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Test inclusi
Atassia spinocerebellare (SCA) – Tipo Terrier
H303
Ichthyosis – Great Dane
H304
Osteopatia craniomandibolare (CMO) - Tipo Terrier
H312
Cortical Cerebellar Abiothrophy (NCCD) – Vizsla
H318
Dental Hypomineralization
H327
Late Onset Ataxia (LOA)
H328
Paralisi Laringea Giovanile e Polineuropatia (JLPP)
H329
Neuronal Ceroid Lipofuscinosis 6 (NCL6) – Australian Shepherd
H330
Juvenile Myoclonic Epilepsy (JME) – Rhodesian Ridgeback
H335
Acral Mutilation Syndrome (AMS)
H336
Ceroidolipofuscinosi neuronale 8-2 (NCL8-2)
H337
Sindrome da Distress Respiratorio Acuto (ARDS)
H338
Congenital Myasthenic Syndrome (CMS) - Labrador Retriever
H339
Polineuropatia (LPN2) – Leonberger
H342
Labbro leporino/Palatoschisi e Sindattilia (CLPS)
H344
Malattia di Von Willebrands tipo 2-2
H345
Chondrodystrophy (CDDY with IVDD Risk)
H346
Glycogen Storage Disease II (GSD2, Pompe) – Dog
H347
Amelogenesi imperfetta (AI) – Levriero
H351
Colore del mantello Panda White spotting
H354
Malformazione Dandy-Walker-Like (DWLM) / Ipoplasia cerebellare (CH) – Eurasier
H355
Condrodisplasia (nanismo)
H356
Progressive Retinal Atrophy (crd1-PRA) – American Staffordshire Terrier
H357
Progressive Retinal Atrophy (crd2-PRA) – American Pit Bull Terrier
H358
Distrofia Muscolare (MD) – Cavalier King Charles Spaniel
H359
Gangliosidosi (GM2 Tipo I) – Chin (Japanese Chin)
H361
Epidermolytic Hyperkeratosis
H363
Acatalasemia
H364
Ipomielinizzazione / Sindrome del cucciolo scosso (SPS) - Weimaraner
H365
Malassorbimento intestinale di cobalamina (ICM, IGS) – Beagle
H366
Malassorbimento intestinale di cobalamina (ICM, IGS) – Border Collie
H367
Inherited Myopathy of Great Danes (IMGD) / Centronuclear Myopathy (CNM, HMLR)
H368
Hereditary Nephritis (HN) – Samoyed
H370
Atrofia Progressiva della Retina (Bas-PRA) - Basenji
H371
Atrofia retinica progressiva (crd-PRA, corretalta a NPHP4) – Bassotto
H372
Iperossaluria primaria
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
Atrofia Retinica Progressiva (ERD-PRA) - Elkhound Norvegese
H382
Glaucoma primario ad angolo aperto (POAG) – Elkhound norvegese
H383
Ichthyosis – German Shepherd
H384
Displasia ectodermica legata al cromosoma X
H385
Achromatopsia 2 (Day Blindness) – German Shepherd
H386
Malattia di Alexander
H389
Atrofia progressiva della retina (CNGA1-PRA) – Cane da pastore Shetland
H390
Congenital Myasthenic Syndrome (CMS) – Heideterrier
H391
Sindrome di Scott canina (CSS)
H392
Colore del mantello Albinismo oculocutaneo (OCA4-3)
H393
Progressive Retinal Atrophy (BBS4-PRA) – Hungarian Puli
H394
Distrofia muscolare dei cingoli (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
Ipotiroidismo congenito con gozzo (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
Distrofia neuroassonale (NAD), correlata a MFN2
H428
Ceroidolipofuscinosi neuronale 10 (NCL10) – Bulldog americano
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
Carenza del fattore VII
H435
Carenza di precallicreina
H439
Trombastenia di Glanzmann (GT) 1 – Cane
H440
Trombopatia – Basset Hound
H442
Trombopatia – Cane eschimese americano
H448
Trombopatia – Landseer
H449
Disturbo piastrinico del recettore P2RY12
H450
Atrofia Progressiva della Retina (PRA3) – Tipo Tibetano
H373
Pyruvate Kinase Deficiency (PKDef) – Pug
H454
Pyruvate Kinase Deficiency (PKDef) – Beagle
H455
Immunodeficienza Combinata Grave (SCID 2) - Cane
H456
Glaucoma primario ad angolo aperto (POAG) / Lussazione primaria del cristallino (PLL) – Shar-Pei
H457
Dilated Cardiomyopathy (DCM, RBM20-related) – Schnauzer
H459
Paracheratosi nasale ereditaria (HNPK) – Levriero (Greyhound)
H460
Distrofia neuroassonale (NAD) – Perro de Agua Español
H462
Acrodermatite letale (LAD)
H463
Miopatia metabolica indotta dall'esercizio
H467
Goniodisgenesi e glaucoma
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
Ipotiroidismo congenito con gozzo (CHG) – Fox Terrier Rat e Toy
H488
Renal Cystadenocarcinoma and Nodular Dermatofibrosis (RCND)
H489
Gangliosidosi (GM2 Tipo II) – Tipo Barboncino
H490
Hereditary Footpad Hyperkeratosis, FAM83G-related
H492
Neuronal Ceroid Lipofuscinosis 1 (NCL1) – Dachshund
H494
Polyneuropathy (AMPN) – Alaskan Malamute
H495
Glaucoma primario ad angolo aperto (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
Malattia del rene policistico (PKD) – Bull Terrier
H509
Displasia scheletrica 2 (SD2) – Labrador Retriever
H510
Atrofia progressiva della retina (rcd4-PRA)
H511
Nevi epidermici verrucosi lineari infiammatori (ILVEN) – Labrador Retriever
H625
Malattia da Accumulo nel Lagotto Romagnolo (LSD)
H627
FN, Familial Nephropathy – English Springer Spaniel
H633
Paroxysmal Dyskinesia (PD) – Irish Soft Coated Wheaten Terrier
H634
Ipofosfatasia
H636
Paralisi laringea (LP) – Tipo Bull Terrier
H641
Malattia di Von-Willebrands, tipo 3 – Kooikerhondje
H642
Cistinuria (Tipo I – A) – Labrador Retriever
H643
Cistinuria (Tipo II – A) – Australian Cattle Dog
H644
Cistinuria (tipo II – B) – Pinscher nano
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
Malattia di Von Willebrand tipo 1
H677
Amelogenesi imperfetta (AI) – Russel Terrier
H679
Amelogenesi imperfetta (AI) – Akita
H680
Progressive Retinal Atrophy (PRA, NECAP1-related) – Schnauzer
H682
Spinocerebellar Ataxia (SCA) – Alpine Dachsbracke
H683
Micro sindrome di Warburg 1 (WARBM1)
H696
Narcolepsy – Doberman
H697
Narcolepsy – Labrador Retriever
H698
Cataratta ereditaria (HC, HSF4-correlata)
H699
Tossicosi da rame (COMMD1 - correlata) – Bedlington Terrier
H701
Gangliosidosi (GM1) – Shiba Inu
H702
Cistinuria (Tipo I – A) – Terranova
H703
Narcolepsy – Dachshund
H707
CLAD (deficit di adesione leucocitaria canina) di tipo I – Setter irlandese
H709
Glycogen Storage Disease VII (GSD7) / Phosphofructokinase Deficiency (PFK Def)
H717
Neuronal Ceroid Lipofuscinosis 5 (NCL5)
H721
Aciduria L-2-idrossiglutarica (L2HGA) – Staffordshire Bull Terrier
H724
Congenital Stationary Night Blindness (CSNB) - Briard
H728
CMR2 (Retinopatia Canina Multifocale)
H730
Fucosidosi
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
Malattia di Von-Willebrands di tipo 3 – Scottish Terrier
H744
X-Linked Severe Combined Immunodeficiency Disease (X-SCID)
H745
Ipertermia maligna (MH) – Cane
H746
Distrofia Muscolare (MD) – Golden Retriever
H747
Mucopolysaccharidosis VII (MPS7) – German Shepherd
H748
Centronuclear Myopathy (CNM) - Labrador Retriever
H749
Sindrome del Collie grigio (Neutropenia ciclica)
H752
Atrofia retinica progressiva (crd4-PRA/cord 1)
H766
Progressive Retinal Atrophy (rcd1-PRA) – Irish Setter
H768
Progressive Retinal Atrophy (rcd1a-PRA) – Sloughi
H769
Atrofia retinica progressiva (rcd3-PRA)
H770
Atrofia retinica progressiva (XL-PRA, X-Linked)
H772
Sindrome da intrappolamento dei neutrofili (TNS)
H787
Oculoskeletal Dysplasia 1 (OSD1) / Retinal Dysplasia – Labrador Retriever
H794
Lipofuscinosi ceroide neuronale 4A (NCL4A) – Atassia cerebellare
H804
Cataratta ereditaria (HC, HSF4) – Australian Shepherd
H809
Iperuricemia (HUU)
H811
Neonatal Encephalopathy (NEWS)
H812
Colore del mantello Locus-A (Agouti) - Cane
H820
Colore del mantello Locus-I (intensità)
H821
Colore del mantello Locus-D 1 - Cane
H847
Mantello improprio/furnishing
H848
Lussazione primaria del cristallino - PLL
H849
Progressive Retinal Atrophy (GR-PRA1) – Golden Retriever
H868
CMR1 (Retinopatia Canina Multifocale)
H871
Nanismo ipofisario – Tipo Cane da pastore
H872
Coat Colour Co-Locus (Cocoa)
H887
Distrofia neuroassonale (NAD) - Rottweiler
H888
Bilateral Deafness and Vestibular Dysfunction (MYO7A, DINGS2) – Doberman
H889
Distrofia Neuroassonale (NAD) - Papillon
H890
Febbre dello Shar-Pei (SPAID)
H891
Coat Colour Oculocutaneous Albinism (OCA2)
H894
Colore del mantello Locus-D 3 - Cane
H897
Atassia ereditaria (correlata a KCNIP4) – Buhund norvegese
H905
Stargardt disease 1
H907
Polyneuropathy (GHPN) – Greyhound
H914
Progressive Retinal Atrophy (g-PRA) – Schapendoes
H915
Achromatopsia 3 (Day Blindness) – Pointer type
H918
Mantello riccio (c1) – Cane
H921
Ventricular Arrhythmias and Sudden Death
H932
Haemophilia A – Rhodesian Ridgeback
H931
Modifier of Copper Toxicosis, ATP7A-related
H824
Sindrome miastenica congenita (CMS) - Jack Russell Terrier
H626
Centronuclear Myopathy (CNM) - Border Collie
H663
Sindrome di Ehlers-Danlos di tipo 1 – Labrador Retriever
H686
Elliptocytosis
H687
Distrofia-Distroglicanopatia Muscolare (MDD) – Labrador Retriever
H688
Myotonia Congenita – Labrador Retriever
H690
Metaemoglobinemia congenita – Tutte le razze
H694
Neuropatia sensoriale - Tutte le razze
H695
Xanthinuria, type 1 - All breeds
H671
Laryngeal paralysis and polyneuropathy, CNTNAP1-related
H693
Leukodystrophy
H708
Malformazione congenita dell'occhio – Golden Retriever
H727
Retinal Dysplasia
H725
Inflammatory Pulmonary Disease
H726
Coat Colour Oculocutaneous Albinism (OCA1)
H751
Neurological defects with dilute coat colour
H716
Colore del mantello Albinismo oculocutaneo (OCA4-1)
H715
Miopatia miotubulare legata all'X (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-mannosidosi – Pastore tedesco
H788
Xanthinuria, type 2 – Manchester Terrier
H789
Sindrome di Ehlers-Danlos tipo 7 – Dobermann
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
Sindrome di Fanconi - 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
Mucopolisaccaridosi VI (MPS6) – Pinscher nano
H886
Osteopatia cranio-mandibolare (CMO) – Basset Hound
H901
Haemophilia A (HEMA-2) – German Shepherd
H780
Pyruvate Kinase Deficiency (PKDef) – Basenji
H445
Coat Colour H-Locus (Harlequin)
H316
Colore del mantello Locus-S (Pezzato)
H326
Colore del mantello Locus-D 2 - Cane
H461
Mantello riccio (c2) – Cane
H681
Coat Colour K-Locus (Dominant Black)
H819
Brachyury (T-Locus, Bobtail naturale)
H487
Haemophilia A (HEMA-1) – German Shepherd
H491
Collasso indotto dall'esercizio, EIC
H672
Mielopatia degenerativa Esone 2 (DM Esone 2)
H673
Atrofia progressiva della retina (prcd-PRA)
H704
Anomalia dell'occhio del collie CEA, CH
H705
Haemophilia B – Rhodesian Ridgeback
H607
Trombocitopenia – Cavalier King Charles Spaniel
H441
Distrofia Corneale Maculare
H317
Mielopatia degenerativa dell'esone 1 (DM Esone 1) – Bovaro del Bernese
H308
Distrofia Muscolare (MD) – Corgi
H419
Dilated Cardiomyopathy (DCM1, PDK4-related) – Doberman
H434
Colore del mantello Merle
H630
Osteochondrodysplasia (OC)
H898
Achromatopsia 3 (Day Blindness)
H904
Sindrome del Mantello Riccio e Occhi Secchi
H913
Sordità ad esordio tardivo nell'adulto EAOD (4 marcatori associati) - Border Collie
H822
Obesity
H895
Wilson Disease, ATP7B-related
H825
Lunghezza del pelo (5 varianti) – Cane
H667
Sindrome di Ehlers-Danlos Tipo 1 – Cane di tutte le razze
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 Farmacoresistenza – Resistenza al fenobarbital (Border Collie)
H754
Colore del mantello Locus-B (Marrone, 4 varianti) – Cane
H857
Lundehund syndrome - LS
H864
Macrotrombocitopenia (MTC)
H879
Achromatopsia 2 (Day Blindness) – Labrador Retriever
H387
May-Hegglin Anomaly (MHA) - Pug
H882
Ichthyosis type 1 & 2 - Golden Retriever
H858
Carcinoma familiare a cellule follicolari tiroidee I & II
H713
Muscular Dystrophy (MD) – Labrador Retriever
H735
Cistinuria (Tipo III) – Tipo Bulldog
H929
Coefficient of Inbreeding
H916
Heterozygosity
H917
Hereditary Ataxia (SCA) - Australian Shepherd
H781
Mucopolysaccharidosis VII (MPS7) – Brazilian Terrier
H451
MDR1 Multi Resistenza ai farmaci - Cane
H629
Sordità dell'adulto ad esordio precoce (Rhodesian Ridgeback)
H756
Glycogen Storage Disease VII (GSD7) – Deutscher Wachtelhund
H397
Alaskan Husky Encephalopathy (AHE)
H404
Ipotiroidismo disormonogenico congenito con gozzo (CDH)
H446
Distrofia muscolare dei cingoli 2D (LGMD2D) – Bassotto
H816
Miopatia miotubulare legata all'X (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
Malassorbimento intestinale di cobalamina (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
Distrofia Muscolare Congenita (CMD) – Piccolo levriero italiano (Italian Greyhound)
H967
Distrofia Muscolare (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
Distrofinopatia da Labradoodle australiano
H759
Ipotiroidismo congenito con gozzo (CHG) – Tenterfield Terrier
H485
Gangliosidosis (GM1) – Portuguese Water Dog
H452
Myeloperoxidase Deficiency
H970
Pyruvate Kinase Deficiency (PKDef) – West Highland White Terrier
H971
Itricosi recessiva (assenza di peli) – American Hairless Terrier
H972
Ipotricosi recessiva (glabra) – Levriero scozzese
H973
Dental-Skeletal-Retinal Anomaly (DSRA)
H974
Atassia ereditaria (correlata all'HACE) – Elkhound norvegese
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
Malattia di Startle - American Shepherd miniatura
H594
Dilated Cardiomyopathy (DCM3) – Doberman
H880
Dilated Cardiomyopathy (DCM4) – Doberman
H881
CMR3 (retinopatia multifocale canina)
H300
Atassia cerebellare (SDCA1 + SDCA2) – Tipo Cane da pastore
H657
Malattia da accumulo di glicogeno IIIa (GSD IIIa) – Retriever a pelo riccio
H813
Specifiche
| Breeds | |
|---|---|
| Organ | |
| specimen | Tampone, Sangue in EDTA, Sangue in Eparina, Sperma, Tessuto |
Informazioni generali
Caratteristiche cliniche
Informazioni aggiuntive
Il nostro pacchetto salute contiene test che non si applicano a tutte le razze. Fare clic sui test per informazioni sull'ampia rilevanza del test.
Riferimenti
Pubmed ID:
Omia ID: