RICKY

Ricky was tested in 2021 - He was also DNA profiled for ASCA, which confirmed his parents are, in fact, his parents. 

• Normal (Clear) Multifocal retinopathy 1 WT/WT
• Normal (Clear) Coagulation factor VII deficiency WT/WT
• Normal (Clear) Degenerative Myelopathy (Common Variant) WT/WT
• Normal (Clear) Progressive retinal atrophy, Progressive rod-cone degeneration WT/WT
• Normal (Clear) Collie eye anomaly WT/WT
• Normal (Clear) Multidrug resistance 1 WT/WT
• Normal (Clear) Exercise-induced collapse WT/WT
• Normal (Clear) Junctional Epidermolysis Bullosa (Australian Shepherd Type) WT/WT
• Normal (Clear) Hereditary cataracts (Australian Shepherd type) WT/WT
• Normal (Clear) Hereditary Ataxia (Australian Shepherd Type) WT/WT
• Carrier Hyperuricosuria SLC2A49 WT/M
• Normal (Clear) Cone degeneration WT/WT
• Normal (Clear) Von Willebrand disease I WT/WT
• Normal (Clear) Neuronal ceroid lipofuscinosis 8 (Australian Shepherd type) WT/WT
• Normal (Clear) Neuronal ceroid lipofuscinosis 6 WT/WT
• Normal (Clear) Neuronal ceroid lipofuscinosis 5 (Herding Dog Type) WT/WT
• Normal (Clear) Intestinal Cobalamin Malabsorption (Australian Shepherd Type) WT/WT
• Normal (Clear) Intestinal Cobalamin Malabsorption (Border Collie Type) WT/WT
• Normal (Clear) Craniomandibular Osteopathy WT/WT
• Normal (Clear) - No CDDY or Increased IVDD Risk Chondrodystrophy with Intervertebral Disc Disease Risk Factor (CDDY with IVDD) WT/WT
•  Normal - No Leg Shortening Associated with CDPAChondrodysplasia (CDPA) cd/cd