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