Alle testen voor genetische ziektes van je honden
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- Acute Respiratory Distress Syndrome
- Alexander disease
- Amelogenesis imperfecta
- Amelogenesis imperfecta 2
- Amelogenesis imperfecta 3
- 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)
- Bleeding disorder (P2RY12)
- Brachyury
- C3 Deficiency
- Canine Multifocal Retinopathy (CMR) 1
- Canine Multifocal Retinopathy (CMR) 2
- Cardiomyopathie met juveniele mortaliteit NEW
- Centronuclear Myopathy, HACD1
- Centronuclear Myopathy, DNM2
- Cerebellar Abiotrophy (NCCD)
- Adult-onset Deafness EAOD (4 markers)
- Cerebellar Ataxia (NCL-A)
- Cerebellar Ataxia (SDCA1)
- Cerebellar Ataxia (SDCA2)
- Cerebellar ataxia, KCNIP4
- Cerebellar Ataxia 1
- Cerebellar Ataxia 2
- Cerebellar Ataxia, early-onset
- Deafness, EPS8L2-related (EOAD)
- Cerebellar Cortical Degeneration
- Cerebellar Hypoplasia Resembling
- Chondrodysplasia
- Chondrodystrophy and Intervertebral Disc Disease
- CLAD Type I
- Muscular dystrophy, Duchenne 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)
- Congenital Cornification Disorder
- Congenital Hypothyroidism 1
- Congenital Hypothyroidism 2
- Cystinuria Bulldog-type
- Congenital Hypothyroidism 4
- Congenital Hypothyroidism 3
- Congenital Stationary Night Blindness, RPE65-related
- Congenital Stationary Night Blindness, LRIT3-related NEW
- Copper toxicosis (Wilson), COMMD1 type
- Copper toxicosis (Wilson), ATP7B type
- Craniomandibular Osteopathy - Terriër
- crd4-PRA (aka cord1-PRA)
- Cystinuria I - A - 1
- Cystinuria type II - A
- Cystinuria type I - A - 2
- Cystinuria type II - B
- Degenerative Myelopathy (DM) 1
- Degenerative Myelopathy (DM) 2
- Dental Hypomineralization (Raine Syndrome)
- Dermatofibrosis
- Dilated Cardiomyopathy PDK4-related
- Dilated Cardiomyopathy RBM20-related
- Dilated Cardiomyopathy TTN-related
- PRA RHO-related
- Dry Eye Curly Coat Syndrome
- Ectodermal dysplasia
- Epidermolysis bullosa, dystrophic (RDEB)
- Epilepsy (BFJ)
- Epilepsy, myoclonic (JME)
- Episodic Falling
- Exercise induced metabolic myopathy
- Exercise Induced Collapse (EIC)
- Haemophilia B
- 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
- PRA CCDC66-related
- Globoid Cell Leukodystrophy (Krabbes Disease)
- Glycogen Storage Disease (GSD) I
- Glycogen Storage Disease (GSD) II
- Glycogen storage disease VII
- Gangliosidosis, GM1 - Shiba
- PRA SLC4A3-related
- PRA TTC8-related
- Goniodysgenesis and glaucoma
- Gray Collie Syndrome (Cyclic Neutropenia)
- Haemophilia A 1 - Duitse herder
- Haemophilia A 2 - Duitse herder NEW
- 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
- Hypocatalasia
- 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
- Multidrug resistance 1 (MDR1)
- Myotubular myopathy 1
- Myotubular myopathy (MTM) 2
- Mucopolysaccharidose Type VII - 2
- Mucopolysaccharidosis Type IIIa
- Mucopolysaccharidosis Type VII
- Multifocal Retinopathy 3 (cmr3) 1
- Multifocal Retinopathy 3 (cmr3) 2
- Muscular Dystrophy (GRMD)
- Muscular Dystrophy, Duchenne (DMD)
- Muscular Dystrophy, Duchenne (MDM)
- 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
- Myopathy
- Myotonia Congenita 1
- Myotonia Congenita 2
- Narcolepsy 1
- Neuroaxonal Dystrophy (NAD) MFN2
- Narcolepsy 2
- Neuroaxonal dystrophy (NAD) PLA2G6
- Narcolepsy 3
- Neuroaxonal Dystrophy (NAD) TECPR2
- Neonatal Encephalopathy
- Nephritis
- Neuroaxonal dystrophy (NAD) 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
- Neuronal ceroid lipofuscinosis, 8 - 1
- Obesitas predispositie
- Oculocutaneous albinism OCA2
- Deafness, bilateral, and vestibular dysfunction (DINGS)
- Leukoencephalomyelopathy (LEMP)
- Oculocutaneous albinism OCA4 1
- Shar-Pei Fever (SPAID)
- Osteogenesis imperfecta 1
- Osteogenesis imperfecta 2
- Osteogenesis imperfecta 3
- Copper toxicosis laag risico 1
- Osteochondrodysplasia
- PRA CNGB1-related
- PRA Type B1 HIVEP3-related
- Paroxysmal Dyskinesia, PIGN-related
- Pituitary dwarfism
- Polycystic kidney disease (PKD1)
- Polyneuropathy 1
- Polyneuropathy 2
- Polyneuropathy 3
- Polyneuropathy 4
- PRA SAG-related
- PRA CNGA1-related
- PRA BBS4-related
- PRA crdPRA
- PRA STK38L-related
- PRA FAM161A-related
- PRA PRCD-related
- Prekallikrein deficiency
- Primary ciliary dyskinesia, CCDC39-related
- Primary glaucoma 1
- Primary glaucoma 2
- Primary glaucoma 3
- Primary glaucoma 4
- Primary Hyperoxaluria
- Primary Lens Luxation (PLL)
- Pyruvate kinase deficiency - Labrador
- Pyruvate kinase deficiency - Mops
- Pyruvate kinase deficiency - Beagle
- Retinal Dysplasia Oculoskeletale Dysplasie (RD OSD) 1
- Rod-cone dysplasia 1 (rcd1)
- Rod-cone dysplasia 1a (rcd1a)
- Rod-cone dysplasia 3 (rcd3)
- Rod-cone dysplasia 4 (rcd4)
- SCID 1
- SCID 2
- Scott syndrome
- Selective Cobalamin Malabsorption 1
- Selective Cobalamin Malabsorption 2
- Sensory Neuropathy 1
- Skeletal Dysplasia 2 (SD2)
- Spinal Dysraphism
- Methaemoglobinaemia 1
- Spinocerebellar ataxia
- CNS atrophy, cerebellar ataxia
- PRA NECAP1-related
- Laryngeal paralysis (LP)
- Spinocerebellar ataxia 2
- Spinocerebellar ataxia, late-onset
- 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 Willebrands Disease Type I
- Von Willebrands Disease Type II - 2
- Von Willebrands Disease Type III - 1
- Warburg Micro Syndrome 1 (WARBM1)
- PRA X-linked, RPGR-related
- X-SCID
- L-2-Hydroxyglutaric aciduria - Yorkshire NEW
- Craniomandibular osteopathy - Basset NEW
- Gangliosidosis, GM1 - Portugese waterhond NEW
- Fecundity NEW
- Neuronal ceroid lipofuscinosis 1 - Cane corso NEW
- Epidermolysis bullosa simplex NEW
- Osteochondromatosis NEW
- CYP1A2 deficiency
- Embryonic lethality, BTBD17-related
- Inflammatory myopathy NEW
- Fanconi syndrome NEW
- Beta-mannosidosis
- Bardet-Biedl syndrome 2 NEW
- Dilated cardiomyopathy PLN-related NEW
- Lundehund syndrome NEW
- Macrothrombocytopenia - Terriër type NEW
- PRA PDE6B-related NEW
- Leukodystrophy, TSEN54-related NEW
- Junctional Epidermolysis Bullosa, LAMB3-related
- May-Hegglin anomaly NEW
- Epidermal keratinocytic nevi, verrucous
- Hyperkeratosis, palmoplantar, DSG1-related
- Pyruvate kinase deficiency - Basenji NEW
- Mucopolysaccharidosis VI NEW
- Haemophilia A - Boxer NEW
- Primary ciliary dyskinesia (PCD), NME5-related
- Eye malformation
- Laryngeal paralysis/polyneuropathy
- Ehlers-Danlos syndrome type7
- Retinal dysplasia
- Inflammatory pulmonary disease
- Diluted coat with neurologic defects
- Oculocutaneous albinism OCA4 2
- Vachtkleur Roan
- Junctional epidermolysis bullosa, LAMA3-related
- Muscular dystrophy, Ullrich
- Spondylocostal dysostosis NEW
- Myeloencephalopathy, PNPLA8 NEW
- Fenobarbital resistentie NEW