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