2,8-Dihydroxyadenine (2,8-DHA) Urolithiasis (APRT) |
clear |
Achromatopsia (CNGA3 Exon 7 German Shepherd Variant) |
clear |
Achromatopsia (CNGA3 Exon 7 Labrador Retriever Variant) |
clear |
Adult-Onset Neuronal Ceroid Lipofuscinosis (ATP13A2) |
clear |
Alanine Aminotransferase (ALT) Activity (GPT) |
clear |
Alaskan Husky Encephalopathy, Subacute Necrotizing Encephalomyelopathy (SLC19A3) |
clear |
Alexander Disease (GFAP) |
clear |
Autosomal Dominant Progressive Retinal Atrophy (RHO) |
clear |
Autosomal Recessive Amelogenesis Imperfecta, Familial Enamel Hypoplasia (Italian Greyhound Variant) |
clear |
Autosomal Recessive Hereditary Nephropathy, Familial Nephropathy (COL4A4 Exon 3) |
clear |
Benign Familial Juvenile Epilepsy, Remitting Focal Epilepsy (LGI2) |
clear |
Canine Elliptocytosis (SPTB Exon 30) |
clear |
Canine Leukocyte Adhesion Deficiency Type III (LAD3) (FERMT3) |
clear |
Canine Multifocal Retinopathy cmr1 (BEST1 Exon 2) |
clear |
Canine Multifocal Retinopathy cmr2 (BEST1 Exon 5) |
clear |
Canine Multifocal Retinopathy cmr3 (BEST1 Exon 10 Deletion) |
clear |
Canine Multifocal Retinopathy cmr3 (BEST1 Exon 10 SNP) |
clear |
Centronuclear Myopathy (PTPLA) |
clear |
Cerebellar Abiotrophy, Neonatal Cerebellar Cortical Degeneration (SPTBN2) |
clear |
Cerebellar Ataxia, Progressive Early-Onset Cerebellar Ataxia (SEL1L) |
clear |
Cerebellar Hypoplasia (VLDLR) |
clear |
Cleft Lip and/or Cleft Palate (ADAMTS20) |
clear |
Collie Eye Anomaly, Choroidal Hypoplasia (NHEJ1) |
clear |
Complement 3 (C3) deficiency (C3) |
clear |
Congenital Hypothyroidism (TPO, Tenterfield Terrier Variant) |
clear |
Congenital Keratoconjunctivitis Sicca and Ichthyosiform Dermatosis (CKCSID), Dry Eye Curly Coat Syndrome (FAM83H Exon 5) |
clear |
Congenital Macrothrombocytopenia (TUBB1 Exon 1, Cavalier King Charles Spaniel Variant) |
clear |
Congenital Myasthenic Syndrome (CHAT) |
clear |
Congenital Myasthenic Syndrome (COLQ) |
clear |
Congenital stationary night blindness (RPE65) |
clear |
Craniomandibular Osteopathy (CMO) (SLC37A2) |
clear |
Cyclic Neutropenia, Gray Collie Syndrome (AP3B1 Exon 20) |
clear |
Cystinuria Type I-A (SLC3A1) |
clear |
Cystinuria Type II-A (SLC3A1) |
clear |
Cystinuria Type II-B (SLC7A9) |
clear |
Deafness and Vestibular Syndrome of Dobermans (DVDob, DINGS) |
clear |
Degenerative Myelopathy (SOD1A) |
clear |
Dilated Cardiomyopathy (DCM1) (PDK4) |
clear |
Dilated Cardiomyopathy (DCM2) (TTN) |
clear |
Dystrophic Epidermolysis Bullosa (COL7A1) |
clear |
Ectodermal Dysplasia, Skin Fragility Syndrome (PKP1) |
clear |
Episodic Falling Syndrome (BCAN) |
clear |
Exercise-Induced Collapse (DNM1) |
clear |
Factor IX Deficiency, Hemophilia B (F9 Exon 7, Rhodesian Ridgeback Variant) |
clear |
Factor IX Deficiency, Hemophilia B (F9 Exon 7, Terrier Variant) |
clear |
Factor VII Deficiency (F7 Exon 5) |
clear |
Factor VIII Deficiency, Hemophilia A (F8 Exon 1, Shepherd Variant 2) |
clear |
Factor VIII Deficiency, Hemophilia A (F8 Exon 10, Boxer Variant) |
clear |
Factor VIII Deficiency, Hemophilia A (F8 Exon 11, Shepherd Variant 1) |
clear |
Fetal-Onset Neonatal Neuroaxonal Dystrophy (MFN2) |
clear |
Focal Non-Epidermolytic Palmoplantar Keratoderma, Pachyonychia Congenita (KRT16) |
clear |
GM1 Gangliosidosis (GLB1 Exon 15 Alaskan Husky Variant) |
clear |
GM1 Gangliosidosis (GLB1 Exon 15 Shiba Inu Variant) |
clear |
GM1 Gangliosidosis (GLB1 Exon 2) |
clear |
GM2 Gangliosidosis (HEXA) |
clear |
GM2 Gangliosidosis (HEXB, Poodle Variant) |
clear |
Glanzmann's Thrombasthenia Type I (ITGA2B Exon 12) |
clear |
Glaucoma Primary Open Angle Glaucoma (ADAMTS10 Exon 17) |
clear |
Glaucoma Primary Open Angle Glaucoma (ADAMTS10 Exon 9) |
clear |
Glaucoma Primary Open Angle Glaucoma (ADAMTS17 Exon 11) |
clear |
Glaucoma Primary Open Angle Glaucoma (ADAMTS17 Exon 2) |
clear |
Globoid Cell Leukodystrophy, Krabbe disease (GALC Exon 5) |
clear |
Glycogen Storage Disease Type II, Pompe's Disease (GAA) |
clear |
Glycogen Storage Disease Type IIIa (GSD IIIa) (AGL) |
clear |
Glycogen Storage Disease Type Ia, Von Gierke Disease (G6PC) |
clear |
Glycogen storage disease Type VII, Phosphofructokinase deficiency (PFKM Wachtelhund Variant) |
clear |
Glycogen storage disease Type VII, Phosphofructokinase deficiency (PFKM Whippet and English Springer Spaniel Variant) |
clear |
Golden Retriever Progressive Retinal Atrophy 1 (SLC4A3) |
clear |
Golden Retriever Progressive Retinal Atrophy 2 (TTC8) |
clear |
Hereditary Cataracts, Early-Onset Cataracts, Juvenile Cataracts (HSF4 Exon 9 Shepherd Variant) |
clear |
Hereditary Footpad Hyperkeratosis (FAM83G) |
clear |
Hereditary Nasal Parakeratosis (SUV39H2) |
clear |
Hereditary Sensory Autonomic Neuropathy (HSAN), Acral Mutilation Syndrome (GDNF-AS) |
clear |
Hereditary Vitamin D-Resistant Rickets (VDR) |
clear |
Hyperuricosuria and Hyperuricemia or Urolithiasis (SLC2A9) |
clear |
Hypocatalasia, Acatalasemia (CAT) |
clear |
Hypomyelination and Tremors (FNIP2) |
clear |
Ichthyosis (NIPAL4) |
clear |
Ichthyosis (PNPLA1) |
clear |
Ichthyosis (SLC27A4) |
clear |
Ichthyosis, Epidermolytic Hyperkeratosis (KRT10) |
clear |
Imerslund-Grasbeck Syndrome, Selective Cobalamin Malabsorption (CUBN Exon 53) |
clear |
Imerslund-Grasbeck Syndrome, Selective Cobalamin Malabsorption (CUBN Exon 8) |
clear |
Inherited Myopathy of Great Danes (BIN1) |
clear |
Juvenile-Onset Polyneuropathy, Leonberger Polyneuropathy 1 (LPN1, ARHGEF10) |
clear |
L-2-Hydroxyglutaricaciduria (L2HGDH) |
clear |
Lagotto Storage Disease (ATG4D) |
clear |
Ligneous Membranitis (PLG) |
clear |
Long QT Syndrome (KCNQ1) |
clear |
MDR1 Drug Sensitivity (MDR1) |
clear |
Macular Corneal Dystrophy (MCD) (CHST6) |
clear |
Malignant Hyperthermia (RYR1) |
clear |
May-Hegglin Anomaly (MYH9) |
clear |
Mucopolysaccharidosis Type IIIA, Sanfilippo Syndrome Type A (SGSH Exon 6 Variant 1) |
clear |
Mucopolysaccharidosis Type IIIA, Sanfilippo Syndrome Type A (SGSH Exon 6 Variant 2) |
clear |
Mucopolysaccharidosis Type VII, Sly Syndrome (GUSB Exon 3) |
clear |
Mucopolysaccharidosis Type VII, Sly Syndrome (GUSB Exon 5) |
clear |
Muscular Dystrophy Cavalier King Charles Spaniel Variant 1 |
clear |
Muscular Dystrophy Muscular Dystrophy (DMD Golden Retriever Variant) |
clear |
Muscular Dystrophy Muscular Dystrophy (DMD Pembroke Welsh Corgi Variant ) |
clear |
Musladin-Lueke Syndrome (ADAMTSL2) |
clear |
Myotonia Congenita (CLCN1 Exon 23) |
clear |
Myotonia Congenita (CLCN1 Exon 7) |
clear |
Myotubular Myopathy 1, X-linked Myotubular Myopathy (MTM1) |
clear |
Narcolepsy (HCRTR2 Intron 6) |
clear |
Neonatal Encephalopathy with Seizures (NEWS) (ATF2) |
clear |
Neuronal Ceroid Lipofuscinosis (CLN5 Golden Retriever Variant) |
clear |
Neuronal Ceroid Lipofuscinosis (CLN8 Australian Shepherd Variant) |
clear |
Neuronal Ceroid Lipofuscinosis (MFSD8) |
clear |
Neuronal Ceroid Lipofuscinosis 1 (CLN5 Border Collie Variant) |
clear |
Neuronal Ceroid Lipofuscinosis 1 (PPT1 Exon 8) |
clear |
Neuronal Ceroid Lipofuscinosis 1, Cerebellar Ataxia - NCL-A (ARSG Exon 2) |
clear |
Neuronal Ceroid Lipofuscinosis 10 (CTSD Exon 5) |
clear |
Neuronal Ceroid Lipofuscinosis 2 (TPP1 Exon 4) |
clear |
Neuronal Ceroid Lipofuscinosis 6 (CLN6 Exon 7) |
clear |
Neuronal Ceroid Lipofuscinosis 8 (CLN8 English Setter Variant) |
clear |
Oculoskeletal Dysplasia 1, Dwarfism-Retinal Dysplasia (COL9A3, Labrador Retriever) |
clear |
Osteochondrodysplasia, Skeletal Dwarfism (SLC13A1) |
clear |
Osteogenesis Imperfecta, Brittle Bone Disease (COL1A1) |
clear |
Osteogenesis Imperfecta, Brittle Bone Disease (COL1A2) |
clear |
Osteogenesis Imperfecta, Brittle Bone Disease (SERPINH1) |
clear |
P2Y12 Receptor Platelet Disorder (P2RY12) |
clear |
Persistent Mullerian Duct Syndrome (AMHR2) |
clear |
Polycystic Kidney Disease (PKD1) |
clear |
Polyneuropathy, NDRG1 Greyhound Variant (NDRG1 Exon 15) |
clear |
Polyneuropathy, NDRG1 Malamute Variant (NDRG1 Exon 4) |
clear |
Prekallikrein Deficiency (KLKB1 Exon 8) |
clear |
Primary Ciliary Dyskinesia (CCDC39 Exon 3) |
clear |
Primary Hyperoxaluria (AGXT) |
clear |
Primary Lens Luxation (ADAMTS17) |
clear |
Progressive Neuronal Abiotrophy (Canine Multiple System Degeneration) (SERAC1 Exon 15) |
clear |
Progressive Neuronal Abiotrophy (Canine Multiple System Degeneration) (SERAC1 Exon 4) |
clear |
Progressive Retinal Atrophy (CNGB1) |
clear |
Progressive Retinal Atrophy (SAG) |
clear |
Progressive Retinal Atrophy - CNGA (CNGA1 Exon 9) |
no call |
Progressive Retinal Atrophy - crd1 (PDE6B) |
clear |
Progressive Retinal Atrophy - crd2 (IQCB1) |
clear |
Progressive Retinal Atrophy - crd4/cord1 (RPGRIP1) |
clear |
Progressive Retinal Atrophy - prcd Progressive rod-cone degeneration (PRCD Exon 1) |
clear |
Progressive Retinal Atrophy - rcd1 Rod-cone dysplasia, rcd1 (PDE6B Exon 21 Irish Setter Variant) |
clear |
Progressive Retinal Atrophy - rcd3 Rod-cone dysplasia, rcd3 (PDE6A) |
clear |
Protein Losing Nephropathy (NPHS1) |
clear |
Pyruvate Dehydrogenase Deficiency (PDP1) |
clear |
Pyruvate Kinase Deficiency (PKLR Exon 10) |
clear |
Pyruvate Kinase Deficiency (PKLR Exon 5) |
clear |
Pyruvate Kinase Deficiency (PKLR Exon 7 Beagle Variant) |
clear |
Pyruvate Kinase Deficiency (PKLR Exon 7 Labrador Variant) |
clear |
Pyruvate Kinase Deficiency (PKLR Exon 7 Pug Variant) |
clear |
Renal Cystadenocarcinoma and Nodular Dermatofibrosis (RCND) (FLCN Exon 7) |
clear |
Severe Combined Immunodeficiency (PRKDC) |
clear |
Severe Combined Immunodeficiency (RAG1) |
clear |
Shaking Puppy Syndrome, X-linked Generalized Tremor Syndrome (PLP) |
clear |
Shar-Pei Autoinflammatory Disease (SPAID, Shar-Pei Fever) (MTBP) |
clear |
Skeletal Dysplasia 2 (COL11A2) |
clear |
Spinocerebellar Ataxia with Myokymia and/or Seizures (KCNJ10) |
clear |
Spinocerebellar Ataxia, Late-Onset Ataxia (CAPN1) |
clear |
Spongy Degeneration with Cerebellar Ataxia 1 (SDCA1), SeSAME/EAST (KCNJ10) |
clear |
Spongy Degeneration with Cerebellar Ataxia 2 (SDCA2) (ATP1B2) |
clear |
Thrombopathia (RASGRP2 Exon 5, American Eskimo Dog Variant) |
clear |
Thrombopathia (RASGRP2 Exon 5, Basset Hound Variant) |
clear |
Thrombopathia (RASGRP2 Exon 8) |
clear |
Trapped Neutrophil Syndrome (VPS13B) |
clear |
Von Willebrand Disease Type I (VWF) |
clear |
Von Willebrand Disease Type II (VWF) |
clear |
Von Willebrand Disease Type III (VWF Exon 4) |
clear |
X-Linked Hereditary Nephropathy (Samoyed Variant 2) (COL4A5 Exon 35) |
clear |
X-linked Ectodermal Dysplasia, Anhidrotic Ectodermal Dysplasia (EDA Intron 8) |
clear |
X-linked Severe Combined Immunodeficiency (IL2RG Variant 1) |
clear |
X-linked Severe Combined Immunodeficiency (IL2RG Variant 2) |
clear |