Hereditary Diseases Cat

Diagnostic spectrum

• Acrodermatitis enteropathica (AE)
• Alpha-Mannosidosis (AMD)
• Autoimmune lymphoproliferative syndrome (ALPS)
• Genetic blood group determination (cat)
• Serological Blood Group Typing (dog, cat)
• Congenital myasthenic syndrome (CMS)
• Cystinuria
• Factor XI deficiency
• Factor XII deficiency (FXII)
• Gangliosidosis (GM 1/GM 2)
• Gangliosidosis (GM2)
• Glycogen storage disease type 4 (GSD4)
• Head defect
• Hypertrophic cardiomyopathy (HCM1)
• Hypertrophic cardiomyopathy (HCM3)
• Hypertrophic cardiomyopathy (HCM4)
• Hypokalaemia
• Hypotrichosis and short life expectancy
• MDR1 gene variant
• Mucopolysaccharidosis type VI (MPS6)
• Mucopolysaccharidosis type VII (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)
• Skeletal dysplasia (SD)
• Spinal muscular atrophy (SMA)