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
- Alexander disease
- Amelogenesis imperfecta
- Amelogenesis imperfecta 2
- Amelogenesis imperfecta 3
- Achromatopsia 2
- Achromatopsia 3
- 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
- Centronuclear Myopathy (CNM)
- Cerebellar Abiotrophy (NCCD)
- Adult-onset Deafness EAOD (4 markers) NEW
- Cerebellar Ataxia (NCL-A)
- Cerebellar Ataxia (SDCA1)
- Cerebellar Ataxia (SDCA2)
- Cerebellar Ataxia 1
- Cerebellar ataxia, KCNIP4
- Cerebellar Ataxia 2
- Cerebellar Ataxia, early-onset
- Cerebellar Cortical Degeneration
- Cerebellar Hypoplasia Resembling
- Chondrodysplasia
- Chondrodystrophy and Intervertebral Disc Disease
- CLAD Type I
- CLAD Type III
- Clept Lip, Palate and Syndactyly
- Collie Eye Anomaly (CEA)
- Cone Degeneration
- Cone-rod dystrophy 1 (crd1)
- Cone-rod dystrophy 2 (crd2)
- Congenital Cornification Disorder
- Congenital Hypothyroidism (CHG) 1
- Congenital Hypothyroidism (CHG) 2
- Congenital Hypothyroidism (CHG) 4
- Congenital Hypothyroidism (CHG) 3
- Cystinuria Bulldog-type
- Congenital Stationary Night Blindness (CSNB)
- Copper toxicosis (Wilson), ATP7B type NEW
- Copper toxicosis (Wilson), COMMD1 type
- Craniomandibular Osteopathy (CMO)
- 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 1 (DCM)
- Dilated Cardiomyopathy 3 (DCM)
- Dilated Cardiomyopathy 2 (DCM)
- Dominant PRA
- Dry Eye Curly Coat Syndrome
- Ectodermal dysplasia
- Epidermolysis bullosa, dystrophic
- Epilepsy (BFJ)
- Epilepsy, myoclonic (JME)
- Episodic Falling
- Exercise Induced Collapse (EIC)
- Exercise induced metabolic myopathy
- Haemophilia B (Factor IX def)
- Factor VII deficiency
- Familial Nephropathy (FN) 1
- Familial Nephropathy (FN) 2
- FBN2
- Thyroid follicular cell carcinoma NEW
- Fucosidosis
- Gallbladder Mucocele
- Gangliosidosis GM2 Type I (B variant)
- Gangliosidosis GM2 type II
- Generalized PRA (gPRA)
- Globoid Cell Leukodystrophy (Krabbes Disease)
- Glycogen Storage Disease (GSD) I
- Glycogen Storage Disease (GSD) II
- Glycogen storage disease VII
- Gangliosidosis, GM1
- Golden Retriever PRA 1
- Golden Retriever PRA 2
- Goniodysgenesis and glaucoma
- Gray Collie Syndrome (Cyclic Neutropenia)
- Ventricular Arrythmias
- Haemophilia A (Factor VIII def) 1
- Haemophilia A (Factor VIII def) 2
- Hereditary Cataract (HSF4) 1
- Hereditary Cataract (HSF4) 2
- Hiplaxity 1
- Hiplaxity 2
- Nasal parakeratosis 2
- Nasal parakeratosis 1
- Hyperkeratosis, epidermolytic
- Hyperkeratosis, palmoplantar 1
- Hyperkeratosis, palmoplantar 2
- Urolthiasis (HUU)
- Hypocatalasia
- Hypocatalasia
- Hypomyelination
- Ichthyosis 2
- Ichthyosis 3
- Ichthyosis 4
- Ichthyosis 5
- Juvenile Laryngeal Paralysis Polyneuropathy
- Limb girdle muscular dystrophy (LGMD2F)
- L-2-Hydroxyglutaric aciduria L2-HGA L2-HGA
- Lafora Disease
- Lagotto storage disease
- Lethal Acrodermatitis
- Macular Corneal Dystrophy
- Maligne Hyperthermia
- Microphtalmia
- Multidrug resistance 1 (MDR1)
- MTM
- 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
- Myasthenic syndrome 1
- Myasthenic syndrome 2
- Myasthenic syndrome 3
- Myopathy
- Myotonia Congenita 1
- Myotonia Congenita 2
- Neuroaxonal Dystrophy (NAD) MFN2
- Narcolepsy 1
- Neuroaxonal dystrophy (NAD) PLA2G6
- Narcolepsy 2
- Narcolepsy 3
- Neuroaxonal Dystrophy (NAD) TECPR2
- Neonatal Encephalopathy
- Nephritis
- Neuroaxonal dystrophy (NAD) VPS11
- Neuronal ceroid lipofuscinosis (NCL) 1
- Neuronal ceroid lipofuscinosis (NCL) 2
- Neuronal ceroid lipofuscinosis (NCL) 5
- Neuronal ceroid lipofuscinosis (NCL) 5 GR
- Neuronal ceroid lipofuscinosis (NCL) 6
- Neuronal ceroid lipofuscinosis (NCL) 8 - 2
- Neuronal ceroid lipofuscinosis (NCL) 10
- Neuronal ceroid lipofuscinosis (NCL) 12
- Neuronal ceroid lipofuscinosis, 8 - 1
- Obesitas predispositie
- Oculocutaneous albinism OCA2
- Shar-Pei Fever (SPAID)
- Leukoencephalomyelopathy (LEMP)
- Deafness, bilateral, and vestibular dysfunction (DINGS)
- Oculocutaneous albinism OCA4
- Osteogenesis imperfecta 1
- Osteogenesis imperfecta 2
- Osteogenesis imperfecta 3
- Osteochondrodysplasia
- Menkes Disease NEW
- PAP-PRA1
- Paroxysmal Dyskinesia
- Pituitary dwarfism
- Polycystic kidney disease (PKD1)
- Polycythemia
- Polyneuropathy 1
- Polyneuropathy 2
- Polyneuropathy 3
- Polyneuropathy 4
- Basenji PRA
- Sheltie PRA
- Puli PRA
- PRA crdPRA
- Early retinal degeneration
- PRA Type 3
- prcd PRA
- Prekallikrein deficiency
- Primary Ciliary dyskinesia
- Primary glaucoma 1
- Primary glaucoma 2
- Primary glaucoma 3
- Primary glaucoma 4
- Primary Hyperoxaluria
- Primary Lens Luxation (PLL)
- Pyruvate Dehydrogenase Phosphatase 1 (PDP1)
- Pyruvate kinase Deficiency 1
- Pyruvatekinase Deficiency 2
- Pyruvatekinase Deficiency 3
- 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
- Skeletal Dysplasia 2 (SD2)
- Spinal Dysraphism
- Methaemoglobinaemia
- Spinocerebellar ataxia
- Laryngeal paralysis (LP)
- PRA NECAP1-related
- Spinocerebellar ataxia 2
- Spinocerebellar ataxia, late-onset
- Stargardt disease 1
- Thrombasthenia 1
- Thrombasthenia 2
- Thrombocytopaenia
- 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)
- X Linked PRA1 (XL PRA1)
- X-SCID