DNA / HEALTH RESULTS
MERCEDES'S HEALTH RESULTS
We have tested MERCEDES's DNA for more than 150 disease-causing mutations. Below is a summary of our findings.
CLEAR - 135Congratulations! MERCEDES inherited zero copies of these disease mutations. Be sure to use our share feature to let your veterinarian know about MERCEDES’s results.
We have tested MERCEDES's DNA for more than 150 disease-causing mutations. Below is a summary of our findings.
CLEAR - 135Congratulations! MERCEDES inherited zero copies of these disease mutations. Be sure to use our share feature to let your veterinarian know about MERCEDES’s results.
Blood
Canine Leukocyte Adhesion Deficiency (CLAD), type III
Canine Scott Syndrome
Factor VII Deficiency
Factor XI Deficiency
Glanzmann Thrombasthenia Type I
Hemophilia A
Hemophilia A
Hemophilia A
Hemophilia A
Hemophilia B
Hemophilia B
Hemophilia B
Hereditary Elliptocytosis
Macrothrombocytopenia
May-Hegglin Anomaly
P2RY12-associated Bleeding Disorder
Phosphofructokinase Deficiency
Prekallikrein Deficiency
Pyruvate Kinase Deficiency
Pyruvate Kinase Deficiency
Pyruvate Kinase Deficiency
Trapped Neutrophil Syndrome
von Willebrand's Disease, type 1
von Willebrand's Disease, type 3
von Willebrand's Disease, type 3
Dental
Amelogenesis Imperfecta
Dental Hypomineralization
Drug response
Multidrug Resistance 1
Eye
Canine Multifocal Retinopathy 1
Canine Multifocal Retinopathy 2
Cone Degeneration
Cone Degeneration
Cone Degeneration
Cone-Rod Dystrophy
Cone-Rod Dystrophy 1
Cone-Rod Dystrophy 2
Dominant Progressive Retinal Atrophy
Primary Lens Luxation
Primary Open Angle Glaucoma
Progressive Retinal Atrophy
Progressive Retinal Atrophy
Progressive Retinal Atrophy Type III
Rod-Cone Dysplasia 1
Rod-Cone Dysplasia 1a
Rod-Cone Dysplasia 3
X-Linked Progressive Retinal Atrophy 2
Heart
QT Syndrome
Hormonal
Congenital Hypothyroidism
Congenital Hypothyroidism
Immune system
Canine Cyclic Neutropenia
Complement 3 Deficiency
Severe Combined Immunodeficiency
X-Linked Severe Combined Immunodeficiency
X-Linked Severe Combined Immunodeficiency
Lung
Primary Ciliary Dyskinesia
Metabolic
Glycogen Storage Disease Type Ia
Hypocatalasia
Imerslund-Gräsbeck Syndrome
Imerslund-Gräsbeck Syndrome
Mucopolysaccharidosis Type IIIA
Mucopolysaccharidosis Type VII
Pyruvate Dehydrogenase Phosphatase 1 Deficiency
Muscle
Centronuclear Myopathy
Centronuclear Myopathy
Muscular Dystrophy
Muscular Dystrophy
Muscular Dystrophy
Muscular Dystrophy
Muscular Hypertrophy
Myotonia Congenita
Myotubular Myopathy
Nervous system
Alaskan Husky Encephalopathy
Bandera's Neonatal Ataxia
Benign Familial Juvenile Epilepsy
Cerebellar Ataxia
Cerebellar Hypoplasia
Degenerative Myelopathy
Fetal Onset Neuroaxonal Dystrophy
Hyperekplexia or Startle Disease
Hypomyelination
L-2-Hydroxyglutaric Aciduria
Lagotto Storage Disease
Narcolepsy
Narcolepsy
Neonatal Cerebellar Cortical Degeneration
Neonatal Encephalopathy with Seizures
Neuroaxonal Dystrophy
Neuronal Ceroid Lipofuscinosis 1
Neuronal Ceroid Lipofuscinosis 10
Neuronal Ceroid Lipofuscinosis 7
Neuronal Ceroid Lipofuscinosis 8
Neuronal Ceroid Lipofuscinosis 8
Sensory Ataxic Neuropathy
Spinal Dysraphism
Spinocerebellar Ataxia (Late-Onset Ataxia)
Spinocerebellar Ataxia with Myokymia and/or Seizures
X-Linked Tremors
Neuromuscular
Congenital Myasthenic Syndrome
Congenital Myasthenic Syndrome
Early-Onset Progressive Polyneuropathy
Episodic Falling Syndrome
Exercise-Induced Collapse
GM2 Gangliosidosis
GM2 Gangliosidosis
Globoid Cell Leukodystrophy
Globoid Cell Leukodystrophy
Reproductive system
Persistent Müllerian Duct Syndrome
Skeletal
Chondrodysplasia
Cleft Lip & Palate with Syndactyly
Cleft Palate
Craniomandibular Osteopathy
Hereditary Vitamin D-Resistant Rickets Type II
Musladin-Lueke Syndrome
Osteochondrodysplasia
Osteogenesis Imperfecta
Osteogenesis Imperfecta
Skeletal Dysplasia 2
Spondylocostal Dysostosis
Van den Ende-Gupta Syndrome
Skin
Dystrophic Epidermolysis Bullosa
Epidermolytic Hyperkeratosis
Focal Non-Epidermolytic Palmoplantar Keratoderma
Hereditary Footpad Hyperkeratosis
Ichthyosis
Lamellar Ichthyosis
Ligneous Membranitis
X-Linked Ectodermal Dysplasia
Urinary
Cystinuria Type I-A
Cystinuria Type II-A
Fanconi Syndrome
Hyperuricosuria
Polycystic Kidney Disease
Protein Losing Nephropathy
Renal Cystadenocarcinoma and Nodular Dermatofibrosis
X-Linked Hereditary Nephropathy
ARTHUR'S HEALTH RESULTS
We have tested ARTHUR's DNA for more than 150 disease-causing mutations. Below is a summary of our findings.
CLEAR - 152Congratulations! ARTHUR inherited zero copies of these disease mutations. Be sure to use our share feature to let your veterinarian know about ARTHUR’s results.. These clear results will help narrow down a future diagnosis if ARTHUR ever gets sick.
Blood
Canine Leukocyte Adhesion Deficiency (CLAD), type III
Canine Scott Syndrome
Factor VII Deficiency
Factor XI Deficiency
Glanzmann Thrombasthenia Type I
Glanzmann Thrombasthenia Type I
Hemophilia A
Hemophilia A
Hemophilia A
Hemophilia A
Hemophilia B
Hemophilia B
Hemophilia B
Hereditary Elliptocytosis
Macrothrombocytopenia
May-Hegglin Anomaly
P2RY12-associated Bleeding Disorder
Phosphofructokinase Deficiency
Prekallikrein Deficiency
Pyruvate Kinase Deficiency
Pyruvate Kinase Deficiency
Pyruvate Kinase Deficiency
Trapped Neutrophil Syndrome
von Willebrand's Disease, type 1
von Willebrand's Disease, type 3
von Willebrand's Disease, type 3
Dental
Amelogenesis Imperfecta
Dental Hypomineralization
Drug response
Multidrug Resistance 1
Eye
Canine Multifocal Retinopathy 1
Canine Multifocal Retinopathy 2
Cone Degeneration
Cone Degeneration
Cone Degeneration
Cone-Rod Dystrophy
Cone-Rod Dystrophy 1
Cone-Rod Dystrophy 2
Dominant Progressive Retinal Atrophy
Primary Lens Luxation
Primary Open Angle Glaucoma
Primary Open Angle Glaucoma and Primary Lens Luxation
Progressive Retinal Atrophy
Progressive Retinal Atrophy
Progressive Retinal Atrophy Type III
Rod-Cone Dysplasia 1
Rod-Cone Dysplasia 1a
Rod-Cone Dysplasia 3
X-Linked Progressive Retinal Atrophy 2
Heart
Dilated Cardiomyopathy
QT Syndrome
Hormonal
Congenital Hypothyroidism
Congenital Hypothyroidism
Immune system
Canine Cyclic Neutropenia
Complement 3 Deficiency
Severe Combined Immunodeficiency
X-Linked Severe Combined Immunodeficiency
X-Linked Severe Combined Immunodeficiency
Lung
Acute Respiratory Distress Syndrome
Primary Ciliary Dyskinesia
Metabolic
Glycogen Storage Disease Type IIIa, (GSD IIIa)
Glycogen Storage Disease Type Ia
Hypocatalasia
Imerslund-Gräsbeck Syndrome
Imerslund-Gräsbeck Syndrome
Mucopolysaccharidosis Type IIIA
Mucopolysaccharidosis Type VII
Pyruvate Dehydrogenase Phosphatase 1 Deficiency
Muscle
Centronuclear Myopathy
Centronuclear Myopathy
Muscular Dystrophy
Muscular Dystrophy
Muscular Dystrophy
Muscular Dystrophy
Muscular Hypertrophy (Double Muscling)
Myotonia Congenita
Myotubular Myopathy
Nemaline Myopathy
X-Linked Myotubular Myopathy
Nervous system
Alaskan Husky Encephalopathy
Alexander Disease
Bandera's Neonatal Ataxia
Benign Familial Juvenile Epilepsy
Cerebellar Ataxia
Cerebellar Cortical Degeneration
Cerebellar Hypoplasia
Degenerative Myelopathy
Fetal Onset Neuroaxonal Dystrophy
Hyperekplexia or Startle Disease
Hypomyelination
Juvenile Laryngeal Paralysis and Polyneuropathy
Juvenile Myoclonic Epilepsy
L-2-Hydroxyglutaric Aciduria
L-2-Hydroxyglutaric Aciduria
Lagotto Storage Disease
Narcolepsy
Narcolepsy
Neonatal Cerebellar Cortical Degeneration
Neonatal Encephalopathy with Seizures
Neuroaxonal Dystrophy
Neuronal Ceroid Lipofuscinosis 1
Neuronal Ceroid Lipofuscinosis 10
Neuronal Ceroid Lipofuscinosis 7
Neuronal Ceroid Lipofuscinosis 8
Neuronal Ceroid Lipofuscinosis 8
Sensory Ataxic Neuropathy
Sensory Neuropathy
Spinal Dysraphism
Spinocerebellar Ataxia (Late-Onset Ataxia)
Spinocerebellar Ataxia with Myokymia and/or Seizures
Spongy Degeneration with Cerebellar Ataxia
X-Linked Tremors
Neuromuscular
Congenital Myasthenic Syndrome
Congenital Myasthenic Syndrome
Early-Onset Progressive Polyneuropathy
Episodic Falling Syndrome
Exercise-Induced Collapse
GM2 Gangliosidosis
GM2 Gangliosidosis (Discovered in the Toy Poodle)
Globoid Cell Leukodystrophy
Globoid Cell Leukodystrophy
Reproductive system
Persistent Müllerian Duct Syndrome
Skeletal
Chondrodysplasia
Cleft Lip & Palate with Syndactyly
Cleft Palate
Craniomandibular Osteopathy
Hereditary Vitamin D-Resistant Rickets Type II
Musladin-Lueke Syndrome
Osteochondrodysplasia
Osteogenesis Imperfecta
Osteogenesis Imperfecta
Skeletal Dysplasia 2
Spondylocostal Dysostosis
Van den Ende-Gupta Syndrome
Skin
Dystrophic Epidermolysis Bullosa
Epidermolytic Hyperkeratosis
Focal Non-Epidermolytic Palmoplantar Keratoderma
Hereditary Footpad Hyperkeratosis
Ichthyosis
Ichthyosis
Lamellar Ichthyosis
Ligneous Membranitis
X-Linked Ectodermal Dysplasia
Urinary
Cystinuria Type I-A
Cystinuria Type II-A
Fanconi Syndrome
Hyperuricosuria
Polycystic Kidney Disease
Protein Losing Nephropathy
Renal Cystadenocarcinoma and Nodular Dermatofibrosis
X-Linked Hereditary Nephropathy
Xanthinuria (Discovered in a mixed breed dog)
Xanthinuria