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 ^{8604 all breeds}

Factor XI deficiency ^{8729 Maine Coon}

Gangliosidosis (GM 1/GM 2) ⁸⁰⁴¹

Gangliosidosis (GM2) ^{8149 Burmese}

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

Head defect ^{8465 Burmese}

Hypertrophic cardiomyopathy (HCM1) Mutation 1 Meurs (G -> C) ⁸⁰⁸⁰

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 ^{8468 MPS6 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}

Skeletal dysplasia (SD) ^{8808 British Shorthair}

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 Genetic blood group, Progressive retinal atrophy (b-PRA), Progressive retinal atrophy (rdAc-PRA), Pyruvate kinase deficiency (PK)}

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

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

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

Combination Burmese ^{8715 Genetic blood group, Gangliosidosis (GM2), Head defect, Hypokalaemia}

Combination Devon Rex ^{8838 genetic blood group, Congenital myasthenic syndrome (CMS), Coat length (short-/long haired), Coat variant Sphynx / Devon Rex (SPH/DRX)}

Combination Maine Coon ^{8718 Genetic blood group, Factor XI deficiency (F11), Hypertrophic cardiomyopathy (HCM1),Pyruvate kinase deficiency (PK), Spinal muscular atrophy (SMA)}

Combination Norwegian Forest Cat ^{8720 Genetic blood group, Glycogen storage disease type 4 (GSD4),Pyruvate kinase deficiency (PK), Amber}

Combination Persian ^{8713 Genetic blood group, Alpha-Mannosidosis (AMD), Polycystic kidney disease (PKD), Progressive retinal atrophy (pd-PRA)}

Combination Ragdoll ^{8719 enetic blood group, Hypertrophic cardiomyopathy (HCM1, HCM3), Polycystic kidney disease (PKD), Progressive retinal atrophy (pd-PRA)}

Combination Siam/Oriental ^{8722 Genetic blood group, Gangliosidosis (GM1), Mucopolysaccharidosis type 6 (MPS6), Primary congenital glaucoma (PCG), Progressive retinal atrophy (rdAc-PRA)}

Combination Siberian ^{8840 genetic blood group, Pyruvate kinase deficiency (PK), Colourpoint, Dilution}

Combination Sphynx ^{8723 Genetic blood group, Congenital myasthenic syndrome (CMS),Hypertrophic cardiomyopathy (HCM4), Hypokalaemia}

Coat colour amber ^{8170 Norwegian Forest Cat}

Coat colour brown (chocolate/cinnamon) ^{8257 all breeds}

Genetic blood group determination ^{8121 analysis: allele b (all breeds except Domestic Shorthair) and allele c (Ragdoll only)}

Serological blood group testing ^{618 only EDTA blood (all breeds)}