Genetic diseases

Dog	Cat	Horse	Cattle	Pig

 
                                                        Tests for specific races, click on the photo 

Dog top

Alaskan Malamute polyneuropathy (AMPN) in Alaskan Malamute

Arrhythmogenic right ventricular cardiomyopathy* (ARVC) in Boxer

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

Centronuclear myopathy (CNM, HMLR) in 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 Landseer and Newfoundland

Degenerative myelopathy (DM) all breed

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

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

Fucosidosis in English Springer Spaniel

Gangliosidosis (GM1) in Husky and Portuguese Waterdog

Globoid cell leukodystrophy (Krabbe disease) Cairn Terrier and West Highland White Terrier

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) in Australian Shepherd and Wäller

Hereditary nasal parakeratosis (HNPK) Labrador Retriever

Hereditary necrotizing myelopathy* (ENM) in Dutch Kooikerhondje

Hereditary polyneuropathy (HN) in Greyhound

Hyperuricosuria and Hyperuricemia (HUU, SLC) all breed

Ichthyosis in Golden Retriever

Imerslund-Gräsbeck syndrome (IGS) in Border Collie

Junctional epidermolysis bullosa (JEB) in German Pointer

Juvenile epilepsy in Lagotto Romagnolo

Juvenile dilated cardiomyopathy* (JDCM) in Portugese Waterdog

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

Maligant Hyperthermia (MH) all breed

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

Mucopolysaccharidosis type VII (MPS) in 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

Polycystic kidney disease (BTPKD) in Bull Terrier

Pituitary dwarfism for breed see info

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 (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* (prcd-PRA) for breed see info

Progressive retinal atrophy (rcd1-PRA) in Irish 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

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

Startle Disease in Irish Wolfhound

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

Hypertrophic cardiomyopathy (HCM) in Maine Coon and Ragdoll

Polycystic kidney disease (PKD) in Persian and related breed

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

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