Alle testen voor genetische ziektes van je honden
Wil je meer dan 2 testen bestellen? Bekijk dan zeker ook onze voordelige pakketen.
- Acute Respiratory Distress Syndrome
- Degenerative Encephalopathy (DEN) NEW
- Skeletal dysplasia, PCYT1A-related
- Alexander disease
- Amelogenesis imperfecta, ENAM-related 1
- Amelogenesis imperfecta, ENAM-related 2
- Amelogenesis imperfecta, ACPT-related
- Methaemoglobinaemia 2
- Achromatopsia 2 variant 1
- Sensory Neuropathy 2
- Muscular dystrophy-dystroglycanopathy
- Ehlers-Danlos syndrome type1 2
- Ehlers-Danlos syndrome type1 1
- Xanthinuria, type I
- Elliptocytosis
- Myotonia congenita 3
- Achromatopsia 2 variant 2
- Achromatopsia cd^AMAL
- Acral mutilation syndrome
- Adult Onset Neuropathy (AON)
- P2RY12 bleeding disorder
- Brachyury
- Complement 3 Deficiency
- Canine Multifocal Retinopathy (CMR) 1
- Canine Multifocal Retinopathy (CMR) 2
- Cardiomyopathie met juveniele mortaliteit
- Centronuclear Myopathy, HACD1
- Centronuclear Myopathy, DNM2
- Cerebellar Abiotrophy (NCCD)
- Adult-onset Deafness EAOD (4 markers)
- Neuronal ceroid lipofuscinosis 4A
- Cerebellar Ataxia (SDCA1+SDCA2)
- Cerebellar Ataxia KCNIP4-related
- Cerebellar Ataxia GRM1-related
- Cerebellar Ataxia RAB24-related
- Cerebellar Ataxia SEL1L-related
- Deafness, EPS8L2-related (EOAD)
- Cerebellar Cortical Degeneration
- Cerebellar Hypoplasia VLDLR
- Chondrodysplasia
- Intervertebral Disc Disease
- CLAD Type I
- Muscular dystrophy 4
- CLAD Type III
- Cleft Lip, Palate and Syndactyly
- Collie Eye Anomaly (CEA)
- Achromatopsia cd^GSPT
- Cone-rod dystrophy 1 (crd1)
- Cone-rod dystrophy 2 (crd2)
- Epidermal keratinocytic nevi, verrucous 3
- Hypothyroidism TPO-related 1
- Hypothyroidism TPO-related 2
- Cystinuria Bulldog-type
- Hypothyroidism TPO-related 4
- Hypothyroidism TPO-related 3
- Congenital Stationary Night Blindness, RPE65-related
- Congenital Stationary Night Blindness, LRIT3-related
- Copper toxicosis (Wilson), COMMD1-related
- Craniomandibular Osteopathy - Terriër
- Cone-rod dystrophy 4
- Cystinuria I - A - 1
- Cystinuria type II - A
- Cystinuria type I - A - 2
- Cystinuria type II - B
- Degenerative Myelopathy (DM Exon 2)
- Degenerative Myelopathy (DM Exon 1)
- Dental Hypomineralization (Raine Syndrome)
- Renal Cystadenocarcinoma, Nodular Dermatofibrosis
- Dilated Cardiomyopathy PDK4-related
- Dilated Cardiomyopathy RBM20-related
- Dilated Cardiomyopathy TTN-related
- Progressive Retinal Atrophy RHO-related
- Dry Eye Curly Coat Syndrome
- Ectodermal dysplasia
- Dystrophic epidermolysis bullosa 1
- Benign juvenile epilepsy
- Epilepsy, myoclonic (JME)
- Episodic Falling
- Exercise induced metabolic myopathy
- Exercise Induced Collapse (EIC)
- Haemophilia B - Rhodesian Ridgeback
- Haemophilia B - Hovawart
- Factor VII deficiency
- Familial Nephropathy variant 1
- Familial Nephropathy variant 2
- Fucosidosis
- Thyroid follicular cell carcinoma
- Gallbladder Mucocele
- Gangliosidosis GM2 type IB
- Gangliosidosis GM2 type II
- Progressive Retinal Atrophy CCDC66-related
- Globoid Cell Leukodystrophy 1
- Glycogen Storage Disease Ia 1
- Glycogen Storage Disease II
- Glycogen storage disease VII 1
- Gangliosidosis, GM1 - Shiba
- Progressive Retinal Atrophy SLC4A3-related
- Progressive Retinal Atrophy TTC8-related
- Goniodysgenesis and glaucoma
- Gray Collie Syndrome (Cyclic Neutropenia)
- Haemophilia A - Duitse herder 1
- Haemophilia A - Duitse herder 2
- Haemophilia A - Rhodesian Ridgeback
- Ventricular Arrythmias
- Hereditary Cataract (HSF4) 1
- Hereditary Cataract (HSF4) 2
- Nasal parakeratosis 2
- Nasal parakeratosis 1
- Hyperkeratosis, epidermolytic
- Hyperkeratosis, palmoplantar FAM83G-related
- Hyperkeratosis, palmoplantar KRT16-related
- Urolthiasis (HUU)
- Hypocatalasia
- Hypophosphatasia
- Hypomyelination
- Ichthyosis, SLC27A4-related
- Ichthyosis, NIPAL4-related
- Ichthyosis, ASPRV1-related
- Juvenile Laryngeal Paralysis Polyneuropathy
- Limb girdle muscular dystrophy (LGMD2F)
- L-2-Hydroxyglutaric aciduria - Bulldog type
- Lafora Disease
- Lagotto storage disease
- Lethal Acrodermatitis
- Macular Corneal Dystrophy
- Maligne Hyperthermia
- Microphtalmia, RBP-related
- Multidrug resistance 1 (MDR1)
- Myotubular myopathy 1
- Myotubular myopathy 2
- Mucopolysaccharidose VII - 2
- Mucopolysaccharidosis IIIa
- Mucopolysaccharidosis VII
- Muscular Dystrophy 3
- Muscular Dystrophy 2
- Muscular Dystrophy 1
- 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
- Centronuclear myopathy
- Myotonia Congenita 1
- Myotonia Congenita 2
- Narcolepsy 1
- Neuroaxonal Dystrophy (NAD) MFN2
- Narcolepsy 2
- Neuroaxonal dystrophy PLA2G6
- Narcolepsy 3
- Neuroaxonal dystrophy TECPR2
- Neonatal Encephalopathy
- Nephritis
- Neuroaxonal dystrophy VPS11
- Neuronal ceroid lipofuscinosis 1 - Teckel
- Neuronal ceroid lipofuscinosis 2
- Neuronal ceroid lipofuscinosis 5
- Neuronal ceroid lipofuscinosis 5 - Golden retriever
- Neuronal ceroid lipofuscinosis 6
- Neuronal ceroid lipofuscinosis 8 - 2
- Neuronal ceroid lipofuscinosis 10
- Neuronal ceroid lipofuscinosis 12 - Tibetaanse terriër
- Neuronal ceroid lipofuscinosis, 8 - 1
- Obesitas predispositie
- Oculocutaneous albinism OCA2
- Deafness, MYO7A-related
- Leukoencephalomyelopathy 1
- Oculocutaneous albinism OCA4 1
- Shar-Pei Fever (SPAID)
- Osteogenesis imperfecta 1
- Osteogenesis imperfecta 2
- Osteogenesis imperfecta 3
- Copper toxicosis low risk 1
- Copper toxicosis Pakket
- Copper toxicosis low risk 1
- Osteochondrodysplasia
- Progressive Retinal Atrophy CNGB1-related
- Progressive Retinal Atrophy Type B1 HIVEP3-related
- Paroxysmal Dyskinesia, PIGN-related
- Pituitary dwarfism LHX3-related
- Polycystic kidney disease (PKD1)
- Polyneuropathy, NDRG1-related 1
- Polyneuropathy, NDRG1-related 2
- Polyneuropathy, ARHGEF10-related
- Polyneuropathy, GJA9-related
- Progressive Retinal Atrophy SAG-related
- Progressive Retinal Atrophy CNGA1-related
- Progressive Retinal Atrophy BBS4-related
- Cone-rod dystrophy, NPHP4-related
- Progressive Retinal Atrophy STK38L-related
- Progressive Retinal Atrophy FAM161A-related
- Progressive Retinal Atrophy PRCD-related
- Prekallikrein deficiency
- Primary ciliary dyskinesia, CCDC39-related
- Primary glaucoma ADAMTS10 1
- Primary glaucoma ADAMTS10 2
- Primary glaucoma ADAMTS17 1
- Primary glaucoma ADAMTS17 2
- Primary Hyperoxaluria
- Primary Lens Luxation (PLL)
- Pyruvate kinase deficiency - Labrador
- Pyruvate kinase deficiency - Mops
- Pyruvate kinase deficiency - Beagle
- Oculoskeletal Dysplasia 1 / Retinal Dysplasia 1
- Rod-cone dysplasia 1 (rcd1)
- Rod-cone dysplasia 1a (rcd1a)
- Rod-cone dysplasia 3 (rcd3)
- Rod-cone dysplasia 4 (rcd4)
- Severe Combined Immuno Deficiency 1
- Severe Combined Immuno Deficiency 2
- Scott syndrome
- Intestinal Cobalamin Malabsorption 1
- Intestinal Cobalamin Malabsorption 2
- Intestinal Cobalamin Malabsorption 3
- Sensory Neuropathy 1
- Skeletal dysplasia COL11A2-related
- Spinal Dysraphism
- Methaemoglobinaemia 1
- Spinocerebellar ataxia KCNJ10-related
- CNS atrophy, cerebellar ataxia
- Progressive Retinal Atrophy NECAP1-related
- Laryngeal paralysis (LP)
- Spinocerebellar ataxia SCN81-related
- Spinocerebellar ataxia CAPN1-related
- Stargardt disease 1
- Thrombasthenia 1
- Thrombasthenia 2
- Macrothrombocytopenia - CKC type
- Thrombopathia 1
- Thrombopathia 2
- Thrombopathia 3
- Trapped Neutrophil Syndrome (TNS)
- Tremor, X-linked
- Vitamin D-deficiency rickets Type II
- Von Willebrand disease Type III - 2
- Von Willebrand Disease Type I
- Von Willebrand Disease Type II - 2
- Von Willebrand Disease Type III - 1
- Warburg Micro Syndrome 1 (WARBM1)
- Progressive Retinal Atrophy X-linked, RPGR-related
- X-linked severe combined immunodeficiency disease
- Charcot-Marie-Tooth Neuropathy NEW
- Myxomatous Valvular Degeneration NEW
- Globoid Cell Leukodystrophy 2 NEW
- Congenital Hypomyelinating Polyneuropathy NEW
- Lysosomal Storage Disease 2 NEW
- Primary Immunodeficiency Type 2
- Ichthyosis, DSP-related
- Juvenile Encephalopathy NEW
- Polymyositis - Kooikerhondje
- Progressive Retinal Atrophy GUCY2D-related NEW
- Deafness, CDH23-related NEW
- Glycogen storage disease Ia 2 NEW
- Van den Ende-Gupta Syndrome NEW
- Microphtalmia, DNAJC21-related NEW
- Protein Losing Nephropathy
- Am Staff Juvenile Laryngeal Paralysis and Polyneuropathy
- Oculoskeletal dysplasia 2 / Retinal Dysplasia NEW
- Hyperekplexia, SLC6A5-related NEW
- Ehlers-Danlos Syndrome, clEDS NEW
- Multiple ocular Defect
- Lysosomal Storage Disease
- Spongiform Leukoencephalomyelopathy
- Cerebral dysfunction
- Alaskan Husky Encephalopathy
- Dilated Cardiomyopathy Risk2
- MCAD Deficiency
- Haemophilia B - Cairnterriër
- Upper airway syndrome
- Pituitary dwarfism POU1F1
- Primary glaucoma ADAMTS17 3
- Hyposegmentation of granulocytes
- Haemophilia A 6
- Cardiac Laminopathy
- Neuroaxonal dystrophy RNF170
- Progressive Retinal Atrophy JPH2-related
- Progressive Retinal Atrophy IFT122-related
- Craniomandibular osteopathy - Basset
- Gangliosidosis, GM1 - Portugese waterhond
- Fecundity
- Ataxia, HACE1-related
- Hypotrichosis, recessive 1
- Myeloperoxidase deficiency
- Paradoxical pseudomyotonia
- Exfoliative cutaneous Lupus erythematosus
- Primary ciliary dyskinesia 3
- Muscular dystrophy, LAMA2-related
- Succinic Semialdehyde Dehydrogenase Deficiency
- Xanthinuria, type II 1
- Bunny Hopping Syndrome 1
- Junctional epidermolysis bullosa, LAMA3-related 2
- Dilated Cardiomyopathy Risk1
- Hyperekplexia, GLRA1-related
- Multifocal retinopathy 3 (2 variants)
- Deafness, PTPRQ-related
- Dyserythropoietic Anemia and Myopathy Syndrome 2
- Cerebellar Degeneration-Myositis Complex
- Immunodeficiency (MAC)
- Paroxysmal dyskinesia, SOD1
- Paroxysmal Exercise-Induced Dyskinesia 2
- Haemophilia B - Lhasa Apso
- Muscular dystrophy, COL6A1-related
- Xanthinuria type II 3
- Xanthinuria, type II 2
- Deafness, LOXHD1-related
- Polyneuropathy SBF2
- Glycogen storage disease VII 2
- Neuronal ceroid lipofuscinosis 1 - Cane corso
- Epidermolysis bullosa simplex
- Osteochondromatosis
- Ectodermal dysplasia X-linked
- Neuronal Ceroid Lipofuscinosis 7
- Haemophilia B - Newfoundlander
- Dental-Skeletal-Retinal Anomaly
- Hypotrichosis, recessive 2
- Pyruvate kinase deficiency - Westie
- Necrotizing Myelopathy
- Oculoskeletal Dysplasia 1 / Retinal Dysplasia 2
- Mucopolysaccharidosis VI 2
- Surfactant metabolism dysfunction
- Muscular dystrophy 5
- Nemaline myopathy
- Haemophilia A - Old English Sheepdog
- Hypothyroidism SLC5A5-related
- Muscular dystrophy
- Mitochondrial Fission Encephalopathy
- PCYT2 deficiency
- Dyserythropoietic Anemia and Myopathy Syndrome 1
- Paroxysmal Exercise-Induced Dyskinesia 1
- Dilated cardiomyopathy ABCC9-related
- Neuronal ceroid lipofuscinosis 12 - Australian Cattle Dog
- Mucopolysaccharidosis I 1
- Neuronal ceroid lipofuscinosis 8 - Saluki
- Hepatorenal fibrocystic disease
- Myotubular myopathy 3
- Persistent Mullerian Duct Syndrome
- CYP1A2 deficiency
- Embryonic lethality, BTBD17-related
- Inflammatory myopathy
- Fanconi syndrome
- Beta-mannosidosis
- Bardet-Biedl syndrome 2
- Dilated cardiomyopathy PLN-related
- Lundehund syndrome
- Leukoencephalomyelopathy 2
- Macrothrombocytopenia - Terriër type
- Progressive Retinal Atrophy PDE6B-related
- Leukodystrophy, TSEN54-related
- Junctional Epidermolysis Bullosa, LAMB3-related
- Mucopolysaccharidosis I 2
- May-Hegglin anomaly
- Pyruvate dehydrogenase deficiency
- Cerebellar hypoplasia RELN-related
- Epidermal keratinocytic nevi, verrucous 1,2
- Hyperkeratosis, palmoplantar, DSG1-related
- Mucopolysaccharidosis VI 1
- Long QT Syndrome
- Pyruvate kinase deficiency - Basenji
- Haemophilia A - Boxer
- Primary ciliary dyskinesia (PCD), NME5-related
- Bald Thigh Syndrome (BTS)
- Osteogenesis imperfecta 4
- Ligneous membranitis NEW
- Eye malformation
- Laryngeal paralysis/polyneuropathy
- Ehlers-Danlos syndrome type 7
- Retinal dysplasia
- Inflammatory pulmonary disease
- Diluted coat with neurologic defects
- Oculocutaneous albinism OCA4 2
- Vachtkleur Roan
- Junctional epidermolysis bullosa, LAMA3-related 1
- Muscular dystrophy, Ullrich
- Spondylocostal dysostosis
- Myeloencephalopathy, PNPLA8
- Fenobarbital resistentie
- alpha-Mannosidosis