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Valentines offer 7th-14th February: Order two packages/tests and get the cheapest free (click to see conditions)
Valentines offer 7th-14th February: Order two packages/tests and get the cheapest free (click to see conditions)

ComprehensiveCanine™ test

Turnaround: 3-4 weeks

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Original price £179.00
Original price £179.00 - Original price £210.00
Original price £179.00
Current price £139.00
£139.00 - £169.00
Current price £139.00

Back by popular demand!

Our ComprehensiveCanine panel is the most up-to-date canine health testing package on the market in 2025 and a dog essential!

The genetic mutations responsible for dog health issues are being discovered continuously and we have made sure our ComprehensiveCaninepanel is the most up-to-date test for dogs on the market today.

This package tests for 282 health disorders with the option to add colour testing or an ISAG 2020 DNA profile as required. 

To see the full list of health tests and colour tests scroll down the page.

 

Disorders tested for in ComprehensiveCanine

Blood disorders
  • Afribrinogenaemia
  • Canine Leukocyte Adhesion Deficiency I (CLAD I)
  • Canine Leukocyte Adhesion Deficiency III (CLAD III)
  • Complement 3 Deficiency (C3)
  • Cyclic neutropaenia (grey collie syndrome)
  • Factor VII (F7) deficiency
  • Glanzma's Thrombasthenia Type 1 (Great Pyrenes and Otterhound variants)
  • Globoid Cell Leukodystrophy (Krabbe disease)
  • Haemophilia A (Boxer, German Shepherd, Old English Sheepdog variants)
  • Haemophilia B (Terrier, Hovawart, Newfoundland and Rhodesian Ridgeback variants)
  • Hereditary Elliptocytosis
  • Macrothrombocytopaenia (Cavalier and terrier variants)
  • May-Hegglin Aomaly
  • Methaemoglobinaemia (Chihuahua and mixed-breed variants)
  • P2RY12-associated bleeding disorder
  • Prekallikrein deficiency
  • Pyruvate Kinase Deficiency (Basenji, Beagle, Labrador, Pug, Terrier variants)
  • Scott Syndrome
  • Thrombopathia (Eskimo dog, basset, landseer variants)
  • Trapped Neutrophil Syndrome
  • von Willebrand Disease, Type I
  • von Willebrand Disease, Type II
  • von Willebrand Disease, Type III

Eye disorders
  • Congenital Stationary Night Blindness
  • Cainine Multifocal Retinopathy 1
  • Canine Multifocal Retinopathy 2
  • Canine Multifocal Retinopathy 3
  • Cone Degeneration (GSD variant)
  • Cone-rod Dystrophy 1
  • Cone-rod Dystrophy 2
  • Congential Eye Malformations
  • Dominant Progressive Retinal Atrophy
  • Early-Onset Progressive Retinal Atrophy
  • Early-Onset Progressive Retinal Atrophy (PDE6b-associated)
  • Generalised PRA
  • Juvenile Hereditary Cataracts (Bulldog and Australian Shepherd variants)
  • Macular Corneal Dystrophy
  • Primary Lens Luxation
  • Primary Open Angle Glaucoma (Basset, Beagle, Elkhound, Griffon, Shar-Pei variants)
  • Progressive Retinal Atrophy (variants: Basenji, Giant Schnauzer, Golden Retriever 1, Golden Retriever 2, IFT122-associated, Miniature schnauzer, papillon, PRCD, shetland sheepdog, bardet-biedle syndrome)
  • Retinal dysplasia
  • Rod-cone dysplasia 1
  • Rod-cone dysplasia 1a
  • Rod-Cone dysplasia 3
  • Stargardt Disease
Metabolic disorders
  • Beta Mannosidosis (GSD and mixed variants)
  • Congenital Dyshormonogenic Hypothyroidism with goitre
  • Congenital hypothyroidism (Frenchn bulldog, terrier, Spanish water dog, variants)
  • Exercise-induced metabolic myopathy
  • Exercise-induced collapse
  • Fucosidosis
  • Glycogen Storage Disease (Types Ia, II, IIIa, VII)
  • GM1 Gangliosidosis (multiple breed variants)
  • GM2 Gangliosidosis (multiple breed variants)
  • Hypocatalasia
  • L-2-hydroxyglutaricacidemia (terrier variant)
  • Lagotto Storage Disease
  • Malignant hyperthermia
  • Mucopolysaccharidosis I, IIIA, VI, VII variants)
  • Myeloperoxidase deficiency
  • Phosphofructokinase Deficiency
  • Pituitary Dwarfism (LHX3 and POU1F1 associated)
  • Porportioate Dwarfism
  • Pyruvate Dehydrogenase Phosphotase 1 deficiency
Musculoskeletal
  • Amelogenesis imperfecta (multiple breed variants)
  • Centronuclear myopathy 1
  • Chondrodysplasia
  • Cleft Lip and Palate
  • Craniomandibular Osteopathy (multiple breed variants)
  • Dental Hypomineralization
  • Dental-Skeletal-Retinal Anomaly
  • Disproportionate dwarfism
  • Hereditary Vitami D resistant rickets type II
  • Hypophosphatasia
  • Inflammatory myopathy
  • Limb-girdle muscular dystrophy
  • Limb-girdle muscular dystrophy, type L3
  • Muscular dystrophy (all known breed variants)
  • Myotonia Congenita (multiple breed variants)
  • Myotubular myopathy 1 (multiple breed variants)
  • Nemaline myopathy
  • Oculoskeletal dysplasia 1
  • Osteochondromatosis
  • Osteogenesis imperfecta (multiple breed variants)
  • skeletal dysplasia 2
  • Spinal dysraphism
  • Van den Ende-Gupta syndrome
Neurological disorders
  • Acral Mutilation Syndrome
  • Alaskan Husky encephalopath
  • Alaskan malamute polyneuropathy
  • Alexander Disease
  • Ataxia, cerebellar (multiple breed variants)
  • Ataxia, HACE1-related
  • Benign Familial Juvenile Epilepsy
  • Cerebellar ataxia
  • Cerebellar Cortical Degeneration
  • Cerebellar Cortical Degeneration
  • Cerebellar hypoplasia
  • Coat Colour dilution and neurological defects
  • Degenerative myelopathy
  • Demyeloinating neuropathy
  • Early-onset progressive polyneuropathy
  • Epilepsy, mitochondrial dysfunction and neurodegeneration
  • Hereditary ataxia (multiple breed variants)
  • Hyperkeplexia
  • Hypomyelination and tremors
  • Juvenile Laryngeal paralysis and polyneuropathy
  • Juveneile Myoclonic epilepsy
  • Juvenile-onset polyneuropathy
  • Leukodystrophy
  • Leukoencephalomyelopathy
  • Narcolepsy (multiple breed variants)
  • Neonatal cerebellar cortical degeneration
  • Neonatal Encephalopathy with seizures
  • Neuronaxonal Dystrophy (multipe breed variants)
  • Neuronal Ceroid Liposufsinosis (1, 10, 12 4a, 5, 6, 8)
  • Progressive early-onset cerebrallar ataxia
  • Sensory neuropathy
  • Spinoscereballar ataxia
  • Spongy degeneration with Cerebellar ataxia
  • X-linked tremors
Neuromuscular disorders
  • Congenital Myasthenic Syndrome (CHAT-associated, CHRNE-associated, Golden Retriever and Labrador variants)
  • Laryngeal Paralysis and Polyneuropathy
  • Paroxysmal Dyskinesia

Other disorders
  • Cardiomyopathy and Juvenile mortality
  • Copper toxicosis (attenuating)
  • Deafness and Vestibular dysfunction (DINGS1 and DINGS2)
  • Dilated cardiomyopathy
  • Dry Eye Curly Coat Syndrome
  • Inflammatory Pulmonary Disease
  • Instestinal Cobalamin Malabsorption (Beagle, Collie and Komondor variants)
  • Lundehund syndrome
  • Lung Developmental Disease
  • MDR1 Medication sensitivity
  • Persistent Mullerian Duct Syndrome
  • Primary Ciliary Dyskinesia (Alaskan Malamute and Old English Sheepdog variants)
  • Renal Cystadenocarcinoma and nodular dermatofibrosis
  • Respiratory Distress syndrome
  • Sensorineural deafness
  • Severe combined Immunodeficiency (multiple variants)
  • Shar-pei autoinflammatory disease
  • Upper airway syndrome
  • Ventricular arrhythmias and sudden death
  • Wilson disease
  • X-linked severe combined immundeficiency (multiple variants)
Renal disorders
  • Cystic renal dysplasia and hepatic fibrosis
  • Cystinuria Type I-A (multiple variants)
  • Cystinuria Type II-A
  • Cystinuria Type II-B
  • Familial nephropathy (Cocker and Spaniel variants)
  • Hyperuricosuria / Urolithiasis
  • Polycystic Kidney Disease
  • Primary Hyperoxaluria
  • X-liked Hereditary ephropathy (multiple variants)
  • Xanthinuria, Type I
  • Xanthinuria, Type II (multiple variants)
Skin disorders
  • Dystrophic Epidermolysis bullosa (multiple variants)
  • Ehlers-Dalos syndrome (multiple variants)
  • Epidermolysis bullosa, simplex
  • Epidermolytic hyperkeratosis
  • Exfoliative cutaneous lupus erythematosus
  • Hereditary Footpad Hyperkeratosis
  • Hereditary Nasal Parakeratosis (Greyhound and labrador variants)
  • Ichthyosis (American Bulldog, German Shepherd, Great dane types)
  • Junctional Epidermolysis Bullosa
  • Lethal acrodermatitis
  • Oculocutaeous albinism
  • Palmoplantar Hyperkeratosis
  • Skin Fragility Syndrome
  • Verrucous epidermal keratinocytic nevi (Chihuahua variants 1 and 2)
  • X-linked ectodermal dysplasia
Colour panel [OPTIONAL]
  • A-Locus (Fawn, Recessive Black, Tan Points)
  • Back muscling and bulk
  • B-Locus Brown / Chocolate / Liver (Australian Shepherd variant, Bc, Bd, Bh, Bs, Be variants)
  • Cocoa
  • Curly coat
  • Dew claws (Eastern and western breed variants)
  • D-Locus Dilution (D1 and D2 variants)
  • Hairlessness
  • Harleuin
  • K-Locus (dominant black)
  • L-Locus (fur length) (L1, L2, L4, L5 variants)
  • Mask
  • Oculocutaneous albinism (two variants)
  • E-Locus (Recessive red) (E1, E2 and E3 variants)
  • I-Locus (red intensity)
  • Saddle tan
  • Screw tail
  • Tail length
  • Widow's peak (Afghan and Saluki)