V záujme zachovania jednotnosti v nomenklatúre, uvádzame v tejto tabuľke názvy chorôb a plemien v anglickom jazyku.

Pes

Dedičné ochorenia psov

BreedGenetic disease
Afghan HoundMalignant Hyperthermia (MH), Degenerative Myelopathy (DM), Chondrodysplasia (CDPA) and -dystrophy (CDDY and IVDD risk), Hyperuricosuria (SLC) Progressive retinal atrophy (prcd-PRA)
Airedale TerrierMalignant Hyperthermia (MH), Degenerative Myelopathy (DM), Chondrodysplasia (CDPA) and -dystrophy (CDDY and IVDD risk), Hyperuricosuria (SLC), Progressive retinal atrophy (prcd-PRA), Lethal lung disease (LAMP3), Faktor VII - deficiency, Protein losing nephropathy (PLN)
AkitaMalignant Hyperthermia (MH), Degenerative Myelopathy (DM), Chondrodysplasia (CDPA) and -dystrophy (CDDY and IVDD risk), Hyperuricosuria (SLC), Progressive retinal atrophy (prcd-PRA), Amelogenesis imperfecta (AI)
Alaskan Klee KaiMalignant Hyperthermia (MH), Degenerative Myelopathy (DM), Chondrodysplasia (CDPA) and -dystrophy (CDDY and IVDD risk), Hyperuricosuria (SLC), Progressive retinal atrophy (prcd-PRA), Faktor VII - deficiency
Alaskan MalamuteMalignant Hyperthermia (MH), Degenerative Myelopathy (DM), Chondrodysplasia (CDPA) and -dystrophy (CDDY and IVDD risk), Hyperuricosuria (SLC), Progressive retinal atrophy (prcd-PRA), Alaskan Malamute Polyneuropathy (AMPN), Primary ciliary dyskinesia (PCD)
Alpine DachsbrackeMalignant Hyperthermia (MH), Degenerative Myelopathy (DM), Chondrodysplasia (CDPA) and -dystrophy (CDDY and IVDD risk), Hyperuricosuria (SLC), Progressive retinal atrophy (prcd-PRA), Spinocerebellar ataxia (SCA)
American AkitaMalignant Hyperthermia (MH), Degenerative Myelopathy (DM), Chondrodysplasia (CDPA) and -dystrophy (CDDY and IVDD risk), Hyperuricosuria (SLC), Progressive retinal atrophy (prcd-PRA), Amelogenesis imperfecta (AI), Hämophilia B (Faktor IX)
American BulldogMalignant Hyperthermia (MH), Degenerative Myelopathy (DM), Chondrodysplasia (CDPA) and -dystrophy (CDDY and IVDD risk), Hyperuricosuria (SLC), Progressive retinal atrophy (prcd-PRA), Neuronal ceroid lipofuscinosis (NCL), Canine multi-focal rethinopathy (CMR), Nemalin myopathy (NM), Ichthyosis, Robinow-like syndrome (DVL2)
American Cocker SpanielMalignant Hyperthermia (MH), Degenerative Myelopathy (DM), Chondrodysplasia (CDPA) and -dystrophy (CDDY and IVDD risk), Hyperuricosuria (SLC), Progressive retinal atrophy (prcd-PRA), Phosphofruktokinase-deficiency (PFKD), Exercise induced collapse (EIC), Macrothrombocytopenia (MTC), Gallbladder mucoceles
American Eskimo DogMalignant Hyperthermia (MH), Degenerative Myelopathy (DM), Chondrodysplasia (CDPA) and -dystrophy (CDDY and IVDD risk), Hyperuricosuria (SLC), Progressive retinal atrophy (prcd-PRA), Primary lens luxation (PLL)
American Hairless TerrierMalignant Hyperthermia (MH), Degenerative Myelopathy (DM), Chondrodysplasia (CDPA) and -dystrophy (CDDY and IVDD risk), Hyperuricosuria (SLC), Progressive retinal atrophy (prcd-PRA), Primary lens luxation (PLL)
American Pitbull TerrierMalignant Hyperthermia (MH), Degenerative Myelopathy (DM), Chondrodysplasia (CDPA) and -dystrophy (CDDY and IVDD risk), Hyperuricosuria (SLC), Progressive retinal atrophy (prcd-PRA), Progressive retinal atrophy (crd2-PRA), Robinow-like syndrome (DVL2)
American Staffordshire TerrierMalignant Hyperthermia (MH), Degenerative Myelopathy (DM), Chondrodysplasia (CDPA) and -dystrophy (CDDY and IVDD risk), Hyperuricosuria (SLC), Progressive retinal atrophy (prcd-PRA), Progressive retinal atrophy (crd1-PRA), Neuronal ceroid lipofuscinosis (NCL), Robinow-like syndrome (DVL2), Muscular dystrophy
Australian Cattle DogMalignant Hyperthermia (MH), Degenerative Myelopathy (DM), Chondrodysplasia (CDPA) and -dystrophy (CDDY and IVDD risk), Hyperuricosuria (SLC), Progressive retinal atrophy (prcd-PRA), Neuronal ceroid lipofuscinosis (NCL), Progressive retinal atrophy (rcd4-PRA), Primary lens luxation (PLL), Myotonia congenita, Cystinuria
Australian KelpieMalignant Hyperthermia (MH), Degenerative Myelopathy (DM), Chondrodysplasia (CDPA) and -dystrophy (CDDY and IVDD risk), Hyperuricosuria (SLC), Progressive retinal atrophy (prcd-PRA), Collie eye anomaly (CEA)
Australian ShepherdMalignant Hyperthermia (MH), Degenerative Myelopathy (DM), Chondrodysplasia (CDPA) and -dystrophy (CDDY and IVDD risk), Hyperuricosuria (SLC), Progressive retinal atrophy (prcd-PRA), 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 DogMalignant Hyperthermia (MH), Degenerative Myelopathy (DM), Chondrodysplasia (CDPA) and -dystrophy (CDDY and IVDD risk), Hyperuricosuria (SLC), Progressive retinal atrophy (prcd-PRA), Brachyuria (stumpy-tail),
Austrian PinscherMalignant Hyperthermia (MH), Degenerative Myelopathy (DM), Chondrodysplasia (CDPA) and -dystrophy (CDDY and IVDD risk), Hyperuricosuria (SLC), Progressive retinal atrophy (prcd-PRA), Brachyuria (stumpy-tail)
BarbetMalignant Hyperthermia (MH), Degenerative Myelopathy (DM), Chondrodysplasia (CDPA) and -dystrophy (CDDY and IVDD risk), Hyperuricosuria (SLC), Progressive retinal atrophy (prcd-PRA)
BarsoiMalignant Hyperthermia (MH), Degenerative Myelopathy (DM), Chondrodysplasia (CDPA) and -dystrophy (CDDY and IVDD risk), Hyperuricosuria (SLC) Progressive retinal atrophy (prcd-PRA)
BasenjiMalignant Hyperthermia (MH), Degenerative Myelopathy (DM), Chondrodysplasia (CDPA) and -dystrophy (CDDY and IVDD risk), Hyperuricosuria (SLC), Progressive retinal atrophy (prcd-PRA), Progressive retinal atrophy (Bas-PRA1), Pyruvatkinase-deficiency (PK), Fanconi Syndrome
Basset Fauve de BretagneMalignant Hyperthermia (MH), Degenerative Myelopathy (DM), Chondrodysplasia (CDPA) and -dystrophy (CDDY and IVDD risk), Hyperuricosuria (SLC), Progressive retinal atrophy (prcd-PRA), Primary open angle glaukoma (POAG)
Basset HoundMalignant Hyperthermia (MH), Degenerative Myelopathy (DM), Chondrodysplasia (CDPA) and -dystrophy (CDDY and IVDD risk), Hyperuricosuria (SLC), Progressive retinal atrophy (prcd-PRA), Thrombopathia, Primary open angle glaukoma (POAG), Lafora disease, X-chromosomal severe combined immuno-deficiency (X-SCID)
BeagleMalignant Hyperthermia (MH), Degenerative Myelopathy (DM), Chondrodysplasia (CDPA) and -dystrophy (CDDY and IVDD risk), Hyperuricosuria (SLC), Progressive retinal atrophy (prcd-PRA), 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 CollieMalignant Hyperthermia (MH), Degenerative Myelopathy (DM), Chondrodysplasia (CDPA) and -dystrophy (CDDY and IVDD risk), Hyperuricosuria (SLC), Progressive retinal atrophy (prcd-PRA), Collie eye anomaly (CEA)
BeauceronMalignant Hyperthermia (MH), Degenerative Myelopathy (DM), Chondrodysplasia (CDPA) and -dystrophy (CDDY and IVDD risk), Hyperuricosuria (SLC), Progressive retinal atrophy (prcd-PRA), 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), Copper storage disease - Copper Toxicosis (CT)
Belgian ShepherdMalignant Hyperthermia (MH), Degenerative Myelopathy (DM), Chondrodysplasia (CDPA) and -dystrophy (CDDY and IVDD risk), Hyperuricosuria (SLC), Progressive retinal atrophy (prcd-PRA), 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 SuisseMalignant Hyperthermia (MH), Degenerative Myelopathy (DM), Chondrodysplasia (CDPA) and -dystrophy (CDDY and IVDD risk), Hyperuricosuria (SLC), Progressive retinal atrophy (prcd-PRA), MDR1 gene variant (Ivermectin hypersensitivity)
Bernese Mountain DogMalignant Hyperthermia (MH), Degenerative Myelopathy (DM), Chondrodysplasia (CDPA) and -dystrophy (CDDY and IVDD risk), Hyperuricosuria (SLC), Progressive retinal atrophy (prcd-PRA), Degenerative Myelopathy Exon 1 (DM Exon 1), von-Willebrand disease type 1 (vWD 1)
Bichon FriseMalignant Hyperthermia (MH), Degenerative Myelopathy (DM), Chondrodysplasia (CDPA) and -dystrophy (CDDY and IVDD risk), Hyperuricosuria (SLC), Progressive retinal atrophy (prcd-PRA), Macrothrombocytopenia (MTC)
Black Russian TerrierMalignant Hyperthermia (MH), Degenerative Myelopathy (DM), Chondrodysplasia (CDPA) and -dystrophy (CDDY and IVDD risk), Hyperuricosuria (SLC), Progressive retinal atrophy (prcd-PRA), Juvenile laryngeal paralysis & polyneuropathy (JLPP)
BobtailMalignant Hyperthermia (MH), Degenerative Myelopathy (DM), Chondrodysplasia (CDPA) and -dystrophy (CDDY and IVDD risk), Hyperuricosuria (SLC), Progressive retinal atrophy (prcd-PRA), Primary ciliary dyskinesia (PCD), Exercise induced collapse (EIC), MDR1 gene variant (Ivermectin hypersensitivity)
BoerboelMalignant Hyperthermia (MH), Degenerative Myelopathy (DM), Chondrodysplasia (CDPA) and -dystrophy (CDDY and IVDD risk), Hyperuricosuria (SLC), Progressive retinal atrophy (prcd-PRA), Canine multi-focal rethinopathy (CMR)
BologneseMalignant Hyperthermia (MH), Degenerative Myelopathy (DM), Chondrodysplasia (CDPA) and -dystrophy (CDDY and IVDD risk), Hyperuricosuria (SLC), Progressive retinal atrophy (prcd-PRA)
Bolonka ZwetnaMalignant Hyperthermia (MH), Degenerative Myelopathy (DM), Chondrodysplasia (CDPA) and -dystrophy (CDDY and IVDD risk), Hyperuricosuria (SLC), Progressive retinal atrophy (prcd-PRA), Progressive retinal atrophy (cord1-PRA)
Border CollieMalignant Hyperthermia (MH), Degenerative Myelopathy (DM), Chondrodysplasia (CDPA) and -dystrophy (CDDY and IVDD risk), Hyperuricosuria (SLC), Progressive retinal atrophy (prcd-PRA), 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 TerrierMalignant Hyperthermia (MH), Degenerative Myelopathy (DM), Chondrodysplasia (CDPA) and -dystrophy (CDDY and IVDD risk), Hyperuricosuria (SLC), Progressive retinal atrophy (prcd-PRA), Spongiform leukoencephalomyelopathy (SLEM)
Boston TerrierMalignant Hyperthermia (MH), Degenerative Myelopathy (DM), Chondrodysplasia (CDPA) and -dystrophy (CDDY and IVDD risk), Hyperuricosuria (SLC), Progressive retinal atrophy (prcd-PRA), Hereditary cataract (HSF4), Robinow-like syndrome (DVL2)
Bouvier des ArdennesMalignant Hyperthermia (MH), Degenerative Myelopathy (DM), Chondrodysplasia (CDPA) and -dystrophy (CDDY and IVDD risk), Hyperuricosuria (SLC), Progressive retinal atrophy (prcd-PRA), Brachyuria (stumpy-tail)
Bouvier des FlandresMalignant Hyperthermia (MH), Degenerative Myelopathy (DM), Chondrodysplasia (CDPA) and -dystrophy (CDDY and IVDD risk), Hyperuricosuria (SLC), Progressive retinal atrophy (prcd-PRA), Exercise induced collapse (EIC)
BoxerMalignant Hyperthermia (MH), Degenerative Myelopathy (DM), Chondrodysplasia (CDPA) and -dystrophy (CDDY and IVDD risk), Hyperuricosuria (SLC), Progressive retinal atrophy (prcd-PRA), Hämophilia A (faktor VIII), Macrothrombocytopenia (MTC)
Boykin SpanielMalignant Hyperthermia (MH), Degenerative Myelopathy (DM), Chondrodysplasia (CDPA) and -dystrophy (CDDY and IVDD risk), Hyperuricosuria (SLC), Progressive retinal atrophy (prcd-PRA), Exercise induced collapse (EIC), Collie eye anomaly (CEA)
Braque du BourbonnaisMalignant Hyperthermia (MH), Degenerative Myelopathy (DM), Chondrodysplasia (CDPA) and -dystrophy (CDDY and IVDD risk), Hyperuricosuria (SLC), Progressive retinal atrophy (prcd-PRA), Brachyuria (stumpy-tail)
Brasilian TerrierMalignant Hyperthermia (MH), Degenerative Myelopathy (DM), Chondrodysplasia (CDPA) and -dystrophy (CDDY and IVDD risk), Hyperuricosuria (SLC), Progressive retinal atrophy (prcd-PRA), Mucopolysaccharidosis type VII (MPS7), Brachyuria (stumpy-tail)
BriardMalignant Hyperthermia (MH), Degenerative Myelopathy (DM), Chondrodysplasia (CDPA) and -dystrophy (CDDY and IVDD risk), Hyperuricosuria (SLC), Progressive retinal atrophy (prcd-PRA), Congenital stationary night blindness (CSNB)
Brittany SpanielMalignant Hyperthermia (MH), Degenerative Myelopathy (DM), Chondrodysplasia (CDPA) and -dystrophy (CDDY and IVDD risk), Hyperuricosuria (SLC), Progressive retinal atrophy (prcd-PRA), C3-deficiency (C3), Brachyuria (stumpy-tail)
BullmastiffMalignant Hyperthermia (MH), Degenerative Myelopathy (DM), Chondrodysplasia (CDPA) and -dystrophy (CDDY and IVDD risk), Hyperuricosuria (SLC), Progressive retinal atrophy (prcd-PRA), Progressive retinal atrophy (dom.-PRA), Canine multi-focal rethinopathy (CMR), Mitochondrial fission encephalopathy
Bull TerrierMalignant Hyperthermia (MH), Degenerative Myelopathy (DM), Chondrodysplasia (CDPA) and -dystrophy (CDDY and IVDD risk), Hyperuricosuria (SLC), Progressive retinal atrophy (prcd-PRA), Polycystic kidney disease (PKD), Lethal acrodermatitis (LAD), Laryngeal paralysis (LP)
Cairn TerrierMalignant Hyperthermia (MH), Degenerative Myelopathy (DM), Chondrodysplasia (CDPA) and -dystrophy (CDDY and IVDD risk), Hyperuricosuria (SLC), Progressive retinal atrophy (prcd-PRA), Globoid cell leukodystrophy (Krabbe-disease), Pyruvatkinase-deficiency (PK), Macrothrombocytopenia (MTC), Cranimandibular osteopathy (CMO), Gallbladder mucoceles
Cardigan Welsh CorgiMalignant Hyperthermia (MH), Degenerative Myelopathy (DM), Chondrodysplasia (CDPA) and -dystrophy (CDDY and IVDD risk), Hyperuricosuria (SLC), Progressive retinal atrophy (prcd-PRA), Brachyuria (stumpy-tail), Progressive retinal atrophy (rcd3-PRA), Lafora disease, X-chromosomal severe combined immuno-deficiency (X-SCID)
Cavalier King Charles SpanielMalignant Hyperthermia (MH), Degenerative Myelopathy (DM), Chondrodysplasia (CDPA) and -dystrophy (CDDY and IVDD risk), Hyperuricosuria (SLC), Progressive retinal atrophy (prcd-PRA), Dry eye curly coat syndrome (CCS), Episodic falling (EF), Macrothrombocytopenia (MTC), Muscular dystrophy (MD), Xanthinurie Typ II, MCAD deficiency, Myxomatous mitral valve disease (MMVD)
Central Asian ShepherdMalignant Hyperthermia (MH), Degenerative Myelopathy (DM), Chondrodysplasia (CDPA) and -dystrophy (CDDY and IVDD risk), Hyperuricosuria (SLC), Progressive retinal atrophy (prcd-PRA), Dystrophic epidermolysis bullosa (DEB)
Chesapeake Bay RetrieverMalignant Hyperthermia (MH), Degenerative Myelopathy (DM), Chondrodysplasia (CDPA) and -dystrophy (CDDY and IVDD risk), Hyperuricosuria (SLC), Progressive retinal atrophy (prcd-PRA), Exercise induced collapse (EIC), Ectodermal dysplasia/Skin fragility syndrome (ED/SFS)
ChihuahuaMalignant Hyperthermia (MH), Degenerative Myelopathy (DM), Chondrodysplasia (CDPA) and -dystrophy (CDDY and IVDD risk), Hyperuricosuria (SLC), Progressive retinal atrophy (prcd-PRA), Macrothrombocytopenia (MTC), Neuronal ceroid lipofuscinosis (NCL), Lafora disease
Chinese Crested DogMalignant Hyperthermia (MH), Degenerative Myelopathy (DM), Chondrodysplasia (CDPA) and -dystrophy (CDDY and IVDD risk), Hyperuricosuria (SLC), Progressive retinal atrophy (prcd-PRA), Canine multiple system degeneration (CMSD), Progressive retinal atrophy (rcd3-PRA), Primary lens luxation (PLL), Neuronal ceroid lipofuscinosis (NCL)
ChinookMalignant Hyperthermia (MH), Degenerative Myelopathy (DM), Chondrodysplasia (CDPA) and -dystrophy (CDDY and IVDD risk), Hyperuricosuria (SLC), Progressive retinal atrophy (prcd-PRA), Chondrodysplasia (Dwarfism)
Chow ChowMalignant Hyperthermia (MH), Degenerative Myelopathy (DM), Chondrodysplasia (CDPA) and -dystrophy (CDDY and IVDD risk), Hyperuricosuria (SLC) Progressive retinal atrophy (prcd-PRA)
Clumber SpanielMalignant Hyperthermia (MH), Degenerative Myelopathy (DM), Chondrodysplasia (CDPA) and -dystrophy (CDDY and IVDD risk), Hyperuricosuria (SLC), Progressive retinal atrophy (prcd-PRA), 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), 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 BulldogMalignant Hyperthermia (MH), Degenerative Myelopathy (DM), Chondrodysplasia (CDPA) and -dystrophy (CDDY and IVDD risk), Hyperuricosuria (SLC), Progressive retinal atrophy (prcd-PRA), Cystinuria, Robinow-like syndrome
Coton de TuléarMalignant 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), Brachyuria (stumpy-tail)
Curly Coated RetrieverMalignant Hyperthermia (MH), Degenerative Myelopathy (DM), Chondrodysplasia (CDPA) and -dystrophy (CDDY and IVDD risk), Hyperuricosuria (SLC), Progressive retinal atrophy (prcd-PRA), 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), 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)
DalmatianMalignant Hyperthermia (MH), Degenerative Myelopathy (DM), Chondrodysplasia (CDPA) and -dystrophy (CDDY and IVDD risk), Hyperuricosuria (SLC), Progressive retinal atrophy (prcd-PRA), Acute respiratory distress syndrome (ARDS), Lysosomal storage disease (LSD)
Danish-Swedish FarmdogMalignant Hyperthermia (MH), Degenerative Myelopathy (DM), Chondrodysplasia (CDPA) and -dystrophy (CDDY and IVDD risk), Hyperuricosuria (SLC), Progressive retinal atrophy (prcd-PRA), Brachyuria (stumpy-tail), Primary lens luxation (PLL)
DeerhoundMalignant Hyperthermia (MH), Degenerative Myelopathy (DM), Chondrodysplasia (CDPA) and -dystrophy (CDDY and IVDD risk), Hyperuricosuria (SLC), Progressive retinal atrophy (prcd-PRA), Faktor VII - deficiency, Delayed postoperative hemorrhage (DEPOH)
DobermannMalignant 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), Disproportionate dwarfism
Dogue de BordeauxMalignant Hyperthermia (MH), Degenerative Myelopathy (DM), Chondrodysplasia (CDPA) and -dystrophy (CDDY and IVDD risk), Hyperuricosuria (SLC), Progressive retinal atrophy (prcd-PRA), Digital hyperkeratosis (DH/HFH), Canine multi-focal rethinopathy (CMR), Robinow-like syndrome (DVL2)
Drentse PatrijshondMalignant 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 ShepherdMalignant Hyperthermia (MH), Degenerative Myelopathy (DM), Chondrodysplasia (CDPA) and -dystrophy (CDDY and IVDD risk), Hyperuricosuria (SLC), Progressive retinal atrophy (prcd-PRA), Spongi degeneration with cerebellar ataxia type 1 (SDCA1) Spongi degeneration with cerebellar ataxia type 2 (SDCA2), Inflammatory myopathy (IM)
EloMalignant Hyperthermia (MH), Degenerative Myelopathy (DM), Chondrodysplasia (CDPA) and -dystrophy (CDDY and IVDD risk), Hyperuricosuria (SLC), Progressive retinal atrophy (prcd-PRA), MDR1 gene variant (Ivermectin hypersensitivity)
English BulldogMalignant Hyperthermia (MH), Degenerative Myelopathy (DM), Chondrodysplasia (CDPA) and -dystrophy (CDDY and IVDD risk), Hyperuricosuria (SLC), Progressive retinal atrophy (prcd-PRA), Canine multi-focal rethinopathy (CMR), Cystinuria, Robinow-like syndrome (DVL2)
English Cocker SpanielMalignant Hyperthermia (MH), Degenerative Myelopathy (DM), Chondrodysplasia (CDPA) and -dystrophy (CDDY and IVDD risk), Hyperuricosuria (SLC), Progressive retinal atrophy (prcd-PRA), Familial nephropathy (FN), Exercise induced collapse (EIC), Macrothrombocytopenia (MTC), Gallbladder mucoceles, Acral mutilation syndrome (AMS), Xanthinurie Typ II, Paradoxical pseudomyotonia (PP)
English PointerMalignant Hyperthermia (MH), Degenerative Myelopathy (DM), Chondrodysplasia (CDPA) and -dystrophy (CDDY and IVDD risk), Hyperuricosuria (SLC), Progressive retinal atrophy (prcd-PRA), Acral mutilation syndrome (AMS)
English SetterMalignant Hyperthermia (MH), Degenerative Myelopathy (DM), Chondrodysplasia (CDPA) and -dystrophy (CDDY and IVDD risk), Hyperuricosuria (SLC), Progressive retinal atrophy (prcd-PRA), Neuronal ceroid lipofuscinosis (NCL), Progressive retinal atrophy (rcd4-PRA)
English ShepherdMalignant Hyperthermia (MH), Degenerative Myelopathy (DM), Chondrodysplasia (CDPA) and -dystrophy (CDDY and IVDD risk), Hyperuricosuria (SLC), Progressive retinal atrophy (prcd-PRA)
English Springer SpanielMalignant Hyperthermia (MH), Degenerative Myelopathy (DM), Chondrodysplasia (CDPA) and -dystrophy (CDDY and IVDD risk), Hyperuricosuria (SLC), Progressive retinal atrophy (prcd-PRA), 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 TerrierMalignant Hyperthermia (MH), Degenerative Myelopathy (DM), Chondrodysplasia (CDPA) and -dystrophy (CDDY and IVDD risk), Hyperuricosuria (SLC), Progressive retinal atrophy (prcd-PRA), Xanthinurie Typ II, Dilated cardiomyopathy (DCM)
Entlebucher Mountain DogMalignant Hyperthermia (MH), Degenerative Myelopathy (DM), Chondrodysplasia (CDPA) and -dystrophy (CDDY and IVDD risk), Hyperuricosuria (SLC), Progressive retinal atrophy (prcd-PRA)
EurasianMalignant Hyperthermia (MH), Degenerative Myelopathy (DM), Chondrodysplasia (CDPA) and -dystrophy (CDDY and IVDD risk), Hyperuricosuria (SLC), Progressive retinal atrophy (prcd-PRA), Dandy-Walker-Like malformation (DWLM)
Field SpanielMalignant Hyperthermia (MH), Degenerative Myelopathy (DM), Chondrodysplasia (CDPA) and -dystrophy (CDDY and IVDD risk), Hyperuricosuria (SLC), Progressive retinal atrophy (prcd-PRA), Adult onset neuropathy (AON)
Finnish HoundMalignant Hyperthermia (MH), Degenerative Myelopathy (DM), Chondrodysplasia (CDPA) and -dystrophy (CDDY and IVDD risk), Hyperuricosuria (SLC), Progressive retinal atrophy (prcd-PRA), Finnish hound ataxia (FHA), Faktor VII - deficiency
Finnish LapphundMalignant Hyperthermia (MH), Degenerative Myelopathy (DM), Chondrodysplasia (CDPA) and -dystrophy (CDDY and IVDD risk), Hyperuricosuria (SLC), Progressive retinal atrophy (prcd-PRA), Glycogen storage disease Type II (Pompe) (GSD II)
Flatcoated RetrieverMalignant Hyperthermia (MH), Degenerative Myelopathy (DM), Chondrodysplasia (CDPA) and -dystrophy (CDDY and IVDD risk), Hyperuricosuria (SLC), Progressive retinal atrophy (prcd-PRA), Obesity
Fox TerrierMalignant Hyperthermia (MH), Degenerative Myelopathy (DM), Chondrodysplasia (CDPA) and -dystrophy (CDDY and IVDD risk), Hyperuricosuria (SLC), Progressive retinal atrophy (prcd-PRA), Primary lens luxation (PLL), Spinocerebellar ataxia (SCA), Congenital Hypothyreosis (CHG), van den Ende-Gupta syndrome (VDEGS)
French BulldogMalignant Hyperthermia (MH), Degenerative Myelopathy (DM), Chondrodysplasia (CDPA) and -dystrophy (CDDY and IVDD risk), Hyperuricosuria (SLC), Progressive retinal atrophy (prcd-PRA), Congenital Hypothyreosis (CHG), Hereditary cataract (HSF4), Canine multi-focal rethinopathy (CMR), Cystinuria, Lafora disease, Robinow-like syndrome (DVL2), Progressive retinal atrophy (cord1-PRA)
French SpanielMalignant Hyperthermia (MH), Degenerative Myelopathy (DM), Chondrodysplasia (CDPA) and -dystrophy (CDDY and IVDD risk), Hyperuricosuria (SLC), Progressive retinal atrophy (prcd-PRA), Acral mutilation syndrome (AMS)
Frisian Water DogMalignant Hyperthermia (MH), Degenerative Myelopathy (DM), Chondrodysplasia (CDPA) and -dystrophy (CDDY and IVDD risk), Hyperuricosuria (SLC), Progressive retinal atrophy (prcd-PRA), Severe combined immuno deficiency (SCID)
Galgo EspanolMalignant Hyperthermia (MH), Degenerative Myelopathy (DM), Chondrodysplasia (CDPA) and -dystrophy (CDDY and IVDD risk), Hyperuricosuria (SLC), Progressive retinal atrophy (prcd-PRA), Startle-disease
German Hunting TerrierMalignant Hyperthermia (MH), Degenerative Myelopathy (DM), Chondrodysplasia (CDPA) and -dystrophy (CDDY and IVDD risk), Hyperuricosuria (SLC), Progressive retinal atrophy (prcd-PRA), Primary lens luxation (PLL), Centronuclear myopathy (CNM)
German PinscherMalignant 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 ShepherdMalignant Hyperthermia (MH), Degenerative Myelopathy (DM), Chondrodysplasia (CDPA) and -dystrophy (CDDY and IVDD risk), Hyperuricosuria (SLC), Progressive retinal atrophy (prcd-PRA), 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 DogMalignant Hyperthermia (MH), Degenerative Myelopathy (DM), Chondrodysplasia (CDPA) and -dystrophy (CDDY and IVDD risk), Hyperuricosuria (SLC), Progressive retinal atrophy (prcd-PRA), 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 DogMalignant Hyperthermia (MH), Degenerative Myelopathy (DM), Chondrodysplasia (CDPA) and -dystrophy (CDDY and IVDD risk), Hyperuricosuria (SLC), Progressive retinal atrophy (prcd-PRA), Familial thyroid follicular cell carcinoma
German SpanielMalignant Hyperthermia (MH), Degenerative Myelopathy (DM), Chondrodysplasia (CDPA) and -dystrophy (CDDY and IVDD risk), Hyperuricosuria (SLC), Progressive retinal atrophy (prcd-PRA), Phosphofructokinase-deficiency (PFKD),
German SpitzMalignant Hyperthermia (MH), Degenerative Myelopathy (DM), Chondrodysplasia (CDPA) and -dystrophy (CDDY and IVDD risk), Hyperuricosuria (SLC), Progressive retinal atrophy (prcd-PRA) Progressive retinal atrophy (GUCY2D-PRA)
German Wirehaired PointerMalignant Hyperthermia (MH), Degenerative Myelopathy (DM), Chondrodysplasia (CDPA) and -dystrophy (CDDY and IVDD risk), Hyperuricosuria (SLC), Progressive retinal atrophy (prcd-PRA), von-Willebrand disease type 2 (vWD 2), Exercise induced collapse (EIC)
Giant SchnauzerMalignant Hyperthermia (MH), Degenerative Myelopathy (DM), Chondrodysplasia (CDPA) and -dystrophy (CDDY and IVDD risk), Hyperuricosuria (SLC), Progressive retinal atrophy (prcd-PRA), Faktor VII - deficiency, Progressive retinal atrophy (NECAP1-PRA), Dilated cardiomyopathy (DCM), Squamous cell carcinoma of the toe - risk estimation
Golden RetrieverMalignant Hyperthermia (MH), Degenerative Myelopathy (DM), Chondrodysplasia (CDPA) and -dystrophy (CDDY and IVDD risk), Hyperuricosuria (SLC), Progressive retinal atrophy (prcd-PRA), 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 SetterMalignant Hyperthermia (MH), Degenerative Myelopathy (DM), Chondrodysplasia (CDPA) and -dystrophy (CDDY and IVDD risk), Hyperuricosuria (SLC), Progressive retinal atrophy (prcd-PRA), Hereditary ataxia (HA), Progressive retinal atrophy (rcd4-PRA), Neuronal ceroid lipofuscinosis (NCL)
Great DaneMalignant Hyperthermia (MH), Degenerative Myelopathy (DM), Chondrodysplasia (CDPA) and -dystrophy (CDDY and IVDD risk), Hyperuricosuria (SLC), Progressive retinal atrophy (prcd-PRA), Congenital Ichthyosis, Leukoencephalomyelopathy (LEMP), Centronuclear myopathy (CNM)
Great PyreneeMalignant Hyperthermia (MH), Degenerative Myelopathy (DM), Chondrodysplasia (CDPA) and -dystrophy (CDDY and IVDD risk), Hyperuricosuria (SLC), Progressive retinal atrophy (prcd-PRA), Canine multi-focal rethinopathy (CMR)
Great Swiss Mountain DogMalignant Hyperthermia (MH), Degenerative Myelopathy (DM), Chondrodysplasia (CDPA) and -dystrophy (CDDY and IVDD risk), Hyperuricosuria (SLC), Progressive retinal atrophy (prcd-PRA), Postoperative hemorrhage (P2Y12)
GreyhoundMalignant Hyperthermia (MH), Degenerative Myelopathy (DM), Chondrodysplasia (CDPA) and -dystrophy (CDDY and IVDD risk), Hyperuricosuria (SLC), Progressive retinal atrophy (prcd-PRA), Greyhound neuropathy (GHN), Hereditary nasal parakeratosis (HNPK), Delayed postoperative hemorrhage (DEPOH)
HavaneseMalignant Hyperthermia (MH), Degenerative Myelopathy (DM), Chondrodysplasia (CDPA) and -dystrophy (CDDY and IVDD risk), Hyperuricosuria (SLC), Progressive retinal atrophy (prcd-PRA), Hämophilia A (faktor VIII), Macrothrombocytopenia (MTC)
HovawartMalignant Hyperthermia (MH), Degenerative Myelopathy (DM), Chondrodysplasia (CDPA) and -dystrophy (CDDY and IVDD risk), Hyperuricosuria (SLC), Progressive retinal atrophy (prcd-PRA), Hämophilia B (Faktor IX)
HuskyMalignant Hyperthermia (MH), Degenerative Myelopathy (DM), Chondrodysplasia (CDPA) and -dystrophy (CDDY and IVDD risk), Hyperuricosuria (SLC), Progressive retinal atrophy (prcd-PRA), Alaskan Husky Encephalopathy (AHE), Progressive retinal atrophy (XL-PRA), Warburg Micro Syndrome 1 (WARBM1), GM1-gangliosidosis
Irish Glen of Imaal TerrierMalignant Hyperthermia (MH), Degenerative Myelopathy (DM), Chondrodysplasia (CDPA) and -dystrophy (CDDY and IVDD risk), Hyperuricosuria (SLC), Progressive retinal atrophy (prcd-PRA), Progressive retinal atrophy (crd3-PRA)
Irish Red and White SetterMalignant Hyperthermia (MH), Degenerative Myelopathy (DM), Chondrodysplasia (CDPA) and -dystrophy (CDDY and IVDD risk), Hyperuricosuria (SLC), Progressive retinal atrophy (prcd-PRA), Canine leukozyte adhesion deficiency (CLAD), Progressive retinal atrophy (rcd1-PRA), Progressive retinal atrophy (rcd4-PRA), von-Willebrand disease type 1 (vWD 1)
Irish Red SetterMalignant Hyperthermia (MH), Degenerative Myelopathy (DM), Chondrodysplasia (CDPA) and -dystrophy (CDDY and IVDD risk), Hyperuricosuria (SLC), Progressive retinal atrophy (prcd-PRA), Canine leukozyte adhesion deficiency (CLAD), Progressive retinal atrophy (rcd1-PRA), Globoid cell leukodystrophy (Krabbe-disease), Progressive retinal atrophy (rcd4-PRA), von-Willebrand disease type 1 (vWD 1)
Irish Soft-Coated Wheaten TerrierMalignant Hyperthermia (MH), Degenerative Myelopathy (DM), Chondrodysplasia (CDPA) and -dystrophy (CDDY and IVDD risk), Hyperuricosuria (SLC), Progressive retinal atrophy (prcd-PRA), Protein losing nephropathy (PLN), Paroxysmal dyskinesia (PxD), Microphthalmia (RBP4)
Irish TerrierMalignant Hyperthermia (MH), Degenerative Myelopathy (DM), Chondrodysplasia (CDPA) and -dystrophy (CDDY and IVDD risk), Hyperuricosuria (SLC), Progressive retinal atrophy (prcd-PRA), Digital hyperkeratosis (DH/HFH)
Irish WolfhoundMalignant Hyperthermia (MH), Degenerative Myelopathy (DM), Chondrodysplasia (CDPA) and -dystrophy (CDDY and IVDD risk), Hyperuricosuria (SLC), Progressive retinal atrophy (prcd-PRA), Startle-disease
Italian Cane CorsoMalignant Hyperthermia (MH), Degenerative Myelopathy (DM), Chondrodysplasia (CDPA) and -dystrophy (CDDY and IVDD risk), Hyperuricosuria (SLC), Progressive retinal atrophy (prcd-PRA), Canine multi-focal rethinopathy (CMR), Neuronal ceroid lipofuscinosis (NCL), Dental-skeletal-retinal anomaly (DSRA)
Italian GreyhoundMalignant Hyperthermia (MH), Degenerative Myelopathy (DM), Chondrodysplasia (CDPA) and -dystrophy (CDDY and IVDD risk), Hyperuricosuria (SLC), Progressive retinal atrophy (prcd-PRA), Amelogenesis imperfecta (AI)
Italian SpinoneMalignant Hyperthermia (MH), Degenerative Myelopathy (DM), Chondrodysplasia (CDPA) and -dystrophy (CDDY and IVDD risk), Hyperuricosuria (SLC), Progressive retinal atrophy (prcd-PRA), Cerebellar ataxia (CA)
Jack Russell TerrierMalignant Hyperthermia (MH), Degenerative Myelopathy (DM), Chondrodysplasia (CDPA) and -dystrophy (CDDY and IVDD risk), Hyperuricosuria (SLC), Progressive retinal atrophy (prcd-PRA), 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 ChinMalignant Hyperthermia (MH), Degenerative Myelopathy (DM), Chondrodysplasia (CDPA) and -dystrophy (CDDY and IVDD risk), Hyperuricosuria (SLC), Progressive retinal atrophy (prcd-PRA), GM2-Gangliosidosis
Karelian Bear DogMalignant Hyperthermia (MH), Degenerative Myelopathy (DM), Chondrodysplasia (CDPA) and -dystrophy (CDDY and IVDD risk), Hyperuricosuria (SLC), Progressive retinal atrophy (prcd-PRA), Brachyuria (stumpy-tail), Chondrodysplasia (Dwarfism), Hypophosphatasia (HPP), Pituitary dwarfism
KeeshondMalignant Hyperthermia (MH), Degenerative Myelopathy (DM), Chondrodysplasia (CDPA) and -dystrophy (CDDY and IVDD risk), Hyperuricosuria (SLC) Progressive retinal atrophy (prcd-PRA),
Kerry Blue TerrierMalignant Hyperthermia (MH), Degenerative Myelopathy (DM), Chondrodysplasia (CDPA) and -dystrophy (CDDY and IVDD risk), Hyperuricosuria (SLC), Progressive retinal atrophy (prcd-PRA), Canine multiple system degeneration (CMSD), von-Willebrand disease type 1 (vWD 1), Factor XI deficiency (F11)
KomondorMalignant Hyperthermia (MH), Degenerative Myelopathy (DM), Chondrodysplasia (CDPA) and -dystrophy (CDDY and IVDD risk), Hyperuricosuria (SLC), Progressive retinal atrophy (prcd-PRA), Imerslund-Gräsbeck syndrom (IGS)
KooikerhondjeMalignant Hyperthermia (MH), Degenerative Myelopathy (DM), Chondrodysplasia (CDPA) and -dystrophy (CDDY and IVDD risk), Hyperuricosuria (SLC), Progressive retinal atrophy (prcd-PRA), von-Willebrand disease type 3 (vWD 3), necrotizing myelopathy (HNM)
KromfohrländerMalignant Hyperthermia (MH), Degenerative Myelopathy (DM), Chondrodysplasia (CDPA) and -dystrophy (CDDY and IVDD risk), Hyperuricosuria (SLC), Progressive retinal atrophy (prcd-PRA), Digital hyperkeratosis (DH/HFH), von-Willebrand disease type 1 (vWD 1)
KuvaszMalignant Hyperthermia (MH), Degenerative Myelopathy (DM), Chondrodysplasia (CDPA) and -dystrophy (CDDY and IVDD risk), Hyperuricosuria (SLC), Progressive retinal atrophy (prcd-PRA)
Labrador RetrieverMalignant Hyperthermia (MH), Degenerative Myelopathy (DM), Chondrodysplasia (CDPA) and -dystrophy (CDDY and IVDD risk), Hyperuricosuria (SLC), Progressive retinal atrophy (prcd-PRA), 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 RomagnoloMalignant Hyperthermia (MH), Degenerative Myelopathy (DM), Chondrodysplasia (CDPA) and -dystrophy (CDDY and IVDD risk), Hyperuricosuria (SLC), Progressive retinal atrophy (prcd-PRA), Lagotto storage disease (LSD), Juvenile epilepsy (JE), Neuroaxonal dystrophy (NAD)
Lakeland TerrierMalignant Hyperthermia (MH), Degenerative Myelopathy (DM), Chondrodysplasia (CDPA) and -dystrophy (CDDY and IVDD risk), Hyperuricosuria (SLC), Progressive retinal atrophy (prcd-PRA), Primary lens luxation (PLL)
Lancashire HeelerMalignant Hyperthermia (MH), Degenerative Myelopathy (DM), Chondrodysplasia (CDPA) and -dystrophy (CDDY and IVDD risk), Hyperuricosuria (SLC), Progressive retinal atrophy (prcd-PRA), Collie eye anomaly (CEA) , Primary lens luxation (PLL)
LandseerMalignant Hyperthermia (MH), Degenerative Myelopathy (DM), Chondrodysplasia (CDPA) and -dystrophy (CDDY and IVDD risk), Hyperuricosuria (SLC), Progressive retinal atrophy (prcd-PRA), Cystinuria, Muscular dystrophy (MD), Thrombopathia
Lapponian HerderMalignant Hyperthermia (MH), Degenerative Myelopathy (DM), Chondrodysplasia (CDPA) and -dystrophy (CDDY and IVDD risk), Hyperuricosuria (SLC), Progressive retinal atrophy (prcd-PRA), Glycogen storage disease type II (Pompe) (GSD II), Canine multi-focal rethinopathy (CMR), Pituitary dwarfism, Progressive retinal atrophy (IFT122-PRA)
Large MünsterländerMalignant Hyperthermia (MH), Degenerative Myelopathy (DM), Chondrodysplasia (CDPA) and -dystrophy (CDDY and IVDD risk), Hyperuricosuria (SLC) Progressive retinal atrophy (prcd-PRA)
LeonbergerMalignant Hyperthermia (MH), Degenerative Myelopathy (DM), Chondrodysplasia (CDPA) and -dystrophy (CDDY and IVDD risk), Hyperuricosuria (SLC), Progressive retinal atrophy (prcd-PRA), Leonberger polyneuropathy 1 (LPN1), Leonberger polyneuropathy 2 (LPN2), Leukoencephalomyelopathy (LEMP), Laryngeal paralysis with polyneuropathy type 3 (LPPN3)
Lhasa ApsoMalignant Hyperthermia (MH), Degenerative Myelopathy (DM), Chondrodysplasia (CDPA) and -dystrophy (CDDY and IVDD risk), Hyperuricosuria (SLC), Progressive retinal atrophy (prcd-PRA), Progressive retinal atrophy (PRA4), Hämophilia B (Faktor IX)
Lucas TerrierMalignant Hyperthermia (MH), Degenerative Myelopathy (DM), Chondrodysplasia (CDPA) and -dystrophy (CDDY and IVDD risk), Hyperuricosuria (SLC), Progressive retinal atrophy (prcd-PRA), Primary lens luxation (PLL)
Magyar ViszlaMalignant Hyperthermia (MH), Degenerative Myelopathy (DM), Chondrodysplasia (CDPA) and -dystrophy (CDDY and IVDD risk), Hyperuricosuria (SLC), Progressive retinal atrophy (prcd-PRA), Neonatal cerebellar abiotrophy (NCCD), Exfoliative cutaneous lupus erythematosus (ECLE), Disproportionate dwarfism
MalteseMalignant Hyperthermia (MH), Degenerative Myelopathy (DM), Chondrodysplasia (CDPA) and -dystrophy (CDDY and IVDD risk), Hyperuricosuria (SLC), Progressive retinal atrophy (prcd-PRA), Glycogen storage disease type Ia (GSD Ia), Macrothrombocytopenia (MTC)
Manchester TerrierMalignant 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)
MarkiesjeMalignant Hyperthermia (MH), Degenerative Myelopathy (DM), Chondrodysplasia (CDPA) and -dystrophy (CDDY and IVDD risk), Hyperuricosuria (SLC), Progressive retinal atrophy (prcd-PRA)
MastiffMalignant Hyperthermia (MH), Degenerative Myelopathy (DM), Chondrodysplasia (CDPA) and -dystrophy (CDDY and IVDD risk), Hyperuricosuria (SLC), Progressive retinal atrophy (prcd-PRA), Progressive retinal atrophy (dom.-PRA), Canine multi-focal rethinopathy (CMR), Cystinuria
McNabMalignant Hyperthermia (MH), Degenerative Myelopathy (DM), Chondrodysplasia (CDPA) and -dystrophy (CDDY and IVDD risk), Hyperuricosuria (SLC), Progressive retinal atrophy (prcd-PRA), MDR1 gene variant (Ivermectin hypersensitivity)
Miniature American ShepherdMalignant Hyperthermia (MH), Degenerative Myelopathy (DM), Chondrodysplasia (CDPA) and -dystrophy (CDDY and IVDD risk), Hyperuricosuria (SLC), Progressive retinal atrophy (prcd-PRA), 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 TerrierMalignant Hyperthermia (MH), Degenerative Myelopathy (DM), Chondrodysplasia (CDPA) and -dystrophy (CDDY and IVDD risk), Hyperuricosuria (SLC), Progressive retinal atrophy (prcd-PRA), Primary lens luxation (PLL), Lethal acrodermatitis (LAD), Laryngeal paralysis (LP)
Miniature PinscherMalignant Hyperthermia (MH), Degenerative Myelopathy (DM), Chondrodysplasia (CDPA) and -dystrophy (CDDY and IVDD risk), Hyperuricosuria (SLC), Progressive retinal atrophy (prcd-PRA), Mucopolysaccharidosis type VI (MPS6), Cystinuria
Miniature PoodleMalignant Hyperthermia (MH), Degenerative Myelopathy (DM), Chondrodysplasia (CDPA) and -dystrophy (CDDY and IVDD risk), Hyperuricosuria (SLC), Progressive retinal atrophy (prcd-PRA), Progressive retinal atrophy (rcd4-PRA), von-Willebrand disease type 1 (vWD 1), GM2-Gangliosidosis, Osteochondrodysplasia (OCD)
Miniature SchnauzerMalignant Hyperthermia (MH), Degenerative Myelopathy (DM), Chondrodysplasia (CDPA) and -dystrophy (CDDY and IVDD risk), Hyperuricosuria (SLC), Progressive retinal atrophy (prcd-PRA), 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)
MudiMalignant Hyperthermia (MH), Degenerative Myelopathy (DM), Chondrodysplasia (CDPA) and -dystrophy (CDDY and IVDD risk), Hyperuricosuria (SLC), Progressive retinal atrophy (prcd-PRA), Brachyuria (stumpy-tail)
NewfoundlandMalignant Hyperthermia (MH), Degenerative Myelopathy (DM), Chondrodysplasia (CDPA) and -dystrophy (CDDY and IVDD risk), Hyperuricosuria (SLC), Progressive retinal atrophy (prcd-PRA), Cystinuria, Lafora disease
Newzealand HuntawayMalignant Hyperthermia (MH), Degenerative Myelopathy (DM), Chondrodysplasia (CDPA) and -dystrophy (CDDY and IVDD risk), Hyperuricosuria (SLC), Progressive retinal atrophy (prcd-PRA), Mucopolysaccharidosis type IIIa (MPS3a)
Norfolk TerrierMalignant Hyperthermia (MH), Degenerative Myelopathy (DM), Chondrodysplasia (CDPA) and -dystrophy (CDDY and IVDD risk), Hyperuricosuria (SLC), Progressive retinal atrophy (prcd-PRA), Primary lens luxation (PLL), Epidermolytic hyperkeratosis (EHK), Muscular dystrophy (MD), Macrothrombocytopenia (MTC)
NorrbottenspitzMalignant Hyperthermia (MH), Degenerative Myelopathy (DM), Chondrodysplasia (CDPA) and -dystrophy (CDDY and IVDD risk), Hyperuricosuria (SLC), Progressive retinal atrophy (prcd-PRA), Finnish hound ataxia (FHA)
Northern InuitMalignant Hyperthermia (MH), Degenerative Myelopathy (DM), Chondrodysplasia (CDPA) and -dystrophy (CDDY and IVDD risk), Hyperuricosuria (SLC), Progressive retinal atrophy (prcd-PRA), Retinal dysplasia (OSD)
Norwegian BuhundMalignant Hyperthermia (MH), Degenerative Myelopathy (DM), Chondrodysplasia (CDPA) and -dystrophy (CDDY and IVDD risk), Hyperuricosuria (SLC), Progressive retinal atrophy (prcd-PRA), Hereditary ataxia (HA)
Norwegian ElkhoundMalignant Hyperthermia (MH), Degenerative Myelopathy (DM), Chondrodysplasia (CDPA) and -dystrophy (CDDY and IVDD risk), Hyperuricosuria (SLC), Progressive retinal atrophy (prcd-PRA), Primary open angle glaukoma (POAG), Chondrodysplasia (Dwarfism), Hereditary ataxia (HA)
Norwegian LundehundMalignant Hyperthermia (MH), Degenerative Myelopathy (DM), Chondrodysplasia (CDPA) and -dystrophy (CDDY and IVDD risk), Hyperuricosuria (SLC), Progressive retinal atrophy (prcd-PRA), Lundehund syndrome (LHS)
Norwich TerrierMalignant Hyperthermia (MH), Degenerative Myelopathy (DM), Chondrodysplasia (CDPA) and -dystrophy (CDDY and IVDD risk), Hyperuricosuria (SLC), Progressive retinal atrophy (prcd-PRA), Primary lens luxation (PLL), Renal dysplasia and hepatic fibrosis (RDHN), Upper airway syndrome (UAS)
Nova Scotia Duck Tolling RetrieverMalignant Hyperthermia (MH), Degenerative Myelopathy (DM), Chondrodysplasia (CDPA) and -dystrophy (CDDY and IVDD risk), Hyperuricosuria (SLC), Progressive retinal atrophy (prcd-PRA), Collie eye anomaly (CEA) , Cleft lip/palate and syndactyly (CLPS), Cerebellar degeneration and myositis complex, Dilated cardiomyopathy (DCM)
Old Danish Pointing DogMalignant Hyperthermia (MH), Degenerative Myelopathy (DM), Chondrodysplasia (CDPA) and -dystrophy (CDDY and IVDD risk), Hyperuricosuria (SLC), Progressive retinal atrophy (prcd-PRA), Congenital myasthenic syndrome (CMS), Progressive retinal atrophy (rcd4-PRA)
Olde English BulldogMalignant Hyperthermia (MH), Degenerative Myelopathy (DM), Chondrodysplasia (CDPA) and -dystrophy (CDDY and IVDD risk), Hyperuricosuria (SLC), Progressive retinal atrophy (prcd-PRA), Cystinuria, Robinow-like syndrome (DVL2)
Old English SheepdogMalignant Hyperthermia (MH), Degenerative Myelopathy (DM), Chondrodysplasia (CDPA) and -dystrophy (CDDY and IVDD risk), Hyperuricosuria (SLC), Progressive retinal atrophy (prcd-PRA), Primary ciliary dyskinesia (PCD), Exercise induced collapse (EIC), Hereditary ataxia (HA), Hämophilia A (faktor VIII), MDR1 gene variant (Ivermectin hypersensitivity), Multiocular defect (MOD)
PapillonMalignant Hyperthermia (MH), Degenerative Myelopathy (DM), Chondrodysplasia (CDPA) and -dystrophy (CDDY and IVDD risk), Hyperuricosuria (SLC), Progressive retinal atrophy (prcd-PRA), Progressive retinal atrophy (pap-PRA1), von-Willebrand disease type 1 (vWD 1) Neuroaxonal dystrophy (NAD), Faktor VII - deficiency
Parson Russell TerrierMalignant Hyperthermia (MH), Degenerative Myelopathy (DM), Chondrodysplasia (CDPA) and -dystrophy (CDDY and IVDD risk), Hyperuricosuria (SLC), Progressive retinal atrophy (prcd-PRA), 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 TerrierMalignant Hyperthermia (MH), Degenerative Myelopathy (DM), Chondrodysplasia (CDPA) and -dystrophy (CDDY and IVDD risk), Hyperuricosuria (SLC), Progressive retinal atrophy (prcd-PRA), Primary lens luxation (PLL), Spinocerebellar ataxia (SCA)
Pembroke Welsh CorgiMalignant Hyperthermia (MH), Degenerative Myelopathy (DM), Chondrodysplasia (CDPA) and -dystrophy (CDDY and IVDD risk), Hyperuricosuria (SLC), Progressive retinal atrophy (prcd-PRA), Brachyuria (stumpy-tail), von-Willebrand disease type 1 (vWD 1), Exercise induced collapse (EIC), Lafora disease, X-chromosomal severe combined immuno-deficiency (X-SCID)
Perro de Presa CanarioMalignant Hyperthermia (MH), Degenerative Myelopathy (DM), Chondrodysplasia (CDPA) and -dystrophy (CDDY and IVDD risk), Hyperuricosuria (SLC), Progressive retinal atrophy (prcd-PRA), Canine multi-focal rethinopathy (CMR)
Petit Basset Griffon VendeenMalignant Hyperthermia (MH), Degenerative Myelopathy (DM), Chondrodysplasia (CDPA) and -dystrophy (CDDY and IVDD risk), Hyperuricosuria (SLC), Progressive retinal atrophy (prcd-PRA), Primary open angle glaukoma (POAG)
PhalèneMalignant Hyperthermia (MH), Degenerative Myelopathy (DM), Chondrodysplasia (CDPA) and -dystrophy (CDDY and IVDD risk), Hyperuricosuria (SLC), Progressive retinal atrophy (prcd-PRA), 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), Brachyuria (stumpy-tail), Progressive retinal atrophy (rcd4-PRA)
PomeranianMalignant Hyperthermia (MH), Degenerative Myelopathy (DM), Chondrodysplasia (CDPA) and -dystrophy (CDDY and IVDD risk), Hyperuricosuria (SLC), Progressive retinal atrophy (prcd-PRA), Progressive retinal atrophy (rcd3-PRA), Vitamin-D dependent rickets (VDR), Gallbladder mucoceles, Methemoglobinemia (MetHg)
Portuguese Water DogMalignant Hyperthermia (MH), Degenerative Myelopathy (DM), Chondrodysplasia (CDPA) and -dystrophy (CDDY and IVDD risk), Hyperuricosuria (SLC), Progressive retinal atrophy (prcd-PRA), Progressive retinal atrophy early onset (eo-PRA), GM1-Gangliosidosis, Improper Coat
Pug DogMalignant Hyperthermia (MH), Degenerative Myelopathy (DM), Chondrodysplasia (CDPA) and -dystrophy (CDDY and IVDD risk), Hyperuricosuria (SLC), Progressive retinal atrophy (prcd-PRA), Pyruvatkinase-deficiency (PK), Pug dog encephalitis (PDE), Primary lens luxation (PLL), May-Hegglin anomaly (MHA)
PuliMalignant Hyperthermia (MH), Degenerative Myelopathy (DM), Chondrodysplasia (CDPA) and -dystrophy (CDDY and IVDD risk), Hyperuricosuria (SLC), Progressive retinal atrophy (prcd-PRA), Progressive retinal atrophy (BBS4-PRA)
Pyrenean Mountain DogMalignant Hyperthermia (MH), Degenerative Myelopathy (DM), Chondrodysplasia (CDPA) and -dystrophy (CDDY and IVDD risk), Hyperuricosuria (SLC), Progressive retinal atrophy (prcd-PRA), Canine multi-focal rethinopathy (CMR), Glanzmann Thrombastenia (GT), Cerebellar ataxia
Pyrenean SheepdogMalignant Hyperthermia (MH), Degenerative Myelopathy (DM), Chondrodysplasia (CDPA) and -dystrophy (CDDY and IVDD risk), Hyperuricosuria (SLC), Progressive retinal atrophy (prcd-PRA), Brachyuria (stumpy-tail)
Rat TerrierMalignant Hyperthermia (MH), Degenerative Myelopathy (DM), Chondrodysplasia (CDPA) and -dystrophy (CDDY and IVDD risk), Hyperuricosuria (SLC), Progressive retinal atrophy (prcd-PRA), Primary lens luxation (PLL), Congenital Hypothyreosis (CHG)
Rhodesian RidgebackMalignant Hyperthermia (MH), Degenerative Myelopathy (DM), Chondrodysplasia (CDPA) and -dystrophy (CDDY and IVDD risk), Hyperuricosuria (SLC), Progressive retinal atrophy (prcd-PRA), Juvenile myoclonic epilepsy (JME), Hämophilia B (Faktor IX), Hämophilia A (faktor VIII), Ventricular Arrhythmia , Hereditary deafness (EOAD)
RottweilerMalignant Hyperthermia (MH), Degenerative Myelopathy (DM), Chondrodysplasia (CDPA) and -dystrophy (CDDY and IVDD risk), Hyperuricosuria (SLC), Progressive retinal atrophy (prcd-PRA), Juvenile laryngeal paralysis & polyneuropathy (JLPP), X-linked Myopathy (XL-MTM), Leukoencephalomyelopathy (LEMP), Neuroaxonal dystrophy (NAD), Hereditary deafness
Saarloos WolfdogMalignant Hyperthermia (MH), Degenerative Myelopathy (DM), Chondrodysplasia (CDPA) and -dystrophy (CDDY and IVDD risk), Hyperuricosuria (SLC), Progressive retinal atrophy (prcd-PRA), Pituitary dwarfism, PRA with neurodegeneration (PCYT2 deficiency)
SalukiMalignant Hyperthermia (MH), Degenerative Myelopathy (DM), Chondrodysplasia (CDPA) and -dystrophy (CDDY and IVDD risk), Hyperuricosuria (SLC), Progressive retinal atrophy (prcd-PRA), Neuronal ceroid lipofuscinosis (NCL), Succinic semialdehyde dehydrogenase deficiency (SSADHD)
SamoyedMalignant Hyperthermia (MH), Degenerative Myelopathy (DM), Chondrodysplasia (CDPA) and -dystrophy (CDDY and IVDD risk), Hyperuricosuria (SLC), Progressive retinal atrophy (prcd-PRA), Familial nephropathy (FN), Progressive retinal atrophy (XL-PRA), Amelogenesis imperfecta / Familial enamel hypoplasia (FEH)
Savoy SheepdogMalignant Hyperthermia (MH), Degenerative Myelopathy (DM), Chondrodysplasia (CDPA) and -dystrophy (CDDY and IVDD risk), Hyperuricosuria (SLC), Progressive retinal atrophy (prcd-PRA), Brachyuria (stumpy-tail)
SchapendoesMalignant Hyperthermia (MH), Degenerative Myelopathy (DM), Chondrodysplasia (CDPA) and -dystrophy (CDDY and IVDD risk), Hyperuricosuria (SLC), Progressive retinal atrophy (prcd-PRA), Progressive retinal atrophy (g-PRA)
SchipperkeMalignant Hyperthermia (MH), Degenerative Myelopathy (DM), Chondrodysplasia (CDPA) and -dystrophy (CDDY and IVDD risk), Hyperuricosuria (SLC), Progressive retinal atrophy (prcd-PRA), Brachyuria (stumpy-tail), Mucopolysaccharidosis type IIIb (MPS3b)
SchnauzerMalignant Hyperthermia (MH), Degenerative Myelopathy (DM), Chondrodysplasia (CDPA) and -dystrophy (CDDY and IVDD risk), Hyperuricosuria (SLC), Progressive retinal atrophy (prcd-PRA), Dilated cardiomyopathy (DCM), Leukoencephalopathy (LEP)
Scottish TerrierMalignant Hyperthermia (MH), Degenerative Myelopathy (DM), Chondrodysplasia (CDPA) and -dystrophy (CDDY and IVDD risk), Hyperuricosuria (SLC), Progressive retinal atrophy (prcd-PRA), von-Willebrand disease type 3 (vWD 3), Cranimandibular osteopathy (CMO)
Sealyham TerrierMalignant Hyperthermia (MH), Degenerative Myelopathy (DM), Chondrodysplasia (CDPA) and -dystrophy (CDDY and IVDD risk), Hyperuricosuria (SLC), Progressive retinal atrophy (prcd-PRA), Primary lens luxation (PLL)
Shar PeiMalignant Hyperthermia (MH), Degenerative Myelopathy (DM), Chondrodysplasia (CDPA) and -dystrophy (CDDY and IVDD risk), Hyperuricosuria (SLC), Progressive retinal atrophy (prcd-PRA), 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 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 InuMalignant Hyperthermia (MH), Degenerative Myelopathy (DM), Chondrodysplasia (CDPA) and -dystrophy (CDDY and IVDD risk), Hyperuricosuria (SLC), Progressive retinal atrophy (prcd-PRA), GM1-Gangliosidosis, GM2-Gangliosidosis
Shih TzuMalignant Hyperthermia (MH), Degenerative Myelopathy (DM), Chondrodysplasia (CDPA) and -dystrophy (CDDY and IVDD risk), Hyperuricosuria (SLC), Progressive retinal atrophy (prcd-PRA), Prekallikrein deficiency (KLK), Macrothrombocytopenia (MTC), Robinow-like syndrome (DVL2), Progressive retinal atrophy (JPH2-PRA)
Silken WindhoundMalignant Hyperthermia (MH), Degenerative Myelopathy (DM), Chondrodysplasia (CDPA) and -dystrophy (CDDY and IVDD risk), Hyperuricosuria (SLC), Progressive retinal atrophy (prcd-PRA), 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), Myostatin-mutation (Bully-Whippet), Phosphofructokinase-deficiency (PFKD), Collie eye anomaly (CEA) , MDR1 gene variant (Ivermectin hypersensitivity)
Silky TerrierMalignant Hyperthermia (MH), Degenerative Myelopathy (DM), Chondrodysplasia (CDPA) and -dystrophy (CDDY and IVDD risk), Hyperuricosuria (SLC), Progressive retinal atrophy (prcd-PRA)
SloughiMalignant Hyperthermia (MH), Degenerative Myelopathy (DM), Chondrodysplasia (CDPA) and -dystrophy (CDDY and IVDD risk), Hyperuricosuria (SLC), Progressive retinal atrophy (prcd-PRA), Progressive retinal atrophy (rcd1a-PRA)
Small MunsterlanderMalignant Hyperthermia (MH), Degenerative Myelopathy (DM), Chondrodysplasia (CDPA) and -dystrophy (CDDY and IVDD risk), Hyperuricosuria (SLC), Progressive retinal atrophy (prcd-PRA), Progressive retinal atrophy (rcd4-PRA)
Spanish Water DogMalignant Hyperthermia (MH), Degenerative Myelopathy (DM), Chondrodysplasia (CDPA) and -dystrophy (CDDY and IVDD risk), Hyperuricosuria (SLC), Progressive retinal atrophy (prcd-PRA), Congenital Hypothyreosis (CHG), Neuroaxonal dystrophy (NAD), Brachyuria (stumpy-tail), Progressive retinal atrophy early onset (eo-PRA)
Saint BernardMalignant Hyperthermia (MH), Degenerative Myelopathy (DM), Chondrodysplasia (CDPA) and -dystrophy (CDDY and IVDD risk), Hyperuricosuria (SLC), Progressive retinal atrophy (prcd-PRA), Laryngeal paralysis with polyneuropathy type 3 (LPPN3)
StabyhounMalignant 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 TerrierMalignant Hyperthermia (MH), Degenerative Myelopathy (DM), Chondrodysplasia (CDPA) and -dystrophy (CDDY and IVDD risk), Hyperuricosuria (SLC), Progressive retinal atrophy (prcd-PRA), L-2-Hydroxy glutaric acid uria (L2HGA), Hereditary cataract (HSF4), Robinow-like syndrome (DVL2)
Standard PoodleMalignant Hyperthermia (MH), Degenerative Myelopathy (DM), Chondrodysplasia (CDPA) and -dystrophy (CDDY and IVDD risk), Hyperuricosuria (SLC), Progressive retinal atrophy (prcd-PRA), Neonatal enzephalopathy with seizures (NEWS), Progressive retinal atrophy (rcd4-PRA), von-Willebrand disease type 1 (vWD 1), Macrothrombocytopenia (MTC), Squamous cell carcinoma of the toe - risk estimation
Sussex SpanielMalignant Hyperthermia (MH), Degenerative Myelopathy (DM), Chondrodysplasia (CDPA) and -dystrophy (CDDY and IVDD risk), Hyperuricosuria (SLC), Progressive retinal atrophy (prcd-PRA), Pyruvat dehydrogenase phosphatase 1 deficiency (PDP1)
Swedish FarmdogMalignant Hyperthermia (MH), Degenerative Myelopathy (DM), Chondrodysplasia (CDPA) and -dystrophy (CDDY and IVDD risk), Hyperuricosuria (SLC), Progressive retinal atrophy (prcd-PRA), Brachyuria (stumpy-tail)
Swedish LapphundMalignant Hyperthermia (MH), Degenerative Myelopathy (DM), Chondrodysplasia (CDPA) and -dystrophy (CDDY and IVDD risk), Hyperuricosuria (SLC), Progressive retinal atrophy (prcd-PRA), Glycogen storage disease Type II (Pompe) (GSD II)
Swedish VallhundMalignant Hyperthermia (MH), Degenerative Myelopathy (DM), Chondrodysplasia (CDPA) and -dystrophy (CDDY and IVDD risk), Hyperuricosuria (SLC), Progressive retinal atrophy (prcd-PRA), Brachyuria (stumpy-tail), Progressive retinal atrophy (MERTK-PRA)
TamaskanMalignant Hyperthermia (MH), Degenerative Myelopathy (DM), Chondrodysplasia (CDPA) and -dystrophy (CDDY and IVDD risk), Hyperuricosuria (SLC), Progressive retinal atrophy (prcd-PRA), Retinal dysplasia (OSD)
Tatra Shepherd DogMalignant Hyperthermia (MH), Degenerative Myelopathy (DM), Chondrodysplasia (CDPA) and -dystrophy (CDDY and IVDD risk), Hyperuricosuria (SLC), Progressive retinal atrophy (prcd-PRA), Progressive retinal atrophy (rcd4-PRA)
Teddy Roosevelt TerrierMalignant Hyperthermia (MH), Degenerative Myelopathy (DM), Chondrodysplasia (CDPA) and -dystrophy (CDDY and IVDD risk), Hyperuricosuria (SLC), Progressive retinal atrophy (prcd-PRA), Primary lens luxation (PLL)
Tenterfield TerrierMalignant Hyperthermia (MH), Degenerative Myelopathy (DM), Chondrodysplasia (CDPA) and -dystrophy (CDDY and IVDD risk), Hyperuricosuria (SLC), Progressive retinal atrophy (prcd-PRA), Congenital Hypothyreosis (CHG), Primary lens luxation (PLL), Spinocerebellar ataxia (SCA), Pituitary dwarfism
Tibetan SpanielMalignant Hyperthermia (MH), Degenerative Myelopathy (DM), Chondrodysplasia (CDPA) and -dystrophy (CDDY and IVDD risk), Hyperuricosuria (SLC), Progressive retinal atrophy (prcd-PRA), Progressive retinal atrophy (PRA3)
Tibetan TerrierMalignant Hyperthermia (MH), Degenerative Myelopathy (DM), Chondrodysplasia (CDPA) and -dystrophy (CDDY and IVDD risk), Hyperuricosuria (SLC), Progressive retinal atrophy (prcd-PRA), Neuronal ceroid lipofuscinosis (NCL), Primary lens luxation (PLL), Progressive retinal atrophy (rcd4-PRA), Pituitary dwarfism Progressive retinal atrophy (PRA3)
Toy Fox TerrierMalignant Hyperthermia (MH), Degenerative Myelopathy (DM), Chondrodysplasia (CDPA) and -dystrophy (CDDY and IVDD risk), Hyperuricosuria (SLC), Progressive retinal atrophy (prcd-PRA), Primary lens luxation (PLL), van den Ende-Gupta syndrome (VDEGS)
Toy PoodleMalignant Hyperthermia (MH), Degenerative Myelopathy (DM), Chondrodysplasia (CDPA) and -dystrophy (CDDY and IVDD risk), Hyperuricosuria (SLC), Progressive retinal atrophy (prcd-PRA), Progressive retinal atrophy (rcd4-PRA), von-Willebrand disease type 1 (vWD 1), GM2-Gangliosidosis
Tschechoslowakian WolfdogMalignant Hyperthermia (MH), Degenerative Myelopathy (DM), Chondrodysplasia (CDPA) and -dystrophy (CDDY and IVDD risk), Hyperuricosuria (SLC), Progressive retinal atrophy (prcd-PRA), Pituitary dwarfism
Volpino ItalianoMalignant Hyperthermia (MH), Degenerative Myelopathy (DM), Chondrodysplasia (CDPA) and -dystrophy (CDDY and IVDD risk), Hyperuricosuria (SLC), Progressive retinal atrophy (prcd-PRA), Primary lens luxation (PLL)
WällerMalignant Hyperthermia (MH), Degenerative Myelopathy (DM), Chondrodysplasia (CDPA) and -dystrophy (CDDY and IVDD risk), Hyperuricosuria (SLC), Progressive retinal atrophy (prcd-PRA), Hereditary cataract (HSF4), MDR1 gene variant (Ivermectin hypersensitivity)
WeimaranerMalignant Hyperthermia (MH), Degenerative Myelopathy (DM), Chondrodysplasia (CDPA) and -dystrophy (CDDY and IVDD risk), Hyperuricosuria (SLC), Progressive retinal atrophy (prcd-PRA), Hypomyelination (Shaking Puppy Syndrome) (SPS), Spinal dysraphism (NTD), Paroxysmal exercise-induced dyskinesia, Bunny Hopping Syndrome (BHS1)
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 SpanielMalignant Hyperthermia (MH), Degenerative Myelopathy (DM), Chondrodysplasia (CDPA) and -dystrophy (CDDY and IVDD risk), Hyperuricosuria (SLC), Progressive retinal atrophy (prcd-PRA), Faktor VII - deficiency, Familial nephropathy (FN), Dilated cardiomyopathy (DCM)
Welsh TerrierMalignant Hyperthermia (MH), Degenerative Myelopathy (DM), Chondrodysplasia (CDPA) and -dystrophy (CDDY and IVDD risk), Hyperuricosuria (SLC), Progressive retinal atrophy (prcd-PRA), Primary lens luxation (PLL)
Westfalia TerrierMalignant Hyperthermia (MH), Degenerative Myelopathy (DM), Chondrodysplasia (CDPA) and -dystrophy (CDDY and IVDD risk), Hyperuricosuria (SLC), Progressive retinal atrophy (prcd-PRA), Primary lens luxation (PLL)
Westhighland White TerrierMalignant Hyperthermia (MH), Degenerative Myelopathy (DM), Chondrodysplasia (CDPA) and -dystrophy (CDDY and IVDD risk), Hyperuricosuria (SLC), Progressive retinal atrophy (prcd-PRA), Globoid cell leukodystrophy (Krabbe-disease), Cranimandibular osteopathy (CMO), Pyruvatkinase-deficiency (PK)
WhippetMalignant Hyperthermia (MH), Degenerative Myelopathy (DM), Chondrodysplasia (CDPA) and -dystrophy (CDDY and IVDD risk), Hyperuricosuria (SLC), Progressive retinal atrophy (prcd-PRA), Myostatin-mutation (Bully-Whippet), Phosphofructokinase-deficiency (PFKD), Collie eye anomaly (CEA) , MDR1 gene variant (Ivermectin hypersensitivity)
White Swiss Shepherd DogMalignant Hyperthermia (MH), Degenerative Myelopathy (DM), Chondrodysplasia (CDPA) and -dystrophy (CDDY and IVDD risk), Hyperuricosuria (SLC), Progressive retinal atrophy (prcd-PRA), MDR1 gene variant (Ivermectin hypersensitivity), Pituitary dwarfism, Cerebellar hypoplasia (CH)
Wire-Haired Pointing Griffon KorthalsMalignant Hyperthermia (MH), Degenerative Myelopathy (DM), Chondrodysplasia (CDPA) and -dystrophy (CDDY and IVDD risk), Hyperuricosuria (SLC), Progressive retinal atrophy (prcd-PRA), Hereditary cataract (HSF4)
Wirehaired Slovakian PointerMalignant Hyperthermia (MH), Degenerative Myelopathy (DM), Chondrodysplasia (CDPA) and -dystrophy (CDDY and IVDD risk), Hyperuricosuria (SLC) Progressive retinal atrophy (prcd-PRA),
Yorkshire TerrierMalignant Hyperthermia (MH), Degenerative Myelopathy (DM), Chondrodysplasia (CDPA) and -dystrophy (CDDY and IVDD risk), Hyperuricosuria (SLC), Progressive retinal atrophy (prcd-PRA), Primary lens luxation (PLL), L-2-Hydroxy glutaric acid uria (L2HGA), Subacute necrotising encephalopathy (SNE)
Mačka

Dedičné ochorenia mačiek

BreedGenetic disease
AbyssinianMDR1-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- / WirehairMDR1-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 MistMDR1-gene variant, Mucopolysaccharidose Typ VII (MPS VII), Myotonia congenita, Cystinuria, Factor XII deficiency (F12), Congenital hypothyroidism (CH), Polydactyly, genetic blood group determination, Hypokalemia
BalineseMDR1-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)
BurmeseMDR1-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
ChartreuxMDR1-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)
ColorpointMDR1-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 RexMDR1-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 RexMDR1-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 LonghairMDR1-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 ShorthairMDR1-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 MauMDR1-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 ShorthairMDR1-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)
JavaneseMDR1-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)
KarthäuserMDR1-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)
KoratMDR1-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 )
LaPermMDR1-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 CoonMDR1-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
MunchkinMDR1-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 MasqueradeMDR1-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)
Norwegian Forest CatMDR1-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)
OcicatMDR1-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 )
PersianMDR1-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)
PeterbaldMDR1-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 )
RagdollMDR1-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 BlueMDR1-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)
SavannahMDR1-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 FoldMDR1-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
SeychelloisMDR1-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 RexMDR1-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)
SiameseMDR1-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)
SibirianMDR1-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)
SingapuraMDR1-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
SomaliMDR1-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)
SphynxMDR1-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)
ThaiMDR1-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)
TonkineseMDR1-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 VanMDR1-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 AngoraMDR1-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

BreedGenetic diseases
Akhal-TekePolysaccharid storage myopathie (PSSM), Naked foal syndrome (NFS)
American SaddlebredPolysaccharid storage myopathie (PSSM), Junctional Epidermolysis Bullosa (JEB2)
AppaloosaPolysaccharid 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 HorsePolysaccharid storage myopathie (PSSM), Severe combined immuno-deficiency (SCID), Lavender foal syndrome (LFS), Cerebellar abiotrophy (CA), Occipitoatlantoaxial Malformation (OAAM)
Ardennes / ArdennaisPolysaccharid storage myopathie (PSSM)
Barb HorsePolysaccharid storage myopathie (PSSM)
Bashkir CurlyPolysaccharid storage myopathie (PSSM), SynchroGait (DMRT3)
Belgian HorsePolysaccharid storage myopathie (PSSM), Junctional epidermolysis bullosa (JEB1), Ocular Squamous Cell Carcinoma (SCC)
Black Forest HorsePolysaccharid storage myopathie (PSSM)
Breton HorsePolysaccharid storage myopathie (PSSM)
Coldblooded TrotterPolysaccharid storage myopathie (PSSM), SynchroGait (DMRT3)
Comtois HorsePolysaccharid storage myopathie (PSSM)
Connemara PonyPolysaccharid storage myopathie (PSSM), Connemara Pony Hoof Wall Separation Disease (HWSD)
Criollo HorsePolysaccharid storage myopathie (PSSM)
Dales PonyPolysaccharid storage myopathie (PSSM), Foal immunodeficency syndrome (FIS)
Dartmoor PonyPolysaccharid storage myopathie (PSSM)
Exmoor PonyPolysaccharid storage myopathie (PSSM)
Fell PonyPolysaccharid storage myopathie (PSSM), Foal immunodeficency syndrome (FIS)
FreibergerPolysaccharid storage myopathie (PSSM)
Frisian HorsePolysaccharid storage myopathie (PSSM), Hydrocephalus, Dwarfism, Distichiasis
Gypsy HorsePolysaccharid storage myopathie (PSSM)
HaflingerPolysaccharid storage myopathie (PSSM), Ocular Squamous Cell Carcinoma (SCC), Warmblood Fragile Foal Syndrome (WFFS)
Hucul PonyPolysaccharid storage myopathie (PSSM)
Icelandic HorsePolysaccharid storage myopathie (PSSM), SynchroGait (DMRT3)
Irish CobPolysaccharid storage myopathie (PSSM)
Kentucky Mountain HorsePolysaccharid storage myopathie (PSSM), SynchroGait (DMRT3)
KonikPolysaccharid storage myopathie (PSSM)
LewitzerPolysaccharid storage myopathie (PSSM)
MangalargaPolysaccharid storage myopathie (PSSM), SynchroGait (DMRT3)
Merens HorsePolysaccharid storage myopathie (PSSM)
Miniature HorsePolysaccharid storage myopathie (PSSM), Dwarfism (ACAN, Chondrodysplasia), Skeletal Atavism (SA), SynchroGait (DMRT3)
Missouri Fox TrotterPolysaccharid storage myopathie (PSSM), SynchroGait (DMRT3), Congenital Stationary Night Blindness (CSNB2)
Morgan HorsePolysaccharid storage myopathie (PSSM), SynchroGait (DMRT3)
MustangPolysaccharid storage myopathie (PSSM), Warmblood Fragile Foal Syndrome (WFFS)
New Forest PonyPolysaccharid storage myopathie (PSSM), Congenital Myotonia
NorikerPolysaccharid storage myopathie (PSSM)
Paint HorsePolysaccharid 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 FinoPolysaccharid storage myopathie (PSSM), SynchroGait (DMRT3), Tiger Eye
PercheronPolysaccharid storage myopathie (PSSM)
Peruvian HorsePolysaccharid storage myopathie (PSSM), SynchroGait (DMRT3)
Pony of the Americas (POA)Polysaccharid storage myopathie (PSSM)
Quater HorsePolysaccharid 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)
Rhenish German ColdbloodPolysaccharid storage myopathie (PSSM)
Rocky Mountain HorsePolysaccharid storage myopathie (PSSM)
SaddlebredPolysaccharid storage myopathie (PSSM), SynchroGait (DMRT3)
Shetland PonyPolysaccharid storage myopathie (PSSM) Dwarfism (ACAN, Chondrodysplasia), Skeletal Atavism (SA)
StandardbredPolysaccharid storage myopathie (PSSM), SynchroGait (DMRT3), Congenital Stationary Night Blindness (CSNB2)
Tennessee Walking HorsePolysaccharid storage myopathie (PSSM), Androgen insensitivity syndrome (AR2, AR3, AR4, AR5), Congenital Stationary Night Blindness (CSNB2), SynchroGait (DMRT3)
Tinker HorsePolysaccharid storage myopathie (PSSM)
ThoroughbredPolysaccharid storage myopathie (PSSM), Tractability, Idiopathic hypocalcemia, Androgen insensitivity syndrome (AR2, AR3, AR4, AR5)
Warmblood HorsesPolysaccharid storage myopathie (PSSM), Warmblood Fragile Foal Syndrome (WFFS), Androgen insensitivity syndrome (AR2, AR3, AR4, AR5)
Welsh PonyPolysaccharid storage myopathie (PSSM)
ZweibrückerPolysaccharid storage myopathie (PSSM)