We offer a limited number of single disease tests for owners and breeders who don't need the comprehensive health testing available in Foresight Health®.
Once you place your order we will send out a cheek swab kit with full instructions on how to collect your dog's DNA and how to register the swab on our site.
The turnaround time for these tests is typically 10-12 working days after the swab arrives at the lab.
If you need more than two tests it is more cost-effective to order Foresight Health®.
Tests available individually:
- Acral Mutilation Syndrome (AMS)
- Alaskan Malamute Polyneuropathy (AMPN)
- CA/NCL4/NCL-A (American Staffordshire Terrier)
- Canine Multifocal Retinopathy (CMR1)
- Centronuclear Myopathy (CNM)
- Collie Eye Anomaly (CEA)
- Copper Toxicosis (CT; Bedlington Terrier)
- Cystinuria (Labrador variant)
- Cyclic neutropaenia (Gray Collie Syndrome, CN)
- Neonatal Ataxia (NA)
- Factor VII deficiency (F7 / FVIID)
- Degenerative Myelopathy (DM)
- Curly Coat / Dry Eye (CC/DE)
- Episodic Falling (EF)
- Glycogen Storage Disease (GSD) (Pompe's Disease)
- Glycogen Storage Disease (GSD) (Von Gierke Disease)
- Gangliosidosis GM1 (Shiba Inu type)
- Gangliosidosis GM2 (Shiba Inu type)
- Golden Retriever Progressive Retinal Atrophy 1 (GR-PRA1)
- Golden Retriever Progressive Retinal Atrophy 2 (GR-PRA2)
- Hereditary Cataracts (JHC / HC)
- Hereditary Nasal Parakeratosis (HNPK)
- Ichthyosis (Golden Retriever type - ICT-A)
- Exercise-Induced Collapse (EIC)
- Familial Nephropathy (FN)
- Fucosidosis (Fuco)
- Hyperuricosuria (HUU)
- Hereditary Footpad Keratosis (Palmoplantar Hyperkeratosis)
- Juvenile Laryngeal Paralysis and Polyneuropathy (JLPP)
- Juvenile Myoclonic Epilepsy (JME)
- L-2-hydroxyglutaricaciduria (L2HGA)
- Lafora's Disease
- Musladin-Lueke Syndrome (MLS)
- Muscular Dystrophy (Cavalier King Charles Spaniel variant)
- Congenital Macrothrombocytopaenia (Cavalier King Charles Spaniel variant)
- Multidrug Resistance (MDR1)
- Narcolepsy
- Neonatal encephalopathy with seizures (NEWS)
- Neuroaxonal Dystrophy (NAD)
- Neuronal Ceroid Lipofuscinosis 8 (NCL8 - Saluki variant)
- Neuronal Ceroid Lipofuscinosis 12 (NCL12 - Tibetan Terrier variant)
- Osteochondrodysplasia (OCD)
- Pyruvate Dehydrogenase Deficiency (PDP1)
- Phosphofructokinase deficiency (PFKD aka Glycogen Storage Disease 7)
- Primary Lens Luxation (PLL)
- Primary Ciliary Dyskinesia (PCD)
- Progressive Retinal Atrophy (PRA-PRCD)
- Progressive Retinal Atrophy (PRA-CORD1/crd4)
- Progressive Retinal Atrophy (PRA-crd3)
- Progressive Retinal Atrophy (PRA-Papillon)
- Progressive Retinal Atrophy (PRA-3)
- Progressive Retinal Atrophy (PRA-RCD4)
- Raine Syndrome (Dental Hypomineralisation)
- Skeletal Dysplasia 2 (SD2)
- Sensory Neuropathy (SN)
- Trapped Neutrophil Syndrome (TNS)
- Von Willebrand Disease 1 (vWD1)
- Von Willebrand Disease 2 (vWD2)
