Genetic diseases

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Dog top

Alaskan Malamute polyneuropathy " "(AMPN) ""in Alaskan Malamute

Brachyuria " "(natural bobtail) ""for breed see info

Brittle bone disease " "(osteogenesis imperfecta) ""in Shorthaired-, Wirehaired Dachshund

Canine leukocyte adhesion deficiency " "(CLAD) ""in Irish Setter and Irish Red- and White Setter

Canine multiple system degeneration " "(CMSD) ""in Chinese Crested Dog and Kerry Blue Terrier

Centronuclear myopathy " "(CNM, HMLR) ""in Great Dane and Labrador Retriever

Collie eye anomaly* " "(CEA) ""for breed see info

Congenital hypothyreosis " "(CHG) ""in Spanish Waterdog

Congenital stationary night blindness " "(CSNB) ""in Briard

Copper toxicosis " "(CT) ""in Bedlington Terrier

Cystinuria ""in Australian Cattle Dog, Labrador Retriever, Landseer, Miniature Pinscher and Newfoundland

Degenerative myelopathy " "(DM) ""all breed

Digital hyperkeratosis " "(DH) ""in Irish Terrier and Kromfohrländer

Dry eye curly coat syndrome " "(CCS) ""in Cavalier King Charles Spaniel

Ectodermal dysplasia/Skin fragility syndrome " "(ED/SFS) ""Chesapeake Bay Retriever

Episodic falling " "(EF) ""in Cavalier King Charles Spaniel

Exercise induced collapse " "(EIC) ""for breed see info

Factor VII deficiency ""for breed see info

Familial Nephropathy* " "(FN) ""in English Cocker Spaniel, English Springer Spaniel and Samojede

Finnish hound ataxia " "(FHA) ""in Finnish Hound

Fucosidosis ""in English Springer Spaniel

Gangliosidosis " "(GM1) ""in Husky and Portuguese Waterdog

Globoid cell leukodystrophy " "(Krabbe disease) ""for breeds see info

Glycogen storage disease type II (Pompe disease) " "(GSDII) ""for breed see info

Glycogen storage disease type IIIa " "(GSDIIIa) ""Curly Coated Retriever

Grey Collie syndrome " "(canine cyclic neutropenia) ""Collie

Haemophilia A " "(factor VIII deficiency) ""in Havanese

Haemophilia B " "(factor IX deficiency) ""in Rhodesian Ridgeback

Hereditary cataract " "(HSF4) ""for breeds see info

Hereditary nasal parakeratosis " "(HNPK) ""Labrador Retriever

Hereditary polyneuropathy " "(HN) ""in Greyhound

Hyperuricosuria and Hyperuricemia " "(HUU, SLC) ""all breed

Hypomyelination " "(Shaking Puppy Syndrome) ""in Weimaraner

Imerslund-Gräsbeck syndrome " "(IGS) ""in Beagle and Border Collie

Junctional epidermolysis bullosa " "(JEB) ""in German Pointer

Juvenile epilepsy ""in Lagotto Romagnolo

L-2-hydroxyglutaric aciduria " "(L-2-HGA) ""in Staffordshire Bull Terrier

Late onset ataxia " "(LOA) ""in Jack Russell Terrier and Parson Russell Terrier

Leonberger Polyneuropathy 1 " "(LPN1) ""in Leonberger

Maligant Hyperthermia " "(MH) ""all breed

MDR1-gene defect* " "(Ivermectin hypersensitivity) ""for breed see info

Mucopolysaccharidosis type VII " "(MPS) ""in Brazilian Terrier and German Shepherd

Muscular Dystrophy " "(MD) ""in Cavalier King Charles Spaniel and Golden Retriever

Musladin-Lueke syndrome " "(MLS) ""in Beagle

Myostatin mutation " "(bully-gene) ""in Whippet

Myotonia congenita ""in Miniature Schnauzer

Narcolepsy ""in Doberman Pinscher and Labrador Retriever

Necrotizing meningoenzephalitis " "(NME) ""in Pug dog

Neonatal cortical cerebellar abiotrophy " "(NCCD) ""in Beagle

Neonatal encephalopathy with seizures " "(NEWS) ""in Standard Poodle

Neuronal ceroid lipofuscinosis " "(NCL) ""for breed see info

Phosphofructokinase deficiency " "(PFKD) ""for breed see info

Pituitary dwarfism ""for breed see info

Polycystic kidney disease " "(BTPKD) ""in Bull Terrier

Primary ciliary dykinesia " "(PCD) ""in Bobtail

Primary lens luxation " "(PLL) ""for breed see info

Primary open angle glaukoma " "(POAG) ""in Beagle

Progressive retinal atrophy " "(PRA) ""general information

Progressive retinal atrophy " "(Bas-PRA1) ""in Basenji
Progressive retinal atrophy " "(crd-PRA) ""in Standard Wirehaired Dachshund
Progressive retinal atrophy " "(dominant-PRA) ""in Bull Mastiff and English Mastiff
Progressive retinal atrophy " "(generalized-PRA) ""in Schapendoes
Progressive retinal atrophy " "(GR-PRA1) ""in Golden Retriever
Progressive retinal atrophy " "(pap-PRA1) ""in Papillon and Phalène
Progressive retinal atrophy* " "(prcd-PRA) ""for breed see info
Progressive retinal atrophy " "(rcd1-PRA) ""in Irish Setter and Irish Red and White Setter
Progressive retinal atrophy " "(rcd1a-PRA) ""in Sloughi
Progressive retinal atrophy* " "(rcd2-PRA) ""in Collie
Progressive retinal atrophy " "(rcd3-PRA) ""in Welsh Corgi
Progressive retinal atrophy " "(rcd4-PRA) ""in Gordon-, Irish Setter and Tibetian Terrier

Protein losing nephropathy " "(PLN) ""in Soft-Coated Wheaten Terrier

Pyruvate dehydrogenase phosphatase 1 deficiency " "(PDP1) ""in Clumber and Sussex Spaniel

Pyruvate kinase deficiency " "(PK) ""for breed see info

Retinal Dysplasia* " "(OSD) ""in Labrador Retriever and Samoyed

Skeletal dysplasia 2 (SD 2) " "(dwarfism) ""in Labrador Retriever

Spinocerebellar ataxia " "(SCA) ""in Jack Russell Terrier and Parson Russell Terrier

Homele Disease ""in Irish Wolfhound

Subvalvular aortic stenosis " "(SAS) ""in Newfoundland

Thrombopathia ""Basset Hound, Landseer

Trapped neutrophil syndrome " "(TNS) ""in Border Collie

von Willebrand disease " "(vWD) ""general information

von Willebrand disease type 1 " "(vWD 1) ""for breed see info
von Willebrand disease type 2 " "(vWD 2) ""for breed see info
von Willebrand disease type 3 " "(vWD 3) ""for breed see info

X-linked severe combined immunodeficiency " "(X-SCID) ""in Basset and Welsh Corgi

Cat top

Gangliosidosis " "(GM1 / GM2) ""in Burmese, Korat, Oriental Shorthair and Siam

Genetic blood group determination ""all breed (exceptions see info)

Glycogen storage disease type IV " "(GSD IV) ""in Norwegian Forest Cat

Head-Defect* ""in Burmese

Hypertrophic cardiomyopathy " "(HCM) ""in Maine Coon and Ragdoll

Hypokalemia ""for breed see info

Polycystic kidney disease " "(PKD) ""for breed see info

Progressive retinal atrophy " "(rdAc-PRA) ""for breed see info

Pyruvatkinase deficiency " "(PK) ""for breed see info

Spinal muscular athrophy " "(SMA) ""in Maine Coon

Horse top

Cerebellar abiotrophy " "(CA) ""in Arabian Horse

Congenital myotonia ""in New Forest Pony

Connemara Pony Hoof Wall Separation Disease " "(HWSD) ""in Connemara Pony

Equine malignant hyperthermia " "(EMH) ""in Appaloosa, Paint Horse and Quarter Horse

Glycogen branching enzyme deficiency " "(GBED) ""in Appaloosa, Paint Horse and Quarter Horse

Greying ""all breed

Hereditary equine regional dermal asthenia " "(HERDA) ""in Appaloosa, Paint Horse and Quarter Horse

Hyperkalemic periodic paralysis " "(HYPP) ""in Appaloosa, Paint Horse and Quarter Horse

Junctional epidermolysis bullosa " "JEB ""in Belgian Draft Horse

Lavender foal syndrome " "(LFS) ""in Arabian Horse

Overo lethal white foal syndrome " "(OLWS) ""in Paint Horse

Polysaccharid storage myopathy " "(PSSM) ""all breed

Severe combined immuno-deficiency " "(SCID) ""in Arabian Horse

Warmblood fragile foal syndrome " "(WFFS) "" in all warmblood breed

Cattle top

Bovine Leukocyte Adhesion Deficiency " "(BLAD) ""in Holstein Cattle

Pig top

Maligant Hyperthermia " "(MHS) ""all breeds

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