Genetic Diseases in Dogs, Cats and Horses

All Genetic Conditions

• Achromatopsia (4)
• Acral Mutilation (1)
• Acrodermatitis (1)
• Acrodermatitis Enteropathica (1)
• Adrenal Hyperplasia (1)
• Afibrinogenaemia (1)
• Agouti (14)
• Albinism (6)
• Alexander Disease (1)
• Alpha-Mannosidosis (1)
• Amber (1)
• Amelogenesis Imperfecta (4)
• ໂຣກ Androgen Insensitivity (5)
• Aoc (1)
• Appaloosa Pattern (1)
• Autoimmune Lymphoproliferative Syndrome (1)
• Bardet-Biedl (1)
• Bernard-Soulier (1)
• Bleeding (1)
• Blood Group (14)
• Bob Tail (1)
• Brachycephaly (2)
• Brain Disease (1)
• Brown (6)
• C3 Deficiency (1)
• Cardiomyopathy (8)
• Cerebellar Abiotrophy (2)
• Cerebellar Ataxia (5)
• Cerebellar Cortical Degeneration (2)
• Cerebellar Degeneration-Myositis Complex (1)
• Cerebellar Hypoplasia (2)
• Champagne (2)
• Chocolate (2)
• Chondrodysplasia (3)
• Cinnamon (1)
• Cleft Palate (2)
• Cocoa (1)
• Colourpoint (2)
• Copal (1)
• Copper Storage Disease (2)
• Copper Toxicosis (2)
• Craniomandibular Osteopathy (2)
• Cream (1)
• Curly (8)
• Cystic Renal Dysplasia And Hepatic Fibrosis (1)
• Cystinuria (11)
• Deafness (5)
• Degenerative Myelopathy (3)
• Dental Hypomineralization (1)
• Dental Skeletal Retinal Anomaly (1)
• Dermatomyositis (2)
• Dihydropyrimidinase Deficiency (1)
• Dilution (5)
• Dominant White (35)
• Dwarfism (16)
• Dyserythropoietic Anemia And Myopathy Syndrome (2)
• Ectodermal Dysplasia (2)
• Encephalopathy (5)
• Epidermolysis Bullosa (9)
• Epidermolytic Hyperkeratosis (1)
• Epilepsy (2)
• Episodic Falling Syndrome (1)
• Exercise-Induced Collapse (1)
• Exfoliative Cutaneous Lupus Erythematosus (1)
• Extension (7)
• Factor Vii Deficiency (1)
• Fanconi Syndrome (1)
• Foal Immunodeficiency Syndrome (1)
• Folded Ears (1)
• Footpad Hyperkeratosis (4)
• Gaitedness (1)
• Gallbladder Mucoceles (1)
• Gangliosidosis (12)
• ການກໍານົດພັນທຸກໍາ
• Glanzmann Thrombasthenia (4)
• Glaucoma (8)
• Gloving (1)
• Glycogen Storage Disease (9)
• Gold (3)
• Grizzle (1)
• Haemophilia (24)
• Hairless (1)
• Hare-Pied And Husky Marking (1)
• Harlequin (1)
• Head Defect (1)
• Hemophilia (4)
• Hereditary Ataxia (4)
• Hereditary Cataract (3)
• Hereditary Equine Regional Dermal Asthenia (2)
• Hereditary Nephritis (1)
• Hoof Wall Separation Disease (1)
• Hydrocephalus (1)
• Hyperkalemic Periodic Paralysis (1)
• Hyperlipoproteinaemia (1)
• Hypertrophic Cardiomyopathy (5)
• Hyperuricosuria (1)
• Hypocatalasia (1)
• Hypokalaemic Periodic Paralysis (1)
• Hypomyelination Of The Central Nervous System (1)
• Hypoparathyroidism (1)
• Hypophosphatasia (1)
• Hyposegmentation Of Granulocytes (1)
• Hypothyroidism (8)
• Hypotrichia (7)
• Hypotrichosis (2)
• Ichthyosis (11)
• Immune Mediated Myositis (1)
• Incontinentia Pigmenti (1)
• Intensity (3)
• Intestinal Cobalamin Malabsorption (5)
• Intestinal Lipid Malabsorption (1)
• Junctionalis Epidermolysis Bullosa (2)
• L-2-Hydroxyglutaric Aciduria (2)
• Laminopathy (1)
• Laryngeal Paralysis (6)
• Late Onset Ataxia (1)
• Lavender Foal Syndrome (1)
• Lethal White Overo Syndrome (1)
• Leucodystrophy (5)
• Leukocyte Adhesion Deficiency (3)
• Leukoencephalomyelopathy (2)
• Locus K (2)
• Long Hair (12)
• Lundehund Syndrome (1)
• Lung Disease (2)
• Lysosomal Storage Disease (3)
• Macchiato (1)
• Macular Corneal Dystrophy (2)
• Malignant Hyperthermia (2)
• Mannosidosis (4)
• May-Hegglin Anomaly (1)
• Methemoglobinemia (4)
• Mucopolysaccharidosis (18)
• Multidrug Resistance (3)
• Multifocal Retinopathy (3)
• Multiocular Defect (1)
• Multiple Drug Resistance (1)
• Multiple System Degeneration (2)
• Muscular Dystrophy (40)
• Muscular Hypertrophy (1)
• Musladin-Lueke Syndrome (1)
• Myasthenic Syndrom (6)
• Mycobacterium Avium Complex (1)
• Myopathy (10)
• Myotonia (12)
• Narcolepsy (3)
• Nasal Parakeratosis (2)
• Nephropathy (7)
• Neuroaxonal Dystrophy (5)
• Neuronal Ceroid Lipofuscinosis (20)
• Neuronal Degeneration (2)
• Niemann-Pick Disease (5)
• Obesity (1)
• Ocular Squamous Cell Carcinoma (1)
• Osteogenesis Imperfecta (6)
• Overo (1)
• Paroxysmal Dyskinesia (2)
• Paroxysmal Exercise-Induced Dyskinesia (2)
• Persistent Mullerian Duct Syndrome (1)
• Pif Infection Risk Modifier (4)
• Polioencephalopathy (1)
• Polycystic Kidney Disease (6)
• Polydactyly (6)
• Polyneuropathy (9)
• Polysaccharide Storage Myopathy (5)
• Porphyria (8)
• Prekallikrein Deficiency (1)
• Primary Ciliary Dyskinesia (3)
• Primary Hyperoxaluria (2)
• Primary Lens Luxation (1)
• Progressive Retinal Atrophy (40)
• Progressive Rod-Cone Degeneration (1)
• Pyruvate Dehydrogenase Phosphatase Deficiency (1)
• Pyruvate Kinase Deficiency (8)
• Pyruvate Kinase Deficiency Of Erythrocyte (1)
• Renal Cystadenocarcinoma And Nodular Fibrosis (1)
• Respiratory Distress (1)
• Retinal Dysplasia (1)
• Russet (1)
• Sabino (1)
• Scott Syndrome (1)
• Screw Tail (1)
• Severe Combined Immunodeficiency Disease (4)
• Shaking Puppy Syndrome (1)
• Shar-Pei Fever (2)
• Shedding (1)
• Silver (1)
• Skeletal Dysplasia (4)
• Snowdrop (1)
• Speed (1)
• Spinocerebellar Ataxia (3)
• Splashed White (12)
• Spondylocostal Dysostosis (1)
• Spongy Degeneration With Cerebellar Ataxia (2)
• Spotting (3)
• Stargardt Disease (1)
• Startle Disease (3)
• Stationary Night Blindness (2)
• Tabby (6)
• Thrombasthenia (2)
• Thrombocytopenia (2)
• Thrombopathia (3)
• Trapped Neutrophil Syndrome (1)
• Upper Airway Syndrome (1)
• Van Den Ende-Gupta Syndrom (1)
• Ventricular Arrhythmias (1)
• Vitamin D-Deficiency Rickets (6)
• Von Willebrand Disease (6)
• Warmblood Foal Fragility Syndrom (1)
• Xanthinuria (5)