Mimi
Born: 19 October 2022
AKC# NP95365601
DNA: V40009853 +h*
*Mimi has been cleared through her DNA for more than 200 genetic diseases. See a more comprehensive analysis at the bottom of her page.
Mimi is our newest addition at Pandora’s and we could not be more proud. We imported Mimi in whelp, bred to ENZO!! Enzo is a compact, gorgeous fluffy merle male! We are so excited to see what Mimi gives us! We had so much fun traveling on the plane with miss Mimi and could not have asked for a better traveling companion. She was patient, listened very well and just wanted cuddles the whole flight from Europe to the US. Mimi is a petite baby who is quite compact and solid in build. She has a well muscled frame with very nice front and rear. Mimi loves to have fun, is fearless with the goats, sheep, and Godzilla bird (Lord Farquaad, our obnoxious goose). She is a free spirit who is just always happy and ready for you to scoop her up for loves. Mimi has a gorgeous brindle coat and is a carrier for fluffy. Bred to Enzo, we are expecting fluffy puppies!! This will be Mimi’s first litter!
We will have some better photos of Mimi soon, but for now, here she is on her way to the United States from Europe <3
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): M/M (at risk)
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
