Full List of Tested Health Conditions – Embark

Embark tests for all of the following health conditions in our Breed + Health Test.

(Updated October 2025)

MDR1 Drug Sensitivity: (Clinical) ABCB1

Alanine Aminotransferase Activity: (Clinical) GPT

Copper Toxicosis (Attenuating): (Clinical) ATP7A, Labrador Retriever

Copper Toxicosis (Attenuating): (Clinical) RETN, Labrador Retriever

P2Y12 Receptor Platelet Disorder: (Blood) P2Y12

Factor IX Deficiency, Hemophilia B: (Blood) F9 Exon 7, Terrier Variant

Factor IX Deficiency, Hemophilia B: (Blood) F9 Exon 7, Rhodesian Ridgeback Variant

Factor VII Deficiency: (Blood) F7 Exon 5

Factor VIII Deficiency, Hemophilia A: (Blood) F8 Exon 10, Boxer Variant

Factor VIII Deficiency, Hemophilia A: (Blood) F8 Exon 11, German Shepherd Variant 1

Factor VIII Deficiency, Hemophilia A: (Blood) F8 Exon 1, German Shepherd Variant 2

Thrombopathia: (Blood) RASGRP1 Exon 5, Basset Hound Variant

Thrombopathia: (Blood) RASGRP1 Exon 8, Landseer Variant

Thrombopathia: (Blood) RASGRP1 Exon 5, American Eskimo Dog Variant

Von Willebrand Disease Type III, Type III vWD: (Blood) VWF Exon 4, Terrier Variant

Von Willebrand Disease Type III, Type III vWD: (Blood) VWF Exon 7, Shetland Sheepdog Variant

Von Willebrand Disease Type I, Type I vWD: (Blood) VWF

Von Willebrand Disease Type III, Type III vWD: (Blood) VWF Intron 16, Nederlandse Kooikerhondje Variant

Von Willebrand Disease Type II, Type II vWD: (Blood) VWF, Pointer Variant

Factor XI Deficiency: (Blood) F11 Exon 7, Kerry Blue Terrier Variant

Canine Leukocyte Adhesion Deficiency Type I, CLAD I: (Blood) ITGB2, Setter Variant

Canine Leukocyte Adhesion Deficiency Type III, CLAD III: (Blood) FERMT3, German Shepherd Variant

Canine Elliptocytosis: (Blood) SPTB Exon 30

Glanzmann's Thrombasthenia Type I: (Blood) ITGA2B Exon 13, Great Pyrenees Variant

Glanzmann's Thrombasthenia Type I: (Blood) ITGA2B Exon 12, Otterhound Variant

May-Hegglin Anomaly: (Blood) MYH9

Congenital Macrothrombocytopenia: (Blood) TUBB1 Exon 1, Cairn and Norfolk Terrier Variant

Prekallikrein Deficiency: (Blood) KLKB1 Exon 8

Pyruvate Kinase Deficiency: (Blood) PKLR Exon 5, Basenji Variant

Pyruvate Kinase Deficiency: (Blood) PKLR Exon 7, Labrador Retriever Variant

Pyruvate Kinase Deficiency: (Blood) PKLR Exon 7, Pug Variant

Pyruvate Kinase Deficiency: (Blood) PKLR Exon 7, Beagle Variant

Pyruvate Kinase Deficiency: (Blood) PKLR Exon 10, Terrier Variant

Trapped Neutrophil Syndrome, TNS: (Blood) VPS13B

Ligneous Membranitis, LM: (Blood) PLG

Platelet Factor X Receptor Deficiency, Scott Syndrome: (Blood) TMEM16F

Methemoglobinemia: (Blood) CYB5R3

Bernard-Soulier Syndrome, BSS: (Blood) GP9, Cocker Spaniel Variant

Methemoglobinemia: (Blood) CYB5R3, Pit Bull Terrier Variant

Congenital Hypothyroidism: (Hormones) TPO, Tenterfield Terrier Variant

Congenital Hypothyroidism with Goiter: (Hormones) TPO Intron 13, French Bulldog Variant

Congenital Hypothyroidism: (Hormones) TPO, Rat, Toy, Hairless Terrier Variant

Congenital Dyshormonogenic Hypothyroidism with Goiter: (Hormones) SLC5A5, Shih Tzu Variant

Pituitary Dwarfism: (Hormones) POU1F1 Intron 4, Karelian Bear Dog Variant

Proportionate Dwarfism: (Hormones) GH1 Exon 5, Chihuahua Variant

Complement 3 Deficiency, C3 Deficiency: (Immune) C3

Severe Combined Immunodeficiency, SCID: (Immune) PRKDC, Terrier Variant

Severe Combined Immunodeficiency, SCID: (Immune) RAG1, Wetterhoun Variant

X-linked Severe Combined Immunodeficiency, X-SCID: (Immune) IL2RG Exon 1, Basset Hound Variant

X-linked Severe Combined Immunodeficiency, X-SCID: (Immune) IL2RG, Corgi Variant

Progressive Retinal Atrophy, rcd1: (Eyes) PDE6B Exon 21, Irish Setter Variant

Progressive Retinal Atrophy, rcd3: (Eyes) PDE6A

Progressive Retinal Atrophy, CNGA: (Eyes) CNGA1 Exon 9

Progressive Retinal Atrophy, prcd: (Eyes) PRCD Exon 1

Progressive Retinal Atrophy, PRA1: (Eyes) CNGB1

Progressive Retinal Atrophy: (Eyes) SAG

Golden Retriever Progressive Retinal Atrophy 1, GR-PRA1: (Eyes) SLC4A3

Golden Retriever Progressive Retinal Atrophy 2, GR-PRA2: (Eyes) TTC8

Progressive Retinal Atrophy, crd1: (Eyes) PDE6B, American Staffordshire Terrier Variant

Progressive Retinal Atrophy, crd4/cord1: (Eyes) RPGRIP1

X-Linked Progressive Retinal Atrophy 1, XL-PRA1: (Eyes) RPGR

Progressive Retinal Atrophy, PRA3: (Eyes) FAM161A

Collie Eye Anomaly, Choroidal Hypoplasia, CEA: (Eyes) NHEJ1

Day Blindness, Cone Degeneration, Achromatopsia: (Eyes) CNGB3 Exon 6, German Shorthaired Pointer Variant

Achromatopsia: (Eyes) CNGA3 Exon 7, German Shepherd Variant

Achromatopsia: (Eyes) CNGA3 Exon 7, Labrador Retriever Variant

Autosomal Dominant Progressive Retinal Atrophy: (Eyes) RHO

Canine Multifocal Retinopathy, cmr1: (Eyes) BEST1 Exon 2

Canine Multifocal Retinopathy, cmr2: (Eyes) BEST1 Exon 5, Coton de Tulear Variant

Canine Multifocal Retinopathy, cmr3: (Eyes) BEST1 Exon 10 Deletion, Finnish and Swedish Lapphund, Lapponian Herder Variant

Primary Open Angle Glaucoma: (Eyes) ADAMTS10 Exon 9, Norwegian Elkhound Variant

Primary Open Angle Glaucoma: (Eyes) ADAMTS10 Exon 17, Beagle Variant

Primary Open Angle Glaucoma: (Eyes) ADAMTS17 Exon 11, Basset Fauve de Bretagne Variant

Primary Open Angle Glaucoma and Primary Lens Luxation: (Eyes) ADAMTS17 Exon 2, Chinese Shar-Pei Variant

Hereditary Cataracts, Early-Onset Cataracts, Juvenile Cataracts: (Eyes) HSF4 Exon 9, Australian Shepherd Variant

Primary Lens Luxation: (Eyes) ADAMTS17

Congenital Stationary Night Blindness: (Eyes) RPE65, Briard Variant

Congenital Stationary Night Blindness: (Eyes) LRIT3, Beagle Variant

Macular Corneal Dystrophy, MCD: (Eyes) CHST6

Goniodysgenesis and Glaucoma, Pectinate Ligament Dysplasia, PLD: (Eyes) OLFM3

Day Blindness, Cone Degeneration, Achromatopsia: (Eyes) CNGB3 Deletion, Alaskan Malamute Variant

Retina Dysplasia and/or Optic Nerve Hypoplasia: (Eyes) SIX6 Exon 1, Golden Retriever Variant

Microphthalmia: (Eyes) RBP4 Exon 2, Soft Coated Wheaten Terrier Variant

Progressive Retinal Atrophy: (Eyes) IFT122 Exon 26, Lapponian Herder Variant

Progressive Retinal Atrophy, Bardet-Biedl Syndrome: (Eyes) BBS2 Exon 11, Shetland Sheepdog Variant

Stargardt Disease: (Eyes) ABCA4 Exon 28, Labrador Retriever Variant

Progressive Retinal Atrophy 5, PRA5: (Eyes) NECAP1 Exon 6, Giant Schnauzer Variant

Hereditary Cataracts, Early-Onset Cataracts, Juvenile Cataracts: (Eyes) FYCO1, Wirehaired Pointing Griffon Variant

2,8-Dihydroxyadenine Urolithiasis, 2,8-DHA Urolithiasis: (Kidney and Bladder APRT

Cystinuria Type I-A: (Kidney and Bladder) SLC3A1, Newfoundland Variant

Cystinuria Type II-A: (Kidney and Bladder) SLC3A1, Australian Cattle Dog Variant

Cystinuria Type II-B: (Kidney and Bladder) SLC7A9, Miniature Pinscher Variant

Hyperuricosuria and Hyperuricemia or Urolithiasis, HUU: (Kidney and Bladder) SLC2A9

Polycystic Kidney Disease, PKD: (Kidney and Bladder) PKD1

Primary Hyperoxaluria: (Kidney and Bladder) AGXT

Protein Losing Nephropathy, PLN: (Kidney and Bladder) NPHS1

X-Linked Hereditary Nephropathy, XLHN: (Kidney and Bladder) COL4A5 Exon 35, Samoyed Variant 2

Autosomal Recessive Hereditary Nephropathy, Familial Nephropathy, ARHN: (Kidney and Bladder) COL4A4 Exon 3, Cocker Spaniel Variant

Autosomal Recessive Hereditary Nephropathy, Familial Nephropathy, ARHN: (Kidney and Bladder) COL4A4 Exon 30, English Springer Spaniel Variant

Fanconi Syndrome: (Kidney and Bladder) FAN1, Basenji Variant

Diffuse Cystic Renal Dysplasia and Hepatic Fibrosis: (Kidney and Bladder) INPP5E Intron 9, Norwich Terrier Variant

Hereditary Xanthinuria, Xanthinuria Type I: (Kidney and Bladder) XDH, Mixed Breed Variant

Primary Ciliary Dyskinesia, PCD: (Multisystem) CCDC39 Exon 3, Old English Sheepdog Variant

Primary Ciliary Dyskinesia, PCD: (Multisystem) NME5, Alaskan Malamute Variant

Congenital Keratoconjunctivitis Sicca and Ichthyosiform Dermatosis, Dry Eye Curly Coat Syndrome, CKCSID: (Multisystem) FAM83H Exon 5

X-linked Ectodermal Dysplasia, Anhidrotic Ectodermal Dysplasia, XHED: (Multisystem) EDA Intron 8

Renal Cystadenocarcinoma and Nodular Dermatofibrosis, RCND: (Multisystem) FLCN Exon 7

Canine Fucosidosis: (Multisystem) FUCA1

Glycogen Storage Disease Type II, Pompe's Disease, GSD II: (Multisystem) GAA, Finnish and Swedish Lapphund, Lapponian Herder Variant

Glycogen Storage Disease Type IA, Von Gierke Disease, GSD IA: (Multisystem) G6PC, Maltese Variant

Glycogen Storage Disease Type IIIA, GSD IIIA: (Multisystem) AGL, Curly Coated Retriever Variant

Mucopolysaccharidosis Type IIIA, Sanfilippo Syndrome Type A, MPS IIIA: (Multisystem) SGSH Exon 6, Dachshund Variant

Mucopolysaccharidosis Type IIIA, Sanfilippo Syndrome Type A, MPS IIIA:(Multisystem) SGSH Exon 6, New Zealand Huntaway Variant

Mucopolysaccharidosis Type VII, Sly Syndrome, MPS VII: (Multisystem) GUSB Exon 5, Terrier Brasileiro Variant

Mucopolysaccharidosis Type VII, Sly Syndrome, MPS VII: (Multisystem) GUSB Exon 3, German Shepherd Variant

Glycogen storage disease Type VII, Phosphofructokinase Deficiency, PFK Deficiency: (Multisystem) PFKM, Whippet and English Springer Spaniel Variant

Glycogen storage disease Type VII, Phosphofructokinase Deficiency, PFK Deficiency: (Multisystem) PFKM, Wachtelhund Variant

Lagotto Storage Disease: (Multisystem) ATG4D

Neuronal Ceroid Lipofuscinosis 1, NCL 1: (Multisystem) PPT1 Exon 8, Dachshund Variant 1

Neuronal Ceroid Lipofuscinosis 2, NCL 2: (Multisystem) TPP1 Exon 4, Dachshund Variant 2

Neuronal Ceroid Lipofuscinosis, Cerebellar Ataxia, NCL4A: (Multisystem) ARSG Exon 2, American Staffordshire Terrier Variant

Neuronal Ceroid Lipofuscinosis 5, NCL 5: (Multisystem) CLN5 Exon 4 SNP, Border Collie Variant

Neuronal Ceroid Lipofuscinosis 6, NCL 6: (Multisystem) CLN6 Exon 7, Australian Shepherd Variant

Neuronal Ceroid Lipofuscinosis 8, NCL 8: (Multisystem) CLN8 Exon 2, English Setter Variant

Neuronal Ceroid Lipofuscinosis 7, NCL 7: (Multisystem) MFSD8, Chihuahua and Chinese Crested Variant

Neuronal Ceroid Lipofuscinosis 8, NCL 8: (Multisystem) CLN8, Australian Shepherd Variant

Neuronal Ceroid Lipofuscinosis 10, NCL 10: (Multisystem) CTSD Exon 5, American Bulldog Variant

Neuronal Ceroid Lipofuscinosis 5, NCL 5: (Multisystem) CLN5 Exon 4 Deletion, Golden Retriever Variant

Late-Onset Neuronal Ceroid Lipofuscinosis, NCL 12: (Multisystem) ATP13A2, Australian Cattle Dog Variant

GM1 Gangliosidosis: (Multisystem) GLB1 Exon 15, Shiba Inu Variant

GM1 Gangliosidosis: (Multisystem) GLB1 Exon 15, Alaskan Husky Variant

GM1 Gangliosidosis: (Multisystem) GLB1 Exon 2, Portuguese Water Dog Variant

GM2 Gangliosidosis: (Multisystem) HEXB, Poodle Variant

GM2 Gangliosidosis: (Multisystem) HEXA, Japanese Chin Variant

Globoid Cell Leukodystrophy, Krabbe disease: (Multisystem) GALC Exon 5, Terrier Variant

Neuronal Ceroid Lipofuscinosis 8, NCL 8: (Multisystem) CLN8 Insertion, Saluki Variant

Mucopolysaccharidosis IIIB, Sanfilippo Syndrome Type B, MPS IIIB: (Multisystem) NAGLU, Schipperke Variant

Primary Ciliary Dyskinesia, PCD: (Multisystem) STK36, Australian Shepherd Variant

Congenital Dyserythropoietic Anemia and Polymyopathy: (Multisystem) EHPB1L1, Labrador Retriever Variant

Glycogen Storage Disease Type IA, Von Gierke Disease, GSD IA: (Multisystem) G6PC1, German Pinscher Variant

Autosomal Recessive Amelogenesis Imperfecta, Familial Enamel Hypoplasia: (Other Systems) ENAM Deletion, Italian Greyhound Variant

Autosomal Recessive Amelogenesis Imperfecta, Familial Enamel Hypoplasia: (Other Systems) ENAM SNP, Parson Russell Terrier Variant

Persistent Mullerian Duct Syndrome, PMDS: (Other Systems) AMHR2

Deafness and Vestibular Syndrome of Dobermans, DVDob, DINGS: (Other Systems) MYO7A

Unilateral Deafness and Vestibular Syndrome: (Other Systems) PTPRQ Exon 39, Doberman Pinscher

Shar-Pei Autoinflammatory Disease, SPAID, Shar-Pei Fever: (Other Systems) MTBP

Neonatal Interstitial Lung Disease: (Other Systems) LAMP3

Recurrent Inflammatory Pulmonary Disease, RIPD: (Other Systems) AKNA, Rough Collie Variant

Early Onset Adult Deafness, EOAD: (Other Systems) EPS8L2 Deletion, Rhodesian Ridgeback Variant

Early Bilateral Deafness: (Other Systems) LOXHD1 Exon 38, Rottweiler Variant

Alaskan Husky Encephalopathy, Subacute Necrotizing Encephalomyelopathy: (Brain and Spinal Cord) SLC19A3

Alexander Disease: (Brain and Spinal Cord) GFAP

Cerebellar Abiotrophy, Neonatal Cerebellar Cortical Degeneration, NCCD: (Brain and Spinal Cord) SPTBN2, Beagle Variant

Cerebellar Ataxia, Progressive Early-Onset Cerebellar Ataxia: (Brain and Spinal Cord) SEL1L, Finnish Hound Variant

Cerebellar Hypoplasia: (Brain and Spinal Cord) VLDLR, Eurasier Variant

Spinocerebellar Ataxia, Late-Onset Ataxia, LoSCA: (Brain and Spinal Cord) CAPN1

Spinocerebellar Ataxia with Myokymia and/or Seizures: (Brain and Spinal Cord) KCNJ10

Hereditary Ataxia, Cerebellar Degeneration: (Brain and Spinal Cord) RAB24, Old English Sheepdog and Gordon Setter Variant

Benign Familial Juvenile Epilepsy, Remitting Focal Epilepsy: (Brain and Spinal Cord) LGI2

Degenerative Myelopathy, DM: (Brain and Spinal Cord) SOD1A

Fetal-Onset Neonatal Neuroaxonal Dystrophy: (Brain and Spinal Cord) MFN2, Giant Schnauzer Variant

Hypomyelination and Tremors: (Brain and Spinal Cord) FNIP2, Weimaraner Variant

Shaking Puppy Syndrome, X-linked Generalized Tremor Syndrome: (Brain and Spinal Cord) PLP1, English Springer Spaniel Vxariant

L-2-Hydroxyglutaricaciduria, L2HGA: (Brain and Spinal Cord) L2HGDH, Staffordshire Bull Terrier Variant

Neonatal Encephalopathy with Seizures, NEWS: (Brain and Spinal Cord) ATF2

Alaskan Malamute Polyneuropathy, AMPN: (Brain and Spinal Cord) NDRG1 SNP

Narcolepsy: (Brain and Spinal Cord) HCRTR2 Intron 4, Doberman Pinscher Variant

Narcolepsy: (Brain and Spinal Cord) HCRTR2 Intron 6, Labrador Retriever Variant

Narcolepsy: (Brain and Spinal Cord) HCRTR2 Exon 1, Dachshund Variant

Progressive Neuronal Abiotrophy, Canine Multiple System Degeneration, CMSD: (Brain and Spinal Cord) SERAC1 Exon 15, Kerry Blue Terrier Variant

Progressive Neuronal Abiotrophy, Canine Multiple System Degeneration, CMSD: (Brain and Spinal Cord) SERAC1 Exon 4, Chinese Crested Variant

Juvenile Laryngeal Paralysis and Polyneuropathy, Polyneuropathy with Ocular Abnormalities and Neuronal Vacuolation, POANV: (Brain and Spinal Cord) RAB3GAP1, Rottweiler Variant

Hereditary Sensory Autonomic Neuropathy, Acral Mutilation Syndrome, AMS: (Brain and Spinal Cord) GDNF-AS, Spaniel and Pointer Variant

Sensory Neuropathy: (Brain and Spinal Cord) FAM134B, Border Collie Variant

Juvenile-Onset Polyneuropathy, Leonberger Polyneuropathy 1, LPN1: (Brain and Spinal Cord) LPN1, ARHGEF10

Juvenile Myoclonic Epilepsy: (Brain and Spinal Cord) DIRAS1

Juvenile-Onset Polyneuropathy, Leonberger Polyneuropathy 2, LPN2: (Brain and Spinal Cord) GJA9

Spongy Degeneration with Cerebellar Ataxia 1, SDCA1, SeSAME/EAST Syndrome: (Brain and Spinal Cord) KCNJ10

Spongy Degeneration with Cerebellar Ataxia 2, SDCA2: (Brain and Spinal Cord) ATP1B2

Neuroaxonal Dystrophy, NAD: (Brain and Spinal Cord) TECPR2, Spanish Water Dog Variant

Neuroaxonal Dystrophy, NAD: (Brain and Spinal Cord) VPS11, Rottweiler Variant

Exercise-Induced Collapse, EIC: (Brain and Spinal Cord) DNM1

Leukodystrophy: (Brain and Spinal Cord) TSEN54 Exon 5, Standard Schnauzer Variant

Spinocerebellar Ataxia: (Brain and Spinal Cord) SCN8A, Alpine Dachsbracke Variant

Hereditary Ataxia: (Brain and Spinal Cord) PNPLA8, Australian Shepherd Variant

Hereditary Cerebellar Ataxia: (Brain and Spinal Cord SELENOP, Belgian Shepherd Variant

Dilated Cardiomyopathy, DCM1: (Heart) PDK4, Doberman Pinscher Variant 1

Dilated Cardiomyopathy, DCM2: (Heart) TTN, Doberman Pinscher Variant 2

Long QT Syndrome: (Heart) KCNQ1

Cardiomyopathy and Juvenile Mortality: (Heart) YARS2

Dilated Cardiomyopathy, DCM: (Heart) RBM20, Schnauzer Variant

Muscular Dystrophy: (Muscular) DMD, Cavalier King Charles Spaniel Variant 1

Muscular Dystrophy: (Muscular) DMD, Golden Retriever Variant

Limb Girdle Muscular Dystrophy: (Muscular) SGCD, Boston Terrier Variant

Ullrich-like Congenital Muscular Dystrophy: (Muscular) COL6A3 Exon 10, Labrador Retriever Variant

Centronuclear Myopathy, CNM: (Muscular) PTPLA

Inherited Myopathy of Great Danes: (Muscular) BIN1

Myostatin Deficiency, Bully Whippet Syndrome: (Muscular) MSTN

Myotonia Congenita: (Muscular) CLCN1 Exon 7, Miniature Schnauzer Variant

Myotonia Congenita: (Muscular) CLCN1 Exon 23, Australian Cattle Dog Variant

Myotubular Myopathy 1, X-linked Myotubular Myopathy, XL-MTM: (Muscular) MTM1, Labrador Retriever Variant

Inflammatory Myopathy: (Muscular) SLC25A12

Nemaline Myopathy: (Muscular) NEB, American Bulldog Variant

Ullrich-like Congenital Muscular Dystrophy: (Muscular) COL6A1 Exon 3, Landseer Variant

Limb-Girdle Muscular Dystrophy 2D: (Muscular) SGCA Exon 3, Miniature Dachshund Variant

Myotonia Congenita: (Muscular) CLCN1 Exon 19, Labrador Retriever Variant

Muscular Dystrophy-Dystroglycanopathy: (Muscular) LARGE1, Labrador Retriever Variant

Congenital Muscular Dystrophy: (Muscular) LAMA2, Italian Greyhound

Hypocatalasia, Acatalasemia: (Metabolic) CAT

Pyruvate Dehydrogenase Deficiency: (Metabolic) PDP1, Spaniel Variant

Malignant Hyperthermia: (Metabolic) RYR1

Mucopolysaccharidosis Type VI, Maroteaux-Lamy Syndrome, MPS VI: (Metabolic) ARSB Exon 5, Miniature Pinscher Variant

Succinic Semialdehyde Dehydrogenase Deficiency: (Metabolic) ALDH5A1 Exon 7, Saluki Variant

β-Mannosidosis: (Metabolic) MANBA Exon 16, Mixed-Breed Variant

Medium-Chain Acyl-CoA Dehydrogenase Deficiency, MCADD: (Metabolic) ACADM, Cavalier King Charles Spaniel Variant

Imerslund-Grasbeck Syndrome, Selective Cobalamin Malabsorption: (Gastrointestinal) CUBN Exon 53, Border Collie Variant

Imerslund-Grasbeck Syndrome, Selective Cobalamin Malabsorption: (Gastrointestinal) CUBN Exon 8, Beagle Variant

Inherited Selected Cobalamin Malabsorption with Proteinuria: (Gastrointestinal) CUBN, Komondor Variant

Lundehund Syndrome: (Gastrointestinal) LEPREL1

Intestinal Lipid Malabsorption: (Gastrointestinal) ACSL5, Australian Kelpie

Copper Toxicosis (Accumulating): (Liver) ATP7B

Congenital Myasthenic Syndrome, CMS: (Neuromuscular) CHAT, Old Danish Pointing Dog Variant

Congenital Myasthenic Syndrome, CMS: (Neuromuscular) COLQ, Labrador Retriever Variant

Congenital Myasthenic Syndrome, CMS: (Neuromuscular) CHRNE, Jack Russell Terrier Variant

Congenital Myasthenic Syndrome, CMS: (Neuromuscular) COLQ, Golden Retriever Variant

Myasthenia Gravis-Like Syndrome: (Neuromuscular) CHRNE, Heideterrier Variant

Episodic Falling Syndrome: (Neuromuscular) BCAN

Paroxysmal Dyskinesia, PxD: (Neuromuscular) PIGN

Demyelinating Polyneuropathy: (Neuromuscular) SBF2/MTRM13

Laryngeal Paralysis: (Neuromuscular) RAPGEF6, Miniature Bull Terrier Variant

Laryngeal Paralysis and Polyneuropathy: (Neuromuscular) CNTNAP1, Leonberger, Saint Bernard, and Labrador Retriever variant

Dystrophic Epidermolysis Bullosa: (Skin & Connective Tissues) COL7A1, Golden Retriever Variant

Dystrophic Epidermolysis Bullosa: (Skin & Connective Tissues) COL7A1, Central Asian Shepherd Dog Variant

Ectodermal Dysplasia, Skin Fragility Syndrome: (Skin & Connective Tissues) PKP1, Chesapeake Bay Retriever Variant

Ichthyosis, Epidermolytic Hyperkeratosis: (Skin & Connective Tissues) KRT10, Terrier Variant

Ichthyosis, ICH1: (Skin & Connective Tissues) PNPLA1, Golden Retriever Variant

Ichthyosis: (Skin & Connective Tissues) SLC27A4, Great Dane Variant

Ichthyosis: (Skin & Connective Tissues) NIPAL4, American Bulldog Variant

Ichthyosis: (Skin & Connective Tissues) ASPRV1 Exon 2, German Shepherd Variant

Focal Non-Epidermolytic Palmoplantar Keratoderma, Pachyonychia Congenita: (Skin & Connective Tissues) KRT16, Dogue de Bordeaux Variant

Hereditary Footpad Hyperkeratosis: (Skin & Connective Tissues) FAM83G, Terrier and Kromfohrlander Variant

Hereditary Footpad Hyperkeratosis: (Skin & Connective Tissues) DSG1, Rottweiler Variant

Hereditary Nasal Parakeratosis, HNPK: (Skin & Connective Tissues) SUV39H2

Musladin-Lueke Syndrome, MLS: (Skin & Connective Tissues) ADAMTSL2

Oculocutaneous Albinism, OCA: (Skin & Connective Tissues) SLC45A2, Small Breed Variant

Bald Thigh Syndrome: (Skin & Connective Tissues) IGFBP5

Lethal Acrodermatitis, LAD: (Skin & Connective Tissues) MKLN1

Ehlers Danlos: (Skin & Connective Tissues) ADAMTS2, Doberman Pinscher Variant

Oculocutaneous Albinism, OCA: (Skin & Connective Tissues) SLC45A2 Exon 6, Bullmastiff Variant

Junctional Epidermolysis Bullosa: (Skin & Connective Tissues) LAMB3 Exon 11, Australian Shepherd Variant

Hereditary Nasal Parakeratosis: (Skin & Connective Tissues) SUV39H2 Intron 4, Greyhound Variant

Junctional Epidermolysis Bullosa: (Skin & Connective Tissues) LAMA3 Exon 66, Australian Cattle Dog Variant

Congenital Cornification Disorder: (Skin & Connective Tissues) NSDHL, Chihuahua Variant

Ehlers-Danlos Syndrome (EDS): (Skin & Connective Tissues) COL5A1, Labrador Retriever Variant

Ichthyosis, ICH2: (Skin & Connective Tissues) ABHD5, Golden Retriever Variant

Darier Disease: (Skin & Connective Tissues) ATP2A2, Irish Terrier Variant

Cleft Lip and/or Cleft Palate: (Skeletal) ADAMTS20, Nova Scotia Duck Tolling Retriever Variant

Hereditary Vitamin D-Resistant Rickets: (Skeletal) VDR

Oculoskeletal Dysplasia 2, Dwarfism-Retinal Dysplasia 2, drd2, OSD2: (Skeletal) COL9A2, Samoyed Variant

Osteogenesis Imperfecta, Brittle Bone Disease: (Skeletal) COL1A2, Beagle Variant

Osteogenesis Imperfecta, Brittle Bone Disease: (Skeletal) SERPINH1, Dachshund Variant

Osteogenesis Imperfecta, Brittle Bone Disease: (Skeletal) COL1A1, Golden Retriever Variant

Osteochondrodysplasia, Skeletal Dwarfism: (Skeletal) SLC13A1, Poodle Variant

Skeletal Dysplasia 2, SD2: (Skeletal) COL11A2, Labrador Retriever Variant

Craniomandibular Osteopathy, CMO: (Skeletal) SLC37A2

Raine Syndrome, Canine Dental Hypomineralization Syndrome: (Skeletal) FAM20C

Chondrodystrophy and Intervertebral Disc Disease, CDDY/IVDD, Type I IVDD: (Skeletal) FGF4 retrogene - CFA12

Chondrodysplasia: (Skeletal) ITGA10, Norwegian Elkhound and Karelian Bear Dog Variant

Hypophosphatasia: (Skeletal) ALPL Exon 9, Karelian Bear Dog Variant

Disproportionate Dwarfism: (Skeletal) PRKG2, Dogo Argentino Variant

Craniomandibular Osteopathy, CMO: (Skeletal) SLC37A2 Intron 16, Basset Hound Variant

Cleft Palate, CP1: (Skeletal) DLX6 intron 2, Nova Scotia Duck Tolling Retriever Variant

Dental-Skeletal-Retinal Anomaly: (Skeletal) MIA3, Cane Corso Variant

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