DISTINCTLY DIFFERENT
BECAUSE OF OUR PARENTS
BO IS FOR SALE

BO IS COMPLETELY CLEAR
OF ALL OF THE FOLLOWING
Genetically based Diseases!
Total of over 170 diseases
BO
MOYEN SIZED PUREBRED POODLE
Bo's Mom
Excellent OFA Hips
Bo's Dad
Excellent OFA Hips


BO'S PARENTS
Von Willebrand Disease Type I (VWF) BLOOD
Seen in Poodle (Standard)s, Poodle (Small)s, but not Lakeshore's Intricate Details.
Congenital Macrothrombocytopenia (TUBB1 Exon 1, Cavalier King Charles Spaniel Variant) BLOOD
Seen in Poodle (Standard)s, Poodle (Small)s, but not Lakeshore's Intricate Details.
Progressive Retinal Atrophy - prcd Progressive rod-cone degeneration (PRCD Exon 1) EYES
Seen in Poodle (Standard)s, Poodle (Small)s, but not Lakeshore's Intricate Details.
GM2 Gangliosidosis (HEXB, Poodle Variant) MULTISYSTEM
Seen in Poodle (Standard)s, Poodle (Small)s, but not Lakeshore's Intricate Details.
Degenerative Myelopathy (SOD1A) BRAIN AND SPINAL CORD
Seen in Poodle (Standard)s, Poodle (Small)s, but not Lakeshore's Intricate Details.
Neonatal Encephalopathy with Seizures (NEWS) (ATF2) BRAIN AND SPINAL CORD
Seen in Poodle (Standard)s, Poodle (Small)s, but not Lakeshore's Intricate Details.
Osteochondrodysplasia, Skeletal Dwarfism (SLC13A1) SKELETAL
Seen in Poodle (Standard)s, Poodle (Small)s, but not Lakeshore's Intricate Details.
MDR1 Drug Sensitivity (MDR1)
Sensitivity to certain classes of drugs, notably the parasiticide ivermectin, as well as certain gastroprotectant and anti-cancer medications, occurs in dogs with mutations in the MDR1 gene. Symptoms can range from vomiting and diarrhea to lethargy, seizures, or coma. MDR1 mutations are particularly common in herding breeds including Australian Shepherds, Collies, and Border Collies, though many other dog breeds are affected. Please note that the dosage of problem drugs in commercially available heartworm, flea, and tick preventatives should not cause symptoms in MDR1 dogs.
ALL GENETICALLY BASED BLOOD ISSUES
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Factor IX Deficiency, Hemophilia B (F9 Exon 7, Terrier Variant)
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Factor IX Deficiency, Hemophilia B (F9 Exon 7, Rhodesian Ridgeback Variant)
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Factor VIII Deficiency, Hemophilia A (F8 Exon 10, Boxer Variant)
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Factor VIII Deficiency, Hemophilia A (F8 Exon 11, Shepherd Variant 1)
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Factor VIII Deficiency, Hemophilia A (F8 Exon 1, Shepherd Variant 2)
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Canine Leukocyte Adhesion Deficiency Type III (LAD3) (FERMT3)
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Congenital Macrothrombocytopenia (TUBB1 Exon 1, Cavalier King Charles Spaniel Variant)
ALL GENETICALLY BASED HORMONE ISSUES
ALL IMMUNE CONDITIONS TESTED FOR
ALL EYE CONDITIONS TESTED FOR
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Progressive Retinal Atrophy - rcd1 Rod-cone dysplasia, rcd1 (PDE6B Exon 21 Irish Setter Variant)
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Progressive Retinal Atrophy Rod-cone dysplasia, rcd1a (PDE6B Exon 21 Sloughi Variant)
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Progressive Retinal Atrophy - rcd3 Rod-cone dysplasia, rcd3 (PDE6A)
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Progressive Retinal Atrophy - prcd Progressive rod-cone degeneration (PRCD Exon 1)
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Hereditary Cataracts, Early-Onset Cataracts, Juvenile Cataracts (HSF4 Exon 9 Shepherd Variant)
Bo is clear of all the Kidney and Bladder conditions that Embark tests for.
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X-Linked Hereditary Nephropathy (Samoyed Variant 2) (COL4A5 Exon 35)
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Autosomal Recessive Hereditary Nephropathy, Familial Nephropathy (COL4A4 Exon 3)
Bo is clear of all the Multisystem conditions that Embark tests for.
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X-linked Ectodermal Dysplasia, Anhidrotic Ectodermal Dysplasia (EDA Intron 8)
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Renal Cystadenocarcinoma and Nodular Dermatofibrosis (RCND) (FLCN Exon 7)
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Mucopolysaccharidosis Type IIIA, Sanfilippo Syndrome Type A (SGSH Exon 6 Variant 1)
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Mucopolysaccharidosis Type IIIA, Sanfilippo Syndrome Type A (SGSH Exon 6 Variant 2)
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Glycogen storage disease Type VII, Phosphofructokinase deficiency (PFKM Wachtelhund Variant)
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Neuronal Ceroid Lipofuscinosis 1, Cerebellar Ataxia - NCL-A (ARSG Exon 2
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Neuronal Ceroid Lipofuscinosis 1 (CLN5 Border Collie Variant)
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Neuronal Ceroid Lipofuscinosis 8 (CLN8 English Setter Variant)
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Neuronal Ceroid Lipofuscinosis (CLN8 Australian Shepherd Variant)
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Neuronal Ceroid Lipofuscinosis (CLN5 Golden Retriever Variant)
Bo is clear of all the Other Systems conditions that Embark tests for.
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Autosomal Recessive Amelogenesis Imperfecta (Italian Greyhound Variant)
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Deafness and Vestibular Syndrome of Dobermans (DVDob, DINGS)
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Shar-Pei Autoinflammatory Disease (SPAID, Shar-Pei Fever) (MTBP)
Bo is clear of all the Brain and Spinal Cord conditions that Embark tests for.
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Alaskan Husky Encephalopathy, Subacute Necrotizing Encephalomyelopathy (SLC19A3)
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Cerebellar Abiotrophy, Neonatal Cerebellar Cortical Degeneration (SPTBN2)
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Cerebellar Ataxia, Progressive Early-Onset Cerebellar Ataxia (SEL1L)
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Spinocerebellar Ataxia with Myokymia and/or Seizures (KCNJ10)
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Benign Familial Juvenile Epilepsy, Remitting Focal Epilepsy (LGI2)
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Shaking Puppy Syndrome, X-linked Generalized Tremor Syndrome (PLP)
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Progressive Neuronal Abiotrophy (Canine Multiple System Degeneration) (SERAC1 Exon 15)
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Progressive Neuronal Abiotrophy (Canine Multiple System Degeneration) (SERAC1 Exon 4)
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Hereditary Sensory Autonomic Neuropathy (HSAN), Acral Mutilation Syndrome (GDNF-AS)
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Juvenile-Onset Polyneuropathy, Leonberger Polyneuropathy 1 (LPN1, ARHGEF10)
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Spongy Degeneration with Cerebellar Ataxia 1 (SDCA1), SeSAME/EAST (KCNJ10)
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Spongy Degeneration with Cerebellar Ataxia 2 (SDCA2) (ATP1B2)
Bo is clear of all the Heart conditions that Embark tests for.
Bo is clear of all the Muscular conditions that Embark tests for.
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Muscular Dystrophy Muscular Dystrophy (DMD Pembroke Welsh Corgi Variant )
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Muscular Dystrophy Muscular Dystrophy (DMD Golden Retriever Variant)
Bo is clear of all the Metabolic conditions that Embark tests for.
Bo is clear of all the Gastrointestinal conditions that Embark tests for.
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Imerslund-Grasbeck Syndrome, Selective Cobalamin Malabsorption (CUBN Exon 53)
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Imerslund-Grasbeck Syndrome, Selective Cobalamin Malabsorption (CUBN Exon 8)
Bo is clear of all the Neuromuscular conditions that Embark tests for.
Bo is clear of all the Skin & Connective Tissues conditions that Embark tests for
Bo is clear of all the Skeletal conditions that Embark tests for.