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 7-10 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) (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)
- 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)
- Neuronal Ceroid Lipofuscinosis 8 (NCL8 - Saluki variant)
- Neuronal Ceroid Lipofuscinosis 12 (NCL12 - Tibetan Terrier variant)
- Osteochondrodysplasia (OCD)
- 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)
