Neuroaxonal Dystrophy (NAD) – Miniature American Shepherd8308RNF170
Neuroaxonal Dystrophy (NAD) – Papillon8308PLA2G6
Neuroaxonal Dystrophy (NAD) – Rottweiler8308VPS11
Neuroaxonal Dystrophy (NAD) – Spanish Water Dog8308TECPR2
Neuronal ceroid lipifuscinosis (NCL) (Partnerlab) – American Staffordshire Terrier8396NCL4A (ARSG)
Neuronal ceroid lipofuscinosis (NCL) – American Bulldog8075CLN10(CTSD)
Neuronal ceroid lipofuscinosis (NCL) – Australian Cattle Dog8133CLN12 (ATP13A2)
Neuronal ceroid lipofuscinosis (NCL) – Australian Shepherd8133CLN6
Neuronal ceroid lipofuscinosis (NCL) – Australian Shepherd 28133CLN8
Neuronal ceroid lipofuscinosis (NCL) – Border Collie8075CLN5
Neuronal ceroid lipofuscinosis (NCL) – Cane Corso8075CLN1 (PPT1)
Neuronal ceroid lipofuscinosis (NCL) – Chinese Crested8075CLN7 (MFSD8)
Neuronal ceroid lipofuscinosis (NCL) – Dachshund 18133CLN1 (PPT1)
Neuronal ceroid lipofuscinosis (NCL) – Dachshund 28133CLN2 (TPP1)
Neuronal ceroid lipofuscinosis (NCL) – English Setter8075CLN8
Neuronal ceroid lipofuscinosis (NCL) – Golden Retriever8075CLN5
Neuronal ceroid lipofuscinosis (NCL) – Tibet Terrier8075CLN12 (ATP13A2)
Osteochondrodysplasia (OCD)8877SLC13A1
Osteogenesis imperfecta (brittle bone disease) – Beagle8215COL1A2
Osteogenesis imperfecta (brittle bone disease) – Dachshund8215SERPINH1
Osteogenesis imperfecta (brittle bone disease) – Golden Retriever8215COL1A1
Panda white spotting8578KIT
Paradoxical pseudomyotonia (PP)8933SLC7A10
Paroxysmal Exercise-Induced Dyskinesia (PED) – Shetland Sheepdog (Sheltie)8690PCK2
Paroxysmal Exercise-Induced Dyskinesia (PED) – Weimaraner8690TNR
Paroxysomal dyskinesia (PxD)8630PIGN
Persistent Müllerian duct syndrome (PMDS)8462AMHR2
Phosphofructokinase Deficiency (PFKD) – English Springer Spaniel8017PFKM
Phosphofructokinase Deficiency (PFKD) – German Spaniel8017PFKM
Pituitary Dwarfism – Karelian Bear Dog8142POU1F1
Polycystic kidney disease (PKD)8476PKD1
Polydactyly SHH
Postoperative hemorrhage (P2Y12) – Great Swiss Mountain Dog8053P2RY12
Prekallikrein deficiency (KLK)8141KLKB1
Primary Ciliary Dyskinesia (PCD) – Alaskan Malamute8483NME5
Primary Ciliary Dyskinesia (PCD) – Old English Sheepdog8483CCDC39
Primary lens luxation (PLL)8226ADAMTS17
Primary Open Angle Glaucoma (POAG) – Basset Fauve de Bretagne8452ADAMTS17
Primary Open Angle Glaucoma (POAG) – Basset Hound8452ADAMTS17
Primary Open Angle Glaucoma (POAG) – Beagle8452ADAMTS10
Primary Open Angle Glaucoma (POAG) – Norwegian Elkhound8452ADAMTS10
Primary open angle glaucoma and lens luxation (POAG/PLL) – Shar Pei8641ADAMTS17
Progressive retinal atrophy (Bas-PRA1) – Basenji8574SAG
Progressive retinal atrophy (BBS2-PRA) – Shetland Sheepdog8773BBS2
Progressive retinal atrophy (BBS4-PRA)8207BBS4
Progressive retinal atrophy (CNGA1-PRA)8375CNGA1
Progressive retinal atrophy (crd1-PRA) – American Staffordshire Terrier8332PDE6B
Progressive retinal atrophy (crd2-PRA) – American Pitbull Terrier8333IQCB1
Progressive retinal atrophy (crd3-PRA) (associated SNP) – Glen of Imaal Terrier ADAM18
Progressive retinal atrophy (crd-PRA)8135NPHP4
Progressive retinal atrophy (dominant PRA) – English Mastiff8355RHO
Progressive retinal atrophy (eo-PRA) – Portuguese Water Dog8617CCDC66
Progressive retinal atrophy (eo-PRA) – Spanish Water Dog8617PDE6B
Progressive retinal atrophy (g-PRA) – Shapendoes8451CCDC66
Progressive retinal atrophy (GR-PRA1) – Golden Retriever8200SLC4A3
Progressive retinal atrophy (GR-PRA2) – Golden Retriever8520TTC8
Progressive retinal atrophy (GUCY2D-PRA) – German Spitz8894GUCY2D
Progressive retinal atrophy (ITF122-PRA) – Lapponian Herder8746IFT122
Progressive retinal atrophy (JHP2-PRA) – Shih Tzu8752JPH2
Progressive retinal atrophy (MERTK-PRA) – Swedish Vallhund (Västgötaspets)8861MERTK
Progressive retinal atrophy (NECAP1-PRA) – Giant Schnauzer8374NECAP1
Progressive retinal atrophy (PAP-PRA) – Papillon8573CNGB1
Progressive retinal atrophy (Prcd-PRA) (Partnerlab)8127PRCD
Progressive retinal atrophy (rcd1) – Irish Setter8042PDE6B
Progressive retinal atrophy (rcd1a) – Sloughi8353PDE6B
Progressive retinal atrophy (rcd3) – Welsh Corgi8354PDE6A
Progressive retinal atrophy (type B1-PRA, HIVEP3) – Miniature Schnauzer8546HIVEP3
Protein losing nephropathy (PLN)8492KIRREL2, NPHS1
Pyruvate dehydrogenase phosphatase 1 deficiency (PDP1)8104PDP1
Pyruvatkinase-Deficiency (PK) – Basenji8015PKLR
Pyruvatkinase-Deficiency (PK) – Beagle8015PKLR
Pyruvatkinase-Deficiency (PK) – Labrador Retriever8015PKLR
Pyruvatkinase-Deficiency (PK) – Pug8015PKLR
Raine syndrome8394FAM20C
Renal cystadenocarcinoma and nodular fibrosis (RCND)8301FLCN
Renal dysplasia and hepatic fibrosis (RDHN)8345INPP5E
Retinal dysplasia (OSD) – Northern Inuit, Tamaskan8677COL9A3
Robinow-like syndrome (DVL2)8747DVL2
Saddle-tan8307RALY
Sensory neuropathy (SN)8596FAM134B
Severe Combined Immunodeficiency (SCID) – Frisian Water Dog8328RAG1
Severe Combined Immunodeficiency (SCID) – Russell Terrier8328PRKDC
Shar Pei autoinflammatory disease (SPAID)8642MTBP
Skeletal dysplasia 2 (Dwarfism) (SD2) – Labrador Retriever8456COL11A2
S-locus (piebald, white spotting)8438MITF
Spinal dysraphism (NTD)8605NKX2-8
Spinocerebellar Ataxia – Belgian Shepherd Mallinois SLC12A6
Spinocerebellar Ataxia (SCA) – Alpine Dachsbracke8537SCN8A
Spinocerebellar Ataxia (SCA) – Terrier8537KCNJ10
Spondylocostal dysostosis (Comma defect)8335HES7
Spongy degeneration with cerebellar ataxia type 1 (SDCA1)8610KCNJ10
Stargardt disease (retinal degeneration) (STGD)8387ABCA4
Startle disease – Galgo Espagnol8191SLC6A5
Succinic semialdehyde dehydrogenase deficiency (SSADHD)8615ALDH5A1
Thrombopathia – Basset Hound8486RASGRP2
Ticking (Roan, Mottle, Spotted)8765USH2A
Trapped neutrophil syndrome (TNS)8143VPS13B
Upper airway syndrome (UAS)8391ADAMTS3
van den Ende-Gupta syndrome (VDEGS)8393SCARF2
Ventricular arrhythmia (IVA)8739MICOS13
Vitamin D dependent rickets (VDR)8302VDR
von-Willebrand disease type I (vWD1)8119VWF
von-Willebrand disease type II (vWD 2)8014VWF
von-Willebrand disease type III (vWD3) – Kooikerhondje8233VWF
von-Willebrand disease type III (vWD3) – Scottish Terrier8233VWF
von-Willebrand disease type III (vWD3) – Shetland Sheepdog (Sheltie)8233VWF
Xanthinuria type II – Cavalier King Charles Spaniel8779MOCOS
Xanthinuria type II – Dachshund (Dackel)8779MOCOS
Xanthinuria type II – Manchester Terrier8779MOCOS
X-chromosomal severe immuno defiziency (X-SCID) – Basset Hound8063IL2RG
X-chromosomal severe immuno defiziency (X-SCID) – Welsh Corgi8063IL2RG
X-linked myopathy (XL-MTM) – Labrador Retriever8305MTM1
X-linked myopathy (XL-MTM) – Rottweiler8305MTM1