Browse Dog Diseases
We test for 40+ dog diseases. Learn more about different dog health disorders and groups from our library!
Congenital myasthenic syndrome, COLQ-related
Congenital muscular dystrophy, LAMA2-related
Nemaline myopathy
Osteochondrodysplasia
Vitamin D-deficiency rickets, type II
Hyperekplexia
Van den Ende-Gupta syndrome
Intervertebral disc disease, type I
Ridge and dermoid sinus
Chondrodystrophy and intervertebral disc disease
Osteochondromatosis
Labrador Retriever muscular dystrophy (LRMD)
Cleft palate
Oculoskeletal dysplasia, COL9A2-related
Ehlers-Danlos syndrome, classic type
Cleft lip with or without cleft palate
Ehlers-Danlos syndrome, Dermatosparaxis type
Ehlers-Danlos syndrome, classic-like type
Musladin-Lueke syndrome
Hypophosphatasia
Inherited Myopathy of Great Danes (IMGD)
Centronuclear myopathy
Myotonia
Skeletal dysplasia 2 (SD2)
Osteogenesis imperfecta, COL1A1-related
Osteogenesis imperfecta, COL1A2-related
Osteogenesis imperfecta, SERPINH1-related
Ullrich congenital muscular dystrophy (UCMD)
Muscular dystrophy, COL6A3-related
Duchenne muscular dystrophy
Australian Labradoodle dystrophinopathy
Muscular dystrophy-dystroglycanopathy
Oculoskeletal dysplasia, COL9A3-related
Exercise-induced collapse syndrome (EIC)
Chondrodysplasia, FGF4-related
Chondrodysplasia, ITGA10-related
Spondylocostal dysostosis
Muscular hypertrophy (double muscling)
Myotubular myopathy
Malignant hyperthermia
Limb-girdle muscular dystrophy, type R3
Limb-girdle muscular dystrophy, type 2F
Inflammatory myopathy
Craniomandibular osteopathy
Progressive retinal atrophy, RHO-related
Renal cystadenocarcinoma and nodular dermatofibrosis
Cataracts, FYCO1-related
Primary open angle glaucoma (POAG), ADAMTS17-related
Leber congenital amaurosis
Rod-cone dysplasia 2 (rcd2)
Microphthalmia with coloboma
Progressive retinal atrophy, PPT1-related
Rod-cone dysplasia 1a (rcd1a), PDB Beta subunit-related
Cone-rod dystrophy, NPHP4-related
Collie eye anomaly
Progressive Retinal Atrophy, MERTK-related
Macular corneal dystrophy
Progressive Retinal Atrophy, IMPG2-related
Cataract, HSF4-related
Progressive retinal atrophy, FAM161A-related
Rod-cone dysplasia 4 (rcd4)
Cone-rod dystrophy 3 (crd3)
Stargardt disease 1
Cone-rod dystrophy 2 (crd2)
Cone-rod dystrophy 4 (crd4)
Primary open-angle glaucoma (POAG), ADAMTS10-related
Lens luxation
Primary open-angle glaucoma (POAG), primary lens luxation (PLL), or both
Multifocal retinopathy 1
Multifocal retinopathy 2
Multifocal retinopathy 3
Progressive retinal atrophy, BBS4-related
Progressive retinal atrophy, CCDC66-related
Progressive retinal atrophy, CNGA1-related
Progressive Retinal Atrophy, CNGB1-related
Progressive Retinal Atrophy, HIVEP3-related
Progressive Retinal Atrophy, IFT122-related
Progressive Retinal Atrophy, NECAP1-related
Progressive retinal atrophy, X-linked, type 1
Progressive retinal atrophy, X-linked, type 2
Progressive Retinal Atrophy, SAG-related
Progressive retinal atrophy, SLC4A3-related
Progressive retinal atrophy, TTC8-related
Achromatopsia, CNGA3-related
Achromatopsia, CNGB3-related
Congenital keratoconjunctivitis sicca and ichthyosiform dermatosis (CKCSID)
Congenital stationary night blindness
X-linked retinal dysplasia
Goniodysgenesis and early-onset glaucoma
Rod-cone dysplasia 3 (rcd3)
Rod-cone dysplasia 1 (rcd1), PDE6B-related
Progressive rod-cone degeneration
Congenital eye malformation
Early retinal degeneration (erd)
Dental-skeletal-retinal anomaly (DSRA)
Pancreatitis, SPINK1-related
XY disorder of sexual development, NR5A1-related
Periodic Fever Syndrome 1
XX disorder of sexual development (testicular and ovotesticular subtype), BTBD17-related
Obesity
Amelogenesis imperfecta, ACP4-related
Leukoencephalomyelopathy
Amelogenesis imperfecta, ENAM-related
Persistent Müllerian duct syndrome
Brachycephaly
Dental hypomineralization
Decreased litter size
Disorder of sexual development, SRY-related
Non-syndromic hearing loss
Deafness, bilateral, and vestibular dysfunction
Deafness, unilateral and vestibular dysfunction
Periodic Fever Syndrome
Multiple Drug Sensitivity (MDR1)
Congenital cornification disorder
Exfoliative cutaneous lupus erythematosus (ECLE)
Ichthyosis, TGM1-related
Ectodermal dysplasia - skin fragility syndrome (ED-SFS)
Ichthyosis, NIPAL4-related
Focal non-epidermolytic palmoplantar keratoderma
Squamous cell carcinoma of the digit
Canine ectodermal dysplasia (CED)
Darier disease
Ichthyosis, ASPRV1-related
Ichthyosis, PNPLA1-related
Ichthyosis, SLC27A4-related
Dystrophic epidermolysis bullosa
Hyperkeratosis, DSG1-related
Hyperkeratosis, FAM83G-related
Hyperkeratosis, KRT10-related
X-linked hypohidrotic ectodermal dysplasia (XHED)
Junctional epidermolysis bullosa, LAMA3-related
Junctional epidermolysis bullosa, LAMB3-related
Lethal acrodermatitis
Inflammatory linear verrucous epidermal nevi (ILVEN)
Epidermolysis bullosa simplex (EBS)
Hypotrichosis
Nasal parakeratosis
Sensory ataxic neuropathy
Paroxysmal dyskinesia, SOD1-related
Cerebellar cortical degeneration
Spinocerebellar ataxia, SLC12A6-related
CNS atrophy and cerebellar ataxia
Polyneuropathy, SBF2-related
Laryngeal paralysis, RAPGEF6-related
Paroxysmal dyskinesia, PIGN-related
Spinal dysraphism
Myoclonus epilepsy of Lafora
Fetal-onset neuroaxonal dystrophy, MFN2-related
Spinocerebellar ataxia, ITPR1-related
Acral mutilation syndrome
Leukodystrophy, CYTB-related
Reduced ability to metabolize cognitive enhancer 5-(3-methoxyphenyl)-3-(5-methyl1,2,4-oxadiazol-3-yl)-2-oxo-1,2-dihydro-1,6-naphthyridine (AC-3933)
Episodic falling syndrome (EFS)
Polyneuropathy, ARHGEF10-related
Polyneuropathy, GJA9-related
Polyneuropathy, NDRG1-related
Polyneuropathy, RAB3GAP1-related
Neurodegenerative vacuolar storage disease
Spongy degeneration with cerebellar ataxia (SDCA)
Spongy degeneration with cerebellar ataxia 1 (SDCA1)
Spinocerebellar ataxia, CAPN1-related
Spinocerebellar ataxia, KCNJ10-related
Spinocerebellar ataxia, SCN8A-related
Spinocerebellar ataxia, SPTBN2-related
Congenital myasthenic syndrome, CHAT-related
Congenital myasthenic syndrome, CHRNE-related
Congenital myasthenic syndrome, COLQ-related
Laryngeal paralysis and polyneuropathy
Generalized myoclonic epilepsy with photosensitivity
Hypomyelination
Krabbe disease
Alexander disease
Bandera's neonatal ataxia (BNAt)
Cerebellar ataxia, KCNIP4-related
Cerebellar ataxia, RAB24-related
Cerebellar ataxia, SEL1L-related
Narcolepsy
L-2-hydroxyglutaricacidemia
Benign familial juvenile epilepsy (BFJE)
Neurological defects, MYO5A-related
Mitochondrial neurodegenerative disease with epileptic encephalopathy
Neuroaxonal dystrophy, PLA2G6-related
Neuroaxonal dystrophy, VPS11-related
Pelizaeus-Merzbacker disease (shaking pup disease)
Multiple system degeneration
Leigh-like subacute necrotizing encephalopathy (SNE)
Degenerative myelopathy
Juvenile-onset neuroaxonal dystrophy, TECPR2-related
Dandy-Walker-like malformation (cerebellar hypoplasia)
Neonatal encephalopathy with seizures
Sensory neuropathy
Myeloperoxidase deficiency
C3 deficiency
Leukodystrophy, TSEN54-related
Leukocyte adhesion deficiency, type III
Leukocyte adhesion deficiency, type I
Severe combined immunodeficiency disease, X-linked
Severe combined immunodeficiency disease, DNA-PKcs-related
Severe combined immunodeficiency disease, RAG1-related
Trapped Neutrophil Syndrome
Bernard-Soulier syndrome, type C
Afibrinogenaemia
Neutropenia
Canine Scott syndrome (CSS)
Methemoglobinaemia
Factor XI deficiency
Factor VII deficiency
Haemophilia B
Haemophilia A
Thrombasthenia
Polycythemia
Prekallikrein deficiency
May-Hegglin anomaly
Bleeding disorder, P2RY12-related
Ligneous membranitis
Thrombopathia
Elliptocytosis
Thrombocytopaenia
Von Willebrand disease I
Von Willebrand disease III
Von Willebrand disease II
Fucosidosis
Wilson's disease, COMMD1-related
Neuronal ceroid lipofuscinosis, CTSD-related
Mucopolysaccharidosis IIIB
Mucopolysaccharidosis I
Exercise induced metabolic myopathy
Glycogen storage disease, type IIIA
Glycogen storage disease, type II
Glycogen storage disease, type VII
Succinic semialdehyde dehydrogenase deficiency
Mucopolysaccharidosis VI
Mucopolysaccharidosis VII
Mucopolysaccharidosis IIIA
Neuronal ceroid lipofuscinosis, CLN8-related
Neuronal ceroid lipofuscinosis, CLN5-related
Neuronal ceroid lipofuscinosis, CLN6-related
Neuronal ceroid lipofuscinosis, ATP13A2-related
Neuronal ceroid lipofuscinosis, ARSG-related
Neuronal ceroid lipofuscinosis, MFSD8-related
Neuronal ceroid lipofuscinosis, PPT1-related
Neuronal ceroid lipofuscinosis, TPP1-related
Wilson's disease, ATP7B-related
Menkes disease
Hypocatalasia (Acatalasemia)
Ciliary dyskinesia, CCDC39-related
Ciliary dyskinesia, NME5-related
Gangliosidosis, GM1
Gangliosidosis, GM2, type I
Gangliosidosis, GM2, type II
Beta-mannosidosis
Xanthinuria, type II
Xanthinuria, type I
Pyruvate dehydrogenase deficiency
Erythrocytic pyruvate kinase (PK) deficiency
Glycogen storage disease, type IA
Recommended by top vets with decades of experience
21 breeds
64 genetic health markers
50 genetic trait markers
