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Tests inclus
Spinocerebellar Ataxia (SCA) – Terrier Type
H303
Ichthyosis – Great Dane
H304
Craniomandibular Osteopathy (CMO) - Terrier Type
H312
Cortical Cerebellar Abiothrophy (NCCD) – Vizsla
H318
Dental Hypomineralization
H327
Late Onset Ataxia (LOA)
H328
Polyneuropathie paralysie laryngée juvéniles(JLPP)
H329
Neuronal Ceroid Lipofuscinosis 6 (NCL6) – Australian Shepherd
H330
Juvenile Myoclonic Epilepsy (JME) – Rhodesian Ridgeback
H335
Syndrome de mutilation acrale (MAM)
H336
Neuronal Ceroid Lipofuscinosis 8-2 (NCL8-2)
H337
Syndôme de détresse respiratoire aiguë (SDRA)
H338
Syndrome myasthénique congénital (SMC) - Labrador Retriever
H339
Polyneuropathy (LPN2) – Leonberger
H342
Fente labiale/palatine et syndactylie (CLPS)
H344
Maladie de Von-Willebrand Type 2-2
H345
Chondrodystrophy (CDDY with IVDD Risk)
H346
Glycogen Storage Disease II (GSD2, Pompe) – Dog
H347
Amelogenesis Imperfecta (AI) – Greyhound
H351
Couleur de la robe Panda "White Spotting"
H354
Dandy-Walker-Like Malformation (DWLM) / Cerebellar Hypoplasia (CH) – Eurasier
H355
Chondrodysplasia (Dwarfism)
H356
Progressive Retinal Atrophy (crd1-PRA) – American Staffordshire Terrier
H357
Progressive Retinal Atrophy (crd2-PRA) – American Pit Bull Terrier
H358
Muscular Dystrophy (MD) – Cavalier King Charles Spaniel
H359
Gangliosidosis (GM2 Type I) – Japanese Chin
H361
Hyperkératose épidermolytique
H363
Hypocatalasie ou acatalasie
H364
Hypomyelination / Shaking Puppy Syndrome (SPS) - Weimaraner
H365
Intestinal Cobalamin Malabsorption (ICM, IGS) – Beagle
H366
Intestinal Cobalamin Malabsorption (ICM, IGS) – Border Collie
H367
Inherited Myopathy of Great Danes (IMGD) / Centronuclear Myopathy (CNM, HMLR)
H368
Hereditary Nephritis (HN) – Samoyed
H370
Progressive Retinal Atrophy (Bas-PRA) - Basenji
H371
Progressive Retinal Atrophy (crd-PRA, NPHP4-related) – Dachshund
H372
Primary hyperoxaluria
H374
Ectodermal Dysplasia / Skin Fragility Syndrome – Chesapeake Bay Retriever Type
H375
Ichthyosis – American Bulldog Type
H378
Polyneuropathy (LPN1)
H379
Neuronal Ceroid Lipofuscinosis 5 (NCL5) – Golden Retriever
H380
Osteogenesis Imperfecta (OI) – Golden Retriever
H381
Progressive Retinal Atrophy (erd-PRA) - Norwegian Elkhound
H382
Primary Open Angle Glaucoma (POAG) – Norwegian Elkhound
H383
Ichthyosis – German Shepherd
H384
La dysplasie ectodermique liée au X
H385
Achromatopsia 2 (Day Blindness) – German Shepherd
H386
Maladie d'Alexander
H389
Progressive Retinal Atrophy (CNGA1-PRA) – Shetland Sheepdog
H390
Congenital Myasthenic Syndrome (CMS) – Heideterrier
H391
Canine Scott Syndrome (CSS)
H392
Coat Colour Oculocutaneous Albinism (OCA4-3)
H393
Progressive Retinal Atrophy (BBS4-PRA) – Hungarian Puli
H394
Limb-Girdle Muscular Dystrophy (LGMD) – Boston Terrier 1
H395
Neonatal Cerebellar Ataxia – Coton de Tulear and Havanese
H410
Cerebellar Ataxia – Finnish Hound
H411
Complement 3 Deficiency (C3) – Brittany Spaniel
H412
Neonatal Cortical Cerebellar Abiotrophy (NCCD) – Beagle
H413
Primary Ciliary Dyskinesia (PCD) – Old English Sheepdog
H414
Glycogen Storage Disease Ia (GSD1a)
H415
Congenital Hypothyroidism with Goiter (CHG) – Spanish Water Dog
H416
Mucopolysaccharidosis IIIa (MPS3a) - Dachshund
H418
Severe Combined Immunodeficiency (SCID) - Dog
H423
Musladin-Lueke Syndroom (MLS)
H424
Congenital Myasthenic Syndrome (CMS) - Old Danish Pointer
H425
X-linked Myotubular Myopathy (XLMTM) – Labrador Retriever
H427
Neuroaxonal Dystrophy (NAD), MFN2-related
H428
Neuronal Ceroid Lipofuscinosis 10 (NCL10) – American Bulldog
H429
Osteogenesis Imperfecta (OI) – Beagle
H430
Osteogenesis Imperfecta (OI) – Dachshund
H431
Hypomyelination / Shaking Puppy Syndrome (SPS) - English Springer Spaniel
H432
Vitamin D-Resistant Rickets (VDR) – German Spitz (Pomeranian)
H433
Déficit en facteur VII
H435
Carence en prékallikréine
H439
Glanzmann’s Thrombasthenia (GT) 1 – Dog
H440
Thrombopathia – Basset Hound
H442
Thrombopathia – American Eskimo Dog
H448
Thrombopathia – Landseer
H449
P2RY12 Receptor Platelet Disorder
H450
Progressive Retinal Atrophy (PRA3) – Tibetan Type
H373
Pyruvate Kinase Deficiency (PKDef) – Pug
H454
Pyruvate Kinase Deficiency (PKDef) – Beagle
H455
Severe Combined Immunodeficiency (SCID 2) - Dog
H456
Primary Open Angle Glaucoma (POAG) / Primary Lens Luxation (PLL) – Shar-Pei
H457
Dilated Cardiomyopathy (DCM, RBM20-related) – Schnauzer
H459
Hereditary Nasal Parakeratosis (HNPK) – Greyhound
H460
Neuroaxonal Dystrophy (NAD) – Spanish Water Dog
H462
Acrodermatite Létale (LAD)
H463
Myopathie métabolique induite par l'exercice
H467
Goniodysgenesie et glaucome
H472
Progressive Retinal Atrophy (GR-PRA2) – Golden Retriever
H473
CLAD (Canine Leukocyte Adhesion Deficiency) Type III – German Shepherd
H484
Juvenile Epilepsy (JE/BFJE) – Lagotto Romagnolo
H486
Congenital Hypothyroidism with Goiter (CHG) – Rat and Toy Fox Terrier
H488
Renal Cystadenocarcinoma and Nodular Dermatofibrosis (RCND)
H489
Gangliosidosis (GM2 Type II) – Poodle Type
H490
Hereditary Footpad Hyperkeratosis, FAM83G-related
H492
Neuronal Ceroid Lipofuscinosis 1 (NCL1) – Dachshund
H494
Polyneuropathy (AMPN) – Alaskan Malamute
H495
Primary Open Angle Glaucoma (POAG) – Beagle
H496
Dystrophic Epidermolysis Bullosa (RDEB) – Golden Retriever
H497
Myotonia Congenita – Australian Cattle Dog and Border Collie
H498
Neuronal Ceroid Lipofuscinosis 2 (NCL2) – Dachshund
H499
Polycystic Kidney Disease (PKD) – Bull Terrier
H509
Skeletal Dysplasia 2 (SD2) – Labrador Retriever
H510
Progressive Retinal Atrophy (rcd4-PRA)
H511
Inflammatory Linear Verrucous Epidermal Nevi (ILVEN) – Labrador Retriever
H625
Lagotto Storage Disease (LSD)
H627
FN, Familial Nephropathy – English Springer Spaniel
H633
Paroxysmal Dyskinesia (PD) – Irish Soft Coated Wheaten Terrier
H634
Hypophosphatasie
H636
Laryngeal Paralysis (LP) – Bull Terrier Type
H641
Von-Willebrands Disease Type 3 – Kooikerhondje
H642
Cystinuria (Type I – A) – Labrador Retriever
H643
Cystinuria (Type II – A) – Australian Cattle Dog
H644
Cystinuria (type II – B) – Miniature Pinscher
H645
Neuronal Ceroid Lipofuscinosis 8-1 (NCL8-1) – English Setter
H652
Hereditary Ataxia (RAB24-related) – Old English Sheepdog and Gordon Setter
H653
FN, Familial Nephropathy – (English) Cocker Spaniel
H676
Maladie de Von Willebrands Type 1
H677
Amelogenesis Imperfecta (AI) – Russel Terrier
H679
Amelogenesis Imperfecta (AI) – Akita
H680
Progressive Retinal Atrophy (PRA, NECAP1-related) – Schnauzer
H682
Spinocerebellar Ataxia (SCA) – Alpine Dachsbracke
H683
Warburg Micro Syndrome 1 (WARBM1)
H696
Narcolepsy – Doberman
H697
Narcolepsy – Labrador Retriever
H698
Hereditary Cataract (HC, HSF4-related)
H699
Copper Toxicosis (COMMD1 - related) – Bedlington Terrier
H701
Gangliosidosis (GM1) – Shiba Inu
H702
Cystinuria (Type I – A) – Newfoundland
H703
Narcolepsy – Dachshund
H707
CLAD (Canine Leukocyte Adhesion Deficiency) Type I – Irish Setter
H709
Glycogen Storage Disease VII (GSD7) / Phosphofructokinase Deficiency (PFK Def)
H717
Neuronal Ceroid Lipofuscinosis 5 (NCL5)
H721
L-2-Hydroxyglutaric Aciduria (L2HGA) – Staffordshire Bull Terrier
H724
Congenital Stationary Night Blindness (CSNB) - Briard
H728
CMR2 (rétinopathie multifocale canine)
H730
L'Alpha-Fucosidose
H736
Globoid Cell Leukodystrophy (GCL, Krabbes disease) – Terrier Type
H737
Myotonia Congenita – Schnauzer
H738
Progressive Retinal Atrophy (Dominant PRA) – Mastiff
H739
Pyruvate Kinase Deficiency (PKDef) – Labrador Retriever
H741
Von-Willebrands Disease Type 3 – Scottish Terrier
H744
X-Linked Severe Combined Immunodeficiency Disease (X-SCID)
H745
Malignant Hyperthermia (MH) – Dog
H746
Muscular Dystrophy (MD) – Golden Retriever
H747
Mucopolysaccharidosis VII (MPS7) – German Shepherd
H748
Centronuclear Myopathy (CNM) - Labrador Retriever
H749
Syndrome du Colley Gris (Neutropénie cyclique)
H752
Progressive Retinal Atrophy (crd4-PRA/cord1)
H766
Progressive Retinal Atrophy (rcd1-PRA) – Irish Setter
H768
Progressive Retinal Atrophy (rcd1a-PRA) – Sloughi
H769
Progressive Retinal Atrophy (rcd3-PRA)
H770
Progressive Retinal Atrophy (XL-PRA, X-Linked)
H772
Syndrome des neutrophiles piégés (TNS)
H787
Oculoskeletal Dysplasia 1 (OSD1) / Retinal Dysplasia – Labrador Retriever
H794
Neuronal Ceroid Lipofuscinosis 4A (NCL4A) – Cerebellar Ataxia
H804
Hereditary Cataract (HC, HSF4-related) – Australian Shepherd
H809
Hyperuricémie (HUU)
H811
Neonatal Encephalopathy (NEWS)
H812
Coat Colour A-Locus (Agouti) - Dog
H820
Coat Colour I-Locus (Intensity)
H821
Coat Colour D-Locus 1 - Dog
H847
Robe incorrecte/Furnishings
H848
Luxation héréditaire primaire du cristallin - PLL
H849
Progressive Retinal Atrophy (GR-PRA1) – Golden Retriever
H868
CMR1 (Canine Multifocal Rethinopathy)
H871
Pituitary Dwarfism – Shepherd Type
H872
Coat Colour Co-Locus (Cocoa)
H887
Neuroaxonal Dystrophy (NAD) - Rottweiler
H888
Bilateral Deafness and Vestibular Dysfunction (MYO7A, DINGS2) – Doberman
H889
Neuroaxonal Dystrophy (NAD) - Papillon
H890
Shar-Pei Fever (SPAID)
H891
Coat Colour Oculocutaneous Albinism (OCA2)
H894
Coat Colour D-Locus 3 - Dog
H897
Hereditary Ataxia (KCNIP4-related) – Norwegian Buhund
H905
Stargardt disease 1
H907
Polyneuropathy (GHPN) – Greyhound
H914
Progressive Retinal Atrophy (g-PRA) – Schapendoes
H915
Achromatopsia 3 (Day Blindness) – Pointer type
H918
Curly Coat (c1) – Dog
H921
Ventricular Arrhythmias and Sudden Death
H932
Haemophilia A – Rhodesian Ridgeback
H931
Modifier of Copper Toxicosis, ATP7A-related
H824
Congenital Myasthenic Syndrome (CMS) - Jack Russell Terrier
H626
Centronuclear Myopathy (CNM) - Border Collie
H663
Ehlers-Danlos Syndrome Type 1 – Labrador Retriever
H686
Elliptocytosis
H687
Muscular Dystrophy-Dystroglycanopathy (MDD) – Labrador Retriever
H688
Myotonia Congenita – Labrador Retriever
H690
Congenital Methemoglobinemia – All breeds
H694
Sensory Neuropathy - All breeds
H695
Xanthinuria, type 1 - All breeds
H671
Laryngeal paralysis and polyneuropathy, CNTNAP1-related
H693
Leukodystrophy
H708
Congenital Eye Malformation – Golden Retriever
H727
Retinal Dysplasia
H725
Inflammatory Pulmonary Disease
H726
Coat Colour Oculocutaneous Albinism (OCA1)
H751
Neurological defects with dilute coat colour
H716
Coat Colour Oculocutaneous Albinism (OCA4-1)
H715
X-linked Myotubular Myopathy (XLMTM) – Rottweiler
H776
Junctional Epidermolysis Bullosa (JEB, LAMA3-related) – Australian Cattle Dog
H718
Coat Colour Roan - Ticked
H763
Hereditary Footpad Hyperkeratosis, DSG1-related
H777
Beta-Mannosidosis – German Shepherd
H788
Xanthinuria, type 2 – Manchester Terrier
H789
Ehlers-Danlos Syndrome Type 7 – Doberman
H732
Progressive Retinal Atrophy (PRA1 Type B, HIVEP3-related) – Schnauzer
H808
Cardiomyopathy and juvenile mortality (CJM) – Belgian Shepherd
H807
Congenital Stationary Night Blindness (CSNB) – Beagle
H814
Fanconi syndrome - FS
H863
Dilated Cardiomyopathy (DCM, PLN-related) – Welsh Springer Spaniel
H865
Progressive Retinal Atrophy (BBS2-PRA) – Shetland Sheepdog
H866
Inflammatory Myopathy (Myositis)
H867
Fecundity
H869
Coat Colour Saddle tan vs black-and-tan IMPROVED
H910
Disproportionate Dwarfism
H876
Progressive Retinal Atrophy Early Onset (eo-PRA) – Spanish Water Dog
H878
Mucopolysaccharidosis VI (MPS6) – Miniature Pinscher
H886
Craniomandibular Osteopathy (CMO) – Basset Hound
H901
Haemophilia A (HEMA-2) – German Shepherd
H780
Pyruvate Kinase Deficiency (PKDef) – Basenji
H445
Coat Colour H-Locus (Harlequin)
H316
Coat Colour S-Locus (Piebald)
H326
Coat Colour D-Locus 2 - Dog
H461
Curly Coat (c2) – Dog
H681
Coat Colour K-Locus (Dominant Black)
H819
Brachyury (T-Locus, Natural Bobtail)
H487
Haemophilia A (HEMA-1) – German Shepherd
H491
Exercise Induced Collapse, EIC
H672
Degenerative Myelopathy Exon 2 (DM Exon 2)
H673
Progressive Retinal Atrophy (prcd-PRA)
H704
Collie Eye Anomaly CEA, CH
H705
Haemophilia B – Rhodesian Ridgeback
H607
Thrombocytopenia – Cavalier King Charles Spaniel
H441
Dystrophie cornéenne maculaire
H317
Degenerative Myelopathy Exon 1 (DM Exon 1) – Bernese Mountain Dog
H308
Muscular Dystrophy (MD) – Corgi
H419
Dilated Cardiomyopathy (DCM1, PDK4-related) – Doberman
H434
Coat Colour Merle
H630
Osteochondrodysplasia (OC)
H898
Achromatopsia 3 (Day Blindness)
H904
Syndrome de sécheresse oculaire robe frisé
H913
Adult Onset Deafness EAOD (4 associated markers) - Border Collie
H822
Obesity
H895
Wilson Disease, ATP7B-related
H825
Hair Length (5 variants) – Dog
H667
Ehlers-Danlos syndrome Type 1 – Dog All Breeds
H689
Junctional Epidermolysis Bullosa (JEB, LAMB3-related) – Australian Shepherd
H778
Metabolizer of a Cognitive Enhancer
H786
Paroxysmal Dyskinesia (PD) - Markiesje
H792
Abortion (embryonic lethality), BTBD17-related
H758
Coat Colour E-Locus (5 variants) - Dog
H791
Spondylocostal Dysostosis (Comma Defect)
H803
MDR1 Multi Drug Resistance – Phenobarbital Resistance (Border Collie)
H754
Coat Colour B-Locus (Brown, 4 variants) – Dog
H857
Lundehund syndrome - LS
H864
Macrothrombocytopenia (MTC)
H879
Achromatopsia 2 (Day Blindness) – Labrador Retriever
H387
May-Hegglin Anomaly (MHA) - Pug
H882
Ichthyosis type 1 & 2 - Golden Retriever
H858
Carcinome folliculaire familial de la thyroïde I & II
H713
Muscular Dystrophy (MD) – Labrador Retriever
H735
Cystinuria (Type III) – Bulldog Type
H929
Coefficient of Inbreeding
H916
Heterozygosity
H917
Hereditary Ataxia (SCA) - Australian Shepherd
H781
Mucopolysaccharidosis VII (MPS7) – Brazilian Terrier
H451
MDR1 Multi Drug Resistance - Dog
H629
Early-onset adult deafness (Rhodesian Ridgeback)
H756
Glycogen Storage Disease VII (GSD7) – Deutscher Wachtelhund
H397
Alaskan Husky Encephalopathy (AHE)
H404
Congenital Dyshormonogenic Hypothyroidism with Goiter (CDH)
H446
Limb-Girdle Muscular Dystrophy 2D (LGMD2D) – Dachshund
H816
X-linked Myotubular Myopathy (XLMTM) – Boykin Spaniel
H859
Unilateral Deafness and Vestibular Dysfunction (PTPRQ, DINGS1) – Doberman
H911
CNS Atrophy with Cerebellar Ataxia (CACA) – Belgian Shepherd
H950
Pituitary Dwarfism – Karelian Bear Dog
H951
Diffuse Cystic Renal Dysplasia and Hepatic Fibrosis
H952
Haemophilia A – Old English Sheepdog
H953
Haemophilia B – Hovawart
H954
Intestinal Cobalamin Malabsorption (ICM, IGS) – Komondor
H955
Neuronal Ceroid Lipofuscinosis 8 (NCL8) – Saluki
H958
Saluki Encephalopathy (SE)
H960
Progressive Retinal Atrophy (IFT122-PRA) – Lapponian Herder
H962
Persistent Mullerian Duct Syndrome (PMDS)
H963
Nonsyndromic Hearing Loss – Rottweiler
H965
Congenital Muscular Dystrophy (CMD) – Italian Greyhound
H967
Muscular Dystrophy (MD) – Border Collie
H912
Verrucous Epidermal Keratinocytic Nevi
H773
Leukodystrophy, TSEN54-related
H870
Haemophilia A - Boxer
H877
Osteochondromatosis
H903
Congenital Methemoglobinemia – German Spitz (Pomeranian)
H908
Australian Labradoodle dystrophinopathy
H759
Congenital Hypothyroidism with Goiter (CHG) – Tenterfield Terrier
H485
Gangliosidosis (GM1) – Portuguese Water Dog
H452
Myeloperoxidase Deficiency
H970
Pyruvate Kinase Deficiency (PKDef) – West Highland White Terrier
H971
Recessive Hypotrichosis (Hairlessness) – American Hairless Terrier
H972
Recessive Hypotrichosis (Hairlessness) – Scottish Deerhound
H973
Dental-Skeletal-Retinal Anomaly (DSRA)
H974
Hereditary Ataxia (HACE-related) – Norwegian Elkhound
H975
Haemophilia B – Lhasa Apso
H976
Haemophilia B – Newfoundland
H977
Neuronal Ceroid Lipofuscinosis 7 (NCL7)
H978
Osteogenesis Imperfecta (OI) – Chow Chow
H964
Pyruvate Dehydrogenase Phosphatase Deficiency (PDP1)
H740
Startle Disease – Miniature American Shepherd
H594
Dilated Cardiomyopathy (DCM3) – Doberman
H880
Dilated Cardiomyopathy (DCM4) – Doberman
H881
CMR3 (Canine Multifocal Retinopathy)
H300
Cerebellar Ataxia (SDCA1 + SDCA2) – Shepherd Type
H657
Glycogen Storage Disease IIIa (GSD IIIa) – Curly Coated Retriever
H813
Caractéristiques
| Breeds | |
|---|---|
| Organ | |
| specimen | Écouvillonnage, sanguin EDTA, sanguine hépariné, sperme, tissu |
Informations générales
Références
Pubmed ID:
Omia ID: