DNA mutation is Autosomal Dominant
Normal: DNA mutation associated with the specific genetic disease is not present. The animal will not develop the condition due to the specific DNA mutation and will not pass the mutation onto its offspring.
Carrier: The animal carries one copy of defective gene and one copy of normal gene. The animal is very likely to develop the condition due to the specific DNA mutation in its lifetime and will pass the mutation onto its offspring 50% of the time.
Affected: The animal carries two copies of the defective gene. The animal is very likely to develop the condition due to the specific DNA mutations in its lifetime and will pass the mutation onto its offspring 100% of the time.
• Amelogenesis Imperfecta (AI) 牙釉質發育不全症
• Canine Cystinuria (Cys) 胱氨酸高尿酸症
• Canine Leukocyte Adhesion Deficiency (CLAD) 白血球黏附缺乏症
• Canine Multifocal Retinopathy Type 1 (CMR1) 犬多焦視網膜病變的一型
• Canine Sensory Neuropathy (SN) 感覺神經元病變
• Centronuclear Myopathy (CNM) 中央核肌肉病變
• Cobalamin Malabsorption (B12) 維他命B12吸收不良
• Collie Eye Anomaly (CEA) 柯利犬眼疾
• Cone Degeneration (CD) 視網膜錐體退化
• Congenital Myotonic (CM) 先天性肌肉收縮症
• Copper Toxicosis (CT) 銅中毒
• Cyclic Neutropenia / Gray Collie Syndrome (CN) 週期性白血球減少
• Degenerative Myelopathy (DM) 退化性脊髓病
• Exercise Induced Collapse (EIC) 運動引發性虛脫
• Hereditary Cataract (HC) 遺傳性白內障
• Hyperuricosuria (HUU) 尿酸過高症
• Malignant Hyperthermia (MH) 麻醉藥物敏感
• Mucopolysaccharidosis VII (MPS VII) 粘多醣貯積病 VII型
• Multi Drug and Ivermectin Sensitivity (MDR1) 多種藥物及杜蟲藥敏感
• Neonatal Encephalopathy with Seizures (NEWS) 新生犬腦病
• Osteogenesis Imperfecta (OI) 骨骼不健全
• Phosphofructokinase Deficiency (PFK) 磷酸果糖激酶缺乏
• Platelet Procoagulant Deficiency (PPD)
• Primary ciliary dyskinesia (PCD) 先天性纖毛運動異常症
• Primary Lens Luxation (PLL) 眼睛晶狀體脫位
• Progressive Retinal Atrophy (PRA) 漸進性視網膜萎縮
• Pug Dog Encephalitis (PDE) 巴哥狗腦炎
• Pyruvate Kinase Deficiency (PKDef) 丙酮酸激酶缺乏貧血症
• von Willebrand's Disease (vWD) 血管性血友病
• Blood Group B (BGB) B血型
• Familial Hypertrophic Cardiomyopathy (HCM) 肥厚性心肌病
• Feline Myotonia Congenita (MC) 先天性肌強直症
• Glycogen Storage Disease Type IV (GSD IV) 第四型肝醣儲積症
• Haemophilia B (HB) 血友病
• Hyperoxaluria (HOU) 高尿酸症
• Polycystic Kidney Disease (PKD) 多囊性腎病
• Progressive Retinal Atrophy (PRA) 漸進性視網膜萎縮
• Pyruvate Kinase Deficiency (PKDef) 丙酮酸激酶缺乏貧血症
• Spinal Muscular Atrophy (SMA) 脊髓性肌肉萎縮症
• Vitamin D-dependent rickets (VDDR) 維他命D依賴軟骨症