Genetic diseases Cat
Please select your animal species. You will then get an overview of the hereditary diseases offered by LABOGEN for the selected animal species. The listed hereditary diseases are presented individually, providing information about the type of disease, an overview of the breeds available, the inheritance and the test duration as estimated by the laboratory.
Genetic diseases Cat
- A
- Acrodermatitis enteropathica (AE)
- Alpha-Mannosidosis (AMD)
- Autoimmune lymphoproliferative syndrome ALPS
- C
- Cat combination Bengal
- Cat combination Birman
- Cat combination British short-/longhair
- Cat combination Burmese
- Cat combination Maine Coon
- Cat combination Norwegian
- Cat combination Persian
- Cat combination Ragdoll
- Cat combination Siam/Oriental
- Cat Combination Sphynx
- Coat variant Sphynx / Devon Rex
- Combination hereditary diseases
- Congenital myasthenic syndrome (CMS)
- Cystinuria (CysK)
- F
- Factor XI deficiency (F11)
- FXII deficiency (FXII)
- G
- Gangliosidosis (GM 1/GM 2)
- Gangliosidosis (GM2)
- Genetic blood group determination
- Glycogen storage disease type IV (GSD4)
- H
- Head defect
- Hypertrophic cardiomyopathy (HCM1)
- Hypertrophic cardiomyopathy (HCM3)
- Hypertrophic cardiomyopathy (HCM4)
- Hypokalemia
- Hypotrichosis and short life expectancy
- M
- MDR1 gene variant
- Mucopolysaccharidosis type VI (MPS6)
- Mucopolysaccharidosis type VII (MPS7)
- Myotonia congenita
- O
- Osteochondrodysplasia (OCD)
- P
- Polycystic kidney disease (PKD)
- Primary congenital glaucoma (PCG)
- Progressive retinal atrophia (b-PRA)
- Progressive retinal atrophy (pd-PRA)
- Progressive retinal atrophy (rdAc-PRA)
- Progressive retinal atrophy (rdy-PRA)
- Pyruvate kinase deficiency (PK)
- S
- Skeletal dysplasia (SD)
- Spinal muscular atrophy (SMA)
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