Lily's DNA Results


Lily's DNA Results
Sugar Run's Princess Lily of Kensington

OFA PRELIM HIPS GOOD - OFA PRELIM ELBOWS NORMAL
ACVO CLEAR / NORMAL - OFA EYE (CAER)
PRCD PROGRESSIVE RETINAL ATROPHY DNA Tested CLEAR/NORMAL
EXERCISED INDUCED COLLAPSE (EIC) DNA TESTED CARRIER/NOT AFFECTED
CENTRONUCLEAR MYOPATHY (CNM) DNA TESTED CLEAR/NORMAL
CYSTINURIA (CY) DNA TESTED CLEAR/NORMAL
DEGENERATIVE MYELOPATHY DNA TESTED CLEAR/NORMAL
HYPERURICOSURIA (HU) DNA TESTED CLEAR/NORMAL
FULL DENTITION - NORMAL
PATELLA - NORMAL

Blood Clearances:
P2y12 Receptor Platelet Disorder - CLEAR/NORMAL
Factor IX Deficiency, Hemophilia B - F9 Exon 7 - CLEAR/NORMAL
Factor VIII Deficiency Hemophilia A - F8 Exon 11 - CLEAR/NORMAL
Factor VIII Deficiency Hemophilia A - F8 Exon 1 - CLEAR/NORMAL
Thrombopathia Exon 5 - CLEAR/NORMAL
Thrombopathia Exon 8 - CLEAR/NORMAL
Von Willebrand Disease Type III - CLEAR/NORMAL
Von Willebrand Disease Type II - CLEAR/NORMAL
Von Willebrand Disease Type I - CLEAR/NORMAL
Canine Leukocyte Adhesion Deficiency Type III (LAD3) - CLEAR/NORMAL
Congenital Macrothrombocytopenia - CLEAR/NORMAL
Canine Elliptocytosis - CLEAR/NORMAL
Canine Neutropenia - CLEAR/NORMAL
Glanzmann's Thrombasthenia Type I - CLEAR/NORMAL
May-Hegglin Anomaly - CLEAR/NORMAL
Prekallikrein Deficiency - CLEAR/NORMAL
Pyruvate Kinase Deficiency Exon 5 - CLEAR/NORMAL
Pyruvate Kinase Deficiency Exon 7 - CLEAR/NORMAL
Pyruvate Kinase Deficiency Exon 10 - CLEAR/NORMAL
Trapped Neutrophil Syndrome - CLEAR/NORMAL
Ligneous Membranitis - CLEAR/NORMAL

Immune Clearances:
Complement 3 (C3) Deficiency - CLEAR/NORMAL
Severe Combined Immunodeficiency - PRKDC - CLEAR/NORMAL
Severe Combined Immunodeficiency - RAG1 - CLEAR/NORMAL
X-Linked Severe Combined Immunodeficiency - Variant 1 - CLEAR/NORMAL
X-Linked Severe Combined Immunodeficiency - Variant 2 - CLEAR/NORMAL

Hormone Clearances:
Congenital Hypothyroidism - CLEAR/NORMA‚ÄčL


Eye Clearances:
Progressive Retinal Atrophy - PRCD1 - CLEAR/NORMAL
Progressive Retinal Atrophy - PRCD3 - CLEAR/NORMAL
Progressive Retinal Atrophy - CNGA - CLEAR/NORMAL
Progressive Retinal Atrophy - PRCD - CLEAR/NORMAL
Progressive Retinal Atrophy - CNGB1 - CLEAR/NORMAL
Progressive Retinal Atrophy - SAG - CLEAR/NORMAL
Progressive Retinal Atrophy 1 - SLC4A3 - CLEAR/NORMAL
Progressive Retinal Atrophy 2 - TTC8 - CLEAR/NORMAL
Progressive Retinal Atrophy - CRD1 - PDE6B - CLEAR/NORMAL
Progressive Retinal Atrophy - CRD2 - IQCB1 - CLEAR/NORMAL
Progressive Retinal Atrophy - CRD4/CORD1 - RPGRIP1 - CLEAR/NORMAL
Choroidal Hypoplasia - NHEJ1 - CLEAR/NORMAL
Achromatopsia - CNGA3 Exon 7 - CLEAR/NORMAL
Autosomal Dominant Progressive Retinal Atrophy - CLEAR/NORMAL
Canine Multifocal Retinopathy - CMR1 - CLEAR/NORMAL
Canine Multifocal Retinopathy - CMR3 - CLEAR/NORMAL

Canine Multifocal Retinopathy - CMR3 - BEST1 EXON 10 SNP - CLEAR/NORMAL
Glaucoma - Primary Open Angle Glaucoma - ADAMTS10 Exon 9 - CLEAR/NORMAL
Glaucoma - Primary Open Angle Glaucoma - ADAMTS10 Exon 17 - CLEAR/NORMAL
Glaucoma - Primary Open Angle Glaucoma - ADAMTS17 Exon 11 - CLEAR/NORMAL
Glaucoma - Primary Open Angle Glaucoma - ADAMTS10 Exon 2 - CLEAR/NORMAL
Hereditary Cataracts, Early Onset Cataracts, Juvenile Cataracts - CLEAR/NORMAL
Primary Lens Luxation - CLEAR/NORMAL
Congenital Stationary Night Blindness - CLEAR/NORMAL
Macular Corneal Dystrophy (MCD) - CLEAR/NORMAL

Clinical Clearances:
MDR1 Drug Sensitivity - CLEAR/NORMAL
Alanine Aminotransfearase (ALT) Activity - CLEAR/NORMAL

MULTISYSTEM CLEARANCES:
Glycogen Storage Disease Von Gierke Disease - CLEAR/NORMAL
Primary Ciliary Dyskinesia - CLEAR/NORMAL
Congenital Keratoconjunctivitis Sicca & Ichthyosiform Dermatosis (CKCSID) - CLEAR/NORMAL
Dry Eye Curly Coat Syndrome - CLEAR/NORMAL
X-Linked Ectodermal Dysplasia - CLEAR/NORMAL
Anhidrotic Ectodermal Dysplasia - CLEAR/NORMAL
Renal Cystadenocarcinoma & Nodular Dermatofibrosis (RCND) - CLEAR/NORMAL
Canine Fucosidosis - CLEAR/NORMAL
Glycogen Storage Disease Type II Pompe's Disease - CLEAR/NORMAL
Glycogen Storage Disease Type IIIa (GSD IIIa) - CLEAR/NORMAL
Mucopolysaccharidosis Type I - CLEAR/NORMAL
Mucopolysaccharidosis Type IIIA Sanflilppo Syndrome Type A - Variant 1 - CLEAR/NORMAL
Mucopolysaccharidosis Type IIIA Sanflilppo Syndrome Type A - Variant 2 - CLEAR/NORMAL
Mucopolysaccharidosis Type VII Exon 3 Sly Syndrome - CLEAR/NORMAL
Mucopolysaccharidosis Type VII Exon 5 Sly Syndrome - CLEAR/NORMAL
Glycogen Storage Disease Type II Phosphofructokinase Deficiency - CLEAR/NORMAL
Lagotto Storage Disease - CLEAR/NORMAL
Neuronal Ceroid Lipofuscinosis 1 - CLEAR/NORMAL
Neuronal Ceroid Lipofuscinosis 2 - CLEAR/NORMAL
Neuronal Ceroid Lipofuscinosis 1 - Cerebellar Ataxia NCL A - CLEAR/NORMAL
Neuronal Ceroid Lipofuscinosis 1 - CLN5 - CLEAR/NORMAL
Neuronal Ceroid Lipofuscinosis 6 - CLN6 Exon 7- CLEAR/NORMAL
Neuronal Ceroid Lipofuscinosis 8 - CLN8 - CLEAR/NORMAL
Neuronal Ceroid Lipofuscinosis - CLEAR/NORMAL
Neuronal Ceroid Lipofuscinosis 10 - CTSD Exon 5 - CLEAR/NORMAL
Adult Onset Neuronal Ceroid Lipofuscinosis - CLEAR/NORMAL
GM1 Gangliosidosis Exon 2 - CLEAR/NORMAL
GM1 Gangliosidosis Exon 15 - CLEAR/NORMAL
GM2 Gangliosidosis Exon 2 - CLEAR/NORMAL
GM2 Gangliosidosis Hexa - CLEAR/NORMAL
Globoid Cell Leukodystrophy, Krabbe Disease - CLEAR/NORMA

BRAIN & SPINAL CORD CLEARANCES:
Alexander Disease - CLEAR/NORMAL
Encephalopathy, Subacute Necrotizing Encephalomyelopathy - CLEAR/NORMAL
Cerebellar Abiotrophy, Neonatal Cerebellar Cortical Degeneration - CLEAR/NORMAL
Cerebellar Ataxia, Progressive Early-Onset Cerebellar Ataxia - CLEAR/NORMAL
Cerebellar Hypoplasia - CLEAR/NORMAL
Spinocerebellar Ataxia, Late-Onset Ataxia - CLEAR/NORMAL
Spinocerebellar Ataxia with Myokymia and/or Seizures - CLEAR/NORMAL
Benign Familial Juvenile Epilepsy, Remitting Focal Epilepsy - CLEAR/NORMAL
Degenerative Myelopathy - CLEAR/NORMAL
Fetal-Onset Neonatal Neuroaxonal Dystrophy - CLEAR/NORMAL
Hypomyelination & Tremors - CLEAR/NORMAL
Shaking Puppy Syndrome, X-Linked Generalized Tremor Syndrome - CLEAR/NORMAL
L-2-Hydroxyglutaric Aciduria - CLEAR/NORMAL
Neonatal Encephalopathy with Seizures (NEWS) - CLEAR/NORMAL
Polyneuropathy, NDRG1 Exon 15 - CLEAR/NORMAL
Polyneuropathy, NDRG1 Exon 4 - CLEAR/NORMAL
Narcolepsy - CLEAR/NORMAL
Progressive Neuronal Abiotrophy (canine Multiple System Degeneration) Exon 4 - CLEAR/NORMAL
Progressive Neuronal Abiotrophy (canine Multiple System Degeneration) Exon 15 - CLEAR/NORMAL
Juvenile Laryngeal Paralysis & Polyneuropathy, Polyneuropathy with Ocular Abnormalities & Neuronal Vacuolation (POANV) - CLEAR/NORMAL
Hereditary Sensory Autonomic Neuropathy (HSAN), Acral Mutilation Syndrome - CLEAR/NORMAL
Juvenile Onset Polyneuropathy, Leonberger Polyneuropathy 1 - CLEAR/NORMAL
Spongy Degeneration with Cerebellar Ataxia 1, SeSAME/EAST - CLEAR/NORMAL
Spongy Degeneration with Cerebellar Ataxia 2, SeSAME/EAST - CLEAR/NORMAL

SKELETAL CLEARANCES:
Cleft Lip and/or Cleft Palate - CLEAR/NORMAL
Hereditary Vitamin D-Resistant Rickets - CLEAR/NORMAL
Oculoskeletal Dysplasia 1, Dwarfism-Retinal Dysplasia - CLEAR/NORMAL
Osteogenesis Imperfecta, Brittle Bone Disease (COL1A1) - CLEAR/NORMAL
Osteogenesis Imperfecta, Brittle Bone Disease (COL1A2) - CLEAR/NORMAL
Osteogenesis Imperfecta, Brittle Bone Disease (SERPINH1) - CLEAR/NORMAL
Osteochondrodysplasia, Skeletal Dwarfism - CLEAR/NORMAL
Skeletal Dysplasia 2 - CLEAR/NORMAL
Craniomandibular Osteopathy (CMO) - CLEAR/NORMAL

HEART CLEARANCES:
Dilated Cardiomyopathy - CLEAR/NORMAL
Long QT Syndrome - CLEAR/NORMAL
MUSCULAR CLEARANCES: Muscular Dystrophy - CLEAR/NORMAL
Centronuclear Myopathy - CLEAR/NORMAL
Exercise-Induced Collapse - CLEAR/NORMAL
Inherited Myopathy - CLEAR/NORMAL
Myostatin Deficiency - CLEAR/NORMAL
Myotonia Congenita Exon 7 - CLEAR/NORMAL
Myotonia Congenita Exon 23 - CLEAR/NORMAL
Myotubular Myopathy 1, X-linked Myotubular Myopathy - CLEAR/NORMAL

METABOLIC CLEARANCES:
Hypocatalasia, Acatalasemia - CLEAR/NORMAL
Pyruvate Dehydrogenase Deficiency - CLEAR/NORMAL
Malignant Hyperthermia - CLEAR/NORMAL

GASTROINTESTINAL CLEARANCES:
Imerslund-Grasbeck Syndrome, Selective Cobalamin Malabsorption Exon 8 - CLEAR/NORMAL
Imerslund-Grasbeck Syndrome, Selective Cobalamin Malabsorption Exon 53 - CLEAR/NORMAL
NEUROMUSCULAR CLEARANCES: Congenital Myasthenic Syndrome CHAT - CLEAR/NORMAL
Congenital Myasthenic Syndrome COLQ - CLEAR/NORMAL
Episodic Falling Syndrome - CLEAR/NORMAL

SKIN & CONNECTIVE TISSUES CLEARANCES:
Dystrophic Epidermolysis BUllosa - CLEAR/NORMAL
Ectodermal Dysplasia, SKin Fragility SYndrome - CLEAR/NORMAL
Ichthyosis, Epidermolytic Hyperkeratosis - CLEAR/NORMAL
Ichthyosis PNPLA1 - CLEAR/NORMAL
Ichthyosis SLC27A4 - CLEAR/NORMAL
Ichthyosis NIPAL4 - CLEAR/NORMAL
Focal Non-Epidermolytic Palmoplantar Keratoderma, Pachyonychia Congenita - CLEAR/NORMAL
Hereditary Footpad Hyperkeratosis - CLEAR/NORMAL
Hereditary Nasal Parakeratosis HNPK - CLEAR/NORMAL
Musladin-Lueke Syndrome - CLEAR/NORMAL 

COAT COLOR CLEARANCES:
E Locus (MC1R) - No dark hairs anywhere
D Locus (MLPH) Does not carry Dilute - CLEAR/NORMAL
B Locus (TYRP1) Produces Black pigment in skin, noses, eye rims and footpads