Kačių genetiniai tyrimai

Acrodermatitis enteropathica (AE) ^{8763 Turkish Van}

Alpha-Mannosidosis (AMD) ^{8239 Persian}

Autoimmune lymphoproliferative syndrome (ALPS) ^{8609 British Shorthair}

Congenital myasthenic syndrome (CMS) ^{8592 Devon Rex, Sphynx}

Cystinuria (all breeds) ⁸⁶⁰⁴

Factor XI deficiency (Maine Coon) ⁸⁷²⁹

Gangliosidosis (GM 1/GM 2) ⁸⁰⁴¹

Gangliosidosis (GM2) (Burmese) ⁸¹⁴⁹

Glycogen storage disease type 4 (GSD4) ^{8113 Norwegian Forest Cat}

Head defect (Burmese) ⁸⁴⁶⁵

Hypertrophic cardiomyopathy (HCM1) Mutation 1 Meurs (G -> C) ^{8080 Maine Coon}

Hypertrophic cardiomyopathy (HCM3) ^{8116 Ragdoll}

Hypertrophic cardiomyopathy (HCM4) ^{8695 Sphynx}

Hypokalaemia ^{8453 Australian Mist, Burmese, Cornish Rex, Devon Rex, Singapura, Sphynx, Tonkinese}

Hypotrichosis and short life expectancy ^{8318 Birman}

MDR1 gene variant ^{8776 (all breeds)}

Mucopolysaccharidosis type VI (MPS6) ^{8468 Balinese, Birman, Domestic Shorthair, Javanese, Oriental Shorthair,Peterbald, Seychellois, Siamese, Thai, Tonkinese}

Mucopolysaccharidosis type VII (MPS7) ^{8473 (all breeds)}

Myotonia congenita ^{8461 (all breeds)}

Osteochondrodysplasia (OCD) ^{8349 Scottish Fold}

Polycystic kidney disease (PKD) ^{8046 Angora, Birman, British Short- and Longhair, Chartreux, Colourpoint, Exotic Shorthair, Persian, Ragdoll, Russian Blue, Scottish Fold, Selkirk Rex}

Primary congenital glaucoma (PCG) ^{8395 Siamese}

Progressive retinal atrophy (b-PRA) ^{8331 Bengal}

Progressive retinal atrophy (pd-PRA) ^{8593 Angora, Birman, British Short- and Longhair, Chartreux, Colourpoint, Exotic Shorthair, Persian, Ragdoll, Russian Blue, Scottish Fold, Selkirk Rex}

Progressive retinal atrophy (rdAc-PRA) ^{8117 Abyssinian, American Curl/Wirehair, Balinese, Bengal, Colourpoint Shorthair, Cornish Rex, Javanese, Munchkin, Ocicat, Oriental Shorthair, Peterbald, Seychellois, Siamese, Singapura, Somali, Thai, Tonkinese}

Progressive retinal atrophy (rdy-PRA) ^{8469 Abyssinian, Ocicat, Somali}

Pyruvate kinase deficiency (PK) ^{8047 Abyssinian, Angora, Bengal, Domestic Shorthair, Egyptian Mau, La Perm, Maine Coon, Norwegian Forest Cat, Ocicat, Savannah, Siberian, Singapura, Somali}

Spinal muscular atrophy (SMA) ^{8123 Maine Coon}

Combination hereditary diseases cat ^{8350 HCM1, HCM3, GSD4, PK, PKD, rdAc-PRA, SMA, genetic blood group}

Combination coat colours cat ^{8280 agouti, burma, mink, chocolate, cinnamon, dilution, siam}

Combination Bengal ^{8717 Progressive retinal atrophy (b-PRA),Progressive retinal atrophy (rdAc-PRA), Pyruvate kinase deficiency (PK)}

Combination coat colours Bengal ^{8281 charcoal, chocolate, cinnamon, dilution, snow}

Combination Birman ^{8716 Hypotrichosis and short life expectancy,Mucopolysaccharidosis type 6 (MPS6), Polycystic kidney disease (PKD), Progressive retinal atrophy (pd-PRA)}

Combination British Short-/Longhair ^{8714 Autoimmune lymphoproliferative syndrome (ALPS),Polycystic kidney disease (PKD), Progressive retinal atrophy (pd-PRA)}