V záujme zachovania jednotnosti v nomenklatúre, uvádzame v tejto tabuľke názvy chorôb a plemien v anglickom jazyku.
Pes
Dedičné ochorenia psov
| Breed | Genetic disease |
|---|---|
| Afghan Hound | Malignant Hyperthermia (MH), Degenerative Myelopathy (DM), Chondrodysplasia (CDPA) and -dystrophy (CDDY and IVDD risk), Hyperuricosuria (SLC) Progressive retinal atrophy (prcd-PRA), von-Willebrand disease type 1 (vWD 1) |
| Airedale Terrier | Malignant Hyperthermia (MH), Degenerative Myelopathy (DM), Chondrodysplasia (CDPA) and -dystrophy (CDDY and IVDD risk), Hyperuricosuria (SLC), Progressive retinal atrophy (prcd-PRA), von-Willebrand disease type 1 (vWD 1), Lethal lung disease (LAMP3), Faktor VII - deficiency, Protein losing nephropathy (PLN) |
| Akita | Malignant Hyperthermia (MH), Degenerative Myelopathy (DM), Chondrodysplasia (CDPA) and -dystrophy (CDDY and IVDD risk), Hyperuricosuria (SLC), Progressive retinal atrophy (prcd-PRA), von-Willebrand disease type 1 (vWD 1), Amelogenesis imperfecta (AI) |
| Alaskan Klee Kai | Malignant Hyperthermia (MH), Degenerative Myelopathy (DM), Chondrodysplasia (CDPA) and -dystrophy (CDDY and IVDD risk), Hyperuricosuria (SLC), Progressive retinal atrophy (prcd-PRA), von-Willebrand disease type 1 (vWD 1), Faktor VII - deficiency |
| Alaskan Malamute | Malignant Hyperthermia (MH), Degenerative Myelopathy (DM), Chondrodysplasia (CDPA) and -dystrophy (CDDY and IVDD risk), Hyperuricosuria (SLC), Progressive retinal atrophy (prcd-PRA), von-Willebrand disease type 1 (vWD 1), Alaskan Malamute Polyneuropathy (AMPN), Primary ciliary dyskinesia (PCD) |
| Alpine Dachsbracke | Malignant Hyperthermia (MH), Degenerative Myelopathy (DM), Chondrodysplasia (CDPA) and -dystrophy (CDDY and IVDD risk), Hyperuricosuria (SLC), Progressive retinal atrophy (prcd-PRA), von-Willebrand disease type 1 (vWD 1), Spinocerebellar ataxia (SCA) |
| American Akita | Malignant Hyperthermia (MH), Degenerative Myelopathy (DM), Chondrodysplasia (CDPA) and -dystrophy (CDDY and IVDD risk), Hyperuricosuria (SLC), Progressive retinal atrophy (prcd-PRA), von-Willebrand disease type 1 (vWD 1), Amelogenesis imperfecta (AI), Hämophilia B (Faktor IX) |
| American Bulldog | Malignant Hyperthermia (MH), Degenerative Myelopathy (DM), Chondrodysplasia (CDPA) and -dystrophy (CDDY and IVDD risk), Hyperuricosuria (SLC), Progressive retinal atrophy (prcd-PRA), von-Willebrand disease type 1 (vWD 1), Neuronal ceroid lipofuscinosis (NCL), Canine multi-focal rethinopathy (CMR), Nemalin myopathy (NM), Ichthyosis, Robinow-like syndrome (DVL2) |
| American Cocker Spaniel | Malignant Hyperthermia (MH), Degenerative Myelopathy (DM), Chondrodysplasia (CDPA) and -dystrophy (CDDY and IVDD risk), Hyperuricosuria (SLC), Progressive retinal atrophy (prcd-PRA), von-Willebrand disease type 1 (vWD 1), Phosphofruktokinase-deficiency (PFKD), Exercise induced collapse (EIC), Macrothrombocytopenia (MTC), Gallbladder mucoceles |
| American Eskimo Dog | Malignant Hyperthermia (MH), Degenerative Myelopathy (DM), Chondrodysplasia (CDPA) and -dystrophy (CDDY and IVDD risk), Hyperuricosuria (SLC), Progressive retinal atrophy (prcd-PRA), von-Willebrand disease type 1 (vWD 1), Primary lens luxation (PLL) |
| American Hairless Terrier | Malignant Hyperthermia (MH), Degenerative Myelopathy (DM), Chondrodysplasia (CDPA) and -dystrophy (CDDY and IVDD risk), Hyperuricosuria (SLC), Progressive retinal atrophy (prcd-PRA), von-Willebrand disease type 1 (vWD 1), Primary lens luxation (PLL) |
| American Pitbull Terrier | Malignant Hyperthermia (MH), Degenerative Myelopathy (DM), Chondrodysplasia (CDPA) and -dystrophy (CDDY and IVDD risk), Hyperuricosuria (SLC), Progressive retinal atrophy (prcd-PRA), von-Willebrand disease type 1 (vWD 1), Progressive retinal atrophy (crd2-PRA), Robinow-like syndrome (DVL2) |
| American Staffordshire Terrier | Malignant Hyperthermia (MH), Degenerative Myelopathy (DM), Chondrodysplasia (CDPA) and -dystrophy (CDDY and IVDD risk), Hyperuricosuria (SLC), Progressive retinal atrophy (prcd-PRA), von-Willebrand disease type 1 (vWD 1), Progressive retinal atrophy (crd1-PRA), Neuronal ceroid lipofuscinosis (NCL), Robinow-like syndrome (DVL2), Muscular dystrophy |
| Australian Cattle Dog | Malignant Hyperthermia (MH), Degenerative Myelopathy (DM), Chondrodysplasia (CDPA) and -dystrophy (CDDY and IVDD risk), Hyperuricosuria (SLC), Progressive retinal atrophy (prcd-PRA), von-Willebrand disease type 1 (vWD 1), Neuronal ceroid lipofuscinosis (NCL), Progressive retinal atrophy (rcd4-PRA), Primary lens luxation (PLL), Myotonia congenita, Cystinuria |
| Australian Kelpie | Malignant Hyperthermia (MH), Degenerative Myelopathy (DM), Chondrodysplasia (CDPA) and -dystrophy (CDDY and IVDD risk), Hyperuricosuria (SLC), Progressive retinal atrophy (prcd-PRA), von-Willebrand disease type 1 (vWD 1), Collie eye anomaly (CEA) |
| Australian Shepherd | Malignant Hyperthermia (MH), Degenerative Myelopathy (DM), Chondrodysplasia (CDPA) and -dystrophy (CDDY and IVDD risk), Hyperuricosuria (SLC), Progressive retinal atrophy (prcd-PRA), von-Willebrand disease type 1 (vWD 1), Neuronal ceroid lipofuscinosis (NCL), Canine multi-focal rethinopathy (CMR), Hereditary cataract (HSF4), Brachyuria (stumpy-tail), Collie eye anomaly (CEA) , Hereditary ataxia (HA), MDR1 gene variant (Ivermectin hypersensitivity), Startle disease |
| Australian Stumpy Tail Cattle Dog | Malignant Hyperthermia (MH), Degenerative Myelopathy (DM), Chondrodysplasia (CDPA) and -dystrophy (CDDY and IVDD risk), Hyperuricosuria (SLC), Progressive retinal atrophy (prcd-PRA), von-Willebrand disease type 1 (vWD 1), Brachyuria (stumpy-tail), |
| Austrian Pinscher | Malignant Hyperthermia (MH), Degenerative Myelopathy (DM), Chondrodysplasia (CDPA) and -dystrophy (CDDY and IVDD risk), Hyperuricosuria (SLC), Progressive retinal atrophy (prcd-PRA), von-Willebrand disease type 1 (vWD 1), Brachyuria (stumpy-tail) |
| Barbet | Malignant Hyperthermia (MH), Degenerative Myelopathy (DM), Chondrodysplasia (CDPA) and -dystrophy (CDDY and IVDD risk), Hyperuricosuria (SLC), Progressive retinal atrophy (prcd-PRA), von-Willebrand disease type 1 (vWD 1) |
| Barsoi | Malignant Hyperthermia (MH), Degenerative Myelopathy (DM), Chondrodysplasia (CDPA) and -dystrophy (CDDY and IVDD risk), Hyperuricosuria (SLC) Progressive retinal atrophy (prcd-PRA), von-Willebrand disease type 1 (vWD 1) |
| Basenji | Malignant Hyperthermia (MH), Degenerative Myelopathy (DM), Chondrodysplasia (CDPA) and -dystrophy (CDDY and IVDD risk), Hyperuricosuria (SLC), Progressive retinal atrophy (prcd-PRA), von-Willebrand disease type 1 (vWD 1), Progressive retinal atrophy (Bas-PRA1), Pyruvatkinase-deficiency (PK), Fanconi Syndrome |
| Basset Fauve de Bretagne | Malignant Hyperthermia (MH), Degenerative Myelopathy (DM), Chondrodysplasia (CDPA) and -dystrophy (CDDY and IVDD risk), Hyperuricosuria (SLC), Progressive retinal atrophy (prcd-PRA), von-Willebrand disease type 1 (vWD 1), Primary open angle glaukoma (POAG) |
| Basset Hound | Malignant Hyperthermia (MH), Degenerative Myelopathy (DM), Chondrodysplasia (CDPA) and -dystrophy (CDDY and IVDD risk), Hyperuricosuria (SLC), Progressive retinal atrophy (prcd-PRA), von-Willebrand disease type 1 (vWD 1), Thrombopathia, Primary open angle glaukoma (POAG), Lafora disease, X-chromosomal severe combined immuno-deficiency (X-SCID) |
| Beagle | Malignant Hyperthermia (MH), Degenerative Myelopathy (DM), Chondrodysplasia (CDPA) and -dystrophy (CDDY and IVDD risk), Hyperuricosuria (SLC), Progressive retinal atrophy (prcd-PRA), von-Willebrand disease type 1 (vWD 1), Musladin-Lueke syndrome (MLS), Primary open angle glaukoma (POAG), Imerslund-Gräsbeck syndrom (IGS), Pyruvatkinase-deficiency (PK), Faktor VII - deficiency, Neonatal cerebellar abiotrophy (NCCD), Actalasemia, Lafora disease, Progressive retinal atrophy (cord1-PRA), Osteogenesis imperfecta (brittle-bone-disease) |
| Bearded Collie | Malignant Hyperthermia (MH), Degenerative Myelopathy (DM), Chondrodysplasia (CDPA) and -dystrophy (CDDY and IVDD risk), Hyperuricosuria (SLC), Progressive retinal atrophy (prcd-PRA), von-Willebrand disease type 1 (vWD 1), Collie eye anomaly (CEA) |
| Beauceron | Malignant Hyperthermia (MH), Degenerative Myelopathy (DM), Chondrodysplasia (CDPA) and -dystrophy (CDDY and IVDD risk), Hyperuricosuria (SLC), Progressive retinal atrophy (prcd-PRA), von-Willebrand disease type 1 (vWD 1), Hereditary deafness |
| Bedlington Terrier | Malignant Hyperthermia (MH), Degenerative Myelopathy (DM), Chondrodysplasia (CDPA) and -dystrophy (CDDY and IVDD risk), Hyperuricosuria (SLC), Progressive retinal atrophy (prcd-PRA), von-Willebrand disease type 1 (vWD 1), Copper storage disease - Copper Toxicosis (CT) |
| Belgian Shepherd | Malignant Hyperthermia (MH), Degenerative Myelopathy (DM), Chondrodysplasia (CDPA) and -dystrophy (CDDY and IVDD risk), Hyperuricosuria (SLC), Progressive retinal atrophy (prcd-PRA), von-Willebrand disease type 1 (vWD 1), Spongi degeneration with cerebellar ataxia type 1 (SDCA1) Spongi degeneration with cerebellar ataxia type 2 (SDCA2), Cardiomyopathy with juvenile mortality (CJM), CNS atrophy with cerebellar ataxia (CACA), Behaviour propensity (Malinois), Cerebellar ataxia (CA1) |
| Berger Blank Suisse | Malignant Hyperthermia (MH), Degenerative Myelopathy (DM), Chondrodysplasia (CDPA) and -dystrophy (CDDY and IVDD risk), Hyperuricosuria (SLC), Progressive retinal atrophy (prcd-PRA), von-Willebrand disease type 1 (vWD 1), MDR1 gene variant (Ivermectin hypersensitivity) |
| Bernese Mountain Dog | Malignant Hyperthermia (MH), Degenerative Myelopathy (DM), Chondrodysplasia (CDPA) and -dystrophy (CDDY and IVDD risk), Hyperuricosuria (SLC), Progressive retinal atrophy (prcd-PRA), von-Willebrand disease type 1 (vWD 1), Degenerative Myelopathy Exon 1 (DM Exon 1) |
| Bichon Frise | Malignant Hyperthermia (MH), Degenerative Myelopathy (DM), Chondrodysplasia (CDPA) and -dystrophy (CDDY and IVDD risk), Hyperuricosuria (SLC), Progressive retinal atrophy (prcd-PRA), von-Willebrand disease type 1 (vWD 1), Macrothrombocytopenia (MTC) |
| Black Russian Terrier | Malignant Hyperthermia (MH), Degenerative Myelopathy (DM), Chondrodysplasia (CDPA) and -dystrophy (CDDY and IVDD risk), Hyperuricosuria (SLC), Progressive retinal atrophy (prcd-PRA), von-Willebrand disease type 1 (vWD 1), Juvenile laryngeal paralysis & polyneuropathy (JLPP) |
| Bobtail | Malignant Hyperthermia (MH), Degenerative Myelopathy (DM), Chondrodysplasia (CDPA) and -dystrophy (CDDY and IVDD risk), Hyperuricosuria (SLC), Progressive retinal atrophy (prcd-PRA), von-Willebrand disease type 1 (vWD 1), Primary ciliary dyskinesia (PCD), Exercise induced collapse (EIC), MDR1 gene variant (Ivermectin hypersensitivity) |
| Boerboel | Malignant Hyperthermia (MH), Degenerative Myelopathy (DM), Chondrodysplasia (CDPA) and -dystrophy (CDDY and IVDD risk), Hyperuricosuria (SLC), Progressive retinal atrophy (prcd-PRA), von-Willebrand disease type 1 (vWD 1), Canine multi-focal rethinopathy (CMR) |
| Bolognese | Malignant Hyperthermia (MH), Degenerative Myelopathy (DM), Chondrodysplasia (CDPA) and -dystrophy (CDDY and IVDD risk), Hyperuricosuria (SLC), Progressive retinal atrophy (prcd-PRA), von-Willebrand disease type 1 (vWD 1) |
| Bolonka Zwetna | Malignant Hyperthermia (MH), Degenerative Myelopathy (DM), Chondrodysplasia (CDPA) and -dystrophy (CDDY and IVDD risk), Hyperuricosuria (SLC), Progressive retinal atrophy (prcd-PRA), von-Willebrand disease type 1 (vWD 1), Progressive retinal atrophy (cord1-PRA), Progressive retinal atrophy (rcd4-PRA) |
| Border Collie | Malignant Hyperthermia (MH), Degenerative Myelopathy (DM), Chondrodysplasia (CDPA) and -dystrophy (CDDY and IVDD risk), Hyperuricosuria (SLC), Progressive retinal atrophy (prcd-PRA), von-Willebrand disease type 1 (vWD 1), Neuronal ceroid lipofuscinosis (NCL), Glaucma and goniodysgenesis (GG), Trapped neutrophil syndrome (TNS), Imerslund-Gräsbeck syndrom (IGS), Collie eye anomaly (CEA) , Sensory neuropathy (SN), Raine syndrome, MDR1 gene variant (Ivermectin hypersensitivity), Myotonia congenita |
| Border Terrier | Malignant Hyperthermia (MH), Degenerative Myelopathy (DM), Chondrodysplasia (CDPA) and -dystrophy (CDDY and IVDD risk), Hyperuricosuria (SLC), Progressive retinal atrophy (prcd-PRA), von-Willebrand disease type 1 (vWD 1), Spongiform leukoencephalomyelopathy (SLEM) |
| Boston Terrier | Malignant Hyperthermia (MH), Degenerative Myelopathy (DM), Chondrodysplasia (CDPA) and -dystrophy (CDDY and IVDD risk), Hyperuricosuria (SLC), Progressive retinal atrophy (prcd-PRA), von-Willebrand disease type 1 (vWD 1), Hereditary cataract (HSF4), Robinow-like syndrome (DVL2) |
| Bouvier des Ardennes | Malignant Hyperthermia (MH), Degenerative Myelopathy (DM), Chondrodysplasia (CDPA) and -dystrophy (CDDY and IVDD risk), Hyperuricosuria (SLC), Progressive retinal atrophy (prcd-PRA), von-Willebrand disease type 1 (vWD 1), Brachyuria (stumpy-tail) |
| Bouvier des Flandres | Malignant Hyperthermia (MH), Degenerative Myelopathy (DM), Chondrodysplasia (CDPA) and -dystrophy (CDDY and IVDD risk), Hyperuricosuria (SLC), Progressive retinal atrophy (prcd-PRA), von-Willebrand disease type 1 (vWD 1), Exercise induced collapse (EIC) |
| Boxer | Malignant Hyperthermia (MH), Degenerative Myelopathy (DM), Chondrodysplasia (CDPA) and -dystrophy (CDDY and IVDD risk), Hyperuricosuria (SLC), Progressive retinal atrophy (prcd-PRA), von-Willebrand disease type 1 (vWD 1), Hämophilia A (faktor VIII), Macrothrombocytopenia (MTC) |
| Boykin Spaniel | Malignant Hyperthermia (MH), Degenerative Myelopathy (DM), Chondrodysplasia (CDPA) and -dystrophy (CDDY and IVDD risk), Hyperuricosuria (SLC), Progressive retinal atrophy (prcd-PRA), von-Willebrand disease type 1 (vWD 1), Exercise induced collapse (EIC), Collie eye anomaly (CEA) |
| Braque du Bourbonnais | Malignant Hyperthermia (MH), Degenerative Myelopathy (DM), Chondrodysplasia (CDPA) and -dystrophy (CDDY and IVDD risk), Hyperuricosuria (SLC), Progressive retinal atrophy (prcd-PRA), von-Willebrand disease type 1 (vWD 1), Brachyuria (stumpy-tail) |
| Brasilian Terrier | Malignant Hyperthermia (MH), Degenerative Myelopathy (DM), Chondrodysplasia (CDPA) and -dystrophy (CDDY and IVDD risk), Hyperuricosuria (SLC), Progressive retinal atrophy (prcd-PRA), von-Willebrand disease type 1 (vWD 1), Mucopolysaccharidosis type VII (MPS7), Brachyuria (stumpy-tail) |
| Briard | Malignant Hyperthermia (MH), Degenerative Myelopathy (DM), Chondrodysplasia (CDPA) and -dystrophy (CDDY and IVDD risk), Hyperuricosuria (SLC), Progressive retinal atrophy (prcd-PRA), von-Willebrand disease type 1 (vWD 1), Congenital stationary night blindness (CSNB) |
| Brittany Spaniel | Malignant Hyperthermia (MH), Degenerative Myelopathy (DM), Chondrodysplasia (CDPA) and -dystrophy (CDDY and IVDD risk), Hyperuricosuria (SLC), Progressive retinal atrophy (prcd-PRA), von-Willebrand disease type 1 (vWD 1), C3-deficiency (C3), Brachyuria (stumpy-tail) |
| Bullmastiff | Malignant Hyperthermia (MH), Degenerative Myelopathy (DM), Chondrodysplasia (CDPA) and -dystrophy (CDDY and IVDD risk), Hyperuricosuria (SLC), Progressive retinal atrophy (prcd-PRA), von-Willebrand disease type 1 (vWD 1), Progressive retinal atrophy (dom.-PRA), Canine multi-focal rethinopathy (CMR), Mitochondrial fission encephalopathy |
| Bull Terrier | Malignant Hyperthermia (MH), Degenerative Myelopathy (DM), Chondrodysplasia (CDPA) and -dystrophy (CDDY and IVDD risk), Hyperuricosuria (SLC), Progressive retinal atrophy (prcd-PRA), von-Willebrand disease type 1 (vWD 1), Polycystic kidney disease (PKD), Lethal acrodermatitis (LAD), Laryngeal paralysis (LP) |
| Cairn Terrier | Malignant Hyperthermia (MH), Degenerative Myelopathy (DM), Chondrodysplasia (CDPA) and -dystrophy (CDDY and IVDD risk), Hyperuricosuria (SLC), Progressive retinal atrophy (prcd-PRA), von-Willebrand disease type 1 (vWD 1), Globoid cell leukodystrophy (Krabbe-disease), Pyruvatkinase-deficiency (PK), Macrothrombocytopenia (MTC), Cranimandibular osteopathy (CMO), Gallbladder mucoceles |
| Cardigan Welsh Corgi | Malignant Hyperthermia (MH), Degenerative Myelopathy (DM), Chondrodysplasia (CDPA) and -dystrophy (CDDY and IVDD risk), Hyperuricosuria (SLC), Progressive retinal atrophy (prcd-PRA), von-Willebrand disease type 1 (vWD 1), Brachyuria (stumpy-tail), Progressive retinal atrophy (rcd3-PRA), Lafora disease, X-chromosomal severe combined immuno-deficiency (X-SCID) |
| Cavalier King Charles Spaniel | Malignant Hyperthermia (MH), Degenerative Myelopathy (DM), Chondrodysplasia (CDPA) and -dystrophy (CDDY and IVDD risk), Hyperuricosuria (SLC), Progressive retinal atrophy (prcd-PRA), von-Willebrand disease type 1 (vWD 1), Dry eye curly coat syndrome (CCS), Episodic falling (EF), Macrothrombocytopenia (MTC), Muscular dystrophy (MD), Xanthinurie Typ II, MCAD deficiency, Myxomatous mitral valve disease (MMVD), Hair shaft dystrophy (HSD), Primary Immunodeficiency type 2 (PIPS2) |
| Central Asian Shepherd | Malignant Hyperthermia (MH), Degenerative Myelopathy (DM), Chondrodysplasia (CDPA) and -dystrophy (CDDY and IVDD risk), Hyperuricosuria (SLC), Progressive retinal atrophy (prcd-PRA), von-Willebrand disease type 1 (vWD 1), Dystrophic epidermolysis bullosa (DEB) |
| Chesapeake Bay Retriever | Malignant Hyperthermia (MH), Degenerative Myelopathy (DM), Chondrodysplasia (CDPA) and -dystrophy (CDDY and IVDD risk), Hyperuricosuria (SLC), Progressive retinal atrophy (prcd-PRA), von-Willebrand disease type 1 (vWD 1), Exercise induced collapse (EIC), Ectodermal dysplasia/Skin fragility syndrome (ED/SFS) |
| Chihuahua | Malignant Hyperthermia (MH), Degenerative Myelopathy (DM), Chondrodysplasia (CDPA) and -dystrophy (CDDY and IVDD risk), Hyperuricosuria (SLC), Progressive retinal atrophy (prcd-PRA), von-Willebrand disease type 1 (vWD 1), Macrothrombocytopenia (MTC), Neuronal ceroid lipofuscinosis (NCL), Lafora disease |
| Chinese Crested Dog | Malignant Hyperthermia (MH), Degenerative Myelopathy (DM), Chondrodysplasia (CDPA) and -dystrophy (CDDY and IVDD risk), Hyperuricosuria (SLC), Progressive retinal atrophy (prcd-PRA), von-Willebrand disease type 1 (vWD 1), Canine multiple system degeneration (CMSD), Progressive retinal atrophy (rcd3-PRA), Primary lens luxation (PLL), Neuronal ceroid lipofuscinosis (NCL) |
| Chinook | Malignant Hyperthermia (MH), Degenerative Myelopathy (DM), Chondrodysplasia (CDPA) and -dystrophy (CDDY and IVDD risk), Hyperuricosuria (SLC), Progressive retinal atrophy (prcd-PRA), von-Willebrand disease type 1 (vWD 1), Chondrodysplasia (Dwarfism) |
| Chow Chow | Malignant Hyperthermia (MH), Degenerative Myelopathy (DM), Chondrodysplasia (CDPA) and -dystrophy (CDDY and IVDD risk), Hyperuricosuria (SLC) Progressive retinal atrophy (prcd-PRA), von-Willebrand disease type 1 (vWD 1) |
| Clumber Spaniel | Malignant Hyperthermia (MH), Degenerative Myelopathy (DM), Chondrodysplasia (CDPA) and -dystrophy (CDDY and IVDD risk), Hyperuricosuria (SLC), Progressive retinal atrophy (prcd-PRA), von-Willebrand disease type 1 (vWD 1), Pyruvat dehydrogenase phosphatase 1 deficiency (PDP1), Exercise induced collapse (EIC), Progressive retinal atrophy (cord1-PRA) |
| Collie (rough and smooth) | Malignant Hyperthermia (MH), Degenerative Myelopathy (DM), Chondrodysplasia (CDPA) and -dystrophy (CDDY and IVDD risk), Hyperuricosuria (SLC), Progressive retinal atrophy (prcd-PRA), von-Willebrand disease type 1 (vWD 1), Grey Collie syndrome (canine zyclic neutropenia), Progressive retinal atrophy (rcd2-PRA), Collie eye anomaly (CEA) , Inflammatory pulmonary disease (IPD), Dermatomyositis (DMS), MDR1 gene variant (Ivermectin hypersensitivity) |
| Continental Bulldog | Malignant Hyperthermia (MH), Degenerative Myelopathy (DM), Chondrodysplasia (CDPA) and -dystrophy (CDDY and IVDD risk), Hyperuricosuria (SLC), Progressive retinal atrophy (prcd-PRA), von-Willebrand disease type 1 (vWD 1), Cystinuria, Robinow-like syndrome |
| Coton de Tuléar | Malignant Hyperthermia (MH), Degenerative Myelopathy (DM), Chondrodysplasia (CDPA) and -dystrophy (CDDY and IVDD risk), Hyperuricosuria (SLC), Progressive retinal atrophy (prcd-PRA), von-Willebrand disease type 1 (vWD 1), Canine multi-focal rethinopathy (CMR), Primary Hyperoxaluria (PH) |
| Croatian Sheepdog (Hrvatski ovčar) | Malignant Hyperthermia (MH), Degenerative Myelopathy (DM), Chondrodysplasia (CDPA) and -dystrophy (CDDY and IVDD risk), Hyperuricosuria (SLC), Progressive retinal atrophy (prcd-PRA), von-Willebrand disease type 1 (vWD 1), Brachyuria (stumpy-tail) |
| Curly Coated Retriever | Malignant Hyperthermia (MH), Degenerative Myelopathy (DM), Chondrodysplasia (CDPA) and -dystrophy (CDDY and IVDD risk), Hyperuricosuria (SLC), Progressive retinal atrophy (prcd-PRA), von-Willebrand disease type 1 (vWD 1), Glycogen storage disease (GSD IIIa), Exercise induced collapse (EIC), Progressive retinal atrophy (cord1-PRA) |
| Dachshund (Dackel) | Malignant Hyperthermia (MH), Degenerative Myelopathy (DM), Chondrodysplasia (CDPA) and -dystrophy (CDDY and IVDD risk), Hyperuricosuria (SLC), Progressive retinal atrophy (prcd-PRA), von-Willebrand disease type 1 (vWD 1), Neuronal ceroid lipofuscinosis (NCL), Progressive retinal atrophy (crd-PRA), Progressive retinal atrophy (cord1-PRA), Lafora disease, Narcolepsy, Osteogenesis imperfecta (brittle-bone-disease), Color dilution and neurological defects, Mucopolysaccharidosis type IIIa (MPS3a), Afibrinogenemia (AFG), Xanthinurie Typ II, Myxomatous mitral valve disease (MMVD), Limb-Girdle Muscular Dystrophy (LGMD) |
| Dalmatian | Malignant Hyperthermia (MH), Degenerative Myelopathy (DM), Chondrodysplasia (CDPA) and -dystrophy (CDDY and IVDD risk), Hyperuricosuria (SLC), Progressive retinal atrophy (prcd-PRA), von-Willebrand disease type 1 (vWD 1), Acute respiratory distress syndrome (ARDS), Lysosomal storage disease (LSD) |
| Danish-Swedish Farmdog | Malignant Hyperthermia (MH), Degenerative Myelopathy (DM), Chondrodysplasia (CDPA) and -dystrophy (CDDY and IVDD risk), Hyperuricosuria (SLC), Progressive retinal atrophy (prcd-PRA), von-Willebrand disease type 1 (vWD 1), Brachyuria (stumpy-tail), Primary lens luxation (PLL) |
| Deerhound | Malignant Hyperthermia (MH), Degenerative Myelopathy (DM), Chondrodysplasia (CDPA) and -dystrophy (CDDY and IVDD risk), Hyperuricosuria (SLC), Progressive retinal atrophy (prcd-PRA), von-Willebrand disease type 1 (vWD 1), Faktor VII - deficiency, Delayed postoperative haemorrhage (DEPOH) |
| Dobermann | Malignant Hyperthermia (MH), Degenerative Myelopathy (DM), Chondrodysplasia (CDPA) and -dystrophy (CDDY and IVDD risk), Hyperuricosuria (SLC), Progressive retinal atrophy (prcd-PRA), von-Willebrand disease type 1 (vWD 1), Hereditary deafness (DINGS1+2), Narcolepsy, Copper storage disease - Copper Toxicosis, Dilated cardiomyopathy (DCM1-4), Lysosomal storage disease (LSD) |
| Dogo Argentino | Malignant Hyperthermia (MH), Degenerative Myelopathy (DM), Chondrodysplasia (CDPA) and -dystrophy (CDDY and IVDD risk), Hyperuricosuria (SLC), Progressive retinal atrophy (prcd-PRA), von-Willebrand disease type 1 (vWD 1), Disproportionate dwarfism |
| Dogue de Bordeaux | Malignant Hyperthermia (MH), Degenerative Myelopathy (DM), Chondrodysplasia (CDPA) and -dystrophy (CDDY and IVDD risk), Hyperuricosuria (SLC), Progressive retinal atrophy (prcd-PRA), von-Willebrand disease type 1 (vWD 1), Digital hyperkeratosis (DH/HFH), Canine multi-focal rethinopathy (CMR), Robinow-like syndrome (DVL2) |
| Drentse Patrijshond | Malignant Hyperthermia (MH), Degenerative Myelopathy (DM), Chondrodysplasia (CDPA) and -dystrophy (CDDY and IVDD risk), Hyperuricosuria (SLC), Progressive retinal atrophy (prcd-PRA), von-Willebrand disease type 1 (vWD 1) |
| Dutch Shepherd | Malignant Hyperthermia (MH), Degenerative Myelopathy (DM), Chondrodysplasia (CDPA) and -dystrophy (CDDY and IVDD risk), Hyperuricosuria (SLC), Progressive retinal atrophy (prcd-PRA), von-Willebrand disease type 1 (vWD 1), Spongi degeneration with cerebellar ataxia type 1 (SDCA1) Spongi degeneration with cerebellar ataxia type 2 (SDCA2), Inflammatory myopathy (IM) |
| Elo | Malignant Hyperthermia (MH), Degenerative Myelopathy (DM), Chondrodysplasia (CDPA) and -dystrophy (CDDY and IVDD risk), Hyperuricosuria (SLC), Progressive retinal atrophy (prcd-PRA), von-Willebrand disease type 1 (vWD 1), MDR1 gene variant (Ivermectin hypersensitivity) |
| English Bulldog | Malignant Hyperthermia (MH), Degenerative Myelopathy (DM), Chondrodysplasia (CDPA) and -dystrophy (CDDY and IVDD risk), Hyperuricosuria (SLC), Progressive retinal atrophy (prcd-PRA), von-Willebrand disease type 1 (vWD 1), Canine multi-focal rethinopathy (CMR), Cystinuria, Robinow-like syndrome (DVL2) |
| English Cocker Spaniel | Malignant Hyperthermia (MH), Degenerative Myelopathy (DM), Chondrodysplasia (CDPA) and -dystrophy (CDDY and IVDD risk), Hyperuricosuria (SLC), Progressive retinal atrophy (prcd-PRA), von-Willebrand disease type 1 (vWD 1), Familial nephropathy (FN), Exercise induced collapse (EIC), Macrothrombocytopenia (MTC), Gallbladder mucoceles, Acral mutilation syndrome (AMS), Xanthinurie Typ II, Paradoxical pseudomyotonia (PP), X-linked retinal dysplasia |
| English Pointer | Malignant Hyperthermia (MH), Degenerative Myelopathy (DM), Chondrodysplasia (CDPA) and -dystrophy (CDDY and IVDD risk), Hyperuricosuria (SLC), Progressive retinal atrophy (prcd-PRA), von-Willebrand disease type 1 (vWD 1), Acral mutilation syndrome (AMS) |
| English Setter | Malignant Hyperthermia (MH), Degenerative Myelopathy (DM), Chondrodysplasia (CDPA) and -dystrophy (CDDY and IVDD risk), Hyperuricosuria (SLC), Progressive retinal atrophy (prcd-PRA), von-Willebrand disease type 1 (vWD 1), Neuronal ceroid lipofuscinosis (NCL), Progressive retinal atrophy (rcd4-PRA) |
| English Shepherd | Malignant Hyperthermia (MH), Degenerative Myelopathy (DM), Chondrodysplasia (CDPA) and -dystrophy (CDDY and IVDD risk), Hyperuricosuria (SLC), Progressive retinal atrophy (prcd-PRA), von-Willebrand disease type 1 (vWD 1) |
| English Springer Spaniel | Malignant Hyperthermia (MH), Degenerative Myelopathy (DM), Chondrodysplasia (CDPA) and -dystrophy (CDDY and IVDD risk), Hyperuricosuria (SLC), Progressive retinal atrophy (prcd-PRA), von-Willebrand disease type 1 (vWD 1), Phosphofructokinase-deficiency (PFKD), Familial nephropathy (FN), Hypomyelination (Shaking Puppy Syndrome), Progressive retinal atrophy (cord1-PRA), Fucosidosis, Acral mutilation syndrome (AMS), Dyserythropoietic anemia and myopathy (DAMS), Paradoxical pseudomyotonia (PP) |
| English Toy Terrier | Malignant Hyperthermia (MH), Degenerative Myelopathy (DM), Chondrodysplasia (CDPA) and -dystrophy (CDDY and IVDD risk), Hyperuricosuria (SLC), Progressive retinal atrophy (prcd-PRA), von-Willebrand disease type 1 (vWD 1), Xanthinurie Typ II, Dilated cardiomyopathy (DCM) |
| Entlebucher Mountain Dog | Malignant Hyperthermia (MH), Degenerative Myelopathy (DM), Chondrodysplasia (CDPA) and -dystrophy (CDDY and IVDD risk), Hyperuricosuria (SLC), Progressive retinal atrophy (prcd-PRA), von-Willebrand disease type 1 (vWD 1) |
| Eurasian | Malignant Hyperthermia (MH), Degenerative Myelopathy (DM), Chondrodysplasia (CDPA) and -dystrophy (CDDY and IVDD risk), Hyperuricosuria (SLC), Progressive retinal atrophy (prcd-PRA), von-Willebrand disease type 1 (vWD 1), Dandy-Walker-Like malformation (DWLM) |
| Field Spaniel | Malignant Hyperthermia (MH), Degenerative Myelopathy (DM), Chondrodysplasia (CDPA) and -dystrophy (CDDY and IVDD risk), Hyperuricosuria (SLC), Progressive retinal atrophy (prcd-PRA), von-Willebrand disease type 1 (vWD 1), Adult onset neuropathy (AON) |
| Finnish Hound | Malignant Hyperthermia (MH), Degenerative Myelopathy (DM), Chondrodysplasia (CDPA) and -dystrophy (CDDY and IVDD risk), Hyperuricosuria (SLC), Progressive retinal atrophy (prcd-PRA), von-Willebrand disease type 1 (vWD 1), Finnish hound ataxia (FHA), Faktor VII - deficiency |
| Finnish Lapphund | Malignant Hyperthermia (MH), Degenerative Myelopathy (DM), Chondrodysplasia (CDPA) and -dystrophy (CDDY and IVDD risk), Hyperuricosuria (SLC), Progressive retinal atrophy (prcd-PRA), von-Willebrand disease type 1 (vWD 1), Glycogen storage disease Type II (Pompe) (GSD II) |
| Flatcoated Retriever | Malignant Hyperthermia (MH), Degenerative Myelopathy (DM), Chondrodysplasia (CDPA) and -dystrophy (CDDY and IVDD risk), Hyperuricosuria (SLC), Progressive retinal atrophy (prcd-PRA), von-Willebrand disease type 1 (vWD 1), Obesity |
| Fox Terrier | Malignant Hyperthermia (MH), Degenerative Myelopathy (DM), Chondrodysplasia (CDPA) and -dystrophy (CDDY and IVDD risk), Hyperuricosuria (SLC), Progressive retinal atrophy (prcd-PRA), von-Willebrand disease type 1 (vWD 1), Primary lens luxation (PLL), Spinocerebellar ataxia (SCA), Congenital Hypothyreosis (CHG), van den Ende-Gupta syndrome (VDEGS) |
| French Bulldog | Malignant Hyperthermia (MH), Degenerative Myelopathy (DM), Chondrodysplasia (CDPA) and -dystrophy (CDDY and IVDD risk), Hyperuricosuria (SLC), Progressive retinal atrophy (prcd-PRA), von-Willebrand disease type 1 (vWD 1), Congenital Hypothyreosis (CHG), Hereditary cataract (HSF4), Canine multi-focal rethinopathy (CMR), Cystinuria, Lafora disease, Robinow-like syndrome (DVL2), Progressive retinal atrophy (cord1-PRA) |
| French Spaniel | Malignant Hyperthermia (MH), Degenerative Myelopathy (DM), Chondrodysplasia (CDPA) and -dystrophy (CDDY and IVDD risk), Hyperuricosuria (SLC), Progressive retinal atrophy (prcd-PRA), von-Willebrand disease type 1 (vWD 1), Acral mutilation syndrome (AMS) |
| Frisian Water Dog | Malignant Hyperthermia (MH), Degenerative Myelopathy (DM), Chondrodysplasia (CDPA) and -dystrophy (CDDY and IVDD risk), Hyperuricosuria (SLC), Progressive retinal atrophy (prcd-PRA), von-Willebrand disease type 1 (vWD 1), Severe combined immuno deficiency (SCID) |
| Galgo Espanol | Malignant Hyperthermia (MH), Degenerative Myelopathy (DM), Chondrodysplasia (CDPA) and -dystrophy (CDDY and IVDD risk), Hyperuricosuria (SLC), Progressive retinal atrophy (prcd-PRA), von-Willebrand disease type 1 (vWD 1), Startle-disease |
| German Hunting Terrier | Malignant Hyperthermia (MH), Degenerative Myelopathy (DM), Chondrodysplasia (CDPA) and -dystrophy (CDDY and IVDD risk), Hyperuricosuria (SLC), Progressive retinal atrophy (prcd-PRA), von-Willebrand disease type 1 (vWD 1), Primary lens luxation (PLL), Centronuclear myopathy (CNM) |
| German Pinscher | Malignant Hyperthermia (MH), Degenerative Myelopathy (DM), Chondrodysplasia (CDPA) and -dystrophy (CDDY and IVDD risk), Hyperuricosuria (SLC), Progressive retinal atrophy (prcd-PRA), von-Willebrand disease type 1 (vWD 1), Glycogen storage disease type Ia (GSD Ia) |
| German Shepherd | Malignant Hyperthermia (MH), Degenerative Myelopathy (DM), Chondrodysplasia (CDPA) and -dystrophy (CDDY and IVDD risk), Hyperuricosuria (SLC), Progressive retinal atrophy (prcd-PRA), von-Willebrand disease type 1 (vWD 1), Mucopolysaccharidosis type VII (MPS7), Achromatopsia (Day blindness) (ACHM), MDR1 gene variant (Ivermectin hypersensitivity), Hemorragic diathesis (Scott Syndrom), Hämophilia A (faktor VIII), Leukocyte adhesion deficiency III (LAD III), Pituitary dwarfism, Renal Cystadenocarcinoma and nodular dermatofibrosis (RCND), Congenital idiopathic megaesophagus (CIM) |
| German Short-haired Pointing Dog | Malignant Hyperthermia (MH), Degenerative Myelopathy (DM), Chondrodysplasia (CDPA) and -dystrophy (CDDY and IVDD risk), Hyperuricosuria (SLC), Progressive retinal atrophy (prcd-PRA), von-Willebrand disease type 1 (vWD 1), Junctional epidermolysis bullosa (JEB), von-Willebrand disease type 2 (vWD 2), Acral mutilation syndrome (AMS), Cone Degeneration (CD), Exfoliative cutaneous lupus erythematosus (ECLE) |
| German Long-haired Pointing Dog | Malignant Hyperthermia (MH), Degenerative Myelopathy (DM), Chondrodysplasia (CDPA) and -dystrophy (CDDY and IVDD risk), Hyperuricosuria (SLC), Progressive retinal atrophy (prcd-PRA), von-Willebrand disease type 1 (vWD 1), Familial thyroid follicular cell carcinoma |
| German Spaniel | Malignant Hyperthermia (MH), Degenerative Myelopathy (DM), Chondrodysplasia (CDPA) and -dystrophy (CDDY and IVDD risk), Hyperuricosuria (SLC), Progressive retinal atrophy (prcd-PRA), von-Willebrand disease type 1 (vWD 1), Phosphofructokinase-deficiency (PFKD), |
| German Spitz | Malignant Hyperthermia (MH), Degenerative Myelopathy (DM), Chondrodysplasia (CDPA) and -dystrophy (CDDY and IVDD risk), Hyperuricosuria (SLC), Progressive retinal atrophy (prcd-PRA) von-Willebrand disease type 1 (vWD 1), Progressive retinal atrophy (GUCY2D-PRA) |
| German Wirehaired Pointer | Malignant Hyperthermia (MH), Degenerative Myelopathy (DM), Chondrodysplasia (CDPA) and -dystrophy (CDDY and IVDD risk), Hyperuricosuria (SLC), Progressive retinal atrophy (prcd-PRA), von-Willebrand disease type 1 (vWD 1), von-Willebrand disease type 2 (vWD 2), Exercise induced collapse (EIC) |
| Giant Schnauzer | Malignant Hyperthermia (MH), Degenerative Myelopathy (DM), Chondrodysplasia (CDPA) and -dystrophy (CDDY and IVDD risk), Hyperuricosuria (SLC), Progressive retinal atrophy (prcd-PRA), von-Willebrand disease type 1 (vWD 1), Faktor VII - deficiency, Progressive retinal atrophy (NECAP1-PRA), Dilated cardiomyopathy (DCM), Squamous cell carcinoma of the toe - risk estimation |
| Golden Retriever | Malignant Hyperthermia (MH), Degenerative Myelopathy (DM), Chondrodysplasia (CDPA) and -dystrophy (CDDY and IVDD risk), Hyperuricosuria (SLC), Progressive retinal atrophy (prcd-PRA), von-Willebrand disease type 1 (vWD 1), Progressive retinal atrophy (GR-PRA1), Progressive retinal atrophy (GR-PRA2), Progressive retinal atrophy (prcd-PRA), Congenital myasthenic syndrome (CMS), Neuronal ceroid lipofuscinosis (NCL), Muscular dystrophy (MD), Ichthyosis, Osteogenesis imperfecta (brittle-bone-disease), Ichthyosis type 2 |
| Gordon Setter | Malignant Hyperthermia (MH), Degenerative Myelopathy (DM), Chondrodysplasia (CDPA) and -dystrophy (CDDY and IVDD risk), Hyperuricosuria (SLC), Progressive retinal atrophy (prcd-PRA), von-Willebrand disease type 1 (vWD 1), Hereditary ataxia (HA), Progressive retinal atrophy (rcd4-PRA), Neuronal ceroid lipofuscinosis (NCL) |
| Great Dane | Malignant Hyperthermia (MH), Degenerative Myelopathy (DM), Chondrodysplasia (CDPA) and -dystrophy (CDDY and IVDD risk), Hyperuricosuria (SLC), Progressive retinal atrophy (prcd-PRA), von-Willebrand disease type 1 (vWD 1), Congenital Ichthyosis, Leukoencephalomyelopathy (LEMP), Centronuclear myopathy (CNM) |
| Great Pyrenee | Malignant Hyperthermia (MH), Degenerative Myelopathy (DM), Chondrodysplasia (CDPA) and -dystrophy (CDDY and IVDD risk), Hyperuricosuria (SLC), Progressive retinal atrophy (prcd-PRA), von-Willebrand disease type 1 (vWD 1), Canine multi-focal rethinopathy (CMR) |
| Great Swiss Mountain Dog | Malignant Hyperthermia (MH), Degenerative Myelopathy (DM), Chondrodysplasia (CDPA) and -dystrophy (CDDY and IVDD risk), Hyperuricosuria (SLC), Progressive retinal atrophy (prcd-PRA), von-Willebrand disease type 1 (vWD 1), Postoperative hemorrhage (P2Y12) |
| Greyhound | Malignant Hyperthermia (MH), Degenerative Myelopathy (DM), Chondrodysplasia (CDPA) and -dystrophy (CDDY and IVDD risk), Hyperuricosuria (SLC), Progressive retinal atrophy (prcd-PRA), von-Willebrand disease type 1 (vWD 1), Greyhound neuropathy (GHN), Hereditary nasal parakeratosis (HNPK), Delayed postoperative hemorrhage (DEPOH) |
| Havanese | Malignant Hyperthermia (MH), Degenerative Myelopathy (DM), Chondrodysplasia (CDPA) and -dystrophy (CDDY and IVDD risk), Hyperuricosuria (SLC), Progressive retinal atrophy (prcd-PRA), von-Willebrand disease type 1 (vWD 1), Hämophilia A (faktor VIII), Macrothrombocytopenia (MTC) |
| Hovawart | Malignant Hyperthermia (MH), Degenerative Myelopathy (DM), Chondrodysplasia (CDPA) and -dystrophy (CDDY and IVDD risk), Hyperuricosuria (SLC), Progressive retinal atrophy (prcd-PRA), von-Willebrand disease type 1 (vWD 1), Hämophilia B (Faktor IX) |
| Hungarian Viszla | Malignant Hyperthermia (MH), Degenerative Myelopathy (DM), Chondrodysplasia (CDPA) and -dystrophy (CDDY and IVDD risk), Hyperuricosuria (SLC), Progressive retinal atrophy (prcd-PRA), von-Willebrand disease type 1 (vWD 1), Neonatal cerebellar abiotrophy (NCCD), Exfoliative cutaneous lupus erythematosus (ECLE), Disproportionate dwarfism |
| Husky | Malignant Hyperthermia (MH), Degenerative Myelopathy (DM), Chondrodysplasia (CDPA) and -dystrophy (CDDY and IVDD risk), Hyperuricosuria (SLC), Progressive retinal atrophy (prcd-PRA), von-Willebrand disease type 1 (vWD 1), Alaskan Husky Encephalopathy (AHE), Progressive retinal atrophy (XL-PRA), Warburg Micro Syndrome 1 (WARBM1), GM1-gangliosidosis |
| Irish Glen of Imaal Terrier | Malignant Hyperthermia (MH), Degenerative Myelopathy (DM), Chondrodysplasia (CDPA) and -dystrophy (CDDY and IVDD risk), Hyperuricosuria (SLC), Progressive retinal atrophy (prcd-PRA), von-Willebrand disease type 1 (vWD 1), Progressive retinal atrophy (crd3-PRA) |
| Irish Red and White Setter | Malignant Hyperthermia (MH), Degenerative Myelopathy (DM), Chondrodysplasia (CDPA) and -dystrophy (CDDY and IVDD risk), Hyperuricosuria (SLC), Progressive retinal atrophy (prcd-PRA), von-Willebrand disease type 1 (vWD 1), Canine leukozyte adhesion deficiency (CLAD), Progressive retinal atrophy (rcd1-PRA), Progressive retinal atrophy (rcd4-PRA) |
| Irish Red Setter | Malignant Hyperthermia (MH), Degenerative Myelopathy (DM), Chondrodysplasia (CDPA) and -dystrophy (CDDY and IVDD risk), Hyperuricosuria (SLC), Progressive retinal atrophy (prcd-PRA), von-Willebrand disease type 1 (vWD 1), Canine leukozyte adhesion deficiency (CLAD), Progressive retinal atrophy (rcd1-PRA), Globoid cell leukodystrophy (Krabbe-disease), Progressive retinal atrophy (rcd4-PRA) |
| Irish Soft-Coated Wheaten Terrier | Malignant Hyperthermia (MH), Degenerative Myelopathy (DM), Chondrodysplasia (CDPA) and -dystrophy (CDDY and IVDD risk), Hyperuricosuria (SLC), Progressive retinal atrophy (prcd-PRA), von-Willebrand disease type 1 (vWD 1), Protein losing nephropathy (PLN), Paroxysmal dyskinesia (PxD), Microphthalmia (RBP4) |
| Irish Terrier | Malignant Hyperthermia (MH), Degenerative Myelopathy (DM), Chondrodysplasia (CDPA) and -dystrophy (CDDY and IVDD risk), Hyperuricosuria (SLC), Progressive retinal atrophy (prcd-PRA), von-Willebrand disease type 1 (vWD 1), Digital hyperkeratosis (DH/HFH) |
| Irish Wolfhound | Malignant Hyperthermia (MH), Degenerative Myelopathy (DM), Chondrodysplasia (CDPA) and -dystrophy (CDDY and IVDD risk), Hyperuricosuria (SLC), Progressive retinal atrophy (prcd-PRA), von-Willebrand disease type 1 (vWD 1), Startle-disease |
| Italian Cane Corso | Malignant Hyperthermia (MH), Degenerative Myelopathy (DM), Chondrodysplasia (CDPA) and -dystrophy (CDDY and IVDD risk), Hyperuricosuria (SLC), Progressive retinal atrophy (prcd-PRA), von-Willebrand disease type 1 (vWD 1), Canine multi-focal rethinopathy (CMR), Neuronal ceroid lipofuscinosis (NCL), Dental-skeletal-retinal anomaly (DSRA) |
| Italian Greyhound | Malignant Hyperthermia (MH), Degenerative Myelopathy (DM), Chondrodysplasia (CDPA) and -dystrophy (CDDY and IVDD risk), Hyperuricosuria (SLC), Progressive retinal atrophy (prcd-PRA), von-Willebrand disease type 1 (vWD 1), Amelogenesis imperfecta (AI) |
| Italian Spinone | Malignant Hyperthermia (MH), Degenerative Myelopathy (DM), Chondrodysplasia (CDPA) and -dystrophy (CDDY and IVDD risk), Hyperuricosuria (SLC), Progressive retinal atrophy (prcd-PRA), von-Willebrand disease type 1 (vWD 1), Cerebellar ataxia (CA) |
| Jack Russell Terrier | Malignant Hyperthermia (MH), Degenerative Myelopathy (DM), Chondrodysplasia (CDPA) and -dystrophy (CDDY and IVDD risk), Hyperuricosuria (SLC), Progressive retinal atrophy (prcd-PRA), von-Willebrand disease type 1 (vWD 1), Spinocerebellar ataxia (SCA), Late onset ataxia (LOA), Congenital myasthenic syndrome (CMS), Primary lens luxation (PLL), Macrothrombocytopenia (MTC), Brachyuria (stumpy-tail), Juvenile brain disease (JBD), Severe combined immuno deficiency (SCID) |
| Japanese Chin | Malignant Hyperthermia (MH), Degenerative Myelopathy (DM), Chondrodysplasia (CDPA) and -dystrophy (CDDY and IVDD risk), Hyperuricosuria (SLC), Progressive retinal atrophy (prcd-PRA), von-Willebrand disease type 1 (vWD 1), GM2-Gangliosidosis |
| Karelian Bear Dog | Malignant Hyperthermia (MH), Degenerative Myelopathy (DM), Chondrodysplasia (CDPA) and -dystrophy (CDDY and IVDD risk), Hyperuricosuria (SLC), Progressive retinal atrophy (prcd-PRA), von-Willebrand disease type 1 (vWD 1), Brachyuria (stumpy-tail), Chondrodysplasia (Dwarfism), Hypophosphatasia (HPP), Pituitary dwarfism |
| Keeshond | Malignant Hyperthermia (MH), Degenerative Myelopathy (DM), Chondrodysplasia (CDPA) and -dystrophy (CDDY and IVDD risk), Hyperuricosuria (SLC) Progressive retinal atrophy (prcd-PRA), von-Willebrand disease type 1 (vWD 1) |
| Kerry Blue Terrier | Malignant Hyperthermia (MH), Degenerative Myelopathy (DM), Chondrodysplasia (CDPA) and -dystrophy (CDDY and IVDD risk), Hyperuricosuria (SLC), Progressive retinal atrophy (prcd-PRA), von-Willebrand disease type 1 (vWD 1), Canine multiple system degeneration (CMSD), Factor XI deficiency (F11) |
| King Charles Spaniel | Malignant Hyperthermia (MH), Degenerative Myelopathy (DM), Chondrodysplasia (CDPA) and -dystrophy (CDDY and IVDD risk), Hyperuricosuria (SLC), Progressive retinal atrophy (prcd-PRA), von-Willebrand disease type 1 (vWD 1), Dry eye curly coat syndrome (CCS), Episodic falling (EF), Macrothrombocytopenia (MTC), Muscular dystrophy (MD), Xanthinurie Typ II, MCAD deficiency, Myxomatous mitral valve disease (MMVD), Hair shaft dystrophy (HSD), Primary Immunodeficiency type 2 (PIPS2) |
| Komondor | Malignant Hyperthermia (MH), Degenerative Myelopathy (DM), Chondrodysplasia (CDPA) and -dystrophy (CDDY and IVDD risk), Hyperuricosuria (SLC), Progressive retinal atrophy (prcd-PRA), von-Willebrand disease type 1 (vWD 1), Imerslund-Gräsbeck syndrom (IGS) |
| Kooikerhondje | Malignant Hyperthermia (MH), Degenerative Myelopathy (DM), Chondrodysplasia (CDPA) and -dystrophy (CDDY and IVDD risk), Hyperuricosuria (SLC), Progressive retinal atrophy (prcd-PRA), von-Willebrand disease type 1 (vWD 1), von-Willebrand disease type 3 (vWD 3), necrotizing myelopathy (HNM) |
| Kromfohrländer | Malignant Hyperthermia (MH), Degenerative Myelopathy (DM), Chondrodysplasia (CDPA) and -dystrophy (CDDY and IVDD risk), Hyperuricosuria (SLC), Progressive retinal atrophy (prcd-PRA), von-Willebrand disease type 1 (vWD 1), Digital hyperkeratosis (DH/HFH) |
| Kuvasz | Malignant Hyperthermia (MH), Degenerative Myelopathy (DM), Chondrodysplasia (CDPA) and -dystrophy (CDDY and IVDD risk), Hyperuricosuria (SLC), Progressive retinal atrophy (prcd-PRA), von-Willebrand disease type 1 (vWD 1) |
| Labrador Retriever | Malignant Hyperthermia (MH), Degenerative Myelopathy (DM), Chondrodysplasia (CDPA) and -dystrophy (CDDY and IVDD risk), Hyperuricosuria (SLC), Progressive retinal atrophy (prcd-PRA), von-Willebrand disease type 1 (vWD 1), Hereditary nasal parakeratosis (HNPK), Exercise induced collapse (EIC), Pyruvatkinase-deficiency (PK), Centronuclear myopathy (CNM), Skeletal dysplasia 2 (SD 2), Retinal dysplasia (OSD), Achromatopsia (Day blindness) (ACHM), Congenital myasthenic syndrome (CMS), Macrothrombocytopenia (MTC), X-linked Myopathy (XL-MTM), Alexander disease (AxD), Obesity, Cystinuria, Narcolepsy, Myotonia congenita, Stargardt disease (STGD, retinal degeneration), Copper storage disease - Copper Toxicosis, Laryngeal paralysis with polyneuropathy type 3 (LPPN3), Macular corneal dystrophy (MCD), Haemophilia A (factor VIII deficiency) |
| Lagotto Romagnolo | Malignant Hyperthermia (MH), Degenerative Myelopathy (DM), Chondrodysplasia (CDPA) and -dystrophy (CDDY and IVDD risk), Hyperuricosuria (SLC), Progressive retinal atrophy (prcd-PRA), von-Willebrand disease type 1 (vWD 1), Lagotto storage disease (LSD), Juvenile epilepsy (JE), Neuroaxonal dystrophy (NAD) |
| Lakeland Terrier | Malignant Hyperthermia (MH), Degenerative Myelopathy (DM), Chondrodysplasia (CDPA) and -dystrophy (CDDY and IVDD risk), Hyperuricosuria (SLC), Progressive retinal atrophy (prcd-PRA), von-Willebrand disease type 1 (vWD 1), Primary lens luxation (PLL) |
| Lancashire Heeler | Malignant Hyperthermia (MH), Degenerative Myelopathy (DM), Chondrodysplasia (CDPA) and -dystrophy (CDDY and IVDD risk), Hyperuricosuria (SLC), Progressive retinal atrophy (prcd-PRA), von-Willebrand disease type 1 (vWD 1), Collie eye anomaly (CEA) , Primary lens luxation (PLL) |
| Landseer | Malignant Hyperthermia (MH), Degenerative Myelopathy (DM), Chondrodysplasia (CDPA) and -dystrophy (CDDY and IVDD risk), Hyperuricosuria (SLC), Progressive retinal atrophy (prcd-PRA), von-Willebrand disease type 1 (vWD 1), Cystinuria, Muscular dystrophy (MD), Thrombopathia |
| Lapponian Herder | Malignant Hyperthermia (MH), Degenerative Myelopathy (DM), Chondrodysplasia (CDPA) and -dystrophy (CDDY and IVDD risk), Hyperuricosuria (SLC), Progressive retinal atrophy (prcd-PRA), von-Willebrand disease type 1 (vWD 1), Glycogen storage disease type II (Pompe) (GSD II), Canine multi-focal rethinopathy (CMR), Pituitary dwarfism, Progressive retinal atrophy (IFT122-PRA) |
| Large Münsterländer | Malignant Hyperthermia (MH), Degenerative Myelopathy (DM), Chondrodysplasia (CDPA) and -dystrophy (CDDY and IVDD risk), Hyperuricosuria (SLC) Progressive retinal atrophy (prcd-PRA), von-Willebrand disease type 1 (vWD 1) |
| Leonberger | Malignant Hyperthermia (MH), Degenerative Myelopathy (DM), Chondrodysplasia (CDPA) and -dystrophy (CDDY and IVDD risk), Hyperuricosuria (SLC), Progressive retinal atrophy (prcd-PRA), von-Willebrand disease type 1 (vWD 1), Leonberger polyneuropathy 1 (LPN1), Leonberger polyneuropathy 2 (LPN2), Leukoencephalomyelopathy (LEMP), Laryngeal paralysis with polyneuropathy type 3 (LPPN3) |
| Lhasa Apso | Malignant Hyperthermia (MH), Degenerative Myelopathy (DM), Chondrodysplasia (CDPA) and -dystrophy (CDDY and IVDD risk), Hyperuricosuria (SLC), Progressive retinal atrophy (prcd-PRA), von-Willebrand disease type 1 (vWD 1), Progressive retinal atrophy (PRA4), Hämophilia B (Faktor IX) |
| Lucas Terrier | Malignant Hyperthermia (MH), Degenerative Myelopathy (DM), Chondrodysplasia (CDPA) and -dystrophy (CDDY and IVDD risk), Hyperuricosuria (SLC), Progressive retinal atrophy (prcd-PRA), von-Willebrand disease type 1 (vWD 1), Primary lens luxation (PLL) |
| Maltese | Malignant Hyperthermia (MH), Degenerative Myelopathy (DM), Chondrodysplasia (CDPA) and -dystrophy (CDDY and IVDD risk), Hyperuricosuria (SLC), Progressive retinal atrophy (prcd-PRA), von-Willebrand disease type 1 (vWD 1), Glycogen storage disease type Ia (GSD Ia), Macrothrombocytopenia (MTC) |
| Manchester Terrier | Malignant Hyperthermia (MH), Degenerative Myelopathy (DM), Chondrodysplasia (CDPA) and -dystrophy (CDDY and IVDD risk), Hyperuricosuria (SLC), Progressive retinal atrophy (prcd-PRA), von-Willebrand disease type 1 (vWD 1), Xanthinurie Typ II, Dilated cardiomyopathy (DCM) |
| Markiesje | Malignant Hyperthermia (MH), Degenerative Myelopathy (DM), Chondrodysplasia (CDPA) and -dystrophy (CDDY and IVDD risk), Hyperuricosuria (SLC), Progressive retinal atrophy (prcd-PRA), von-Willebrand disease type 1 (vWD 1) |
| Mastiff | Malignant Hyperthermia (MH), Degenerative Myelopathy (DM), Chondrodysplasia (CDPA) and -dystrophy (CDDY and IVDD risk), Hyperuricosuria (SLC), Progressive retinal atrophy (prcd-PRA), von-Willebrand disease type 1 (vWD 1), Progressive retinal atrophy (dom.-PRA), Canine multi-focal rethinopathy (CMR), Cystinuria |
| McNab | Malignant Hyperthermia (MH), Degenerative Myelopathy (DM), Chondrodysplasia (CDPA) and -dystrophy (CDDY and IVDD risk), Hyperuricosuria (SLC), Progressive retinal atrophy (prcd-PRA), von-Willebrand disease type 1 (vWD 1), MDR1 gene variant (Ivermectin hypersensitivity) |
| Miniature American Shepherd | Malignant Hyperthermia (MH), Degenerative Myelopathy (DM), Chondrodysplasia (CDPA) and -dystrophy (CDDY and IVDD risk), Hyperuricosuria (SLC), Progressive retinal atrophy (prcd-PRA), von-Willebrand disease type 1 (vWD 1), Neuronal ceroid lipofuscinosis (NCL), Canine multi-focal rethinopathy (CMR), Hereditary cataract (HSF4), Brachyuria (stumpy-tail), Collie eye anomaly (CEA) , Hereditary ataxia (HA), MDR1 gene variant (Ivermectin hypersensitivity), Startle disease, Neuroaxonal dystrophy (NAD) |
| Miniature Bull Terrier | Malignant Hyperthermia (MH), Degenerative Myelopathy (DM), Chondrodysplasia (CDPA) and -dystrophy (CDDY and IVDD risk), Hyperuricosuria (SLC), Progressive retinal atrophy (prcd-PRA), von-Willebrand disease type 1 (vWD 1), Primary lens luxation (PLL), Lethal acrodermatitis (LAD), Laryngeal paralysis (LP) |
| Miniature Pinscher | Malignant Hyperthermia (MH), Degenerative Myelopathy (DM), Chondrodysplasia (CDPA) and -dystrophy (CDDY and IVDD risk), Hyperuricosuria (SLC), Progressive retinal atrophy (prcd-PRA), von-Willebrand disease type 1 (vWD 1), Mucopolysaccharidosis type VI (MPS6), Cystinuria |
| Miniature Poodle | Malignant Hyperthermia (MH), Degenerative Myelopathy (DM), Chondrodysplasia (CDPA) and -dystrophy (CDDY and IVDD risk), Hyperuricosuria (SLC), Progressive retinal atrophy (prcd-PRA), von-Willebrand disease type 1 (vWD 1), Progressive retinal atrophy (rcd4-PRA), GM2-Gangliosidosis, Osteochondrodysplasia (OCD) |
| Miniature Schnauzer | Malignant Hyperthermia (MH), Degenerative Myelopathy (DM), Chondrodysplasia (CDPA) and -dystrophy (CDDY and IVDD risk), Hyperuricosuria (SLC), Progressive retinal atrophy (prcd-PRA), von-Willebrand disease type 1 (vWD 1), Persistent Müllerian duct syndrome (PMDS), Myotonia congenita, Progressive retinal atrophy (type B1-PRA, HIVEP3), Spondylocostal Dysostosis (Comma Defect), Mycobacterium avium complex sensitivity (MAC), Charcot-Marie-Tooth Neuropathy (CMT) |
| Mudi | Malignant Hyperthermia (MH), Degenerative Myelopathy (DM), Chondrodysplasia (CDPA) and -dystrophy (CDDY and IVDD risk), Hyperuricosuria (SLC), Progressive retinal atrophy (prcd-PRA), von-Willebrand disease type 1 (vWD 1), Brachyuria (stumpy-tail) |
| Newfoundland | Malignant Hyperthermia (MH), Degenerative Myelopathy (DM), Chondrodysplasia (CDPA) and -dystrophy (CDDY and IVDD risk), Hyperuricosuria (SLC), Progressive retinal atrophy (prcd-PRA), von-Willebrand disease type 1 (vWD 1), Cystinuria, Lafora disease |
| Newzealand Huntaway | Malignant Hyperthermia (MH), Degenerative Myelopathy (DM), Chondrodysplasia (CDPA) and -dystrophy (CDDY and IVDD risk), Hyperuricosuria (SLC), Progressive retinal atrophy (prcd-PRA), von-Willebrand disease type 1 (vWD 1), Mucopolysaccharidosis type IIIa (MPS3a) |
| Norfolk Terrier | Malignant Hyperthermia (MH), Degenerative Myelopathy (DM), Chondrodysplasia (CDPA) and -dystrophy (CDDY and IVDD risk), Hyperuricosuria (SLC), Progressive retinal atrophy (prcd-PRA), von-Willebrand disease type 1 (vWD 1), Primary lens luxation (PLL), Epidermolytic hyperkeratosis (EHK), Muscular dystrophy (MD), Macrothrombocytopenia (MTC) |
| Norrbottenspitz | Malignant Hyperthermia (MH), Degenerative Myelopathy (DM), Chondrodysplasia (CDPA) and -dystrophy (CDDY and IVDD risk), Hyperuricosuria (SLC), Progressive retinal atrophy (prcd-PRA), von-Willebrand disease type 1 (vWD 1), Finnish hound ataxia (FHA) |
| Northern Inuit | Malignant Hyperthermia (MH), Degenerative Myelopathy (DM), Chondrodysplasia (CDPA) and -dystrophy (CDDY and IVDD risk), Hyperuricosuria (SLC), Progressive retinal atrophy (prcd-PRA), von-Willebrand disease type 1 (vWD 1), Retinal dysplasia (OSD) |
| Norwegian Buhund | Malignant Hyperthermia (MH), Degenerative Myelopathy (DM), Chondrodysplasia (CDPA) and -dystrophy (CDDY and IVDD risk), Hyperuricosuria (SLC), Progressive retinal atrophy (prcd-PRA), von-Willebrand disease type 1 (vWD 1), Hereditary ataxia (HA) |
| Norwegian Elkhound | Malignant Hyperthermia (MH), Degenerative Myelopathy (DM), Chondrodysplasia (CDPA) and -dystrophy (CDDY and IVDD risk), Hyperuricosuria (SLC), Progressive retinal atrophy (prcd-PRA), von-Willebrand disease type 1 (vWD 1), Primary open angle glaukoma (POAG), Chondrodysplasia (Dwarfism), Hereditary ataxia (HA) |
| Norwegian Lundehund | Malignant Hyperthermia (MH), Degenerative Myelopathy (DM), Chondrodysplasia (CDPA) and -dystrophy (CDDY and IVDD risk), Hyperuricosuria (SLC), Progressive retinal atrophy (prcd-PRA), von-Willebrand disease type 1 (vWD 1), Lundehund syndrome (LHS) |
| Norwich Terrier | Malignant Hyperthermia (MH), Degenerative Myelopathy (DM), Chondrodysplasia (CDPA) and -dystrophy (CDDY and IVDD risk), Hyperuricosuria (SLC), Progressive retinal atrophy (prcd-PRA), von-Willebrand disease type 1 (vWD 1), Primary lens luxation (PLL), Renal dysplasia and hepatic fibrosis (RDHN), Upper airway syndrome (UAS) |
| Nova Scotia Duck Tolling Retriever | Malignant Hyperthermia (MH), Degenerative Myelopathy (DM), Chondrodysplasia (CDPA) and -dystrophy (CDDY and IVDD risk), Hyperuricosuria (SLC), Progressive retinal atrophy (prcd-PRA), von-Willebrand disease type 1 (vWD 1), Collie eye anomaly (CEA) , Cleft lip/palate and syndactyly (CLPS, CP1), Cerebellar degeneration and myositis complex, Dilated cardiomyopathy (DCM) |
| Old Danish Pointing Dog | Malignant Hyperthermia (MH), Degenerative Myelopathy (DM), Chondrodysplasia (CDPA) and -dystrophy (CDDY and IVDD risk), Hyperuricosuria (SLC), Progressive retinal atrophy (prcd-PRA), von-Willebrand disease type 1 (vWD 1), Congenital myasthenic syndrome (CMS), Progressive retinal atrophy (rcd4-PRA) |
| Olde English Bulldog | Malignant Hyperthermia (MH), Degenerative Myelopathy (DM), Chondrodysplasia (CDPA) and -dystrophy (CDDY and IVDD risk), Hyperuricosuria (SLC), Progressive retinal atrophy (prcd-PRA), von-Willebrand disease type 1 (vWD 1), Cystinuria, Robinow-like syndrome (DVL2) |
| Old English Sheepdog | Malignant Hyperthermia (MH), Degenerative Myelopathy (DM), Chondrodysplasia (CDPA) and -dystrophy (CDDY and IVDD risk), Hyperuricosuria (SLC), Progressive retinal atrophy (prcd-PRA), von-Willebrand disease type 1 (vWD 1), Primary ciliary dyskinesia (PCD), Exercise induced collapse (EIC), Hereditary ataxia (HA), Hämophilia A (faktor VIII), MDR1 gene variant (Ivermectin hypersensitivity), Multiocular defect (MOD), Startle disease |
| Papillon | Malignant Hyperthermia (MH), Degenerative Myelopathy (DM), Chondrodysplasia (CDPA) and -dystrophy (CDDY and IVDD risk), Hyperuricosuria (SLC), Progressive retinal atrophy (prcd-PRA), von-Willebrand disease type 1 (vWD 1), Progressive retinal atrophy (pap-PRA1), Neuroaxonal dystrophy (NAD), Faktor VII - deficiency |
| Parson Russell Terrier | Malignant Hyperthermia (MH), Degenerative Myelopathy (DM), Chondrodysplasia (CDPA) and -dystrophy (CDDY and IVDD risk), Hyperuricosuria (SLC), Progressive retinal atrophy (prcd-PRA), von-Willebrand disease type 1 (vWD 1), Spinocerebellar ataxia (SCA), Late onset ataxia (LOA), Congenital myasthenic syndrome (CMS), Primary lens luxation (PLL), Macrothrombocytopenia (MTC), Brachyuria (stumpy-tail), Juvenile brain disease (JBD), Severe combined immuno deficiency (SCID), Amelogenesis imperfecta (AI) |
| Patterdale Terrier | Malignant Hyperthermia (MH), Degenerative Myelopathy (DM), Chondrodysplasia (CDPA) and -dystrophy (CDDY and IVDD risk), Hyperuricosuria (SLC), Progressive retinal atrophy (prcd-PRA), von-Willebrand disease type 1 (vWD 1), Primary lens luxation (PLL), Spinocerebellar ataxia (SCA) |
| Pembroke Welsh Corgi | Malignant Hyperthermia (MH), Degenerative Myelopathy (DM), Chondrodysplasia (CDPA) and -dystrophy (CDDY and IVDD risk), Hyperuricosuria (SLC), Progressive retinal atrophy (prcd-PRA), von-Willebrand disease type 1 (vWD 1), Brachyuria (stumpy-tail), Exercise induced collapse (EIC), Lafora disease, X-chromosomal severe combined immuno-deficiency (X-SCID), Degenerative myelopathy risk modifier |
| Perro de Presa Canario | Malignant Hyperthermia (MH), Degenerative Myelopathy (DM), Chondrodysplasia (CDPA) and -dystrophy (CDDY and IVDD risk), Hyperuricosuria (SLC), Progressive retinal atrophy (prcd-PRA), von-Willebrand disease type 1 (vWD 1), Canine multi-focal rethinopathy (CMR) |
| Petit Basset Griffon Vendeen | Malignant Hyperthermia (MH), Degenerative Myelopathy (DM), Chondrodysplasia (CDPA) and -dystrophy (CDDY and IVDD risk), Hyperuricosuria (SLC), Progressive retinal atrophy (prcd-PRA), von-Willebrand disease type 1 (vWD 1), Primary open angle glaukoma (POAG) |
| Phalène | Malignant Hyperthermia (MH), Degenerative Myelopathy (DM), Chondrodysplasia (CDPA) and -dystrophy (CDDY and IVDD risk), Hyperuricosuria (SLC), Progressive retinal atrophy (prcd-PRA), von-Willebrand disease type 1 (vWD 1), Progressive retinal atrophy (pap-PRA1) |
| Polish Lowland Sheepdog (PON) | Malignant Hyperthermia (MH), Degenerative Myelopathy (DM), Chondrodysplasia (CDPA) and -dystrophy (CDDY and IVDD risk), Hyperuricosuria (SLC), Progressive retinal atrophy (prcd-PRA), von-Willebrand disease type 1 (vWD 1), Brachyuria (stumpy-tail), Progressive retinal atrophy (rcd4-PRA) |
| Pomeranian | Malignant Hyperthermia (MH), Degenerative Myelopathy (DM), Chondrodysplasia (CDPA) and -dystrophy (CDDY and IVDD risk), Hyperuricosuria (SLC), Progressive retinal atrophy (prcd-PRA), von-Willebrand disease type 1 (vWD 1), Progressive retinal atrophy (rcd3-PRA), Vitamin-D dependent rickets (VDR), Gallbladder mucoceles, Methaemoglobinaemia (MetHg) |
| Portuguese Water Dog | Malignant Hyperthermia (MH), Degenerative Myelopathy (DM), Chondrodysplasia (CDPA) and -dystrophy (CDDY and IVDD risk), Hyperuricosuria (SLC), Progressive retinal atrophy (prcd-PRA), von-Willebrand disease type 1 (vWD 1), Progressive retinal atrophy early onset (eo-PRA), GM1-Gangliosidosis, Improper Coat, Microphthalmia |
| Pug Dog | Malignant Hyperthermia (MH), Degenerative Myelopathy (DM), Chondrodysplasia (CDPA) and -dystrophy (CDDY and IVDD risk), Hyperuricosuria (SLC), Progressive retinal atrophy (prcd-PRA), von-Willebrand disease type 1 (vWD 1), Pyruvatkinase-deficiency (PK), Pug dog encephalitis (PDE), Primary lens luxation (PLL), May-Hegglin anomaly (MHA) |
| Puli | Malignant Hyperthermia (MH), Degenerative Myelopathy (DM), Chondrodysplasia (CDPA) and -dystrophy (CDDY and IVDD risk), Hyperuricosuria (SLC), Progressive retinal atrophy (prcd-PRA), von-Willebrand disease type 1 (vWD 1), Progressive retinal atrophy (BBS4-PRA) |
| Pyrenean Mountain Dog | Malignant Hyperthermia (MH), Degenerative Myelopathy (DM), Chondrodysplasia (CDPA) and -dystrophy (CDDY and IVDD risk), Hyperuricosuria (SLC), Progressive retinal atrophy (prcd-PRA), von-Willebrand disease type 1 (vWD 1), Canine multi-focal rethinopathy (CMR), Glanzmann Thrombastenia (GT), Cerebellar ataxia |
| Pyrenean Sheepdog | Malignant Hyperthermia (MH), Degenerative Myelopathy (DM), Chondrodysplasia (CDPA) and -dystrophy (CDDY and IVDD risk), Hyperuricosuria (SLC), Progressive retinal atrophy (prcd-PRA), von-Willebrand disease type 1 (vWD 1), Brachyuria (stumpy-tail) |
| Rat Terrier | Malignant Hyperthermia (MH), Degenerative Myelopathy (DM), Chondrodysplasia (CDPA) and -dystrophy (CDDY and IVDD risk), Hyperuricosuria (SLC), Progressive retinal atrophy (prcd-PRA), von-Willebrand disease type 1 (vWD 1), Primary lens luxation (PLL), Congenital Hypothyreosis (CHG) |
| Rhodesian Ridgeback | Malignant Hyperthermia (MH), Degenerative Myelopathy (DM), Chondrodysplasia (CDPA) and -dystrophy (CDDY and IVDD risk), Hyperuricosuria (SLC), Progressive retinal atrophy (prcd-PRA), von-Willebrand disease type 1 (vWD 1), Juvenile myoclonic epilepsy (JME), Hämophilia B (Faktor IX), Hämophilia A (faktor VIII), Ventricular Arrhythmia , Hereditary deafness (EOAD) |
| Rottweiler | Malignant Hyperthermia (MH), Degenerative Myelopathy (DM), Chondrodysplasia (CDPA) and -dystrophy (CDDY and IVDD risk), Hyperuricosuria (SLC), Progressive retinal atrophy (prcd-PRA), von-Willebrand disease type 1 (vWD 1), Juvenile laryngeal paralysis & polyneuropathy (JLPP), X-linked Myopathy (XL-MTM), Leukoencephalomyelopathy (LEMP), Neuroaxonal dystrophy (NAD), Hereditary deafness |
| Saarloos Wolfdog | Malignant Hyperthermia (MH), Degenerative Myelopathy (DM), Chondrodysplasia (CDPA) and -dystrophy (CDDY and IVDD risk), Hyperuricosuria (SLC), Progressive retinal atrophy (prcd-PRA), von-Willebrand disease type 1 (vWD 1), Pituitary dwarfism, PRA with neurodegeneration (PCYT2 deficiency) |
| Saluki | Malignant Hyperthermia (MH), Degenerative Myelopathy (DM), Chondrodysplasia (CDPA) and -dystrophy (CDDY and IVDD risk), Hyperuricosuria (SLC), Progressive retinal atrophy (prcd-PRA), von-Willebrand disease type 1 (vWD 1), Neuronal ceroid lipofuscinosis (NCL), Succinic semialdehyde dehydrogenase deficiency (SSADHD) |
| Samoyed | Malignant Hyperthermia (MH), Degenerative Myelopathy (DM), Chondrodysplasia (CDPA) and -dystrophy (CDDY and IVDD risk), Hyperuricosuria (SLC), Progressive retinal atrophy (prcd-PRA), von-Willebrand disease type 1 (vWD 1), Familial nephropathy (FN), Progressive retinal atrophy (XL-PRA), Amelogenesis imperfecta / Familial enamel hypoplasia (FEH) |
| Savoy Sheepdog | Malignant Hyperthermia (MH), Degenerative Myelopathy (DM), Chondrodysplasia (CDPA) and -dystrophy (CDDY and IVDD risk), Hyperuricosuria (SLC), Progressive retinal atrophy (prcd-PRA), von-Willebrand disease type 1 (vWD 1), Brachyuria (stumpy-tail) |
| Schapendoes | Malignant Hyperthermia (MH), Degenerative Myelopathy (DM), Chondrodysplasia (CDPA) and -dystrophy (CDDY and IVDD risk), Hyperuricosuria (SLC), Progressive retinal atrophy (prcd-PRA), von-Willebrand disease type 1 (vWD 1), Progressive retinal atrophy (g-PRA), Neuronal ceroid lipofuscinosis (NCL) |
| Schipperke | Malignant Hyperthermia (MH), Degenerative Myelopathy (DM), Chondrodysplasia (CDPA) and -dystrophy (CDDY and IVDD risk), Hyperuricosuria (SLC), Progressive retinal atrophy (prcd-PRA), von-Willebrand disease type 1 (vWD 1), Brachyuria (stumpy-tail), Mucopolysaccharidosis type IIIb (MPS3b) |
| Schnauzer | Malignant Hyperthermia (MH), Degenerative Myelopathy (DM), Chondrodysplasia (CDPA) and -dystrophy (CDDY and IVDD risk), Hyperuricosuria (SLC), Progressive retinal atrophy (prcd-PRA), von-Willebrand disease type 1 (vWD 1), Dilated cardiomyopathy (DCM), Leukoencephalopathy (LEP) |
| Scottish Terrier | Malignant Hyperthermia (MH), Degenerative Myelopathy (DM), Chondrodysplasia (CDPA) and -dystrophy (CDDY and IVDD risk), Hyperuricosuria (SLC), Progressive retinal atrophy (prcd-PRA), von-Willebrand disease type 1 (vWD 1), von-Willebrand disease type 3 (vWD 3), Cranimandibular osteopathy (CMO) |
| Sealyham Terrier | Malignant Hyperthermia (MH), Degenerative Myelopathy (DM), Chondrodysplasia (CDPA) and -dystrophy (CDDY and IVDD risk), Hyperuricosuria (SLC), Progressive retinal atrophy (prcd-PRA), von-Willebrand disease type 1 (vWD 1), Primary lens luxation (PLL) |
| Shar Pei | Malignant Hyperthermia (MH), Degenerative Myelopathy (DM), Chondrodysplasia (CDPA) and -dystrophy (CDDY and IVDD risk), Hyperuricosuria (SLC), Progressive retinal atrophy (prcd-PRA), von-Willebrand disease type 1 (vWD 1), Shar Pei autoinflammatory disease (SPAID), Primary open angle glaukoma and lens luxation (POAG/PLL) |
| Shetland Sheepdog (Sheltie) | Malignant Hyperthermia (MH), Degenerative Myelopathy (DM), Chondrodysplasia (CDPA) and -dystrophy (CDDY and IVDD risk), Hyperuricosuria (SLC), Progressive retinal atrophy (prcd-PRA), von-Willebrand disease type 1 (vWD 1), von-Willebrand disease type 3 (vWD 3), Collie eye anomaly (CEA) , Dermatomyositis (DMS), Gallbladder mucoceles, Progressive retinal atrophy (CNGA1-PRA), Paroxysmal exercise-induced dyskinesia (PED), MDR1 gene variant (Ivermectin hypersensitivity), Progressive retinal atrophy (BBS2-PRA), Maxillary canine tooth mesioversion (MCM) |
| Shiba Inu | Malignant Hyperthermia (MH), Degenerative Myelopathy (DM), Chondrodysplasia (CDPA) and -dystrophy (CDDY and IVDD risk), Hyperuricosuria (SLC), Progressive retinal atrophy (prcd-PRA), von-Willebrand disease type 1 (vWD 1), GM1-Gangliosidosis, GM2-Gangliosidosis |
| Shih Tzu | Malignant Hyperthermia (MH), Degenerative Myelopathy (DM), Chondrodysplasia (CDPA) and -dystrophy (CDDY and IVDD risk), Hyperuricosuria (SLC), Progressive retinal atrophy (prcd-PRA), von-Willebrand disease type 1 (vWD 1), Prekallikrein deficiency (KLK), Macrothrombocytopenia (MTC), Robinow-like syndrome (DVL2), Progressive retinal atrophy (JPH2-PRA) |
| Silken Windhound | Malignant Hyperthermia (MH), Degenerative Myelopathy (DM), Chondrodysplasia (CDPA) and -dystrophy (CDDY and IVDD risk), Hyperuricosuria (SLC), Progressive retinal atrophy (prcd-PRA), von-Willebrand disease type 1 (vWD 1), MDR1 gene variant (Ivermectin hypersensitivity), Collie eye anomaly (CEA) |
| Silken Windsprite (Long Haired-Whippet) | Malignant Hyperthermia (MH), Degenerative Myelopathy (DM), Chondrodysplasia (CDPA) and -dystrophy (CDDY and IVDD risk), Hyperuricosuria (SLC), Progressive retinal atrophy (prcd-PRA), von-Willebrand disease type 1 (vWD 1), Myostatin-mutation (Bully-Whippet), Phosphofructokinase-deficiency (PFKD), Collie eye anomaly (CEA) , MDR1 gene variant (Ivermectin hypersensitivity) |
| Silky Terrier | Malignant Hyperthermia (MH), Degenerative Myelopathy (DM), Chondrodysplasia (CDPA) and -dystrophy (CDDY and IVDD risk), Hyperuricosuria (SLC), Progressive retinal atrophy (prcd-PRA), von-Willebrand disease type 1 (vWD 1) |
| Sloughi | Malignant Hyperthermia (MH), Degenerative Myelopathy (DM), Chondrodysplasia (CDPA) and -dystrophy (CDDY and IVDD risk), Hyperuricosuria (SLC), Progressive retinal atrophy (prcd-PRA), von-Willebrand disease type 1 (vWD 1), Progressive retinal atrophy (rcd1a-PRA) |
| Small Munsterlander | Malignant Hyperthermia (MH), Degenerative Myelopathy (DM), Chondrodysplasia (CDPA) and -dystrophy (CDDY and IVDD risk), Hyperuricosuria (SLC), Progressive retinal atrophy (prcd-PRA), von-Willebrand disease type 1 (vWD 1), Progressive retinal atrophy (rcd4-PRA) |
| Small Swiss Hound | Malignant Hyperthermia (MH), Degenerative Myelopathy (DM), Chondrodysplasia (CDPA) and -dystrophy (CDDY and IVDD risk), Hyperuricosuria (SLC), Progressive retinal atrophy (prcd-PRA), von-Willebrand disease type 1 (vWD 1), Neuronal ceroid lipofuscinosis (NCL) |
| Spanish Water Dog | Malignant Hyperthermia (MH), Degenerative Myelopathy (DM), Chondrodysplasia (CDPA) and -dystrophy (CDDY and IVDD risk), Hyperuricosuria (SLC), Progressive retinal atrophy (prcd-PRA), von-Willebrand disease type 1 (vWD 1), Congenital Hypothyreosis (CHG), Neuroaxonal dystrophy (NAD), Brachyuria (stumpy-tail), Progressive retinal atrophy early onset (eo-PRA) |
| Saint Bernard | Malignant Hyperthermia (MH), Degenerative Myelopathy (DM), Chondrodysplasia (CDPA) and -dystrophy (CDDY and IVDD risk), Hyperuricosuria (SLC), Progressive retinal atrophy (prcd-PRA), von-Willebrand disease type 1 (vWD 1), Laryngeal paralysis with polyneuropathy type 3 (LPPN3) |
| Stabyhoun | Malignant Hyperthermia (MH), Degenerative Myelopathy (DM), Chondrodysplasia (CDPA) and -dystrophy (CDDY and IVDD risk), Hyperuricosuria (SLC), Progressive retinal atrophy (prcd-PRA), von-Willebrand disease type 1 (vWD 1), Cerebral dysfunction |
| Staffordshire Bull Terrier | Malignant Hyperthermia (MH), Degenerative Myelopathy (DM), Chondrodysplasia (CDPA) and -dystrophy (CDDY and IVDD risk), Hyperuricosuria (SLC), Progressive retinal atrophy (prcd-PRA), von-Willebrand disease type 1 (vWD 1), L-2-Hydroxy glutaric acid uria (L2HGA), Hereditary cataract (HSF4), Robinow-like syndrome (DVL2) |
| Standard Poodle | Malignant Hyperthermia (MH), Degenerative Myelopathy (DM), Chondrodysplasia (CDPA) and -dystrophy (CDDY and IVDD risk), Hyperuricosuria (SLC), Progressive retinal atrophy (prcd-PRA), von-Willebrand disease type 1 (vWD 1), Neonatal enzephalopathy with seizures (NEWS), Progressive retinal atrophy (rcd4-PRA), Macrothrombocytopenia (MTC), Squamous cell carcinoma of the toe - risk estimation |
| Sussex Spaniel | Malignant Hyperthermia (MH), Degenerative Myelopathy (DM), Chondrodysplasia (CDPA) and -dystrophy (CDDY and IVDD risk), Hyperuricosuria (SLC), Progressive retinal atrophy (prcd-PRA), von-Willebrand disease type 1 (vWD 1), Pyruvat dehydrogenase phosphatase 1 deficiency (PDP1) |
| Swedish Farmdog | Malignant Hyperthermia (MH), Degenerative Myelopathy (DM), Chondrodysplasia (CDPA) and -dystrophy (CDDY and IVDD risk), Hyperuricosuria (SLC), Progressive retinal atrophy (prcd-PRA), von-Willebrand disease type 1 (vWD 1), Brachyuria (stumpy-tail) |
| Swedish Lapphund | Malignant Hyperthermia (MH), Degenerative Myelopathy (DM), Chondrodysplasia (CDPA) and -dystrophy (CDDY and IVDD risk), Hyperuricosuria (SLC), Progressive retinal atrophy (prcd-PRA), von-Willebrand disease type 1 (vWD 1), Glycogen storage disease Type II (Pompe) (GSD II) |
| Swedish Vallhund | Malignant Hyperthermia (MH), Degenerative Myelopathy (DM), Chondrodysplasia (CDPA) and -dystrophy (CDDY and IVDD risk), Hyperuricosuria (SLC), Progressive retinal atrophy (prcd-PRA), von-Willebrand disease type 1 (vWD 1), Brachyuria (stumpy-tail), Progressive retinal atrophy (MERTK-PRA) |
| Tamaskan | Malignant Hyperthermia (MH), Degenerative Myelopathy (DM), Chondrodysplasia (CDPA) and -dystrophy (CDDY and IVDD risk), Hyperuricosuria (SLC), Progressive retinal atrophy (prcd-PRA), von-Willebrand disease type 1 (vWD 1), Retinal dysplasia (OSD) |
| Tatra Shepherd Dog | Malignant Hyperthermia (MH), Degenerative Myelopathy (DM), Chondrodysplasia (CDPA) and -dystrophy (CDDY and IVDD risk), Hyperuricosuria (SLC), Progressive retinal atrophy (prcd-PRA), von-Willebrand disease type 1 (vWD 1), Progressive retinal atrophy (rcd4-PRA) |
| Teddy Roosevelt Terrier | Malignant Hyperthermia (MH), Degenerative Myelopathy (DM), Chondrodysplasia (CDPA) and -dystrophy (CDDY and IVDD risk), Hyperuricosuria (SLC), Progressive retinal atrophy (prcd-PRA), von-Willebrand disease type 1 (vWD 1), Primary lens luxation (PLL) |
| Tenterfield Terrier | Malignant Hyperthermia (MH), Degenerative Myelopathy (DM), Chondrodysplasia (CDPA) and -dystrophy (CDDY and IVDD risk), Hyperuricosuria (SLC), Progressive retinal atrophy (prcd-PRA), von-Willebrand disease type 1 (vWD 1), Congenital Hypothyreosis (CHG), Primary lens luxation (PLL), Spinocerebellar ataxia (SCA), Pituitary dwarfism |
| Tibetan Spaniel | Malignant Hyperthermia (MH), Degenerative Myelopathy (DM), Chondrodysplasia (CDPA) and -dystrophy (CDDY and IVDD risk), Hyperuricosuria (SLC), Progressive retinal atrophy (prcd-PRA), von-Willebrand disease type 1 (vWD 1), Progressive retinal atrophy (PRA3) |
| Tibetan Terrier | Malignant Hyperthermia (MH), Degenerative Myelopathy (DM), Chondrodysplasia (CDPA) and -dystrophy (CDDY and IVDD risk), Hyperuricosuria (SLC), Progressive retinal atrophy (prcd-PRA), von-Willebrand disease type 1 (vWD 1), Neuronal ceroid lipofuscinosis (NCL), Primary lens luxation (PLL), Progressive retinal atrophy (rcd4-PRA), Pituitary dwarfism Progressive retinal atrophy (PRA3) |
| Toy Fox Terrier | Malignant Hyperthermia (MH), Degenerative Myelopathy (DM), Chondrodysplasia (CDPA) and -dystrophy (CDDY and IVDD risk), Hyperuricosuria (SLC), Progressive retinal atrophy (prcd-PRA), von-Willebrand disease type 1 (vWD 1), Primary lens luxation (PLL), van den Ende-Gupta syndrome (VDEGS) |
| Toy Poodle | Malignant Hyperthermia (MH), Degenerative Myelopathy (DM), Chondrodysplasia (CDPA) and -dystrophy (CDDY and IVDD risk), Hyperuricosuria (SLC), Progressive retinal atrophy (prcd-PRA), von-Willebrand disease type 1 (vWD 1), Progressive retinal atrophy (rcd4-PRA), GM2-Gangliosidosis |
| Tschechoslowakian Wolfdog | Malignant Hyperthermia (MH), Degenerative Myelopathy (DM), Chondrodysplasia (CDPA) and -dystrophy (CDDY and IVDD risk), Hyperuricosuria (SLC), Progressive retinal atrophy (prcd-PRA), von-Willebrand disease type 1 (vWD 1), Pituitary dwarfism |
| Volpino Italiano | Malignant Hyperthermia (MH), Degenerative Myelopathy (DM), Chondrodysplasia (CDPA) and -dystrophy (CDDY and IVDD risk), Hyperuricosuria (SLC), Progressive retinal atrophy (prcd-PRA), von-Willebrand disease type 1 (vWD 1), Primary lens luxation (PLL) |
| Wäller | Malignant Hyperthermia (MH), Degenerative Myelopathy (DM), Chondrodysplasia (CDPA) and -dystrophy (CDDY and IVDD risk), Hyperuricosuria (SLC), Progressive retinal atrophy (prcd-PRA), von-Willebrand disease type 1 (vWD 1), Hereditary cataract (HSF4), MDR1 gene variant (Ivermectin hypersensitivity) |
| Weimaraner | Malignant Hyperthermia (MH), Degenerative Myelopathy (DM), Chondrodysplasia (CDPA) and -dystrophy (CDDY and IVDD risk), Hyperuricosuria (SLC), Progressive retinal atrophy (prcd-PRA), von-Willebrand disease type 1 (vWD 1), Hypomyelination (Shaking Puppy Syndrome) (SPS), Spinal dysraphism (NTD), Paroxysmal exercise-induced dyskinesia, Bunny Hopping Syndrome (BHS1), Lysosomal storage disease (LSD) |
| Welsh Corgi (see Cardigan or Pembroke) | Malignant Hyperthermia (MH), Degenerative Myelopathy (DM), Chondrodysplasia (CDPA) and -dystrophy (CDDY and IVDD risk), Hyperuricosuria (SLC), Progressive retinal atrophy (prcd-PRA), von-Willebrand disease type 1 (vWD 1), Progressive retinal atrophy (rcd3-PRA), Brachyuria (stumpy-tail), Lafora disease, X-chromosomal severe combined immuno-deficiency (X-SCID) |
| Welsh Springer Spaniel | Malignant Hyperthermia (MH), Degenerative Myelopathy (DM), Chondrodysplasia (CDPA) and -dystrophy (CDDY and IVDD risk), Hyperuricosuria (SLC), Progressive retinal atrophy (prcd-PRA), von-Willebrand disease type 1 (vWD 1), Faktor VII - deficiency, Familial nephropathy (FN), Dilated cardiomyopathy (DCM) |
| Welsh Terrier | Malignant Hyperthermia (MH), Degenerative Myelopathy (DM), Chondrodysplasia (CDPA) and -dystrophy (CDDY and IVDD risk), Hyperuricosuria (SLC), Progressive retinal atrophy (prcd-PRA), von-Willebrand disease type 1 (vWD 1), Primary lens luxation (PLL) |
| Westfalia Terrier | Malignant Hyperthermia (MH), Degenerative Myelopathy (DM), Chondrodysplasia (CDPA) and -dystrophy (CDDY and IVDD risk), Hyperuricosuria (SLC), Progressive retinal atrophy (prcd-PRA), von-Willebrand disease type 1 (vWD 1), Primary lens luxation (PLL) |
| Westhighland White Terrier | Malignant Hyperthermia (MH), Degenerative Myelopathy (DM), Chondrodysplasia (CDPA) and -dystrophy (CDDY and IVDD risk), Hyperuricosuria (SLC), Progressive retinal atrophy (prcd-PRA), von-Willebrand disease type 1 (vWD 1), Globoid cell leukodystrophy (Krabbe-disease), Cranimandibular osteopathy (CMO), Pyruvatkinase-deficiency (PK) |
| Whippet | Malignant Hyperthermia (MH), Degenerative Myelopathy (DM), Chondrodysplasia (CDPA) and -dystrophy (CDDY and IVDD risk), Hyperuricosuria (SLC), Progressive retinal atrophy (prcd-PRA), von-Willebrand disease type 1 (vWD 1), Myostatin-mutation (Bully-Whippet), Phosphofructokinase-deficiency (PFKD), Collie eye anomaly (CEA) , MDR1 gene variant (Ivermectin hypersensitivity) |
| White Swiss Shepherd Dog | Malignant Hyperthermia (MH), Degenerative Myelopathy (DM), Chondrodysplasia (CDPA) and -dystrophy (CDDY and IVDD risk), Hyperuricosuria (SLC), Progressive retinal atrophy (prcd-PRA), von-Willebrand disease type 1 (vWD 1), MDR1 gene variant (Ivermectin hypersensitivity), Pituitary dwarfism, Cerebellar hypoplasia (CH) |
| Wire-Haired Pointing Griffon Korthals | Malignant Hyperthermia (MH), Degenerative Myelopathy (DM), Chondrodysplasia (CDPA) and -dystrophy (CDDY and IVDD risk), Hyperuricosuria (SLC), Progressive retinal atrophy (prcd-PRA), von-Willebrand disease type 1 (vWD 1), Hereditary cataract (HSF4) |
| Wirehaired Slovakian Pointer | Malignant Hyperthermia (MH), Degenerative Myelopathy (DM), Chondrodysplasia (CDPA) and -dystrophy (CDDY and IVDD risk), Hyperuricosuria (SLC) Progressive retinal atrophy (prcd-PRA), von-Willebrand disease type 1 (vWD 1) |
| Yorkshire Terrier | Malignant Hyperthermia (MH), Degenerative Myelopathy (DM), Chondrodysplasia (CDPA) and -dystrophy (CDDY and IVDD risk), Hyperuricosuria (SLC), Progressive retinal atrophy (prcd-PRA), von-Willebrand disease type 1 (vWD 1), Primary lens luxation (PLL), L-2-Hydroxy glutaric acid uria (L2HGA), Subacute necrotising encephalopathy (SNE) |
Mačka
Dedičné ochorenia mačiek
| Breed | Genetic disease |
|---|---|
| Abyssinian | MDR1-gene variant, Mucopolysaccharidose Typ VII (MPS VII), Myotonia congenita, Cystinuria, Factor XII deficiency (F12), Congenital hypothyroidism (CH), Polydactyly, genetic blood group determination, Progressive retinal atrophy (rdAc-PRA), Progressive retinal atrophy (rdy-PRA), Pyruvate kinase deficiency (PK) |
| American Curl- / Wirehair | MDR1-gene variant, Mucopolysaccharidose Typ VII (MPS VII), Myotonia congenita, Cystinuria, Factor XII deficiency (F12), Congenital hypothyroidism (CH), Polydactyly, genetic blood group determination, Progressive retinal atrophy (rdAc-PRA) |
| Australian Mist | MDR1-gene variant, Mucopolysaccharidose Typ VII (MPS VII), Myotonia congenita, Cystinuria, Factor XII deficiency (F12), Congenital hypothyroidism (CH), Polydactyly, genetic blood group determination, Hypokalemia |
| Balinese | MDR1-gene variant, Mucopolysaccharidose Typ VII (MPS VII), Myotonia congenita, Cystinuria, Factor XII deficiency (F12), Congenital hypothyroidism (CH), Polydactyly, genetic blood group determination, Progressive retinal atrophy (rdAc-PRA), Mucopolysaccharidose Typ VI (MPS VI), Gangliosidosis (GM1) |
| Bengal (Leopard cat) | MDR1-gene variant, Mucopolysaccharidose Typ VII (MPS VII), Myotonia congenita, Cystinuria, Factor XII deficiency (F12), Congenital hypothyroidism (CH), Polydactyly, genetic blood group determination, Progressive retinal atrophy (rdAc-PRA), Progressive retinal atrophy (PRA-b), Pyruvate kinase deficiency (PK) |
| Birman (Sacred cat of Burma) | MDR1-gene variant, Mucopolysaccharidose Typ VII (MPS VII), Myotonia congenita, Cystinuria, Factor XII deficiency (F12), Congenital hypothyroidism (CH), Polydactyly, genetic blood group determination, Mucopolysaccharidose Typ VI (MPS VI), Polyzystic kidney disease (PKD), Progressive retinal atrophy (pd-PRA), Hypotrichose and short life expectancy |
| British Shorthair (BSH) | MDR1-gene variant, Mucopolysaccharidose Typ VII (MPS VII), Myotonia congenita, Cystinuria, Factor XII deficiency (F12), Congenital hypothyroidism (CH), Polydactyly, genetic blood group determination, Polyzystic kidney disease (PKD), Progressive retinal atrophy (pd-PRA), Skeletal dyplasia (SD), Autoimmune lymphoproliferative syndrome (ALPS) |
| British Longhair (BLH) | MDR1-gene variant, Mucopolysaccharidose Typ VII (MPS VII), Myotonia congenita, Cystinuria, Factor XII deficiency (F12), Congenital hypothyroidism (CH), Polydactyly, genetic blood group determination, Polyzystic kidney disease (PKD), Progressive retinal atrophy (pd-PRA) |
| Burmese | MDR1-gene variant, Mucopolysaccharidose Typ VII (MPS VII), Myotonia congenita, Cystinuria, Factor XII deficiency (F12), Congenital hypothyroidism (CH), Polydactyly, genetic blood group determination, Gangliosidosis (GM2), Head-Defect, Hypokalemia |
| Chartreux | MDR1-gene variant, Mucopolysaccharidose Typ VII (MPS VII), Myotonia congenita, Cystinuria, Factor XII deficiency (F12), Congenital hypothyroidism (CH), Polydactyly, genetic blood group determination, Polyzystic kidney disease (PKD), Progressive retinal atrophy (pd-PRA) |
| Colorpoint | MDR1-gene variant, Mucopolysaccharidose Typ VII (MPS VII), Myotonia congenita, Cystinuria, Factor XII deficiency (F12), Congenital hypothyroidism (CH), Polydactyly, genetic blood group determination, Progressive retinal atrophy (rdAc-PRA), Polyzystic kidney disease (PKD), Progressive retinal atrophy (pd-PRA) |
| Cornish Rex | MDR1-gene variant, Mucopolysaccharidose Typ VII (MPS VII), Myotonia congenita, Cystinuria, Factor XII deficiency (F12), Congenital hypothyroidism (CH), Polydactyly, genetic blood group determination, Progressive retinal atrophy (rdAc-PRA), Hypokalemia |
| Devon Rex | MDR1-gene variant, Mucopolysaccharidose Typ VII (MPS VII), Myotonia congenita, Cystinuria, Factor XII deficiency (F12), Congenital hypothyroidism (CH), Polydactyly, genetic blood group determination, Hypokalemia, Congenital myasthenic syndrome (CMS) |
| Domestic Longhair | MDR1-gene variant, Mucopolysaccharidose Typ VII (MPS VII), Myotonia congenita, Cystinuria, Factor XII deficiency (F12), Congenital hypothyroidism (CH), Polydactyly, genetic blood group determination, Pyruvate kinase deficiency (PK), Polyzystic kidney disease (PKD), Progressive retinal atrophy (pd-PRA) |
| Domestic Shorthair | MDR1-gene variant, Mucopolysaccharidose Typ VII (MPS VII), Myotonia congenita, Cystinuria, Factor XII deficiency (F12), Congenital hypothyroidism (CH), Polydactyly, Mucopolysaccharidose Typ VI (MPS VI), Pyruvate kinase deficiency (PK) |
| Egyptian Mau | MDR1-gene variant, Mucopolysaccharidose Typ VII (MPS VII), Myotonia congenita, Cystinuria, Factor XII deficiency (F12), Congenital hypothyroidism (CH), Polydactyly, genetic blood group determination, Pyruvate kinase deficiency (PK) |
| Exotic Shorthair | MDR1-gene variant, Mucopolysaccharidose Typ VII (MPS VII), Myotonia congenita, Cystinuria, Factor XII deficiency (F12), Congenital hypothyroidism (CH), Polydactyly, genetic blood group determination, Polyzystic kidney disease (PKD), Progressive retinal atrophy (pd-PRA) |
| Javanese | MDR1-gene variant, Mucopolysaccharidose Typ VII (MPS VII), Myotonia congenita, Cystinuria, Factor XII deficiency (F12), Congenital hypothyroidism (CH), Polydactyly, genetic blood group determination, Progressive retinal atrophy (rdAc-PRA), Mucopolysaccharidose Typ VI (MPS VI), Gangliosidosis (GM1) |
| Karthäuser | MDR1-gene variant, Mucopolysaccharidose Typ VII (MPS VII), Myotonia congenita, Cystinuria, Factor XII deficiency (F12), Congenital hypothyroidism (CH), Polydactyly, genetic blood group determination, Polyzystic kidney disease (PKD), Progressive retinal atrophy (pd-PRA) |
| Korat | MDR1-gene variant, Mucopolysaccharidose Typ VII (MPS VII), Myotonia congenita, Cystinuria, Factor XII deficiency (F12), Congenital hypothyroidism (CH), Polydactyly, genetic blood group determination, Gangliosidosis (GM1 ), Gangliosidosis (GM2 ) |
| LaPerm | MDR1-gene variant, Mucopolysaccharidose Typ VII (MPS VII), Myotonia congenita, Cystinuria, Factor XII deficiency (F12), Congenital hypothyroidism (CH), Polydactyly, genetic blood group determination, Pyruvate kinase deficiency (PK) |
| Maine Coon | MDR1-gene variant, Mucopolysaccharidose Typ VII (MPS VII), Myotonia congenita, Cystinuria, Factor XII deficiency (F12), Congenital hypothyroidism (CH), Polydactyly, genetic blood group determination, Hypertrophic cardiomyopathy (HCM), Spinal muscular atrophy (SMA), Pyruvate kinase deficiency (PK), Factor XI deficiency, Blue eyes |
| Munchkin | MDR1-gene variant, Mucopolysaccharidose Typ VII (MPS VII), Myotonia congenita, Cystinuria, Factor XII deficiency (F12), Congenital hypothyroidism (CH), Polydactyly, genetic blood group determination, Progressive retinal atrophy (rdAc-PRA) |
| Neva Masquerade | MDR1-gene variant, Mucopolysaccharidose Typ VII (MPS VII), Myotonia congenita, Cystinuria, Factor XII deficiency (F12), Congenital hypothyroidism (CH), Polydactyly, genetic blood group determination, Pyruvate kinase deficiency (PK), Polycystic kidney disease (PKD2) |
| Norwegian Forest Cat | MDR1-gene variant, Mucopolysaccharidose Typ VII (MPS VII), Myotonia congenita, Cystinuria, Factor XII deficiency (F12), Congenital hypothyroidism (CH), Polydactyly, genetic blood group determination, Glycogen storage disease (GSD4), Pyruvate kinase deficiency (PK) |
| Ocicat | MDR1-gene variant, Mucopolysaccharidose Typ VII (MPS VII), Myotonia congenita, Cystinuria, Factor XII deficiency (F12), Congenital hypothyroidism (CH), Polydactyly, genetic blood group determination, Progressive retinal atrophy (rdAc-PRA), Progressive retinal atrophy (rdy-PRA), Mucopolysaccharidose Typ VI (MPS VI), Pyruvate kinase deficiency (PK), Gangliosidosis (GM1 ) |
| Oriental Shorthair (OSH) | MDR1-gene variant, Mucopolysaccharidose Typ VII (MPS VII), Myotonia congenita, Cystinuria, Factor XII deficiency (F12), Congenital hypothyroidism (CH), Polydactyly, genetic blood group determination, Progressive retinal atrophy (rdAc-PRA), Mucopolysaccharidose Typ VI (MPS VI), Gangliosidosis (GM1 ) |
| Persian | MDR1-gene variant, Mucopolysaccharidose Typ VII (MPS VII), Myotonia congenita, Cystinuria, Factor XII deficiency (F12), Congenital hypothyroidism (CH), Polydactyly, genetic blood group determination, Alpha-Mannosidosis (AMD), Polyzystic kidney disease (PKD), Progressive retinal atrophy (pd-PRA) |
| Peterbald | MDR1-gene variant, Mucopolysaccharidose Typ VII (MPS VII), Myotonia congenita, Cystinuria, Factor XII deficiency (F12), Congenital hypothyroidism (CH), Polydactyly, genetic blood group determination, Progressive retinal atrophy (rdAc-PRA), Mucopolysaccharidose Typ VI (MPS VI), Gangliosidosis (GM1 ) |
| Ragdoll | MDR1-gene variant, Mucopolysaccharidose Typ VII (MPS VII), Myotonia congenita, Cystinuria, Factor XII deficiency (F12), Congenital hypothyroidism (CH), Polydactyly, genetic blood group determination, Hypertrophic cardiomyopathy (HCM), Mucopolysaccharidose Typ VI (MPS VI), Polyzystic kidney disease (PKD), Progressive retinal atrophy (pd-PRA), Mucopolysaccharidose Typ VI (MPS VI), |
| Russian Blue | MDR1-gene variant, Mucopolysaccharidose Typ VII (MPS VII), Myotonia congenita, Cystinuria, Factor XII deficiency (F12), Congenital hypothyroidism (CH), Polydactyly, genetic blood group determination Polyzystic kidney disease (PKD), Progressive retinal atrophy (pd-PRA) |
| Savannah | MDR1-gene variant, Mucopolysaccharidose Typ VII (MPS VII), Myotonia congenita, Cystinuria, Factor XII deficiency (F12), Congenital hypothyroidism (CH), Polydactyly, genetic blood group determination, Pyruvate kinase deficiency (PK) |
| Scottish Fold | MDR1-gene variant, Mucopolysaccharidose Typ VII (MPS VII), Myotonia congenita, Cystinuria, Factor XII deficiency (F12), Congenital hypothyroidism (CH), Polydactyly, genetic blood group determination, Polyzystic kidney disease (PKD), Progressive retinal atrophy (pd-PRA), Osteochondrodysplasia, Autoimmune lymphoproliferative syndrome, Skeletal dyplasia |
| Seychellois | MDR1-gene variant, Mucopolysaccharidose Typ VII (MPS VII), Myotonia congenita, Cystinuria, Factor XII deficiency (F12), Congenital hypothyroidism (CH), Polydactyly, genetic blood group determination, Progressive retinal atrophy (rdAc-PRA), Mucopolysaccharidose Typ VI (MPS VI), Gangliosidosis (GM1 ) |
| Selkirk Rex | MDR1-gene variant, Mucopolysaccharidose Typ VII (MPS VII), Myotonia congenita, Cystinuria, Factor XII deficiency (F12), Congenital hypothyroidism (CH), Polydactyly, genetic blood group determination, Polyzystic kidney disease (PKD), Progressive retinal atrophy (pd-PRA) |
| Siamese | MDR1-gene variant, Mucopolysaccharidose Typ VII (MPS VII), Myotonia congenita, Cystinuria, Factor XII deficiency (F12), Congenital hypothyroidism (CH), Polydactyly, genetic blood group determination, Progressive retinal atrophy (rdAc-PRA), Mucopolysaccharidose Typ VI (MPS VI), Gangliosidosis (GM1), Primary congenital glaucoma (PCG) |
| Sibirian | MDR1-gene variant, Mucopolysaccharidose Typ VII (MPS VII), Myotonia congenita, Cystinuria, Factor XII deficiency (F12), Congenital hypothyroidism (CH), Polydactyly, genetic blood group determination, Pyruvate kinase deficiency (PK), Polycystic kidney disease (PKD2) |
| Singapura | MDR1-gene variant, Mucopolysaccharidose Typ VII (MPS VII), Myotonia congenita, Cystinuria, Factor XII deficiency (F12), Congenital hypothyroidism (CH), Polydactyly, genetic blood group determination, Progressive retinal atrophy (rdAc-PRA), Pyruvate kinase deficiency (PK), Hypokalemia |
| Somali | MDR1-gene variant, Mucopolysaccharidose Typ VII (MPS VII), Myotonia congenita, Cystinuria, Factor XII deficiency (F12), Congenital hypothyroidism (CH), Polydactyly, genetic blood group determination, Progressive retinal atrophy (rdAc-PRA), Progressive retinal atrophy (rdy-PRA), Pyruvate kinase deficiency (PK) |
| Sphynx | MDR1-gene variant, Mucopolysaccharidose Typ VII (MPS VII), Myotonia congenita, Cystinuria, Factor XII deficiency (F12), Congenital hypothyroidism (CH), Polydactyly, genetic blood group determination, Hypertrophic cardiomyopathy (HCM), Hypokalemia, Congenital myasthenic syndrome (CMS) |
| Thai | MDR1-gene variant, Mucopolysaccharidose Typ VII (MPS VII), Myotonia congenita, Cystinuria, Factor XII deficiency (F12), Congenital hypothyroidism (CH), Polydactyly, genetic blood group determination, Progressive retinal atrophy (rdAc-PRA), Mucopolysaccharidose Typ VI (MPS VI), Gangliosidosis (GM1) |
| Tonkinese | MDR1-gene variant, Mucopolysaccharidose Typ VII (MPS VII), Myotonia congenita, Cystinuria, Factor XII deficiency (F12), Congenital hypothyroidism (CH), Polydactyly, genetic blood group determination, Progressive retinal atrophy (rdAc-PRA), Mucopolysaccharidose Typ VI (MPS VI), Gangliosidosis (GM1 ), Gangliosidosis (GM2), Head-Defect, Hypokalemia |
| Turkish Van | MDR1-gene variant, Mucopolysaccharidose Typ VII (MPS VII), Myotonia congenita, Cystinuria, Factor XII deficiency (F12), Congenital hypothyroidism (CH), Polydactyly, genetic blood group determination, Acrodermatitis enteropathica |
| Turkish Angora | MDR1-gene variant, Mucopolysaccharidose Typ VII (MPS VII), Myotonia congenita Cystinuria, Factor XII deficiency (F12), Congenital hypothyroidism (CH), Polydactyly, genetic blood group determination |
Kôň
Dedičné ochorenia koní
| Breed | Genetic diseases |
|---|---|
| Akhal-Teke | Polysaccharid storage myopathie (PSSM), Naked foal syndrome (NFS) |
| American Saddlebred | Polysaccharid storage myopathie (PSSM), Junctional Epidermolysis Bullosa (JEB2) |
| Appaloosa | Polysaccharid storage myopathie (PSSM), Equine malignant hyperthermia (EMH), Hereditary equine regional dermal asthenia (HERDA), Glycogen branching enzyme deficiency (GBED), Hyperkalemic periodic paralysis (HYPP), Androgen Insensitivity Syndrome (AIS), Warmblood Fragile Foal Syndrome (WFFS), Immune Mediated Myositis & MYH1 Myopathy (MYHM), SynchroGait (DMRT3) |
| Arabian Horse | Polysaccharid storage myopathie (PSSM), Severe combined immuno-deficiency (SCID), Lavender foal syndrome (LFS), Cerebellar abiotrophy (CA), Occipitoatlantoaxial Malformation (OAAM) |
| Ardennes / Ardennais | Polysaccharid storage myopathie (PSSM) |
| Barb Horse | Polysaccharid storage myopathie (PSSM) |
| Bashkir Curly | Polysaccharid storage myopathie (PSSM), SynchroGait (DMRT3) |
| Belgian Horse | Polysaccharid storage myopathie (PSSM), Junctional epidermolysis bullosa (JEB1), Ocular Squamous Cell Carcinoma (SCC) |
| Black Forest Horse | Polysaccharid storage myopathie (PSSM) |
| Breton Horse | Polysaccharid storage myopathie (PSSM) |
| Coldblooded Trotter | Polysaccharid storage myopathie (PSSM), SynchroGait (DMRT3) |
| Comtois Horse | Polysaccharid storage myopathie (PSSM) |
| Connemara Pony | Polysaccharid storage myopathie (PSSM), Connemara Pony Hoof Wall Separation Disease (HWSD) |
| Criollo Horse | Polysaccharid storage myopathie (PSSM) |
| Dales Pony | Polysaccharid storage myopathie (PSSM), Foal immunodeficency syndrome (FIS) |
| Dartmoor Pony | Polysaccharid storage myopathie (PSSM) |
| Exmoor Pony | Polysaccharid storage myopathie (PSSM) |
| Fell Pony | Polysaccharid storage myopathie (PSSM), Foal immunodeficency syndrome (FIS) |
| Freiberger | Polysaccharid storage myopathie (PSSM) |
| Frisian Horse | Polysaccharid storage myopathie (PSSM), Hydrocephalus, Dwarfism, Distichiasis |
| Gypsy Horse | Polysaccharid storage myopathie (PSSM) |
| Haflinger | Polysaccharid storage myopathie (PSSM), Ocular Squamous Cell Carcinoma (SCC), Warmblood Fragile Foal Syndrome (WFFS) |
| Hucul Pony | Polysaccharid storage myopathie (PSSM) |
| Icelandic Horse | Polysaccharid storage myopathie (PSSM), SynchroGait (DMRT3) |
| Irish Cob | Polysaccharid storage myopathie (PSSM) |
| Kentucky Mountain Horse | Polysaccharid storage myopathie (PSSM), SynchroGait (DMRT3) |
| Konik | Polysaccharid storage myopathie (PSSM) |
| Lewitzer | Polysaccharid storage myopathie (PSSM) |
| Mangalarga | Polysaccharid storage myopathie (PSSM), SynchroGait (DMRT3) |
| Merens Horse | Polysaccharid storage myopathie (PSSM) |
| Miniature Horse | Polysaccharid storage myopathie (PSSM), Dwarfism (ACAN, Chondrodysplasia), Skeletal Atavism (SA), SynchroGait (DMRT3) |
| Missouri Fox Trotter | Polysaccharid storage myopathie (PSSM), SynchroGait (DMRT3), Congenital Stationary Night Blindness (CSNB2) |
| Morgan Horse | Polysaccharid storage myopathie (PSSM), SynchroGait (DMRT3) |
| Mustang | Polysaccharid storage myopathie (PSSM), Warmblood Fragile Foal Syndrome (WFFS) |
| New Forest Pony | Polysaccharid storage myopathie (PSSM), Congenital Myotonia |
| Noriker | Polysaccharid storage myopathie (PSSM) |
| Paint Horse | Polysaccharid storage myopathie (PSSM), Equine malignant hyperthermia (EMH), Hereditary equine regional dermal asthenia (HERDA), Glycogen branching enzyme deficiency (GBED), Hyperkalemic periodic paralysis (HYPP), Overo lethal white foal syndrome (OLWS) Warmblood Fragile Foal Syndrome (WFFS), Immune Mediated Myositis & MYH1 Myopathy (MYHM), SynchroGait (DMRT3) |
| Paso Fino | Polysaccharid storage myopathie (PSSM), SynchroGait (DMRT3), Tiger Eye |
| Percheron | Polysaccharid storage myopathie (PSSM) |
| Peruvian Horse | Polysaccharid storage myopathie (PSSM), SynchroGait (DMRT3) |
| Pony of the Americas (POA) | Polysaccharid storage myopathie (PSSM) |
| Quater Horse | Polysaccharid storage myopathie (PSSM), Equine malignant hyperthermia (EMH), Hereditary equine regional dermal asthenia (HERDA), Glycogen branching enzyme deficiency (GBED), Hyperkalemic periodic paralysis (HYPP), Androgen Insensitivity Syndrome (AIS), Warmblood Fragile Foal Syndrome (WFFS), Immune Mediated Myositis & MYH1 Myopathy (MYHM), SynchroGait (DMRT3),Equine Juvenile Spinozerebelläre Ataxie (EJSCA) |
| Rhenish German Coldblood | Polysaccharid storage myopathie (PSSM) |
| Rocky Mountain Horse | Polysaccharid storage myopathie (PSSM) |
| Saddlebred | Polysaccharid storage myopathie (PSSM), SynchroGait (DMRT3) |
| Shetland Pony | Polysaccharid storage myopathie (PSSM) Dwarfism (ACAN, Chondrodysplasia), Skeletal Atavism (SA) |
| Standardbred | Polysaccharid storage myopathie (PSSM), SynchroGait (DMRT3), Congenital Stationary Night Blindness (CSNB2) |
| Tennessee Walking Horse | Polysaccharid storage myopathie (PSSM), Androgen insensitivity syndrome (AR2, AR3, AR4, AR5), Congenital Stationary Night Blindness (CSNB2), SynchroGait (DMRT3) |
| Tinker Horse | Polysaccharid storage myopathie (PSSM) |
| Thoroughbred | Polysaccharid storage myopathie (PSSM), Tractability, Idiopathic hypocalcemia, Androgen insensitivity syndrome (AR2, AR3, AR4, AR5) |
| Warmblood Horses | Polysaccharid storage myopathie (PSSM), Warmblood Fragile Foal Syndrome (WFFS), Androgen insensitivity syndrome (AR2, AR3, AR4, AR5) |
| Welsh Pony | Polysaccharid storage myopathie (PSSM) |
| Zweibrücker | Polysaccharid storage myopathie (PSSM) |
