Callname: Denali
Gender: Female
Color: BLK
Coat Genotype: Black - No Hidden Color - EEBB
Whelp Date: 4/14/2020
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