Lillehammer Denali
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Callname: Denali Gender: Female Color: BLK coat Genotype: Black - No Hidden Color - EEBB Whelp Date: 4/14/2020 Date of Death: 0/0/0 Owner: Tim Culhane Breeder: SheriLinn Whitman |
AKC reg: SS18103302 OFA Hips: LR-280713E60F-P-VPI (Excellent) Eye CERF/CAER: LR-EYE33656/61F-VPI (Normal) OFA Elbow: LR-EL127355F60-P-VPI (Normal) CNM: Normal/Clear EIC: LR-EIC8843/61F-VPI (Normal/Clear) PRA: Normal/Clear OSD: Normal/Clear Cardiac: Normal/Clear Other Health Certifications: NORMAL/CLEAR on ALL Royal Canin Genetic Conditions (including the following): Genetic Condition 2,8-dihydroxyadenine (DHA) Urolithiasis Acral Mutilation Syndrome Acute Respiratory Distress Syndrome Alexander Disease Bandera's Neonatal Ataxia Benign Familial Juvenile Epilepsy Canine Congenital Stationary Night Canine Leukocyte Adhesion Deficiency (CLAD), type III Canine Multifocal Retinopathy 1 Canine Multifocal Retinopathy 2 Canine Multifocal Retinopathy 3 Cardiomyopathy and Juvenile Mortality Centronuclear Myopathy Cerebellar Ataxia Cerebellar Cortical Degeneration Cerebellar Hypoplasia Cerebral Dysfunction Chondrodysplasia Chondrodystrophy (CDDY) and Intervertebral Disc Disease (IVDD) Risk Cleft Lip & Palate with Syndactyly Cleft Palate CNS Atrophy with Cerebellar Ataxia Coat Color Dilution and Neurological Defects Cone Degeneration Cone-Rod Dystrophy 1 & 2 Congenital Cornification Congenital Dyshormonogenic Hypothyroidism with Goiter Congenital Eye Malformations Congenital Hypothyroidism Congenital Muscular Dystrophy Congenital Myasthenic Syndrome Cystic Renal Dysplasia and Hepatic Fibrosis Cystinuria Type I & II-A Deafness and Vestibular Dysfunction (DINGS1/DINGS2) Degenerative Myelopathy Demyelinating Neuropathy Dental Hypomineralization Dilated Cardiomyopathy Dominant Progressive Retinal Atrophy Early Retinal Degeneration Early-Onset Adult Deafness Early-Onset Progressive Polyneuropathy Ehlers-Danlos Syndrome Epidermolytic Hyperkeratosis Episodic Falling Syndrome Exercise-Induced Collapse Factor VII Deficiency Factor XI Deficiency Fetal Onset Neuroaxonal Dystrophy Focal Non-Epidermolytic Palmoplantar Globoid Cell Leukodystrophy Glycogen Storage Disease Type Ia & IIIa Hemophilia A & B Hereditary Calcium Oxalate Urolithiasis, Type 1 Hereditary Elliptocytosis Hereditary Footpad Hyperkeratosis Hereditary Nasal Parakeratosis Hereditary Vitamin D-Resistant Rickets Type II Hypomyelination Hypophosphatasia Ichthyosis, Type 1 & 2 Inflammatory Myopathy Inflammatory Pulmonary Disease Juvenile Cataract Juvenile Dilated Cardiomyopathy Juvenile Laryngeal Paralysis and Polyneuropathy Juvenile Myoclonic Epilepsy Laryngeal Paralysis Leigh-like Subacute Necrotizing Encephalopathy Leukodystrophy Ligneous Membranitis Limb-girdle Muscular Dystrophy Lung Developmental Disease May-Hegglin Anomaly MDR1 Medication Sensitivity Microphthalmia Mucopolysaccharidosis Type VI & VII Muscular Dystrophy Muscular Dystrophy-Dystroglycanopathy Muscular Hypertrophy (Double Muscling) Musladin-Lueke Syndrome Myotonia Congenita Myotubular Myopathy Narcolepsy Nemaline Myopathy Neonatal Cerebellar Cortical Degeneration Neonatal Encephalopathy with Seizures Neuroaxonal Dystrophy Neuronal Ceroid Lipofuscinosis 1, 2, 5, 7, & 8 Obesity risk (POMC) Osteochondrodysplasia Osteogenesis Imperfecta P2RY12-associated Bleeding Disorder Paroxysmal Dyskinesia Polycystic Kidney Disease Prekallikrein Deficiency Primary Open Angle Glaucoma and Lens Luxation Progressive Early-Onset Cerebellar Ataxia Progressive Retinal Atrophy GR-PRA1/GR-PRA2/BBS2/CNGA1 Protein Losing Nephropathy Pyruvate Dehydrogenase Phosphatase 1 Deficiency QT Syndrome Renal Cystadenocarcinoma and Nodular Dermatofibrosis Rod-Cone Dysplasia 1,1a, & 3 Sensory Neuropathy Severe Combined Immunodeficiency Skeletal Dysplasia 2 Spinocerebellar Ataxia (Late-Onset Ataxia) Spinocerebellar Ataxia with Myokymia and/or Seizures Spondylocostal Dysostosis Stargardt Disease Startle Disease Trapped Neutrophil Syndrome Van den Ende-Gupta Syndrome von Willebrand's Disease, type 1, 2, & 3 X-Linked Ectodermal Dysplasia X-Linked Hereditary Nephropathy X-Linked Myotubular Myopathy X-Linked Progressive Retinal Atrophy 1 & 2 X-Linked Severe Combined Immunodeficiency X-Linked Tremors Xanthinuria |
Pedigree:
| Lillehammer Denali | HRCH Cascade Ranges High Hunts Low MH QAA ( BLK ) |
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| Aleksia Lillehammer Jewel Of Boring SH ( BLK ) |
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Provided to you by Hunting Lab Pedigree