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- Aanleg zwaarlijvigheid
- Achromatopsia 2 variant 1
- Achromatopsia 2 variant 2
- Achromatopsia cd^AMAL
- Achromatopsia cd^GSPT
- Acral mutilation syndrome
- ACTH
- ACTH stimulatietest [2xS]
- Acute Respiratory Distress Syndrome
- Adult Onset Neuropathy (AON)
- Adult-onset Deafness EAOD (4 markers)
- Aerobe kultuur
- Alaskan Husky Encephalopathy
- Albumine
- Aldosteron
- Alexander disease
- Alfa-Foetoproteïne AFP
- ALP
- alpha-Mannosidosis
- ALT
- Amelogenesis imperfecta, ACPT-related
- Amelogenesis imperfecta, ENAM-related 1
- Amelogenesis imperfecta, ENAM-related 2
- Ammoniak
- Amylase
- Amylase
- Anaerobe kultuur
- Anaplasma phagocytophilum PCR
- Anaplasma phagocytophylum as (EIA)
- Anaplasma platys PCR
- Angiostrongylus vasorum ag
- Anti-2M as
- Anti-acetylcholine receptor as
- Anti-Mülleriaan hormoon (AMH)
- Anti-nucleaire factor
- Anti-thrombocyten as
- Antidiuretisch hormoon
- aPTT + PT
- Ascites
- Aspergillus as
- Aspergillus PCR
- AST
- AST
- Ataxia, HACE1-related
- Autopsie (excl bijkomend OZ)
- Autopsie Unif (excl bijkomend OZ)
- Babesia canis as (EIA)
- Babesia PCR
- Bactec
- Bardet-Biedl syndrome 2
- Bartonella hensellae PCR
- Beenmergcytologie
- Benign juvenile epilepsy
- Benign juvenile epilepsy
- Beperkte screening Hond
- Beta-mannosidosis
- Bicarbonaat
- Bilirubine
- Bilirubine totaal
- Bloedgroep Hond
- Bordetella bronchoseptica PCR
- Borrelia as (IF)
- Borrelia as (Western Blot)
- Borrelia PCR
- Brachyury
- Brucella canis as (AT)
- Brucella canis as (IF)
- Brucella PCR
- Bunny Hopping Syndrome 1 NEW
- C-Reactive Protein
- Calcium
- Calcium geïoniseerd
- Campylobacter kultuur
- Canine Multifocal Retinopathy (CMR) 1
- Canine Multifocal Retinopathy (CMR) 2
- Carcino-embryonaal antigen (CEA)
- Cardiac Laminopathy NEW
- Cardiomyopathie met juveniele mortaliteit
- CAV (adeno) as (IF)
- CAV-1 (adeno) PCR
- CB Akita
- CB Beauceron NEW
- CBC (telling+diff+retic)
- CCoV (corona) PCR
- CDV (distemper) PCR
- CDV (hondenziekte) as (IF)
- Celtelling
- Centronuclear myopathy
- Centronuclear Myopathy, DNM2
- Centronuclear Myopathy, HACD1
- Cerebellar Abiotrophy (NCCD)
- Cerebellar Ataxia (SDCA1+SDCA2)
- Cerebellar Ataxia GRM1-related
- Cerebellar Ataxia KCNIP4-related
- Cerebellar Ataxia RAB24-related
- Cerebellar Ataxia SEL1L-related
- Cerebellar Cortical Degeneration
- Cerebellar Degeneration-Myositis Complex NEW
- Cerebellar hypoplasia RELN-related
- Cerebellar Hypoplasia VLDLR
- Cerebral dysfunction
- Chlamydia spp. PCR
- Chloride
- Cholesterol
- Cholesterol/Triglyceriden
- Cholinesterase
- Chondrodysplasia
- CHV (herpes) as (IF)
- CHV (herpes) PCR
- CLAD Type I
- CLAD Type III
- Cleft Lip, Palate and Syndactyly
- CNS atrophy, cerebellar ataxia
- Collie Eye Anomaly (CEA)
- CombiBreed Alaska-malamute UPDATED
- CombiBreed Amerikaanse buldog
- CombiBreed Amerikaanse cockerspaniël
- CombiBreed Amerikaanse staffordshireterriër UPDATED
- CombiBreed Aussiedoodle NEW
- CombiBreed Australische Cobberdog
- CombiBreed Australische herder UPDATED
- CombiBreed Australische veedrijvershond UPDATED
- CombiBreed Barbet NEW
- CombiBreed Basenji UPDATED
- CombiBreed Basset Hound
- CombiBreed Beagle UPDATED
- CombiBreed Bearded Collie
- CombiBreed Belgische herder UPDATED
- CombiBreed Bernedoodle
- CombiBreed Berner sennenhond
- CombiBreed Bichon Frisé
- CombiBreed Bloedhond
- CombiBreed Bordeauxdog
- CombiBreed Bordercollie UPDATED
- CombiBreed Bostonterriër
- CombiBreed Boxer UPDATED
- CombiBreed Bullmastiff UPDATED
- CombiBreed Bulterriër UPDATED
- CombiBreed Cairnterriër UPDATED
- CombiBreed Cane corso
- CombiBreed Cavalier King Charles-spaniël UPDATED
- CombiBreed Cavapoo
- CombiBreed Chihuahua UPDATED
- CombiBreed Chinese gekuifde naakthond
- CombiBreed Cockapoo
- CombiBreed Collie, gladharig
- CombiBreed Collie, ruwharig UPDATED
- CombiBreed Continentale dwergspaniel
- CombiBreed Continentale dwergspaniel (Phalène)
- CombiBreed Coton de Tulear
- CombiBreed Curly coated retriever UPDATED
- CombiBreed Dalmatiër UPDATED
- CombiBreed Dobermann UPDATED
- CombiBreed Duitse Dog UPDATED
- CombiBreed Duitse Herder UPDATED
- CombiBreed Duitse spitz
- CombiBreed Duitse staande hond, korthaar
- CombiBreed Duitse staande hond, langhaar
- CombiBreed Dwergpinscher
- CombiBreed Engelse buldog
- CombiBreed Engelse cockerspaniël + AON
- CombiBreed Engelse cockerspaniël UPDATED
- CombiBreed Engelse setter NEW
- CombiBreed Engelse springerspaniël UPDATED
- CombiBreed Epagneul breton
- CombiBreed Finse lappenhond
- CombiBreed Franse buldog UPDATED
- CombiBreed Golden retriever
- CombiBreed Goldendoodle
- CombiBreed Gordon Setter
- CombiBreed Griffon Bruxellois
- CombiBreed Grote Zwitserse sennenhond
- CombiBreed Health Hond UPDATED
- CombiBreed Hollandse herder
- CombiBreed Hongaarse Vizsla, draadharig
- CombiBreed Hovawart NEW
- CombiBreed Ierse setter
- CombiBreed Ierse terriër
- CombiBreed Irish soft-coated wheaten terriër
- CombiBreed Italiaans windhondje
- CombiBreed Jackrussellterriër
- CombiBreed Kooikerhondje
- CombiBreed Labernese
- CombiBreed Labradoodle
- CombiBreed Labrador UPDATED
- CombiBreed Lagotto romagnolo
- CombiBreed Landseer UPDATED
- CombiBreed Leonberger
- CombiBreed Lhasa Apso
- CombiBreed Maltezer
- CombiBreed Manchesterterriër UPDATED
- CombiBreed Markiesje
- CombiBreed Mastiff
- CombiBreed Miniatuur Bulterriër
- CombiBreed Mopshond
- CombiBreed Newfoundlander
- CombiBreed Noorse Elkhound
- CombiBreed Norfolkterriër
- CombiBreed Nova Scotia duck tolling retriever + DEN
- CombiBreed Nova Scotia duck tolling retriever UPDATED
- CombiBreed Old English Sheepdog (Bobtail)
- CombiBreed Parson Russell-terriër
- CombiBreed Patent Pack Hond
- CombiBreed Poedel
- CombiBreed Pomeranian
- CombiBreed Pomsky
- CombiBreed Portugese waterhond
- CombiBreed Pyrenese berghond
- CombiBreed Rhodesian Ridgeback
- CombiBreed Rottweiler
- CombiBreed Saarlooswolfhond UPDATED
- CombiBreed Samojeed
- CombiBreed Schapendoes
- CombiBreed Schipperke
- CombiBreed Schnauzer UPDATED
- CombiBreed Shar Pei
- CombiBreed Shetland Sheepdog
- CombiBreed Shiba Inu
- CombiBreed Shih tzu
- CombiBreed Siberische husky
- CombiBreed Sint-bernard
- CombiBreed Spaanse waterhond
- CombiBreed Staffordshire-Bulterriër
- CombiBreed Teckel
- CombiBreed Tibetaanse spaniël
- CombiBreed Tibetaanse terriër
- CombiBreed Toy Poedel NEW
- CombiBreed Vacht Hond UPDATED
- CombiBreed Vizsla, kortharig
- CombiBreed Weimaraner UPDATED
- CombiBreed Welsh corgi Pembroke
- CombiBreed Welsh terriër
- CombiBreed West Highland white terriër
- CombiBreed Whippet
- CombiBreed Yorkshireterriër UPDATED
- CombiBreed Zwitserse witte herder
- Complement 3 Deficiency
- Cone-rod dystrophy 1 (crd1)
- Cone-rod dystrophy 2 (crd2)
- Cone-rod dystrophy 4
- Cone-rod dystrophy, NPHP4-related
- Congenital Stationary Night Blindness, LRIT3-related
- Congenital Stationary Night Blindness, RPE65-related
- Coombs direct
- Copper toxicosis (Wilson), COMMD1-related
- Copper toxicosis low risk 1
- Copper toxicosis low risk 1
- Copper toxicosis low risk 1
- Copper toxicosis Pakket NEW
- Corona ag
- Cortisol basaal
- Cortisol na dexa [3xS]
- Cortisol/creatinine urine
- COX-2 expressie
- CPiV (parainfluenza) PCR
- cPLI
- cPSE
- CPV (parvo) as (IF)
- CPV (parvo) PCR
- Craniomandibular osteopathy – Basset
- Craniomandibular Osteopathy – Terriër
- Creatine kinase (CK)
- Creatine kinase (CK)
- Creatinine
- Cryptosporidium PCR
- CSV
- cTLI
- cTSH
- CYP1A2 deficiency
- Cystatine C
- Cystatine C:creatinine urine
- Cystinuria Bulldog-type
- Cystinuria I – A – 1
- Cystinuria type I – A – 2
- Cystinuria type II – A
- Cystinuria type II – B
- Cytologie
- Cytologie cytospin
- Cytologie hemato
- Deafness, EPS8L2-related (EOAD)
- Deafness, LOXHD1-related
- Deafness, MYO7A-related
- Deafness, PTPRQ-related
- Degenerative Myelopathy (DM Exon 1)
- Degenerative Myelopathy (DM Exon 2)
- Dental Hypomineralization (Raine Syndrome)
- Dental-Skeletal-Retinal Anomaly
- Dermatofyten (schimmel) PCR
- Diagnose chronische diarree Hond
- Diagnose hypothyroïdie Hond
- Diagnose Pu/Pd Hond
- Diarree mestprofiel Hond
- Digoxine
- Dilated cardiomyopathy ABCC9-related
- Dilated Cardiomyopathy PDK4-related
- Dilated cardiomyopathy PLN-related
- Dilated Cardiomyopathy RBM20-related
- Dilated Cardiomyopathy Risk1 NEW
- Dilated Cardiomyopathy Risk2 NEW
- Dilated Cardiomyopathy TTN-related
- Diluted coat with neurologic defects
- Dirofilaria PCR
- DNAprofiel SNP (ASCA)
- DNAprofiel SNP (ASCA) + ouderschap
- DNAprofiel SNP (ISAG)
- DNAprofiel STR (ISAG)
- DNAprofiel STR + Ouderschap Hond
- DNAprofiel STR + SNP (ISAG)
- Dry Eye Curly Coat Syndrome
- Dyserythropoietic Anemia and Myopathy Syndrome 1
- Dyserythropoietic Anemia and Myopathy Syndrome 2 NEW
- Dystrophic epidermolysis bullosa 1
- Ectodermal dysplasia
- Ectodermal dysplasia X-linked
- Ectoparasieten
- Ehlers-Danlos syndrome type 7
- Ehlers-Danlos syndrome type1 1
- Ehlers-Danlos syndrome type1 2
- Ehrlichia canis as (EIA)
- Ehrlichia PCR
- Eiwit + elektroforese
- Eiwit totaal
- Eiwit totaal
- Eiwit/creatinine urine
- Eiwitelektroforese
- Elliptocytosis
- Embryonic lethality, BTBD17-related
- Endoparasieten (Wo+Fl+Co)
- Epidermal keratinocytic nevi, verrucous 1,2
- Epidermal keratinocytic nevi, verrucous 3
- Epidermolysis bullosa simplex
- Epilepsy, myoclonic (JME)
- Episodic Falling
- Erytropoëtine
- Exercise Induced Collapse (EIC)
- Exercise induced metabolic myopathy
- Exfoliative cutaneous Lupus erythematosus
- Eye malformation
- Factor IX
- Factor VII deficiency
- Factor VIII
- Faeces BO
- Familial Nephropathy variant 1
- Familial Nephropathy variant 2
- Fanconi syndrome
- Fecundity
- Fenobarbital
- Fenobarbital resistentie
- Fibrinogeen+D-dimeren
- Fit-4-Life
- Folaat
- Fosfaat
- Fosfaatesters
- Fructosamine
- Fucosidosis
- Gallbladder Mucocele
- Galzuren
- Galzuren t0+t2
- Gangliosidosis GM2 type IB
- Gangliosidosis GM2 type II
- Gangliosidosis, GM1 – Portugese waterhond
- Gangliosidosis, GM1 – Shiba
- Gekrulde Vacht 1
- Gekrulde Vacht 2
- Genitaal BO
- Genitaal mycologisch onderzoek
- Gewrichtsvocht
- GGT
- GGT/creatinine urine
- Giardia PCR
- Giardia zoönitische stam PCR
- GLDH
- Globoid Cell Leukodystrophy
- Glucose
- Glucose
- Glutengevoeligheid
- Glycogen Storage Disease Ia
- Glycogen Storage Disease II
- Glycogen storage disease VII 1
- Glycogen storage disease VII 2
- Goniodysgenesis and glaucoma
- Gray Collie Syndrome (Cyclic Neutropenia)
- Haemophilia A – Boxer
- Haemophilia A – Duitse herder 1
- Haemophilia A – Duitse herder 2
- Haemophilia A – Old English Sheepdog
- Haemophilia A – Rhodesian Ridgeback
- Haemophilia A 6
- Haemophilia B – Cairnterriër
- Haemophilia B – Hovawart
- Haemophilia B – Lhasa Apso
- Haemophilia B – Newfoundlander
- Haemophilia B – Rhodesian Ridgeback
- Hemokultuur
- Hepatorenal fibrocystic disease
- Hepatozoon PCR
- Hereditary Cataract (HSF4) 1
- Hereditary Cataract (HSF4) 2
- Histopathologie Bioptie
- Hond – Atopie
- Hond – Mastocytoma
- Huid BO
- Hyperekplexia
- Hyperkeratosis, epidermolytic
- Hyperkeratosis, palmoplantar FAM83G-related
- Hyperkeratosis, palmoplantar KRT16-related
- Hyperkeratosis, palmoplantar, DSG1-related
- Hypocatalasia
- Hypocatalasia
- Hypomyelination
- Hyposegmentation of granulocytes NEW
- Hypothyroidism SLC5A5-related
- Hypothyroidism TPO-related 1
- Hypothyroidism TPO-related 2
- Hypothyroidism TPO-related 3
- Hypothyroidism TPO-related 4
- Hypotrichosis, recessive 1
- Hypotrichosis, recessive 2
- Ichthyosis, ASPRV1-related
- Ichthyosis, NIPAL4-related
- Ichthyosis, SLC27A4-related
- Ichthyosis, type 1 & 2 Golden Retriever
- IgA
- IgA
- IGF-1
- IgG + IgM
- Ijzer
- Immuno-histochemie
- Immunodeficiency (MAC) NEW
- Immunoscreen 12
- Immunoscreen 12
- Immunoscreen 24
- Immunoscreen 24
- Immunoscreen Labrador Nauka Dx
- Improper Coat / Furnishings
- Infectieus hoestprofiel Hond
- Inflammatory myopathy
- Inflammatory pulmonary disease
- Influenza A PCR
- Insecticiden
- Insuline
- Intervertebral Disc Disease
- Intestinal Cobalamin Malabsorption 1
- Intestinal Cobalamin Malabsorption 2
- Intestinal Cobalamin Malabsorption 3
- Junctional epidermolysis bullosa, LAMA3-related 1
- Junctional epidermolysis bullosa, LAMA3-related 2
- Junctional Epidermolysis Bullosa, LAMB3-related
- Juvenile Laryngeal Paralysis Polyneuropathy
- Kalium
- KBr
- Koper
- L-2-Hydroxyglutaric aciduria – Bulldog type
- Lactaat
- Lafora Disease
- Lagotto storage disease
- Laryngeal paralysis (LP)
- Laryngeal paralysis/polyneuropathy
- LDH
- LDH
- Leishmania as sneltest
- Leishmania as titer (EIA)
- Leishmania as titer (IF)
- Leishmania PCR
- Leptospira as titer (MAT)
- Leptospira IgM (sneltest)
- Leptospira PCR
- Lethal Acrodermatitis
- Leukodystrophy, CYTB-related
- Leukodystrophy, TSEN54-related
- Leukoencephalomyelopathy 1
- Leukoencephalomyelopathy 2
- LH
- Lichaamsgrootte NEW
- Limb girdle muscular dystrophy (LGMD2F)
- Lipase
- Longwormen
- Lood
- Lundehund syndrome
- Lysosomal Storage Disease NEW
- Macrothrombocytopenia – CKC type
- Macrothrombocytopenia – Terriër type
- Macular Corneal Dystrophy
- Magnesium
- Maligne Hyperthermia
- Mangaan
- May-Hegglin anomaly
- MCAD Deficiency
- Methaemoglobinaemia 1
- Methaemoglobinaemia 2
- Microphtalmia
- Mitochondrial Fission Encephalopathy NEW
- Monitoring bijnier Hond
- Monitoring diabetes
- Monitoring epilepsie Hond
- Monitoring lever
- Monitoring nier Hond
- Monitoring schildklier Hond
- Mucopolysaccharidose VII – 2
- Mucopolysaccharidosis I 1
- Mucopolysaccharidosis I 2
- Mucopolysaccharidosis IIIa
- Mucopolysaccharidosis VI 1
- Mucopolysaccharidosis VI 2
- Mucopolysaccharidosis VII
- Multidrug resistance 1 (MDR1)
- Multifocal retinopathy 3 (2 variants)
- Muscular dystrophy
- Muscular Dystrophy 1
- Muscular Dystrophy 2
- Muscular Dystrophy 3
- Muscular dystrophy 4
- Muscular dystrophy 5
- Muscular dystrophy-dystroglycanopathy
- Muscular dystrophy, COL6A1-related
- Muscular dystrophy, LAMA2-related
- Muscular dystrophy, Ullrich
- Muscular hypertrophy (double muscling)
- Musladin-Lueke syndrome (MLS)
- Myasthenic Syndrome, CHAT-related
- Myasthenic syndrome, CHRNE-related 1
- Myasthenic syndrome, CHRNE-related 2
- Myasthenic syndrome, COLQ-related
- Mycoplasma spp. PCR
- Myeloencephalopathy, PNPLA8
- Myeloperoxidase deficiency
- Myotonia Congenita 1
- Myotonia Congenita 2
- Myotonia congenita 3
- Myotubular myopathy 1
- Myotubular myopathy 2
- Myotubular myopathy 3
- Narcolepsy 1
- Narcolepsy 2
- Narcolepsy 3
- Nasal parakeratosis 1
- Nasal parakeratosis 2
- Natrium
- Necrotizing Myelopathy
- Nemaline myopathy
- Neonatal Encephalopathy
- Neospora caninum as (IF)
- Neospora caninum PCR
- Nephritis
- Neuroaxonal Dystrophy (NAD) MFN2
- Neuroaxonal dystrophy PLA2G6
- Neuroaxonal dystrophy RNF170 NEW
- Neuroaxonal dystrophy TECPR2
- Neuroaxonal dystrophy VPS11
- Neurologisch CSV-profiel Hond
- Neuronal ceroid lipofuscinosis 1 – Cane corso
- Neuronal ceroid lipofuscinosis 1 – Teckel
- Neuronal ceroid lipofuscinosis 10
- Neuronal ceroid lipofuscinosis 12 – Australian Cattle Dog
- Neuronal ceroid lipofuscinosis 12 – Tibetaanse terriër
- Neuronal ceroid lipofuscinosis 2
- Neuronal ceroid lipofuscinosis 4A
- Neuronal ceroid lipofuscinosis 5
- Neuronal ceroid lipofuscinosis 5 – Golden retriever
- Neuronal ceroid lipofuscinosis 6
- Neuronal Ceroid Lipofuscinosis 7
- Neuronal ceroid lipofuscinosis 8 – 2
- Neuronal ceroid lipofuscinosis 8 – Saluki
- Neuronal ceroid lipofuscinosis, 8 – 1
- Neus BO
- Neus MO
- Nier diagnoseprofiel
- NT-proBNP (quant)
- Obesitas predispositie
- Occult bloed
- Oculocutaneous albinism OCA2
- Oculocutaneous albinism OCA4 1
- Oculocutaneous albinism OCA4 2
- Oculoskeletal Dysplasia / Retinal Dysplasia
- Oculoskeletal dysplasia 3
- Oestradiol
- Oog BO
- Oor BO + gisten
- Orofarynx BO
- Osmolaliteit
- Osmolaliteit urine
- Osteochondrodysplasia
- Osteochondromatosis
- Osteogenesis imperfecta 1
- Osteogenesis imperfecta 2
- Osteogenesis imperfecta 3
- Osteogenesis imperfecta 4
- P2RY12 bleeding disorder
- Papillomavirus PCR
- Paradoxical pseudomyotonia
- Paroxysmal Dyskinesia, PIGN-related
- Paroxysmal dyskinesia, SOD1
- Paroxysmal Exercise-Induced Dyskinesia 1
- Paroxysmal Exercise-Induced Dyskinesia 2
- Parvovirus ag
- PCR Antigen Receptor Rearrangements (PARR)
- PCYT2 deficiency
- Persistent Mullerian Duct Syndrome
- Pituitary dwarfism LHX3-related
- Pituitary dwarfism POU1F1
- Pleuraalvocht
- Pleuraalvocht 2 (vocht+serum)
- Polycystic kidney disease (PKD1)
- Polydactyly
- Polyneuropathy SBF2
- Polyneuropathy, ARHGEF10-related
- Polyneuropathy, GJA9-related
- Polyneuropathy, NDRG1-related 1
- Polyneuropathy, NDRG1-related 2
- Prekallikrein deficiency
- Primary ciliary dyskinesia (PCD), NME5-related
- Primary ciliary dyskinesia 3
- Primary ciliary dyskinesia, CCDC39-related
- Primary glaucoma ADAMTS10 1
- Primary glaucoma ADAMTS10 2
- Primary glaucoma ADAMTS17 1
- Primary glaucoma ADAMTS17 2
- Primary glaucoma ADAMTS17 3
- Primary Hyperoxaluria
- Primary Lens Luxation (PLL)
- Progesteron
- Progressive Retinal Atrophy BBS4-related
- Progressive Retinal Atrophy CCDC66-related
- Progressive Retinal Atrophy CNGA1-related
- Progressive Retinal Atrophy CNGB1-related
- Progressive Retinal Atrophy FAM161A-related
- Progressive Retinal Atrophy IFT122-related
- Progressive Retinal Atrophy JPH2-related
- Progressive Retinal Atrophy NECAP1-related
- Progressive Retinal Atrophy PDE6B-related
- Progressive Retinal Atrophy PRCD-related
- Progressive Retinal Atrophy RHO-related
- Progressive Retinal Atrophy SAG-related
- Progressive Retinal Atrophy SLC4A3-related
- Progressive Retinal Atrophy STK38L-related
- Progressive Retinal Atrophy TTC8-related
- Progressive Retinal Atrophy Type B1 HIVEP3-related
- Progressive Retinal Atrophy X-linked, RPGR-related
- PTH intact
- PTH-rP
- Punctievocht BO
- Pyruvate dehydrogenase deficiency
- Pyruvate kinase deficiency – Basenji
- Pyruvate kinase deficiency – Beagle
- Pyruvate kinase deficiency – Labrador
- Pyruvate kinase deficiency – Mops
- Pyruvate kinase deficiency – Westie
- Ras Identificatie Hond
- Relaxine
- Renal Cystadenocarcinoma, Nodular Dermatofibrosis
- Reproductieprofiel Hond
- Respiratoir PCR-profiel Hond
- Reticulocyten
- Retinal dysplasia
- Reumafactor
- Rickettsia conorii as (IF)
- Rickettsia PCR
- Rickettsia rickettsii as (IF)
- Rod-cone dysplasia 1 (rcd1)
- Rod-cone dysplasia 1a (rcd1a)
- Rod-cone dysplasia 3 (rcd3)
- Rod-cone dysplasia 4 (rcd4)
- Rotavirus ag
- Sarcoptes as
- SARS-Cov-2 PCR
- Schimmel/gist kultuur
- Scott syndrome
- SDMA
- Selenium
- Senior screening Hond
- Sensitest voeding IgE/IgG Hond
- Sensory Neuropathy 1
- Sensory Neuropathy 2
- Severe Combined Immuno Deficiency 1
- Severe Combined Immuno Deficiency 2
- Shar-Pei Fever (SPAID)
- Skeletal dysplasia COL11A2-related
- Skeletal dysplasia, PCYT1A-related
- Spinal Dysraphism
- Spinocerebellar ataxia CAPN1-related
- Spinocerebellar ataxia KCNJ10-related
- Spinocerebellar ataxia SCN81-related
- Spoeling
- Spoeling BO
- Spondylocostal dysostosis
- Spongiform Leukoencephalomyelopathy NEW
- Stargardt disease 1
- Steenanalyse
- Stollingsprofiel
- Strychnine
- Succinic Semialdehyde Dehydrogenase
Deficiency
- Surfactant metabolism dysfunction
- T3 totaal (Triiodothyronine)
- T3 vrij
- Taurine
- TBEV as (IF)
- TBEV IgG (EIA)
- Teek PCR-profiel
- Tekenserologie hond
- Testosteron
- Thallium
- Thrombasthenia 1
- Thrombasthenia 2
- Thromboelastografie
- Thrombopathia 1
- Thrombopathia 2
- Thrombopathia 3
- Thymidinekinase
- Thyroglobuline as
- Thyroid follicular cell carcinoma
- Thyroxine totaal (T4)
- Thyroxine vrij
- Tick-borne Encephalitis Virus (TBEV) PCR
- Toxoplasma as (EIA)
- Toxoplasma gondii PCR
- Trapped Neutrophil Syndrome (TNS)
- Tremor, X-linked
- Triglyceriden
- Troponine I
- Upper airway syndrome
- Ureum
- Ureum
- Urine BO
- Urine sediment + biochemie
- Urineonderzoek
- Urinezuur
- Urolthiasis (HUU)
- Vaccinatiestatus Hond
- Vachtkleur A-locus
- Vachtkleur B-locus
- Vachtkleur Cocoa
- Vachtkleur D-locus 1
- Vachtkleur D-locus 2
- Vachtkleur D-locus 3
- Vachtkleur E-locus
- Vachtkleur H-locus
- Vachtkleur Himalayan
- Vachtkleur I-locus
- Vachtkleur K-locus
- Vachtkleur Merle
- Vachtkleur Panda White Spotting
- Vachtkleur Roan
- Vachtkleur S-locus Piebald
- Vachtkleur Saddle tan/black-and-tan
- Vachtlengte Hond
- Vachttype SD-Locus NEW
- Vector-borne ziektes Hond
- Ventricular Arrythmias
- Vertering
- Vitamin D-deficiency rickets Type II
- Vitamine B12
- Vitamine D
- Volledige screening Hond
- Von Willebrand Disease Type I
- Von Willebrand Disease Type II – 2
- Von Willebrand Disease Type III – 1
- Von Willebrand disease Type III – 2
- Voucher
- vWF ag
- Warburg Micro Syndrome 1 (WARBM1)
- Wonde/Abces BO
- X-linked severe combined immunodeficiency disease
- Xanthinuria type II 3
- Xanthinuria, type I
- Xanthinuria, type II 1
- Xanthinuria, type II 2
- Zink
