
Harry Potter Ewabo
*Optimal Selection™ Tested*
DNA Health Testing
Optimal Selection™ Panel - CLEAR
*HIGHLIGHTS*
Blood Disorders
- Canine Scott Syndrome (CSS)
- Hemophilia A (Factor VIII Deficiency)
- Hemophilia B (Factor IX Deficiency)
- Phosphofructokinase Deficiency (PFK)
- Prekallikrein Deficiency
- Pyruvate kinase deficiency (PKD)
- Von Willebrand's Disease (vWD), type 1, type 2, type 3
Ocular Disorders
- Juvenile Hereditary Cataracts (JHC - HSF4)
- Primary Hereditary Cataract, (PHC)
- Canine Multifocal Retinopathy 1 (CMR1), Canine Multifocal Retinopathy 2 (CMR2), Canine Multifocal Retinopathy 3 (CMR3)
- Cone Degeneration, (CD)
- Cone-Rod Dystrophy (CRD), Cone-Rod Dystrophy 1 (CRD1), Cone-Rod Dystrophy 2 (CRD2)
- Dominant Progressive Retinal Atrophy (DPRA)
- Early retinal degeneration (ERD)
- Generalized progressive retinal atrophy (GPRA)
- Goniodysgenesis and Glaucoma
- Primary Lens Luxation (PLL)
- Primary Open Angle Glaucoma (POAG)
- Progressive Retinal Atrophy, (PRA), Progressive Retinal Atrophy 1, Progressive Retinal Atrophy III
- Progressive Rod Cone Degeneration (prcd-PRA)
- X-Linked Progressive Retinal Atrophy 1 (XLPRA1), X-Linked Progressive Retinal Atrophy 2 (XLPRA2)
- Rod-Cone Dysplasia 1, Rod-Cone Dysplasia (rcd1a), Rod-Cone Dysplasia 3 (rcd3)
Cardiac Disorders
- Dilated cardiomyopathy (DCM)
- Long QT Syndrome (LQTS)
Endocrine Disorders
- Congenital Dyshormonogenic Hypothyroidism (CDH)
- Congenital Hypothyroidism
Immunological Disorders
- Severe Combined Immunodeficiency (ARSCID), Severe Combined Immunodeficiency (SCID)
- X-linked Severe Combined Immunodeficiency (XSCID)
Renal Disorders
- 2,8-dihydroxyadenine (DHA) Urolithiasis
- Renal Cystadenocarcinoma and Nodular Dermatofibrosis (RCND)
- Protein Losing Nephropathy (PLN)
- Polycystic Kidney Disease (PKD)
- Cystinuria Type I-A, Cystinuria Type II-A
- Cystic Renal Dysplasia and Hepatic Fibrosis
- Hyperuricosuria, (HUU)
Metabolic Disorders
- Glycogen Storage Disease Type IIIa, (GSD IIIa), Glycogen Storage Disease Type Ia
- Intestinal Cobalamin Malabsorption (ICM) or Imerslund-Gräsbeck Syndrome
- Pyruvate Dehydrogenase Phosphatase 1 (PDP1) Deficiency
Muscular Disorders
- Muscular Dystrophy
- Centronuclear Myopathy (CNM)
Neurological Disorders
- Benign Familial Juvenile Epilepsy (BFJE)
- Juvenile Myoclonic Epilepsy
- Juvenile Encephalopathy
- Neonatal Encephalopathy with Seizures (NEWS)
- Spongiform LeucoEncephaloMyelopathy (SLEM) (Shaking Puppy Syndrome)
- Spinocerebellar Ataxia with Myokymia and/or Seizures (SAMS)
- Degenerative Myelopathy (DM)
Neuromuscular Disorders
- Congenital Myasthenic Syndrome (CMS)
- Exercise-Induced Collapse (EIC)
- GM1 Gangliosidosis, GM2 Gangliosidosis
Skeletal Disorders
- Chondrodysplasia
- Cleft Lip & Palate with Syndactyly (CLPS)
- Cleft Palate (CP)
- Craniomandibular Osteopathy (CMO)
- Osteochondrodysplasia
- Osteogenesis Imperfecta (OI)
- Hypophosphatasia
- Skeletal Dysplasia 2 (SD2)
- Spondylocostal Dysostosis
Dermal Disorders
- Dystrophic Epidermolysis Bullosa
- Epidermolytic Hyperkeratosis
- Ichthyosis
- Lamellar Ichthyosis, (LI)
- Lethal Acrodermatitis, (LAD)
Other Disorders
- Acute respiratory distress syndrome (ARDS)
- Amelogenesis Imperfecta (AI)
- Lung Developmental Disease
- Primary Ciliary Dyskinesia (PCD)
- MDR1 Medication Sensitivity
Traits
- Piebald Gene
Non-DNA Testing/Polygenetic Disease
Patellas - 0/0 - BTR-PA2830/22M/P-VPI
Sire | Lord Bibi Black Beauty Of Pamita |
---|---|
Dam | Diva Daniella Ewabo |
Gender | Male |
Name | Harry |
Coat | Brindle and white |
Owner | Bedford Kennel |
Breeder | Eva Belkova - Ewabo Kennel |
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