Pandora’s Obsession

Born: 20 May 2023
AKC# NP95589501
DNA: V10103771 +h*
*Obsession has been cleared through her DNA for more than 200 genetic diseases. A more comprehensive analysis is included at the bottom of her page.

I am infatuated with this beauty! We picked her up in Italy and had the best time. She is an absolute doll and ever so gorgeous. She is a carrier for fluffy, so we hope for some fluffy babies that we can also become obsessed over!

Acral Mutilation Syndrome: WT/WT (clear)
Acute Respiratory Distress Syndrome: WT/WT (clear)
Adult Paroxysmal Dyskinesia: WT/WT (clear)
Afibrinogenemia: WT/WT (clear)
Alaskan Husky Encephalopathy: WT/WT (clear)
Alaskan Malamute Polyneuropathy : WT/WT (clear)
Amelogenesis Imperfecta: WT/WT (clear)
Ataxia: WT/WT (clear)
Benign Familial Juvenile Epilepsy: WT/WT (clear)
Benard-Soulier Syndrome: WT/WT (clear)
Canine Multiple System Degeneration: WT/WT (clear)
Canine Scott Syndrome: WT/WT (clear)
Cardiomyopathy and Juvenile Mortality: WT/WT (clear)
Catalase Deficiency: WT/WT (clear)
Centronuclear Myopathy: WT/WT (clear)
Cerebellar Ataxia: WT/WT (clear)
Cerebellar Ataxia 1 : WT/WT (clear)
Cerebellar Ataxia 2 : WT/WT (clear)
Cerebellar Cortical Degeneration: WT/WT (clear)
Cerebellar Degeneration: WT/WT (clear)
Charcot-Marie-Tooth Disease: WT/WT (clear)
Chondrodysplasia: WT/WT (clear)
Cleft Palate and Syndactyly: WT/WT (clear)
Coagulation Factor VII Deficiency: WT/WT (clear)
Collie Eye Anomaly: WT/WT (clear)
Complement 3 Deficiency: WT/WT (clear)
Cone Degeneration: WT/WT (clear)
Congenital Hypothyroidism with Goiter: WT/WT (clear)
Congenital Macrothrombocytopenia: WT/WT (clear)
Congenital Methemoglobinemia: WT/WT (clear)
Congenital Myasthenic Syndrome: WT/WT (clear)
Congenital Stationary Night Blindness: WT/WT (clear)
Copper Storage Disease: WT/WT (clear)
Craniomandibular Osteopathy: WT/WT (clear)
Cyclic Neutropenia: WT/WT (clear)
Cystinuria: WT/WT (clear)
Cystinuria Type 3 (Bulldog Type Risk Factor, Variant 3): WT/WT (clear)
Cystinuria Type 3 (Bulldog Type Risk Factor, Variants 1 and 2): 1 copy carrier
Dandy-Walker-Like Malformation: WT/WT (clear)
Darier Disease and Associated Infundibular Cyst Formation: WT/WT (clear)
Deafness and Vestibular Dysfunction: WT/WT (clear)
Degenerative Myelopathy WT/WT (clear)
Degenerative Myelopathy Early-Onset Risk Modifier: WT/WT (clear)
Dental Hypomineralization: WT/WT (clear)
Diffuse Cystic Renal Dysplasia and Hepatic Fibrosis: WT/WT (clear)
Dilated Cardiomyopathy: WT/WT (clear)
Dry Eye Curly Coat Syndrome: WT/WT (clear)
Dystrophic Epidermolysis Bullosa: WT/WT (clear)
Early Onset Adult Deafness: WT/WT (clear)
Early Retinal Degeneration: WT/WT (clear)
Early-Onset Epilepsy: WT/WT (clear)
Ectodermal Dysplasia: WT/WT (clear)
Ectodermal Dysplasia, X-Linked: WT/WT (clear)
Ehlers-Danlos Syndrome: WT/WT (clear)
Elliptocytosis: WT/WT (clear)
Epidermolytic Hyperkeratosis: WT/WT (clear)
Episodic Falling Syndrome: WT/WT (clear)
Exercise-Induced Collapse: WT/WT (clear)
Exfoliative Cutaneous Lupus Erythematosus (ECLE): WT/WT (clear)
Factor XI Deficiency: WT/WT (clear)
Familial Nephropathy: WT/WT (clear)
Fucosidosis: WT/WT (clear)
Gallbladder Mucoceles: WT/WT (clear)
Glanzmann’s Thrombasthenia: WT/WT (clear)
Glaucoma: WT/WT (clear)
Globoid Cell Leukodystrophy: WT/WT (clear)
Glycogen Storage Disease Ia: WT/WT (clear)
Glycogen Storage Disease IIIa: WT/WT (clear)
Glycogen Storage Disease VII: WT/WT (clear)
Glycogen Storage Disease VII, PFK Deficiency: WT/WT (clear)
GM1 Gangliosidosis: WT/WT (clear)
GM2 Gangliosidosis: WT/WT (clear)
Greyhound Polyneuropathy: WT/WT (clear)
Hemophilia A: WT/WT (clear)
Hemophilia B: WT/WT (clear)
Hereditary Ataxia: WT/WT (clear)
Hereditary Cataracts: WT/WT (clear)
Hereditary Footpad Hyperkeratosis: WT/WT (clear)
Hereditary Nasal Parakeratosis: WT/WT (clear)
Hereditary Nephritis: WT/WT (clear)
Hyperuricosuria: WT/WT (clear)
Hypomyelination: WT/WT (clear)
Ichthyosis: WT/WT (clear)
Inflammatory Myopathy: WT/WT (clear)
Intervertebral Disc Disease Risk Factor and Chondrodystrophy (CDDY with IVDD): WT/WT (clear)
Intestinal Cobalamin Malabsorption: WT/WT (clear)
Intestinal Lipid Malabsorption: WT/WT (clear)
Junctional Epidermolysis Bullosa: WT/WT (clear)
Juvenile Laryngeal Paralysis and Polyneuropathy (JLPP): WT/WT (clear)
Juvenile Myoclonic Epilepsy: WT/WT (clear)
L-2-Hydroxyglutaric Aciduria: WT/WT (clear)
Lagotto Storage Disease: WT/WT (clear)
Laryngeal Paralysis and Polyneuropathy: WT/WT (clear)
Late Onset Ataxia: WT/WT (clear)
Lethal Acrodermatitis: WT/WT (clear)
Leukocyte Adhesion Deficiency, Type I: WT/WT (clear)
Leukocyte Adhesion Deficiency, Type III: WT/WT (clear)
Ligneous Membranitis: WT/WT (clear)
Limb-Girdle Muscular Dystrophy: WT/WT (clear)
Lundehund Syndrome: WT/WT (clear)
Macular Corneal Dystrophy: WT/WT (clear)
Mammary Tumors: WT/WT (clear)
May-Hegglin Anomaly: WT/WT (clear)
Microphthalmia: WT/WT (clear)
Mucopolysaccharidosis I: WT/WT (clear)
Mucopolysaccharidosis IIIA: WT/WT (clear)
Mucopolysaccharidosis IIIB: WT/WT (clear)
Mucopolysaccharidosis VI: WT/WT (clear)
Mucopolysaccharidosis VII: WT/WT (clear)
Multidrug Resistance 1: WT/WT (clear)
Multifocal Retinopathy1: WT/WT (clear)
Multifocal Retinopathy 2: WT/WT (clear)
Multifocal Retinopathy 3: WT/WT (clear)
Muscular Dystrophy: WT/WT (clear)
Musladin-Lueke Syndrome: WT/WT (clear)
Myostatin Deficiency: WT/WT (clear)
Mytonia Congenita: WT/WT (clear)
Myotubular Myopathy 1: WT/WT (clear)
Narcolepsy: WT/WT (clear)
Neonatal Ataxia: WT/WT (clear)
Neonatal Cerebellar Cortical Degeneration: WT/WT (clear)
Neonatal Encephalopathy with Seizures: WT/WT (clear)
Neuroaxonal Dystrophy: WT/WT (clear)
Neuronal Ceroid Lipofuscinosis 1: WT/WT (clear)
Neuronal Ceroid Lipofuscinosis 10: WT/WT (clear)
Neuronal Ceroid Lipofuscinosis 12: WT/WT (clear)
Neuronal Ceroid Lipofuscinosis 2: WT/WT (clear)
Neuronal Ceroid Lipofuscinosis 4A: WT/WT (clear)
Neuronal Ceroid Lipofuscinosis 5: WT/WT (clear)
Neuronal Ceroid Lipofuscinosis 6: WT/WT (clear)
Neuronal Ceroid Lipofuscinosis 7: WT/WT (clear)
Neuronal Ceroid Lipofuscinosis 8: WT/WT (clear)
Nonsyndromic Hearing Loss: WT/WT (clear)
Oculocutaneous Albinism: WT/WT (clear)
Osteochondrodysplasia: WT/WT (clear)
Osteogenesis Imperfecta: WT/WT (clear)
P2RY12 Receptor Platelet Disorder: WT/WT (clear)
Pancreatitis: WT/WT (clear)
Pembroke Welsh Corgi Duchenne Muscular Dystrophy: WT/WT (clear)
Persistent Mullerian Duct Syndrome: WT/WT (clear)
Pituitary Dwarfism: WT/WT (clear)
Polyneuropathy: WT/WT (clear)
Polyneuropathy with Ocular Abnormalities and Neuronal Vacuolation: WT/WT (clear)
Pompe Disease: WT/WT (clear)
Prekallikrein Deficiency: WT/WT (clear)
Primary Ciliary Dyskinesia: WT/WT (clear)
Primary Hyperoxaluria: WT/WT (clear)
Primary Lens Luxation: WT/WT (clear)
Primary Open Angle Glaucoma: WT/WT (clear)
Primary Open Angle Glaucoma and Primary Lens Luxation: WT/WT (clear)
Progressive Retinal Atrophy: WT/WT (clear)
Progressive Retinal Atrophy, Cone-Rod Dystrophy: WT/WT (clear)
Progressive Retinal Atrophy, Cone-Rod Dystrophy 1: WT/WT (clear)
Progressive Retinal Atrophy, Cone-Rod Dystrophy 2: WT/WT (clear)
Progressive Retinal Atrophy, Cone-Rod Dystrophy 3: WT/WT (clear)
Progressive Retinal Atrophy, Cone-Rod Dystrophy 4: WT/WT (clear)
Progressive Retinal Atrophy, Early Onset: WT/WT (clear)
Progressive Retinal Atrophy, Generalized: WT/WT (clear)
Progressive Retinal Atrophy, Late-Onset: WT/WT (clear)
Progressive Retinal Atrophy, PRA1: WT/WT (clear)
Progressive Retinal Atrophy, PRA3: WT/WT (clear)
Progressive Retinal Atrophy, Progressive Cone-Rod Degeneration (prcd): WT/WT (clear)
Progressive Retinal Atrophy, Cone-Rod Dysplasia 3: WT/WT (clear)
Progressive Retinal Atrophy, Cone-Rod Dysplasia 4: WT/WT (clear)
Progressive Retinal Atrophy, Syndromic Retinal Degeneration: WT/WT (clear)
Progressive Retinal Atrophy, X-Linked 1: WT/WT (clear)
Progressive Retinal Atrophy, X-Linked 2: WT/WT (clear)
Protein Losing Nephropathy: WT/WT (clear)
Pyruvate Dehydrogenase Deficiency: WT/WT (clear)
Pyruvate Kinase Deficiency: WT/WT (clear)
Recurrent Inflammatory Pulmonary Disease: WT/WT (clear)
Renal Cystadenocarcinoma and Nodular Dermatofibrosis: WT/WT (clear)
Retinal Dysplasia/Oculoskeletal Dysplasia 1: WT/WT (clear)
Dysplasia/Oculoskeletal Dysplasia 2: WT/WT (clear)
Sensory Neuropathy: WT/WT (clear)
Severe Combined Immunodeficiency Disease: WT/WT (clear)
Severe Combined Immunodeficiency Disease, X-Linked: WT/WT (clear)
Shar-Pei Autoinflammatory Disease: WT/WT (clear)
Skeletal Dysplasia 2: WT/WT (clear)
Spinal Dysraphism: WT/WT (clear)
Spinocerebellar Ataxia: WT/WT (clear)
Spondylocostal Dysostosis: WT/WT (clear)
Stargardt Disease: WT/WT (clear)
Startle Disease: WT/WT (clear)
Subacute Necrotizing Encephalopathy: WT/WT (clear)
Thrombopathia: WT/WT (clear)
Trapped Neutrophil Syndrome: WT/WT (clear)
Ullrich Congenital Muscular Dystrophy (LR Type 1): WT/WT (clear)
Ullrich Congenital Muscular Dystrophy (LR Type 2): WT/WT (clear)
Urolithiasis: WT/WT (clear)
Van Den Ende-Gupta Syndrome: WT/WT (clear)
Von Willebrand Disease 1: WT/WT (clear)
Von Willebrand Disease II: WT/WT (clear)
Von Willebrand Disease III: WT/WT (clear)

Eyes:
Hereditary Cataracts: WT/WT (clear)
Hyperuricosuria: WT/WT (clear)
Multifocal Retinopathy 1: WT/WT (clear)
Oculocutaneous Albinism: WT/WT (clear)
Progressive Retinal Atrophy, Cone-Rod Dystrophy 4: WT/WT (clear)

Coat:
A Locus: AyAt- (Sable/fawn; carries tricolor/black & tan)
B Locos: B/b- (Black coat, nose, foot pads; carries 1 copy brown)
Co Locos: CO/CO- Black coat, nose & foot pads (does not carry cocoa)
Cu Locos: Cu/Cu- Straight coat
D Locus: D/d- Carries one copy dilute color
E Locus: E/e- Carrier Melanistic Mask (face color), yellow/red
L Locus: Sh/Sh- Does not carry Fluffy
M Locus: m/m- Non Merle
S Locus: S/S- No white spotting, flash, parti or piebald
SD Locus: sd/sd- Low Shedding

Polydactyly: pd/pd- normal, likely no rear dew claws

Social Behavior: WT/WT; WT/M- May demonstrate more social behavior

T Locus (Natural Bobtail): t/t- Normal Frenchie Tail