Foresight Health® Dog

by The Pet Genetics Lab

£125.00

Quantity

Description

The results of DNA testing with Foresight Health are accepted by The Kennel Club

Please note this product is in the process of being phased out. Please search for your breed in the box at the top of the page to find your breed-specific package (we are adding breed packages regularly).

Our proprietary next-generation testing method tests each mutation thousands of times to ensure accuracy while making DNA testing more affordable than ever.

If you want to check which inherited diseases in Foresight Health are applicable to your breed, please use the search bar to find the DNA testing guide for your breed.
Foresight Health covers the DNA tests currently required for breed testing schemes offered by the Kennel Club (search for your breed to find out more).
We want to make sure your DNA testing experience is simple yet high quality. The expert geneticists who developed our advanced DNA tests are available for any questions you may have.

How long does it take?

We aim to turn around Foresight Health samples in 15 working days from when the swab arrives back at the lab. However, this is a guideline turnaround and while it can sometimes be a few days quicker, it can also be a few days slower, depending on how busy the lab is. Our next-generation testing methods take a little longer than the older methods used by other labs but we believe that good things are worth waiting for.

What happens when I order?

We will send you out one of our eco-friendly (and totally recyclable) kits for swabbing your dog's cheek to collect DNA. You activate your kit on our website and send the swab back to us. We begin testing your dog's DNA and you'll be kept updated by our online system and by email as the testing progresses. Once your results are ready you'll be able to see them in a fantastic interactive report on our dedicated results site.

Included tests: Blood and Heart

Coagulation Factor VII deficiency (F7)
Phosphofructokinase deficiency (PFKD)
Coagulation Factor VIII Deficiency (Haemophilia A)
Canine Leucocyte Adhesion Deficiency Type I (CLAD)
Malignant Histiocytosis
Prekallikrein deficiency (KTK)
Pyruvate kinase deficiency (PKDef)
Arrythmogenic Right Ventricular Cardiomyopathy (ARVC)
Glanzmann's Thrombasthenia Type I
Congenital Macrothrombocytopaniea
Thrombopathia
Von Willebrand disease I (vWD1)
Von Willebrand disease II (vWD2)
Von Willebrand disease III (vWD3)
Canine Scott Syndrome
Trapped Neutrophil Syndrome (TNS)
Coagulopathy P2RY12-related
May-Hegglin anomaly
Methemoglobinaemia

Included tests: Dental

Amelogenesis Imperfecta (AI)
Dental hypomineralisation

Included tests: Drug Response

Malignant hyperthermia (MH)

Included tests: Eye

Achromatopsia (Cone Degeneration, originally discovered in Alaskan Malamute)
Achromatopsia (Cone Degeneration, Hemeralopia, originally discovered in the German Shorthaired Pointer)
Achromatopsia 2
Bardet-Biedle syndrome 4 (PRA in Puli)
Canine Multifocal Retinopathy 1 (CMR1)
Canine Multifocal Retinopathy 2 (CMR2)
Canine Multifocal Retinopathy 3 (CMR3)
Ichthyosis
Juvenile Hereditary Cataracts (JHC, Early onset Cataracts)
Macular corneal dystrophy
Microphthalmia
Primary Lens Luxation (PLL)
Primary Open Angle Glaucoma (POAG, originally discovered in Beagle)
Primary Open Angle Glaucoma (POAG, originally discovered in Basset Hound)
Progressive Retinal Atrophy

CNGB1 variant (Papillon)
SAG variant (Basenji)
CNGA1 variant (Shetland Sheepdog)
GRPRA2 variant (Golden Retriever)
Autosomal Dominant
cone-rod dystrophy 1 (crd1)
cone-rod dystrophy 2 (crd2)
rod-cone dysplasia (rcd1)
rod-cone dysplasia (rcd1a)
rod-cone dysplasia (rcd3)

Included tests: Hormonal

Congenital Hypothyroidism

Included tests: Immune system

Complement 3 (C3) deficiency
Cyclic Neutropaenia (CN, Gray Collie Syndrome)
Severe Combined Immunodeficiency (PRKDC variant)
Severe Combined Immunodeficiency (RAG1 variant)
X-linked Severe Combined Immunodeficiency

Included tests: Metabolic

Cobalamin malabsorption
Fucosidosis
Gallbladder mucoceles
Glycogen Storage Disease Ia (Von Gierke Disease)
Glycogen Storage Disease II (Pompe's Disease)
Glycogen Storage Disease IIIa
Hypocatalasia
Imerslund-Grasbeck Syndrome (IGS, Cobalamin malabsorption)
Labrador obesity susceptibility
Lagotto Storage Disease
Lundehund syndrome
Menke's disease
Mucopolysaccharidosis I
Mucopolysaccharidosis IIIA
Mucopolysaccharidosis VI
Mucopolysaccharidosis VII
Periodic Fever Syndrome
Pyruvate dehydrogenase deficiency
Wilson's Disease (Copper toxicosis)

Included tests: Muscle

Inherited myopathy of Great Danes
Muscular Dystrophy
Muscular hypertrophy (Bully whippet syndrome)
Myotonia Congenita
Myotubular myopathy 1
Nemaline myopathy

Included tests: Nervous system

Acral Mutilation Syndrome
Alaskan Husky Encephalopathy (Subacute nectrotising encephalopathy of Leigh)
Alexander disease
Axonal Disease Hypomyelination and Tremor
Benign Familiar Juvenile Epilepsy
Cerebellar Ataxia (RAB24 variant)
Cerebellar Ataxia (KCNJ10 variant)
Cerebellar Ataxia (ATP1B2 variant)
Cerebellar cortical degeneration
Deafness and vestibular dysfunction
Foetal-onset / neonatal neuroaxonal dystrophy
Generalised myoclonic epilepsy with photosensitivity
Juvenile euroaxonal dystrophy
L-2-hydroxyglutaricaciduria (L-2-HGA)
Leonberger Polyneuropathy
Narcolepsy
Neonatal Ataxia (NA, Bandera's Neonatal Ataxia, BNAt)
Neonatal Encephalopathy with seizures (NEWS)
Neuroaxonal dystrophy (PLA2G6 variant)
Neuroaxonal dystrophy (VPS11 variant)
Neuronal Ceroid Lipofuscinosis (NCL) variants 1, 10, 12, 2, 4A, 6, 7 and 8
Sensory Ataxic Neuropathy (SAN)
Shaking puppy syndrome (X-linked generalised tremor syndrome)
Spinocerebellar Ataxia (KCNJ10 variant - Late Onset Ataxia)

Included tests: Neuromuscular

Congenital myasthenic syndrome (CMS, CHRNE variant)
Congenital myasthenic syndrome (CMS, COLQ variant)
Congenital myasthenic syndrome (CMS, CHAT variant)
Exercise-induced metabolic myopathy
Gangliosidosis GM1
Gangliosidosis GM2 (HEXA variant)
Gangliosidosis GM2 (HEXB variant)
Globoid Cell Leukodystrophy (Krabbe's Disease)
Greyhound Polyneuropathy
Leucodystrophy
Leukoencephalomyelopahty
Muscular Dystrophy (Limb-girdle type 2F)
Paroxysmal Dyskenesia

Included tests: Reproductive

BTBD17-related embryonic lethality
Persistent Mullerian Duct Syndrome

Included tests: Respiratory

Primary Ciliary Dyskinesia
Acute Respiratory Distress Syndrome (ARDS)

Included tests: Skeletal

Brachycephaly
Chondrodysplasia
Craniomandibular osteopathy
Hereditary Vitamin D-resistant rickets
Musladin-Lueke syndrome (MLS)
Osteochondromatosis
Osteogeneisis Imperfecta (3 variants)
Skeletal dysplasia
Spondylocostal dysostosis

Included tests: Skin

Albinism (OCA2 and SLC45A2 variants)
Anhidrotic Ectodermal Dysplasia
Dry Eye Curly Coat Syndrome
Dystrophic epidermolysis bullosa
Ectodermal dysplasia
Epidermolytic Hyperkeratosis
Focal non-epidermolytic palmoplantar keratoderma
Icthyosis
Lethal acrodermatitis
Ligneous membranitis
Palmoplantar hyperkeratosis (Hereditary footpad keratosis)
Recessive Hypotrichosis

Included tests: Urinary

Cystinuria Type I-A
Cystinuria Type II-A
Cystinuria Type II-B
Familial Nephropathy (FN)
Hyperuricosuria (HUU)
Primary Hyperoxaluria
Renal Cystadenocarcinoma and Nodular Dermatofibrosis
X-linked nephropathy

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