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Breed
Columba livia
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Condition or trait
2,8-Dihydroxyadenine Urolithiasis Achromatopsia 2 (Day Blindness) – German Shepherd Achromatopsia 2 (Day Blindness) – Labrador Retriever Achromatopsia 3 (Day Blindness) Achromatopsia 3 (Day Blindness) – Pointer type Acral Mutilation Syndrome (AMS) Acrodermatitis Enteropathica (AE) Acute Intermittent Porphyria (AIP) – 1 Acute Intermittent Porphyria (AIP) – 2 Acute Intermittent Porphyria (AIP) – 3 Acute Intermittent Porphyria (AIP) – 4 Acute Intermittent Porphyria (AIP) – 5 Acute Intermittent Porphyria (AIP) – 6 Acute Respiratory Distress Syndrome (ARDS) Adult Onset Deafness 1 – Border Collie Adult Onset Deafness 2 – Border Collie Adult Onset Deafness 3 – Border Collie Adult Onset Deafness 4 – Border Collie Alaskan Husky Encephalopathy (AHE) Alexander Disease Alpha-Mannosidosis (AMD) – Cat Alpha-Mannosidosis (AMD) – Doberman Am Staff Juvenile Laryngeal Paralysis and Polyneuropathy (ALPP) Amelogenesis Imperfecta (AI) – (American) Akita Amelogenesis Imperfecta (AI) – Greyhound Amelogenesis Imperfecta (AI) – Russel Terrier Androgen Insensitivity Syndrome – AIS Androgen Insensitivity Syndrome – AIS 2 Australian Labradoodle dystrophinopathy Autoimmune Lymphoproliferative Syndrome – ALPS Bald Thigh Syndrome (BTS) – Sighthound Type Bernard-Soulier Syndrome (BSS) – Cocker Spaniel Type Beta-Mannosidosis – German Shepherd Bilateral Deafness and Vestibular Dysfunction (MYO7A, DINGS2) – Doberman Body Size 1 (IGF1-AS-related) – Dog Body Size 2 (IGF1R-related) – Dog Body Size 3 (STC2-related) – Dog Body Size 4 (GHR-E191K-related) – Dog Body Size 5 (GHR-P177L-related) – Dog Bully Whippet – Whippet Double Muscling Burmese Head Defect Burmese Hypokalemia Canine Atopic Dermatitis (cAD) Canine Ectodermal Dysplasia (CED), FOXI3 Canine Multiple System Degeneration (CMSD) – Chinese Crested Canine Multiple System Degeneration (CMSD) – Kerry Blue Terrier Canine Scott Syndrome (CSS) Cardiac Laminopathy (CLAM) – Nova Scotia Duck Tolling Retriever Cardiomyopathy and juvenile mortality (CJM) – Belgian Shepherd Centronuclear Myopathy (CNM) – Border Collie Centronuclear Myopathy (CNM) – Labrador Retriever Cerebellar Abiotrophy (CA) – Horse Cerebellar Abiotrophy (CA) – Kelpie Cerebellar Ataxia (CA1, RALGAPA1-related) – Belgian Shepherd Cerebellar Ataxia (LINGO3-related) – Kelpie Cerebellar Ataxia (SDCA1) – Belgian Shepherd Cerebellar Ataxia (SDCA2) – Belgian Shepherd Cerebellar Ataxia – Finnish Hound Cerebellar Ataxia – Flat-Coated Retriever Cerebellar Degeneration-Myositis Complex (CDMC) – NSDTR Cerebellar Hypoplasia (CH) – White Swiss Shepherd Charcot-Marie-Tooth Neuropathy (CMT, DP, SBF2-related) – Schnauzer Charcot-Marie-Tooth Neuropathy (CMT, ITPR3-related) – Lancashire Heeler Chondrodysplasia (CDPA) Chondrodysplasia (Dwarfism) Chondrodystrophy (CDDY with IVDD Risk) CLAD (Canine Leukocyte Adhesion Deficiency) Type I – Irish Setter CLAD (Canine Leukocyte Adhesion Deficiency) Type III – German Shepherd Cleft Lip / Palate and Syndactyly (CLPS) Cleft Palate (CP1) CMR1 (Canine Multifocal Retinopathy) CMR2 (Canine Multifocal Retinopathy) CMR3 (Canine Multifocal Retinopathy) 1 CMR3 (Canine Multifocal Retinopathy) 2 CNS Atrophy with Cerebellar Ataxia (CACA) – Belgian Shepherd Coat Colour A-Locus (Agouti) – Cat Coat Colour A-Locus (Agouti) – Dog Coat Colour A-Locus (Agouti) – Horse Coat Colour A-Locus (Charcoal) Coat Colour A-Locus – a1 (ASIP_325-381del57) Coat Colour A-Locus – a2 (ASIP_C292T) Coat Colour A-Locus – a3 (ASIP_G353A) Coat Colour Appaloosa Pattern 1 – PATN1 Coat Colour B-Locus Coat Colour B-Locus (Chocolate, Cinnamon) – Cat Coat Colour B-Locus – Australian Shepherd Coat Colour B-Locus Be Coat Colour B-Locus Bh Coat Colour Brindle (BR1) Coat Colour C-Locus (Albinism c) Coat Colour C-Locus (Albinism c2) Coat Colour C-Locus Colourpoint (Siam, Mink, Burma) Coat Colour Champagne Coat Colour Classic Grey – Alpaca Coat Colour Cocoa (HPS3-related) Coat Colour Cream Dilution (Cremello, Pearl) Coat Colour D-Locus (Dilution) – Cat Coat Colour D-Locus 1 – Dog Coat Colour D-Locus 2 – Dog Coat Colour D-Locus 3 – Dog Coat Colour Dun Dilution Coat Colour E-Locus (Amber) Coat Colour E-Locus (Russet) Coat Colour E-locus – e (Chestnut) Coat Colour E-Locus – e1 (MC1R_C901T) Coat Colour E-Locus – e1 (red/yellow) Coat Colour E-Locus – e2 (Australian Cattle Dog cream colour variant) Coat Colour E-Locus – e2 (MC1R_A82G) Coat Colour E-Locus – e3 (Husky pale yellow/white variant) Coat Colour E-Locus – e3 (MC1R_224-227delACTT) Coat Colour E-locus – e^a (Chestnut) Coat Colour E-Locus – Eg (Grizzle) Coat Colour E-Locus – eH (Sable) Coat Colour E-Locus – Em (Melanistic Mask) Coat Colour Frame Overo – OLWS Coat Colour G-Locus (Grey) – Horse Coat Colour G-Locus (White Gloves) – Birman Coat Colour Glitter Coat Colour Gold (Copper) Coat Colour Gold (Extreme Sunshine) Coat Colour Gold (Sunshine) Coat Colour H-Locus (Harlequin) Coat Colour I-Locus (Intensity) Coat Colour K-Locus (Dominant Black) Coat Colour Merle Coat Colour Mushroom Coat Colour O-Locus (Orange) Coat Colour Oculocutaneous Albinism (OCA1) Coat Colour Oculocutaneous Albinism (OCA2) Coat Colour Oculocutaneous Albinism (OCA4-1) Coat Colour Oculocutaneous Albinism (OCA4-3) Coat Colour Panda White Spotting Coat Colour Roan – Horse Coat Colour Roan – Ticked Coat Colour S-Locus (Piebald) Coat Colour Sabino 1 Coat Colour Saddle tan vs black-and-tan IMPROVED Coat Colour Salmiak Coat Colour Silver Dilution (MCOA) Coat Colour Snowdrop Coat Colour Splashed White 1 Coat Colour Splashed White 2 Coat Colour Splashed White 3 Coat Colour Tabby (Mackerel, Blotched, Marble) – 3 variants Coat Colour Ticked (Ti^A) – Cat Coat Colour Ticked (Ti^CK) – Cat Coat Colour Tobiano Coat Colour W-Locus (Dominant White KIT gene) Coat Colour White Spotting – W10 Coat Colour White Spotting – W15 Coat Colour White Spotting – W18 Coat Colour White Spotting – W19 Coat Colour White Spotting – W20 Coat Colour White Spotting – W21 Coat Colour White Spotting – W4 Coat Type SD-Locus (Shedding MC5R) Collie Eye Anomaly CEA, CH Complement 3 Deficiency (C3) – Brittany Spaniel Congenital Adrenal Hyperplasia – CAH Congenital Cornification Disorder (ILVEN) – Chihuahua 1 Congenital Cornification Disorder (ILVEN) – Chihuahua 2 Congenital Cornification Disorder (ILVEN) – Labrador Retriever Congenital Dyshormonogenic Hypothyroidism with Goiter (CDH) Congenital Erythropoietic Porphyria (CEP) 1 Congenital Erythropoietic Porphyria (CEP) 2 Congenital Eye Malformation (CEM) – Golden Retriever Congenital Hypomyelinating Polyneuropathy (MPZ-related) Congenital Hypomyelinating Polyneuropathy (MTMR2-related) Congenital Hypomyelinating Polyneuropathy (SH3TC2-related) Congenital Hypothyroidism – Cat 1 Congenital Hypothyroidism – Cat 2 Congenital Hypothyroidism with Dwarfism (CH) – Rottweiler Congenital Hypothyroidism with Goiter (CHG) – French Bulldog Congenital Hypothyroidism with Goiter (CHG) – Rat and Toy Fox Terrier Congenital Hypothyroidism with Goiter (CHG) – Spanish Water Dog Congenital Hypothyroidism with Goiter (CHG) – Tenterfield Terrier Congenital Idiopathic Megaesophagus (CIM) – German Shepherd Congenital Methemoglobinemia – All breeds Congenital Methemoglobinemia – German Spitz (Pomeranian) Congenital Mirror Movement Disorder 1 (CMM1, EFNB3-related) Congenital Muscular Dystrophy (CMD) – Italian Greyhound Congenital Myasthenic Syndrome (CMS) – Cat Congenital Myasthenic Syndrome (CMS) – Heideterrier Congenital Myasthenic Syndrome (CMS) – Jack Russell Terrier Congenital Myasthenic Syndrome (CMS) – Labrador Retriever Congenital Myasthenic Syndrome (CMS) – Old Danish Pointer Congenital Stationary Night Blindness (CSNB) – Beagle Congenital Stationary Night Blindness (CSNB) – Briard Congenital Stationary Night Blindness 2 (CSNB2) – Horse Copper Toxicosis (Accumulating Variant, ATP7B-related) Copper Toxicosis (Accumulating Variant, COMMD1 – related) – Bedlington Terrier Copper Toxicosis (Modifier, ATP7A-related) Copper Toxicosis (Modifier, RETN-related) Cortical Cerebellar Abiothrophy (NCCD) – Vizsla Craniomandibular Osteopathy (CMO) – Basset Hound Craniomandibular Osteopathy (CMO) – Terrier Type Craniomandibular Osteopathy (CMO) – Weimaraner Curly Coat (c1) – Dog Curly Coat (c2) – Dog Curly Coat – Cornish Rex Curly Coat – Selkirk Rex Curly Coat with or without Hypotrichosis (SP6- and KRT25-related) – Horse Curly Coat/Hairless Coat – Devon Rex and Sphynx Cystinuria (Type I – A) – Cat Cystinuria (Type I – A) – Labrador Retriever Cystinuria (Type I – A) – Newfoundland Cystinuria (Type II – A) – Australian Cattle Dog Cystinuria (type II – B) – Miniature Pinscher Cystinuria (Type III) – Bulldog Type – 1 Cystinuria (Type III) – Bulldog Type – 2 Cystinuria (Type III) – Bulldog Type – 3 Cystinuria Type B Variant 1 – Cat Cystinuria Type B Variant 2 – Cat Cystinuria Type B Variant 3 – Cat Dandy-Walker-Like Malformation (DWLM) / Cerebellar Hypoplasia (CH) – Eurasier Degenerative Encephalopathy (DEN) Degenerative Myelopathy Exon 1 (DM Exon 1) – Bernese Mountain Dog Degenerative Myelopathy Exon 2 (DM Exon 2) Degenerative Myelopathy Exon 2 (DM Exon 2) (External Patent Lab) Degenerative Myelopathy Risk Modifier (DMRM) – variant 1 Degenerative Myelopathy Risk Modifier (DMRM) – variant 2 Degenerative Myelopathy Risk Modifier (DMRM) – variant 3 Degenerative Myelopathy Risk Modifier (DMRM) – variant 4 Degenerative Myelopathy Risk Modifier (DMRM) – variant 5 Delayed Postoperative Hemorrhage – DEPOH, SERPINF2-related (External lab) Dental Hypomineralization Dental-Skeletal-Retinal Anomaly (DSRA) Diffuse Cystic Renal Dysplasia and Hepatic Fibrosis Dihydropyrimidinase Deficiency Dilated Cardiomyopathy (DCM, PLN-related) – Welsh Springer Spaniel Dilated Cardiomyopathy (DCM, RBM20-related) – Schnauzer Dilated Cardiomyopathy (DCM1, PDK4-related) – Doberman Dilated Cardiomyopathy (DCM2, TTN-related) – Doberman Dilated Cardiomyopathy (DCM3) – Doberman Dilated Cardiomyopathy (DCM4) – Doberman Disproportionate Dwarfism – Dalmatian Disproportionate Dwarfism – Dogo Argentino Distichiasis Dominant Blue Eyes (DBE-RE) Dominant Blue Eyes Agosto (DBE-AGO) Dominant Blue Eyes Altai (DBE-ALT) Double Coat (Coat Composition, CFA28-related) Dry Eye Curly Coat Syndrome (CCS, DE-CC) Dwarfism ACAN D1, D2, D3 IMPROVED, D4 Dwarfism ACAN D5 Dwarfism Friesian Dyserythropoietic Anemia and Myopathy Syndrome (DAMS) – English Springer Spaniel Dyserythropoietic Anemia and Myopathy Syndrome (DAMS) – Labrador Retriever Dystrophic Epidermolysis Bullosa (RDEB) – Central Asian Shepherd Dystrophic Epidermolysis Bullosa (RDEB) – Golden Retriever Early Onset Progressive Polyneuropathy (EOPP) Early-Onset Adult Deafness (EOAD) – Rhodesian Ridgeback Ectodermal Dysplasia / Skin Fragility Syndrome – Chesapeake Bay Retriever Type Ehlers-Danlos Syndrome (EDS, COL5A1-related) – Bengal Ehlers-Danlos Syndrome (EDS, COL5A1-related) – Dog Ehlers-Danlos Syndrome (EDS, TNXB-related) – Dog (variant 1) Ehlers-Danlos Syndrome (EDS, TNXB-related) – Dog (variant 2) Ehlers-Danlos Syndrome Type 1 – Cat All Breeds Ehlers-Danlos Syndrome Type 1 – Labrador Retriever Ehlers-Danlos Syndrome Type 7 – Doberman Elliptocytosis Epidermolysis Bullosa Simplex (EBS) Epidermolytic Hyperkeratosis (EHK) and Ichthyosis – Norfolk Terrier Epileptic Encephalopathy (EE) – Bengal Episodic Falling Disease – EFS (External Lab) Episodic Falling Disease – EFS (External Patent Lab) Exercise Induced Collapse, EIC Exercise Induced Collapse, EIC (External Patent Lab) Exercise Induced Metabolic Myopathy Exfoliative Cutaneous Lupus Erythematosus (ECLE) Factor VII deficiency Factor XI deficiency – Maine Coon Factor XII deficiency – variant 147 Factor XII deficiency – variant 533 Familial Thyroid Follicular Cell Carcinoma I Familial Thyroid Follicular Cell Carcinoma II Fanconi syndrome – FS Fecundity FN, Familial Nephropathy – (English) Cocker Spaniel FN, Familial Nephropathy – English Springer Spaniel Foal Immunodeficiency Syndrome Fucosidosis Gangliosidosis (GM1) – Korat and Siamese Gangliosidosis (GM1) – Portuguese Water Dog Gangliosidosis (GM1) – Shiba Inu Gangliosidosis (GM2 Type I) – Japanese Chin Gangliosidosis (GM2 Type II) – Burmese Gangliosidosis (GM2 Type II) – Cat All Breeds Gangliosidosis (GM2 Type II) – Japanese Domestic Gangliosidosis (GM2 Type II) – Korat Gangliosidosis (GM2 Type II) – Poodle Type Gangliosidosis (GM2, Sandhoff Disease) – Shiba Inu Gangliosidosis (GM2A) – Cat All Breeds Glanzmann’s Thrombasthenia (GT) 1 – Dog Glanzmann’s Thrombasthenia (GT) 1 – Horse Glanzmann’s Thrombasthenia (GT) 2 – Dog Glanzmann’s Thrombasthenia (GT) 2 – Horse Globoid Cell Leukodystrophy (GCL, Krabbes disease) – Irish Setter Globoid Cell Leukodystrophy (GCL, Krabbes disease) – Terrier Type Glycogen Branching Enzyme Deficiency – GBED Glycogen Storage Disease (GSD-PGBM1) – Basset Hound Glycogen Storage Disease Ia (GSD1a) – German Pinscher Glycogen Storage Disease Ia (GSD1a) – Maltese Glycogen Storage Disease II (GSD2, Pompe) – Dog Glycogen Storage Disease IIIa (GSD IIIa) – Curly Coated Retriever Glycogen Storage Disease IV (GSD4) – Norwegian Forest Cat Glycogen Storage Disease VII (GSD7) – Deutscher Wachtelhund Glycogen Storage Disease VII (GSD7) / Phosphofructokinase Deficiency (PFK Def) Goniodysgenesis and Glaucoma (GG) Gray Collie Syndrome (Cyclic Neutropenia) Haemophilia A (HEMA-1) – German Shepherd Haemophilia A (HEMA-2) – German Shepherd Haemophilia A – Border Collie Haemophilia A – Boxer Haemophilia A – Labrador Retriever Haemophilia A – Old English Sheepdog Haemophilia A – Rhodesian Ridgeback Haemophilia B – Cairn Terrier Haemophilia B – Hovawart Haemophilia B – Lhasa Apso Haemophilia B – Newfoundland Haemophilia B – Rhodesian Ridgeback Haemophilia B 1 – Cat Haemophilia B 2 – Cat Hair Length – 1 Hair Length – 2 Hair Length – 3 Hair Length – 4 Hair Length – 5 Hair Length Cat – All Breeds Hair Length Cat – Maine Coon Hair Length Cat – Norwegian Forest Hair Length Cat – Ragdoll Hair Length Cat – Ragdoll / Maine Coon Hair Shaft Dysplasia type 1 Hair Shaft Dysplasia type 2 Hereditary Ataxia (HACE-related) – Norwegian Elkhound Hereditary Ataxia (KCNIP4-related) – Norwegian Buhund Hereditary Ataxia (RAB24-related) – Old English Sheepdog and Gordon Setter Hereditary Ataxia (SCA) – Australian Shepherd Hereditary Cataract (HC, HSF4-1) Hereditary Cataract (HC, HSF4-2) Hereditary Deafness (CDH23) – Beauceron Hereditary Equine Regional Dermal Asthenia – HERDA Hereditary Footpad Hyperkeratosis ( FNEPPK1, KRT16-related) – Dogue de Bordeaux Hereditary Footpad Hyperkeratosis (DSG1-related) – Rottweiler Hereditary Footpad Hyperkeratosis (FAM83G-related) Hereditary Nasal Parakeratosis (HNPK) – Greyhound Hereditary Necrotizing Myelopathy (HNM) Hereditary Nephritis (HN) – Samoyed HNPK (External Lab) HNPK (External Patent Lab) Hoof Wall Separation Disease – HWSD Hydrocephalus – Friesian Hyperkalemic Periodic Paralysis – HYPP Hyperlipoproteinaemia Hyperthrophic Cardiomyopathy (HCM MYH7-related) Hypertrophic Cardiomyopathy (HCM) – Golden Retriever Hypertrophic Cardiomyopathy 1 (HCM1) Hypertrophic Cardiomyopathy 3 (HCM3) Hyperuricemia (HUU, SLC2A9-related) Hypocatalasia (CAT) Hypomyelination / Shaking Puppy Syndrome (SPS) – English Springer Spaniel Hypomyelination / Shaking Puppy Syndrome (SPS) – Weimaraner Hypophosphatasia Hyposegmentation of Granulocytes (HG) – Australian Shepherd Hypotrichosis and Short Life Expectancy – Cat Ichthyosis – American Bulldog Type Ichthyosis – German Shepherd Ichthyosis – Golden Retriever Type 1 Ichthyosis – Golden Retriever Type 2 Ichthyosis – Great Dane Ichthyosis – Jack Russell Terrier Type Ichthyosis – Poodle Type Improper Coat/Furnishings Incontinentia pigmenti – IP Inflammatory Myopathy (Myositis) Inflammatory Pulmonary Disease Inherited Myopathy of Great Danes (IMGD) / Centronuclear Myopathy (CNM, HMLR) Intestinal Cobalamin Malabsorption (ICM, IGS) – Beagle Intestinal Cobalamin Malabsorption (ICM, IGS) – Border Collie Intestinal Cobalamin Malabsorption (ICM, IGS) – Komondor Intestinal Lipid Malabsorption (ILM) – Kelpie Junctional Epidermolysis Bullosa (JEB, LAMA3-related) – Australian Cattle Dog Junctional Epidermolysis Bullosa (JEB, LAMA3-related) – German Pointer Junctional Epidermolysis Bullosa (JEB, LAMA3-related) – Horse Junctional Epidermolysis Bullosa (JEB, LAMB3-related) – Australian Shepherd Junctional Epidermolysis Bullosa (JEB, LAMC2-related) – Horse Juvenile Addison’s Disease (JADD) Juvenile Brain Disease (JBD) – Juvenile Encephalopathy Juvenile Cataract – Wirehaired Pointing Griffon Juvenile Dilated Cardiomyopathy (JDCM) – Manchester Terrier Juvenile Epilepsy (JE/BFJE) – Lagotto Romagnolo Juvenile Laryngeal Paralysis Polyneuropathy (JLPP) Juvenile Myoclonic Epilepsy (JME) – Rhodesian Ridgeback L-2-Hydroxyglutaric Aciduria (L2HGA) – Staffordshire Bull Terrier Lafora disease Lagotto Storage Disease (LSD) Laryngeal Paralysis (LP) – Bull Terrier Type Laryngeal Paralysis and polyneuropathy (LPPN3, CNTNAP1-related) Late Onset Ataxia (LOA) Lavender Foal Syndrome – LFS Leopard Complex Spotting (LP) and Congenital Stationary Night Blindness (CSNB1) Lethal Acrodermatitis (LAD) Lethal Lung Disease (LAMP3) – Airedale Terrier Leukodystrophy (CYTB-related) Leukodystrophy (LEP, TSEN54-related) – Schnauzer Leukoencephalomyelopathy (LEMP) – Leonberger Leukoencephalomyelopathy (LEMP) – Rottweiler and Great Dane Ligneous Membranitis (LM) – Scottish Terrier Limb-Girdle Muscular Dystrophy (LGMD) – Boston Terrier 1 Limb-Girdle Muscular Dystrophy 2D (LGMD2D) – Dachshund Long QT Syndrome Lundehund syndrome – LS Lysosomal Storage Disease (LSD) – Dalmatian Lysosomal Storage Disease (LSD) – Weimaraner Macrothrombocytopenia (MTC) – Cairn and Norfolk Terrier Macrothrombocytopenia (MTC) – Cavalier King Charles Spaniel Macular Corneal Dystrophy (MCD) Malignant Hyperthermia (MH) – American Quarter Horse Malignant Hyperthermia (MH) – Dog May-Hegglin Anomaly (MHA) – Pug MCAD Deficiency – Cavalier King Charles Spaniel MDR1 Multi Drug Resistance – Cat MDR1 Multi Drug Resistance – Dog Metabolizer of a Cognitive Enhancer Microphtalmia (RBP4-related) – Irish Soft Coated Wheaten Terrier Microphthalmia (DNAJC21-related) – Portuguese Water Dog Mitochondrial Fission Encephalopathy (MFE) – Bullmastiff Mucopolysacchardidosis VII (MPS7) type 1 – Cat Mucopolysacchardidosis VII (MPS7) type 3 – Cat Mucopolysaccharidosis I (MPS1) – Boston Terrier Mucopolysaccharidosis I (MPS1) – Cat Mucopolysaccharidosis I (MPS1) – Plott Hound Mucopolysaccharidosis IIIa (MPS3a) – Dachshund Mucopolysaccharidosis IIIB (MPS3B) – Schipperke Mucopolysaccharidosis VI (MPS6) – Cat (2 variants) Mucopolysaccharidosis VI (MPS6) – Great Dane Mucopolysaccharidosis VI (MPS6) – Miniature Pinscher Mucopolysaccharidosis VII (MPS7) – Brazilian Terrier Mucopolysaccharidosis VII (MPS7) – German Shepherd Mucopolysaccharidosis VII (MPS7) type 2 – Cat Multiocular Defect (MOD) – Old English Sheepdog Muscular Dystrophy (MD) – American Staffordshire Terrier Muscular Dystrophy (MD) – Border Collie Muscular Dystrophy (MD) – Cavalier King Charles Spaniel Muscular Dystrophy (MD) – Corgi Muscular Dystrophy (MD) – French Bulldog Muscular Dystrophy (MD) – Golden Retriever Muscular Dystrophy (MD) – Labrador Retriever 1 Muscular Dystrophy (MD) – Labrador Retriever 2 Muscular Dystrophy (MD) – Landseer Muscular Dystrophy-Dystroglycanopathy (MDD) – Labrador Retriever Musladin-Lueke Syndroom (MLS) Muzzle Length (Brachycephaly, BMP3-related) – Dog Mycobacterium Avium Complex (MAC) – Schnauzer Myeloperoxidase Deficiency Myosin Heavy Chain Myopathy (MYHM) Myotonia Congenita – Australian Cattle Dog and Border Collie Myotonia Congenita – French Bulldog Myotonia Congenita – Labrador Retriever Myotonia Congenita – New Forest Pony Myotonia Congenita – Schnauzer Myotonia Congenita Variant 1 – Cat Myotonia Congenita Variant 2 – Cat Myotonia Congenita Variant 3 – Cat Myxomatous Valvular Degeneration (MMVD, NEBL1) Myxomatous Valvular Degeneration (MMVD, NEBL2) Myxomatous Valvular Degeneration (MMVD, NEBL3) Naked Foal Syndrome (NFS) – Akhal-Teke Narcolepsy – Dachshund Narcolepsy – Doberman Narcolepsy – Labrador Retriever Nemaline Myopathy – American Bulldog Neonatal Cerebellar Ataxia – Coton de Tulear and Havanese Neonatal Cortical Cerebellar Abiotrophy (NCCD) – Beagle Neonatal Encephalopathy (NEWS) Neuroaxonal Dystrophy (NAD) – Miniature American Shepherd Neuroaxonal Dystrophy (NAD) – Papillon Neuroaxonal Dystrophy (NAD) – Rottweiler Neuroaxonal Dystrophy (NAD) – Schnauzer and Beagle Neuroaxonal Dystrophy (NAD) – Spanish Water Dog Neurological defects with dilute coat colour Neuronal Ceroid Lipofuscinosis 1 (NCL1) – Cane Corso Neuronal Ceroid Lipofuscinosis 1 (NCL1) – Dachshund Neuronal Ceroid Lipofuscinosis 10 (NCL10) – American Bulldog Neuronal Ceroid Lipofuscinosis 12 (NCL12) – Australian Cattle Dog Neuronal Ceroid Lipofuscinosis 12 (NCL12) – Tibetan Terrier Neuronal Ceroid Lipofuscinosis 2 (NCL2) – Dachshund Neuronal Ceroid Lipofuscinosis 4A (NCL4A) – Cerebellar Ataxia Neuronal Ceroid Lipofuscinosis 5 (NCL5) Neuronal Ceroid Lipofuscinosis 5 (NCL5) – Golden Retriever Neuronal Ceroid Lipofuscinosis 6 (NCL6) – Australian Shepherd Neuronal Ceroid Lipofuscinosis 6 (NCL6) – Schapendoes Neuronal Ceroid Lipofuscinosis 7 (NCL7) Neuronal Ceroid Lipofuscinosis 8 (NCL8) – Alpine Dachsbracke Neuronal Ceroid Lipofuscinosis 8 (NCL8) – Australian Shepherd Type Neuronal Ceroid Lipofuscinosis 8 (NCL8) – English Setter Neuronal Ceroid Lipofuscinosis 8 (NCL8) – Saluki Niemann-Pick Disease C1 – All Breeds 1 Niemann-Pick Disease C1 – All Breeds 2 Nonsyndromic Hearing Loss – Rottweiler Obesity (DENND1B-related) Obesity (POMC-related) Occipitoatlantoaxial Malformation – OAAM Ocular Squamous Cell Carcinoma (SCC) Oculoskeletal Dysplasia (OSD) / Retinal Dysplasia (RD) – Northern Inuit Dog Oculoskeletal Dysplasia 1 (OSD1) / Retinal Dysplasia (RD) – Labrador Retriever Oculoskeletal Dysplasia 2 (OSD2) / Retinal Dysplasia (RD) – Samoyed Osteochondrodysplasia (OC) Osteochondrodysplasia – Scottish Fold Osteochondromatosis Osteogenesis Imperfecta (OI) – Beagle Osteogenesis Imperfecta (OI) – Cat Osteogenesis Imperfecta (OI) – Chow Chow Osteogenesis Imperfecta (OI) – Dachshund Osteogenesis Imperfecta (OI) – Golden Retriever P2RY12 Receptor Platelet Disorder Paradoxical Pseudomyotonia (PPM) Paroxysmal Dyskinesia (PD) – Irish Soft Coated Wheaten Terrier Paroxysmal Dyskinesia (PD) – Markiesje Paroxysmal Exercise-Induced Dyskinesia (PED) – Shetland Sheepdog Paroxysmal Exercise-Induced Dyskinesia (PED) – Weimaraner Persistent Mullerian Duct Syndrome (PMDS) Pigeon Performance Gene CASK Pigeon Performance Gene CRY-1 Pigeon Performance Gene DRD4-1 Bst4CI Pigeon Performance Gene DRD4-2 MnLI Pigeon Performance Gene GSR Expression Pigeon Performance Gene LDHA Pigeon Performance Gene LRP8 Pituitary Dwarfism – Karelian Bear Dog Pituitary Dwarfism – Shepherd Type Polioencephalopathy (PE) – Eurasier Polycystic Kidney Disease (PKD) – Bull Terrier Polycystic Kidney Disease type 1 (PKD) – Cat Polycystic Kidney Disease type 2 (PKD) – Siberian Polydactyly (DC-2) – Dog Polydactyly Hw – Cat Polydactyly UK1 – Cat Polydactyly UK2 – Cat Polymyositis 1 (PM1) – Kooikerhondje Polymyositis 2 (PM2) – Kooikerhondje Polyneuropathy (AMPN) – Alaskan Malamute Polyneuropathy (LPN1) Polyneuropathy (LPN2) – Leonberger Polysaccharide Storage Myopathy – PSSM1 Polysaccharide Storage Myopathy – PSSM1 (External Patent Lab) Predictive Height (LCORL-related) Prekallikrein Deficiency (KLK) Primary Ciliary Dyskinesia (PCD) – Alaskan Malamute Primary Ciliary Dyskinesia (PCD) – Australian Shepherd Primary Ciliary Dyskinesia (PCD) – Eurasier Primary Ciliary Dyskinesia (PCD) – Nova Scotia Duck Tolling Retriever Primary Ciliary Dyskinesia (PCD) – Old English Sheepdog Primary Congenital Glaucoma (PCG) – Siamese Primary hyperoxaluria Primary hyperoxaluria II Primary Immunodeficiency Type 2 (PIPS2, CARMIL2-related) – CKCS Primary Lens Luxation – PLL Primary Open Angle Glaucoma (POAG) – Basset Fauve de Bretagne Primary Open Angle Glaucoma (POAG) – Basset Hound Primary Open Angle Glaucoma (POAG) – Beagle Primary Open Angle Glaucoma (POAG) – Norwegian Elkhound Primary Open Angle Glaucoma (POAG) – Petit Basset Griffon Vendéen Primary Open Angle Glaucoma (POAG) / Primary Lens Luxation (PLL) – Shar-Pei Progressive Retinal Atrophy (Bas-PRA, SAG-related) – Basenji Progressive Retinal Atrophy (BBS2-PRA) – Shetland Sheepdog Progressive Retinal Atrophy (BBS4-PRA) – Hungarian Puli Progressive Retinal Atrophy (bPRA) – Bengal Progressive Retinal Atrophy (CNGA1-PRA) – Shetland Sheepdog Progressive Retinal Atrophy (crd-PRA, NPHP4-related) – Dachshund Progressive Retinal Atrophy (crd1-PRA) – American Staffordshire Terrier Progressive Retinal Atrophy (crd2-PRA) – American Pit Bull Terrier Progressive Retinal Atrophy (crd4-PRA, MAP9-related) Progressive Retinal Atrophy (crd4-PRA/cord1) Progressive Retinal Atrophy (D-PRA, Dominant PRA) – Mastiff Progressive Retinal Atrophy (erd-PRA) – Norwegian Elkhound Progressive Retinal Atrophy (g-PRA) – Schapendoes Progressive Retinal Atrophy (GR-PRA1) Progressive Retinal Atrophy (GR-PRA2) Progressive Retinal Atrophy (GTPBP2-PRA) Progressive Retinal Atrophy (GUCY2D-PRA) Progressive Retinal Atrophy (IFT122-PRA) – Lapponian Herder Progressive Retinal Atrophy (JPH2 – PRA) – Shih-Tzu Progressive Retinal Atrophy (MERTK-PRA) Progressive Retinal Atrophy (PAP-PRA1) Progressive Retinal Atrophy (PCYT2-Deficiency) – Saarloos Wolfdog Progressive Retinal Atrophy (pd-PRA) – Cat Progressive Retinal Atrophy (PRA, NECAP1-related) – Schnauzer Progressive Retinal Atrophy (PRA1 Type B, HIVEP3-related) – Schnauzer Progressive Retinal Atrophy (PRA3) – Tibetan Type Progressive Retinal Atrophy (prcd-PRA) Progressive Retinal Atrophy (rcd1-PRA) – Irish Setter Progressive Retinal Atrophy (rcd1a-PRA) – Sloughi Progressive Retinal Atrophy (rcd2-PRA) (External Lab) – Collie Type Progressive Retinal Atrophy (rcd3-PRA) Progressive Retinal Atrophy (rcd4-PRA) Progressive Retinal Atrophy (rdAc-PRA) Progressive Retinal Atrophy (rdy-PRA) – Cat Progressive Retinal Atrophy (XL-PRA, X-Linked) Progressive Retinal Atrophy Early Onset (eo-PRA) – Spanish Water Dog Protein Losing Nephropathy (PLN, KIRREL2-related) Protein Losing Nephropathy (PLN, NPHS1-related) Pug Dog Encephalitis (PDE) / Necrotizing Meningoencephalitis (NME) Risk Factor Pyruvate Dehydrogenase Phosphatase Deficiency (PDP1) Pyruvate Kinase Deficiency (PKDef) – Basenji Pyruvate Kinase Deficiency (PKDef) – Beagle Pyruvate Kinase Deficiency (PKDef) – Cat Pyruvate Kinase Deficiency (PKDef) – Labrador Retriever Pyruvate Kinase Deficiency (PKDef) – Pug Pyruvate Kinase Deficiency (PKDef) – West Highland White Terrier Recessive Hypotrichosis (Hairlessness) – American Hairless Terrier Recessive Hypotrichosis (Hairlessness) – Scottish Deerhound Recessive Lethal (FH10) – Friesian Recessive Lethal (FH4) – Friesian REM Sleep Behaviour Disorder (RBD) – Russian Blue Renal Cystadenocarcinoma and Nodular Dermatofibrosis (RCND) Resistance to Phenobarbital Therapy – Border Collie Retinal Dysplasia Retinopathy with Vitamin E Deficiency Ridge Predisposition (External Lab) Robinow-like Syndrome (DVL2) Saluki Encephalopathy (SE) Sebaceous Gland Dysplasia, SOAT1-related Sensory Neuropathy – All breeds Sensory Neuropathy – Border Collie Severe Combined Immuno Deficiency (SCID) – Horse Severe Combined Immunodeficiency (SCID, PRKDC-related) – Jack Russel Terrier Severe Combined Immunodeficiency (SCID, RAG1-related) – Wetterhoun Sex Determination – Pigeon Shar-Pei Fever (SPAID) Skeletal Dysplasia (SD3) – Vizsla Skeletal Dysplasia 2 (SD2) – Labrador Retriever Spastic Ataxia (SACS-related) – Great Pyrenees Spinal Dysraphism (SD) / Neural Tube Defects (NTD) Spinal Muscular Atrophie – SMA Spinocerebellar Ataxia (SCA) – Alpine Dachsbracke Spinocerebellar Ataxia (SCA) – Terrier Type Spondylocostal Dysostosis (Comma Defect) Spongiform Leukoencephalomyelopathy (SLEM) – Border Terrier (External Lab) Stargardt disease 1 Startle Disease – Miniature American Shepherd Startle Disease – Old English Sheepdog Subacute Necrotizing Encephalopathy (SNE) – Yorkshire Terrier SynchroGait (DMRT3-related) Tail Length (Brachyury, T-Locus, Natural Bobtail) – Dog Thrombopathia – American Eskimo Dog Thrombopathia – Basset Hound Thrombopathia – Landseer Trapped Neutrophil Syndrome (TNS) Unilateral Deafness and Vestibular Dysfunction (PTPRQ, DINGS1) – Doberman Upper Airway Syndrome (UAS, NTUAS) Van den Ende-Gupta Syndrome (VDEGS) Ventricular Arrhythmias and Sudden Death Vitamin D-Resistant Rickets (VDR) – Cat Vitamin D-Resistant Rickets (VDR) – German Spitz (Pomeranian) Vitamin D-Resistant Rickets (VDR) – Pug Von Willebrand Disease Type 1 Von Willebrand Disease Type 2-2 Von Willebrand Disease Type 3 – Kooikerhondje Von Willebrand Disease Type 3 – Scottish Terrier Von Willebrand Disease Type 3 – Shetland Sheepdog Warburg Micro Syndrome 1 (WARBM1) Warmblood Fragile Foal Syndrome – WFFS X-Linked Ectodermal Dysplasia (XHED) – Shepherd Type X-linked Myotubular Myopathy (XLMTM) – Boykin Spaniel X-linked Myotubular Myopathy (XLMTM) – Labrador Retriever X-linked Myotubular Myopathy (XLMTM) – Maine Coon X-linked Myotubular Myopathy (XLMTM) – Rottweiler X-linked Progressive Retinal Atrophy (XLPRA) – English Cocker Spaniel X-Linked Severe Combined Immunodeficiency Disease (XSCID) – Cardigan Welsh Corgi Xanthinuria type 2 – Dachshund Xanthinuria, type 1 – All breeds Xanthinuria, type 2 – Manchester Terrier Xanthinuria, type 2 – Spaniel variant
Gene
ABCA4 ABCB1 ABCC9 ABHD5 ACADM ACADVL ACAN ACPT ACSL5 ADAMTS10 ADAMTS17 ADAMTS2 ADAMTS20 ADAMTS3 ADAMTSL2 AGL AGXT AIPL1 AKNA ALDH5A1 ALPL ALX1 AMHR2 ANLN ANO6 AP3B1 APRT AR ARHGAP36 ARHGEF10 ARSB ARSG ASIP ASPRV1 ATF2 ATG4D ATP13A2 ATP1B2 ATP7A ATP7B B3GALNT2 B4GALT7 BBS2 BBS4 BCAN BEST1 BIN1 BMP3 BTBD17 C12ORF35 C3 CACNA1F CAD CAPN1 CARD9 CARMIL2 CASK CAT CBD103 CCDC39 CCDC66 CDH23 CEP290 CHAT CHRNE CLCN1 CLN5 CLN6 CLN8 CMAH CNGA1 CNGA3 CNGB1 CNGB3 CNP CNTNAP1 COL11A1 COL11A2 COL1A1 COL1A2 COL4A4 COL4A5 COL5A1 COL6A1 COL6A3 COL7A1 COL9A2 COL9A3 COLQ COMMD1 CORIN CREB3L1 CRX CRY-1 CTSD CUBN CYB5R3 CYP11B1 CYP1A2 CYP27B1 CYTB DDB2 DENND1B DIRAS1 DKK4 DLA-DPB1 DLX6 DMD DMRT3 DNAJC21 DNM1 DNM2 DPYS DRD4 DSG1 DSG4 DSP DVL2 EDA EDNRB EFNB3 EHBP1L1 ENAM EPS8L2 EXT2 F11 F12 F7 F8 F9 FAM134B FAM161A FAM20C FAM83G FAM83H FAM8A1 FAN1 FASLG FERMT3 FGF4L1 FGF4L2 FGF5 FGFR2 FLCN FNIP2 FOXI3 FOXN1 FUCA1 FYCO1 G6PC GAA GALC GBE1 GDF9 GDNF GFAP GHR GJA9 GLB1 GLRA1 GM2A GP9 GRHPR GRM1 GRM6 GSR GTPBP2 GUCY2D GUSB GYS1 HACD1/PTPLA HACE1 HCRTR2 HES7 HEXA HEXB HIVEP3 HMBS HOXD3 HPS3 HS3ST2 HSF4 IBA57 IDUA IFT122 IGF1-AS IGF1R IGFBP5 IKBKG IL2RG INPP5E IQCB1 ITGA10 ITGA2B ITGB2 ITPR3 JPH2 KCNIP4 KCNJ10 KCNQ1 KIF3B KIRREL2 KIT KLKB1 KRT10 KRT16 KRT25; SP6 KRT71 L2HGDH LAMA2 LAMA3 LAMB3 LAMC2 LAMP3 Large insertion on Chr18 LARGE1 LCORL LDHA LGI2 LHX3 LINGO3 LIX1 LMBR1 LMBR1L LMNA lncRNA upstream of ADRB1 LOC102156622 LOC489707 LOXHD1 LPAR6 LPL LRIT3 LRP8 LTBP2 LVRN MAN2B1 MANBA MAP9 MBTPS2 MC1R MC5R MCHR2 MECR MERTK MET MFF MFN2 MFSD12 MFSD8 MIA3 MITF MKLN1 MLPH MOCOS MPO MPZ MSTN MTBP MTM1 MTMR2 MUTYH MYBPC3 MYH1 MYH7 MYH9 MYO5A MYO7A NAGLU NAPEPLD ncRNA’s, SLC28A3, SPATA31 NDP NDRG1 NEB NEBL NECAP1 NHEJ1 NHLRC1 NIPAL4 NKX2-8 NME5 NPC1 NPHP4 NPHS1 NSDHL OCA2 OLFML3 P2RY12 P3H2 PAOX PAX3 PCARE PCK2 PCYT1A PCYT2 PDE6A PDE6B PDK4 PDP1 PFKM PIGN PITRM1 PKD1 PKD2 PKLR PKP1 PLA2G6 PLEC PLG PLN PLOD1 PLP PMEL PNPLA1 PNPLA8 POMC POU1F1 PPIB PPT1 PRCD PRKDC PRKG2 PSMB7 PTPRQ QIL1 RAB24 RAB3GAP1 RAG1 RALGAPA1 RALY RAPGEF6 RASGRP2 RB1CC1 RBBP6 RBCK1 RBM20 RBP4 RD3 RELN RETN RFWD3 RHO RNF170 RNF207 RPE65 RPGR RPGRIP1 RSPO2 RYR1 SACS SAG SBF2 SCARF2 SCN4A SCN8A SEL1L SEPP1 a.k.a. SELENOP SERAC-1 SERAC1 SERPINB11 SERPINF2 SERPINH1 SGCA SGCD SGK3 SGSH SH3TC2 SIX6 SLAMF1 SLC13A1 SLC19A3 SLC25A12 SLC27A4 SLC2A9 SLC35D1 SLC36A1 SLC37A2 SLC39A4 SLC3A1 SLC45A2 SLC4A3 SLC5A3 SLC5A5 SLC6A5 SLC7A10 SLC7A9 SNX14 SOAT1 SOD1 SP110 SPTB SPTBN2 ST14 STC2 STK36 STK38L STX17 SUV39H2 T TBX3 TECPR2 TG TGM1 TNNI3 TNR TNXB TPO TPP1 TRPM1 TRPV4 TSEN54 TTC8 TTN TTPA TUBB1 TYR TYRP1 UNC93B1 unpublished upstream of IL21/IL2 locus UROS USH2A USP31 VDR VLDLR VMP1 VPS11 VPS13B VWF WNK4 XDH YARS2 ZMYND10 ZW chromosomes
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