Hereditary Diseases Cat
Diagnostic spectrum
- Genetic blood group determination
- Alpha-Mannosidosis (AMD)
- Autoimmune lymphoproliferative syndrome (ALPS)
- Congenital myasthenic syndrome (CMS)
- Cystinuria
- Factor XI deficiency
- Gangliosidosis (GM 1/GM 2)
- Gangliosidosis (GM2)
- Glycogen storage disease type 4 (GSD4)
- Head defect
- Hypertrophic cardiomyopathy (HCM1)
- Hypertrophic cardiomyopathy (HCM3)
- Hypertrophic cardiomyopathy (HCM4)
- Hypokalemia
- Hypotrichosis and short life expectancy
- Mucopolysaccharidosis type 6 (MPS6)
- Mucopolysaccharidosis type 7 (MPS7)
- Myotonia congenita
- Osteochondrodysplasia (OCD)
- Polycystic kidney disease (PKD)
- Primary congenital glaucoma (PCG)
- Progressive retinal atrophy (b-PRA)
- Progressive retinal atrophy (pd-PRA)
- Progressive retinal atrophy (rdAc-PRA)
- Progressive retinal atrophy (rdy-PRA)
- Pyruvate kinase deficiency (PK)
- Serological Blood Group Typing
- Spinal muscular atrophy (SMA)
* Partner laboratory
