|
2,8-Dihydroxyadenine Urolithiasis, 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, Tibetan Terrier Variant) |
clear |
|
Alanine Aminotransferase Activity (GPT) |
at risk, homozygote codominant |
|
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 Amelogenesis Imperfecta, Familial Enamel Hypoplasia (Parson Russell Terrier Variant) |
clear |
|
Autosomal Recessive Hereditary Nephropathy, Familial Nephropathy, ARHN (COL4A4 Exon 3) |
clear |
|
Bald Thigh Syndrome (IGFBP5) |
clear |
|
Benign Familial Juvenile Epilepsy, Remitting Focal Epilepsy (LGI2) |
clear |
|
Canine Elliptocytosis (SPTB Exon 30) |
clear |
|
Canine Fucosidosis (FUCA1) |
clear |
|
Canine Leukocyte Adhesion Deficiency Type I, CLADI (ITGB2) |
clear |
|
Canine Leukocyte Adhesion Deficiency Type III, CLADIII (FERMT3) |
clear |
|
Canine Multifocal Retinopathy (BEST1 Exon 10 Deletion) |
clear |
|
Canine Multifocal Retinopathy (BEST1 Exon 10 SNP) |
clear |
|
Canine Multifocal Retinopathy (BEST1 Exon 2) |
clear |
|
Canine Multifocal Retinopathy (BEST1 Exon 5) |
clear |
|
Centronuclear Myopathy (PTPLA) |
clear |
|
Cerebellar Abiotrophy, Neonatal Cerebellar Cortical Degeneration, NCCD (SPTBN2) |
clear |
|
Cerebellar Ataxia, Progressive Early-Onset Cerebellar Ataxia (SEL1L) |
clear |
|
Cerebellar Hypoplasia (VLDLR) |
clear |
|
Chondrodystrophy and Intervertebral Disc Disease, CDDY/IVDD, Type I IVDD (FGF4 retrogene - CFA12) |
clear |
|
Chondrodystrophy, Norwegian Elkhound and Karelian Bear Dog Variant (ITGA10) |
clear |
|
Cleft Lip and/or Cleft Palate (ADAMTS20) |
clear |
|
Coefficient Of Inbreeding |
0.00992945 |
|
Collie Eye Anomaly, Choroidal Hypoplasia, CEA (NHEJ1) |
carrier, heterozygote recessive |
|
Complement 3 Deficiency, C3 Deficiency (C3) |
clear |
|
Congenital Hypothyroidism (TPO, Rat, Toy, Hairless Terrier Variant) |
clear |
|
Congenital Hypothyroidism (TPO, Tenterfield Terrier Variant) |
clear |
|
Congenital Keratoconjunctivitis Sicca and Ichthyosiform Dermatosis, Dry Eye Curly Coat Syndrome, CKCSID (FAM83H Exon 5) |
clear |
|
Congenital Macrothrombocytopenia (TUBB1 Exon 1, Cairn and Norfolk Terrier Variant) |
clear |
|
Congenital Myasthenic Syndrome (CHAT) |
clear |
|
Congenital Myasthenic Syndrome (COLQ) |
clear |
|
Congenital Stationary Night Blindness (RPE65) |
clear |
|
Craniomandibular Osteopathy, CMO (SLC37A2) |
clear |
|
Cystinuria Type I-A (SLC3A1) |
clear |
|
Cystinuria Type II-A (SLC3A1) |
clear |
|
Cystinuria Type II-B (SLC7A9) |
clear |
|
Day blindness, Cone Degeneration, Achromatopsia (CNGB3 Exon 6) |
clear |
|
Deafness and Vestibular Syndrome of Dobermans, DVDob, DINGS (MYO7A) |
clear |
|
Degenerative Myelopathy, DM (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 (ADAMTS10 Exon 17) |
clear |
|
Glaucoma (ADAMTS10 Exon 9) |
clear |
|
Glaucoma (ADAMTS17 Exon 11) |
clear |
|
Glaucoma (ADAMTS17 Exon 2) |
clear |
|
Globoid Cell Leukodystrophy, Krabbe disease (GALC Exon 5) |
clear |
|
Glycogen Storage Disease Type IA, Von Gierke Disease, GSD IA (G6PC) |
clear |
|
Glycogen Storage Disease Type II, Pompe's Disease, GSD II (GAA) |
clear |
|
Glycogen Storage Disease Type IIIA, GSD IIIA (AGL) |
clear |
|
Glycogen storage disease Type VII, Phosphofructokinase Deficiency, PFK Deficiency (PFKM Wachtelhund Variant) |
clear |
|
Glycogen storage disease Type VII, Phosphofructokinase Deficiency, PFK Deficiency (PFKM Whippet and English Springer Spaniel Variant) |
clear |
|
Golden Retriever Progressive Retinal Atrophy 1, GR-PRA1 (SLC4A3) |
clear |
|
Golden Retriever Progressive Retinal Atrophy 2, GR-PRA2 (TTC8) |
clear |
|
Goniodysgenesis and Glaucoma (OLFM3) |
clear |
|
Hereditary Ataxia (RAB24) |
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, Acral Mutilation Syndrome, AMS (GDNF-AS) |
clear |
|
Hereditary Vitamin D-Resistant Rickets (VDR) |
clear |
|
Hyperuricosuria and Hyperuricemia or Urolithiasis, HUU (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 Laryngeal Paralysis and Polyneuropathy, Polyneuropathy with Ocular Abnormalities and Neuronal Vacuolation, POANV (RAB3GAP1, Rottweiler Variant) |
clear |
|
Juvenile Myoclonic Epilepsy (DIRAS1) |
clear |
|
Juvenile-Onset Polyneuropathy, Leonberger Polyneuropathy 1, LPN1 (LPN1, ARHGEF10) |
clear |
|
Juvenile-Onset Polyneuropathy, Leonberger Polyneuropathy 2, LPN2 (GJA9) |
clear |
|
L-2-Hydroxyglutaricaciduria, L2HGA (L2HGDH) |
clear |
|
Lagotto Storage Disease (ATG4D) |
clear |
|
Late-Onset Neuronal Ceroid Lipofuscinosis (ATP13A2, Australian Cattle Dog Variant) |
clear |
|
Ligneous Membranitis, LM (PLG) |
clear |
|
Limb Girdle Muscular Dystrophy (SGCD, Boston Terrier Variant) |
clear |
|
Long QT Syndrome (KCNQ1) |
clear |
|
Lundehund Syndrome (LEPREL1) |
clear |
|
MDR1 Drug Sensitivity (MDR1) |
clear |
|
MHC Class II - DLA DQA1 and DQB1 |
2 |
|
MHC Class II - DLA DRB1 |
2 |
|
Macular Corneal Dystrophy, MCD (CHST6) |
clear |
|
Malignant Hyperthermia (RYR1) |
clear |
|
May-Hegglin Anomaly (MYH9) |
clear |
|
Methemoglobinemia CYB5R3 |
clear |
|
Mucopolysaccharidosis Type I, MPS I (IDUA) |
clear |
|
Mucopolysaccharidosis Type IIIA, Sanfilippo Syndrome Type A, MPS IIIA (SGSH Exon 6 Variant 1) |
clear |
|
Mucopolysaccharidosis Type IIIA, Sanfilippo Syndrome Type A, MPS IIIA (SGSH Exon 6 Variant 2) |
clear |
|
Mucopolysaccharidosis Type VII, Sly Syndrome, MPS VII (GUSB Exon 3) |
clear |
|
Mucopolysaccharidosis Type VII, Sly Syndrome, MPS VII (GUSB Exon 5) |
clear |
|
Muscular Dystrophy (DMD Golden Retriever Variant) |
clear |
|
Muscular Dystrophy (DMD Pembroke Welsh Corgi Variant ) |
clear |
|
Muscular Dystrophy (DMD, Cavalier King Charles Spaniel Variant 1) |
clear |
|
Musladin-Lueke Syndrome (ADAMTSL2) |
clear |
|
Myostatin Deficiency, Bully Whippet Syndrome (MSTN) |
clear |
|
Myotonia Congenita (CLCN1 Exon 23) |
clear |
|
Myotonia Congenita (CLCN1 Exon 7) |
clear |
|
Myotubular Myopathy 1, X-linked Myotubular Myopathy, XL-MTM (MTM1, Labrador Variant) |
clear |
|
Narcolepsy (HCRTR2 Intron 6) |
clear |
|
Neonatal Encephalopathy with Seizures, NEWS (ATF2) |
clear |
|
Neuroaxonal Dystrophy, NAD (Rottweiler Variant) |
clear |
|
Neuroaxonal Dystrophy, NAD (Spanish Water Dog Variant) |
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, Cerebellar Ataxia, NCL4A (ARSG Exon 2) |
clear |
|
Neuronal Ceroid Lipofuscinosis 1, NCL 1 (PPT1 Exon 8) |
clear |
|
Neuronal Ceroid Lipofuscinosis 1, NCL 5 (CLN5 Border Collie Variant) |
clear |
|
Neuronal Ceroid Lipofuscinosis 10, NCL 10 (CTSD Exon 5) |
clear |
|
Neuronal Ceroid Lipofuscinosis 2, NCL 2 (TPP1 Exon 4) |
clear |
|
Neuronal Ceroid Lipofuscinosis 6, NCL 6 (CLN6 Exon 7) |
clear |
|
Neuronal Ceroid Lipofuscinosis 8, NCL 8 (CLN8 English Setter Variant) |
clear |
|
Oculocutaneous Albinism, OCA2 (Pekingese Type) |
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 (P2Y12) |
clear |
|
Paroxysmal Dyskinesia, PxD (PGIN) |
clear |
|
Persistent Mullerian Duct Syndrome, PMDS (AMHR2) |
clear |
|
Platelet factor X receptor deficiency, Scott Syndrome (TMEM16F) |
clear |
|
Polycystic Kidney Disease, PKD (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, PCD (CCDC39 Exon 3) |
clear |
|
Primary Hyperoxaluria (AGXT) |
clear |
|
Primary Lens Luxation (ADAMTS17) |
clear |
|
Progressive Neuronal Abiotrophy, Canine Multiple System Degeneration, CMSD (SERAC1 Exon 15) |
clear |
|
Progressive Neuronal Abiotrophy, Canine Multiple System Degeneration, CMSD (SERAC1 Exon 4) |
clear |
|
Progressive Retinal Atrophy (CNGB1) |
clear |
|
Progressive Retinal Atrophy (SAG) |
clear |
|
Progressive Retinal Atrophy - crd4/cord1 (RPGRIP1) |
clear |
|
Progressive Retinal Atrophy, CNGA (CNGA1 Exon 9) |
clear |
|
Progressive Retinal Atrophy, PRA3 (FAM161A) |
clear |
|
Progressive Retinal Atrophy, crd1 (PDE6B) |
clear |
|
Progressive Retinal Atrophy, prcd (PRCD Exon 1) |
clear |
|
Progressive Retinal Atrophy, rcd1 (PDE6B Exon 21 Irish Setter Variant) |
clear |
|
Progressive Retinal Atrophy, rcd3 (PDE6A) |
clear |
|
Protein Losing Nephropathy, PLN (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, SD2 (COL11A2) |
clear |
|
Spinocerebellar Ataxia with Myokymia and/or Seizures (KCNJ10) |
clear |
|
Spinocerebellar Ataxia, Late-Onset Ataxia, LoSCA (CAPN1) |
clear |
|
Spongy Degeneration with Cerebellar Ataxia 1, SDCA1, SeSAME/EAST Syndrome (KCNJ10) |
clear |
|
Spongy Degeneration with Cerebellar Ataxia 2, SDCA2 (ATP1B2) |
clear |
|
Thrombopathia (RASGRP1 Exon 5, American Eskimo Dog Variant) |
clear |
|
Thrombopathia (RASGRP1 Exon 5, Basset Hound Variant) |
clear |
|
Thrombopathia (RASGRP1 Exon 8) |
clear |
|
Trapped Neutrophil Syndrome (VPS13B) |
clear |
|
Von Willebrand Disease Type I (VWF) |
clear |
|
Von Willebrand Disease Type II, Type II vWD (VWF) |
clear |
|
Von Willebrand Disease Type III, Type III vWD (VWF Exon 4) |
clear |
|
Von Willebrand Disease Type III, Type III vWD (VWF Exon 7) |
clear |
|
X-Linked Hereditary Nephropathy, XLHN (COL4A5 Exon 35, Samoyed Variant 2) |
clear |
|
X-Linked Progressive Retinal Atrophy 1, XL-PRA1 (RPGR) |
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 |
