Inherited diseases in dogs

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- Make Selection - Affenpinscher Afghan Hound Airedale Terrier Akita Alaskan Husky Alaskan Malamute Alaskan sled dog American Bulldog American Eskimo dog American Foxhound American Staffordshire Terrier Anatolian Shepherd Dog Australian Cattle Dog Australian Kelpie Australian Shepherd Australian Silky Terrier Basenji Basset Griffon Vendeen Basset Hound Bavarian Mountain Dog Beagle Bearded Collie Beauceron Bedlington Terrier Belgian Shepherd (Groenendael, also known as Belgian sheepdog)) Belgian Shepherd (Malanois) Belgian Shepherd (Tervueren) Berger Picard Bernese Mountain Dog Bichon Frise Black Russian Terrier Bloodhound Blue Heeler Bluetick Hound Boerboel Border Collie Border Terrier Borzoi Boston Terrier Bouvier des Flandres Boxer Boykin Spaniel Briard Briquet Griffon Vendeen Brittany Spaniel Brussels Griffon Bull Terrier Bull Terrier (miniature) Bulldog Bullmastiff (or Bull Mastiff) Cairn Terrier Canaan Dog Cane Corso Mastiff Cardigan Welsh Corgi Carelian Bear Dog Catahoula Leopard Dog Cavalier King Charles Spaniel Chihuahua Chinese Crested Chinook Chow Chow Collie Collie (Rough) Collie (Smooth) Coonhound (Black and Tan) Coonhound Coton de Tulear Dachshund Dachshund (and Miniature Long Haired Dachshund) Dachshund (Dappled) Dachshund (Longhaired) Dachshund (Minature) Dachshund (Miniature Long Haired) Dachshund (Wire-haired) Dachshund (miniature wire haired) Dachshund (Rough coated) Dalmatian Dandie Dinmont Terrier Danish-Swedish Farm Hound Dobermann Doberman Pinscher Dogo Argentino Dogue de Bordeaux Drever Hunting Dog Drentse Partrijshond Dunker Elo English Bulldog English Mastiff English Setter Entlebucher mountain dog Eskimo spitz Estrela mountain dog Eurasian Fila Brasiliero Finnish Harrier Finnish Lapphund Finnish Spitz Flat-coated Retriever Foxhound (American) Foxhound (English) Fox Terrier Fox Terrier (toy) French Bulldog Gammel Dansk Honsehund Garafiano Shepherd German Pinscher German Shepherd German Shorthaired Pointer German Spitz (Klein) German Spitz (Mittel) German Wirehaired Pointer Giant Schnauzer Glen of Imaal Terrier Gordon Setter Grand Basset Griffon Vendeen Great Dane Great Dane (Harlequin) Great Pyrenees Greater Swiss Mountain Dog Greyhound Greyhound (piebald) Griffon Bruxellois Havanese Hovawart Hungarian Kuvasz Hungarian Puli Hygenhund Ibizan Hound Irish Red & White Setter Irish Setter Irish Setter x Poodle Irish Terrier Irish Wolfhound Italian Greyhound Italian Griffin Italian Spinone Jack Russell Terrier Jagdterrier Japanese Chin Japanese Spaniel Japanese Spitz Karabash Keeshond Kerry Blue Terrier King Charles Spaniel Komondorok Kooikerhondje (Dutch Kooiker) Korean Jindo Kromfohrlander Lakeland Terrier Lancashire Heeler Landseer Lagotto Romagnolo Lapland Spitz Lapponian Herder Large Munsterlander Leonberger Lhasa Apso Long Haired Whippet Lowchen Lundehund Maltese Manchester Terrier Many Breeds Mastiff Mexican Hairless Mixed breed dog Munsterlander Neapolitan Mastiff Newfoundland New Zealand Huntaway Norfolk Terrier Norwegian Buhund Norwegian Dunkerhound Norwegian Elkhound Norwegian Spitz Norwich Terrier Nova Scotia Duck-Tolling Retriever Old Danish Pointing Dog Old English Sheepdog Old English Shepherd Ormskirk Terrier Others Otterhound Papillon Parson Russell Terrier Patterdale Terrier Pekingese Pembroke Welsh Corgi Pharoah Hound Pinscher (German) Pinscher (Miniature) Pit Bull mixed breed Pit Bull Terrier Plott Hound Pointer (English, short haired) Pointer (German, wire haired) Pointer Polish Owczarec Nizinny (PON) Pomeranian Poodle Poodle (mainly minature and toy) Poodle (miniature and toy) Poodle (miniature) Poodle (standard) Poodle (standard, miniature and toy) Poodle (toy) Portuguese Podenco Portuguese Water Dog Pug Pyrenean Mountain Dog Pyrenean Sheepdog (Pyrenees Shepherd Dog) Rat terrier Retriever (Chesapeake Bay) Retriever (Curly Coated) Retriever (Golden) Retriever (Labrador) Rhodesian Ridgeback Rottweiler Russian Terrier Saint Bernard Saluki Samoyed Sapsaree Schappendoes Schipperke Schnauzer Schnauzer (Giant and Standard) Schnauzer (miniature) Scottish Deerhound Scottish Terrier Sealyham Terrier Shar Pei Shetland Sheepdog Shiba Dog Shiba Inu Shih Tzu Shropshire Terrier Siberian Husky Silken Windhound Skye Terrier Sloughi Dog (Arabian Greyhound) Smooth Fox Terrier Soft Coated Wheaton Terrier Spaniel (American Cocker) Spaniel (Clumber) Spaniel (Cocker) Spaniel (English Cocker -AKC recognised) Spaniel (English Springer) Spaniel (French) Spaniel (Irish Water) Spaniel (Japanese) Spaniel (Sussex) Spaniel (Welsh Springer) Spanish Catalan sheepdog Spanish Picard Spanish water dog Spinoni Italiano Spitz Staffordshire Bull Terrier Swedish Elkhound Swedish Lapland Dog Swedish Lapphund Swedish Vallhund Sydney Silkie Terrier Tibetan Mastiff Tibetan Spaniel Tibetan Terrier Vizsla Weimaraner Welsh Terrier West Highland White Terrier Whippet White Swiss Shepherd Wire Haired Fox Terrier Yorkshire Terrier   

 

or you can browse by genetic anomaly:

- Make Selection - Absence of optic chiasma Acepromazine sensitivity Achalasia Achondrogenesis Achondroplasia Achromatopsia type 3 Acinar atrophy Acne vulgaris Acral mutilation Addison’s disease Adrenal gland dysplasia Adrenal hyperplasia Afibrinogenaemia Afibrinogenemia Aging Aggressive temperament Aggression Alabama rot Alexander disease Alopecia Alopecia X Alport syndrome Amblyopia Amyloidosis Anaemia Anemia Aniridia Ankyloglossia Anury (absence of tail) Aortic aneurysm Aortic stenosis Arnold-Chiari malformation Arteritis Aseptic meningitis Asthma Ataxia and myelopathy Atherosclerosis Atopic dermatitis Atrial septal defect Atrioventricular heart block Attention deficit disorder Autoimmune disorders (multiple) Autoimmune haemolytic anaemia Autoimmune polyendocrine syndrome (APS) Autoimmune thyroiditis Axonal neuropathy Basset thrombopathia B-cell non-Hodgkin's lymphoma Beagle pain syndrome Beta adrenoreceptor insensitivity Bilateral sensorial deafness Birt-Hogg-Dube syndrome Black hair follicular dysplasia Black skin disease Blindness with ocular developmental anomalies Bloat Blue-eye Bob-tail trait Brachycephalic airway syndrome Brachycephaly Brachygnathia Brachyury Bradyarrhythmia Brittle bone disease Calcinosis circumscripta Calcium excess mediated bone disease Cancer Canine adenovirus type 1 (CAV1) sensitivity Canine hereditary multi-systems atrophy (CHMSA) Canine leukocyte adhesion deficiency (CLAD) Canine motor neurone disease Canine multifocal retinopathy (cmr1) Canine multifocal retinopathy (cmr2) Canine multifocal retinopathy (cmr3) Cardiac arrhythmias Cardiac valvular defects Cardiomyopathy Caroli's disease Carpus subluxation Catalase deficiency Cataract Central core myopathy Centronuclear myopathy (cnm) Cerebellar abiotrophy Cerebellar and cerebral cortical degeneration Cerebellar ataxia Cerebellar ataxia - extrapyramidal abiotrophy Cerebellar cortical abiotrophies Cerebellar degeneration Cerebellar degeneration (immune mediated) Ceroid lipofuscinosis Ceroid lipofuscinosis type 2 Ceroid lipofuscinosis (ceroidal retinal degeneration) Cervical disc prolapse Charcot-Marie-Tooth disease Cherry Eye Chondrodysplasia Chondrodystrophia Choroidal hypoplasia Chronic pancreatitis Chronic superficial keratitis Chronic superficial keratitis of the cornea Chronic valvular disease Chylothorax Ciliary dyskinesia Ciliary dyskinesia (Kartagener’s syndrome) Cleft palate Clotting disorder Cobalamin malabsorption Coeliac disease Collie eye anomaly (CEA) Colour dilution alopecia (CDA) Cone-rod dystrophy Congenital adrenal hyperplasia syndrome Comedones Common variable immunodeficiency Complement (C3) deficiency Cone degeneration (cd) Congenital sensorineural deafness Congenital sensorineural deafness with microphthalmia Congenital Stationary Night Blindness (CSNB) Conotruncal defect Conjunctivitis Coonhound paralysis Copper associated liver disease Copper toxicosis Cori disease Corneal dystrophy Corneal endothelial dystrophy Corneal oedema Corneal ulcers Cornification and multiple congenital defects Cornification defect Cornifying epithelioma (Keratocanthoma) Cranial cruciate ligament rupture Cranio-mandibular osteopathy Cranioschisis Cricopharyngeal achalasia Cricopharangeal dysfunction Cryptorchidism Cushing syndrome (congenital) Cutaneous asthenia (Ehlers Danlos syndrome) Cutaneous lupus erythematosis Cutaneous vasculopathy Cyclic hematopoiesis Cyclic neutropenia Cysteine and urate uroliths Cystic bone lesions Cystic Kidney disease Cystine and urate uroliths Cystinuria Dancing Doberman disease Degenerative encephalomyelopathy Degenerative myelopathy Demodicosis Demyelination Dermatitis Dermatofibrosis (nodular) Dermatomyositis Dewclaw D-glyceric acidurea D-glycericacidaemia D-glycerate kinase deficiency Diabetes Diabetes mellitus Diabetes mellitus (gestational) Diabetes insipidus Dilated cardiomyopathy Displaced canine teeth Distal myopathy Distal polyneuropathy Distichiasis Doberman hepatitis Double Muscling Dry eye Dwarfism: pseudoachondroplastic dysplasia Dyskinesia Dyskinesia in pups Dysphagia Dysraphic spine Dystocia Ear Inflammation Ectodermal dysplasia Ectopia lentis Ectopic ureters Ectrodactyly Ehlers Danlos syndrome Elbow deformity Elbow dysplasia Elbow incongruity Elliptocytosis Emphysema with bronchial hypoplasia Encephalitis Encephalomyelopathy Entropion Epidermolysis bullosa Epilepsy Episodic Falling episodic Head TremorEssential hypertension Everted membrane nictitans Exercise induced collapse Exocrine pancreatic insufficiency Factor I (Fibrinogen) deficiency Factor II (Prothrombin) deficiency Factor VII (Proconvertin) deficiency Factor X (Stuart-Prower Factor) deficiency Factor XI (Plasma Thromboplastin Antecedent) deficiency Factor XII (Hageman Factor) deficiency Familial focal seizures Familial nephropathy Familial renal disease Fanconi syndrome Fibrodysplasia Ossificans Fibrinoid Leukodystrophy Fibrosarcoma Forbes disease Fractures of humeral condyle Fucosidosis (alpha) Galactocerebrosidosis Galactosialidosis Gastric carcinoma Gastric dilatation/ volvulus Gastropathy Gaucher’s disease I Generalised tremor Giant axonal neuropathy Gingival hypertrophy Glanzmann’s-type I thrombasthenia Glaucoma Glaucoma - pigmentary Glaucoma - secondary Glaucoma with ciliary body cysts Globoid cell leukodystrophy Glomerulonephropathy Glomerulonephritis Glucosuria Glutathione-S-Transferase deficiency Gluten sensitive enteropathy Glycogen storage disease Ia Glycogen storage disease II Glycogen storage disease type IIIa Glycogen storage disease IV Glycogen storage disease VII, (Phosphofructokinase deficiency) GM1 gangliosidosis GM2 gangliosidosis GM2 gangliosidosis (type AB) (Tay Sachs disease, AB variant) GM2 gangliosidosis (type B) (Sandhoff disease) Goniodysgenesis Granulomatous sebaceous adenitis GSTT1 deficiency Grey matter spongy degeneration Guillaine Barre syndrome Haemophilia A Haemophilia B Hair loss Hairless, defective teeth Hairless, small litter size Halothane sensitivity Hemeralopia Hemimelia Hemivertebrae Hemophagocytic histiocytic sarcoma Hemophilia Hepatitis (chronic active) Hepatocerebellar degeneration Hepatoportal microvascular dysplasia Hereditary ataxia Hereditary myelopathy Hereditary myopathy Hereditary necrotizing myelopathy Hereditary nephritis Hereditary polyneuropathy Hereditary spinal muscular atrophy (“Canine motor neurone disease”) Hereditary ventricular tachycardia Hexosaminidase B deficiency High K erythrocytes Hindlimb lameness Hip dysplasia Histiocytic sarcoma Histiocytic ulcerative colitis Horner’s syndrome Hunter syndrome Hurler-Scheie syndrome Hyaluronan accumulation Hydroxyglutaric acidurea (1-2-HGA) Hydrocephalus and hypertrichosis Hydronephrosis Hyperadrenocorticism Hypercalcemia Hyperlipidaemia Hyperlipoproteinaemia Hyperparathyroidism and renal cortical hypoplasia Hyperparathyroidism and renal cortical hypoplasia (juvenile) Hyperparathyroidism- neoplasia Hyperphosphatasemia Hypertonic myopathies Hypertonic myopathies (Scotty Cramp) Hypertrophic cardiomyopathy Hypertrophic neuropathy Hypertrophic osteodystrophy/ hydroxylapetite deposition disease Hyperuricosuria Hypoadrenocorticism Hypochondrodysplasia Hypochondroplastic dwarfism Hypofibrinogenemia Hypofibrinogenaemia Hypomyelinating neuropathy Hypomyelination Hypospadias Hypothyroidism Hypothyroidism with hyperlipoproteinaemia Hypothyroidism with hypomyelination Ichthyosis Idiopathic haemorrhagic pericardial effusion Idiopathic polyneuropathy Idiopathic thrombocytopenic purpura (ITP) IgA deficiency IgA deficiency – inflammatory enteropathy Imerslund-Grasbeck syndrome Immune mediated thrombocytopenia Immunodeficiency syndrome Immunodeficient dwarfism Immunoproliferative enteropathy Incomplete ossification of humeral condyle Infertility Inflammatory bowel disease Intradural haemorrhage Intradural vasculitis Interdog dominance aggression Interstitial lung disease Intervertebral disc calcification Intervertebral disc herniation Intraocular xanthogranuloma Intrinsic platelet function defect Iris cysts Ivermectin sensitivity Juvenile dilated cardiomyopathy Juvenile myopathy Juvenile nephropathy Juvenile onset polyarthritis Juvenile polyarteritis Juvenile renal disease Kartagener’s syndrome Keratoconjunctivitis sicca Keratinisation defect Kidney stones Knee problems Knobbed acrosome defect Knock knees Krabbe disease Lafora's disease Laryngeal paralysis Laryngeal paralysis-polyneuropathy Leber congenital amaurosis Legg-Calve Perthe disease Leishmania susceptibility Lens luxation Lentiginosis profusa Lethal acrodermatitis Lethal astrocytosis Leukodystrophy Leukoencephalo-myelopathy Leukopenia Lipid storage disease (Wolman disease) Lissencephaly Lobster Claw Deformity Longevity Lower motor neuron disease Low Glutathione-S-Transferase Lumbosacral osteochondrosis Lung lobe torsion Lymphocytic thyroiditis Lymphoedema Lymphoma Lymphosarcoma Malignant histiocytosis Malignant hyperthermia Masticatory muscle myositis Medullary thyroid carcinoma Megaoesophagus Meningoencephalitis Metaphyseal osteopathy Microphthalmia and anterior segment defects Microphthalmia with coloboma Microphthalmia with multiple ocular defects Mitochondrial encephalomyopathy Mitochondrial myopathy Mitral (left atrio-ventricular) valve defects Mitral (left atrio-ventricular) valve dysplasia Mitral stenosis Motor neuron abiotrophy Mucinosis Mucopolysaccharidosis I (Hurler-Scheie syndrome) Mucopolysaccharidosis II (Hunter syndrome) Mucopolysaccharidosis IIIa (Sanfilippo syndrome) Mucopolysaccharidosis IIIb (Sanfilippo syndrome) Mucopolysaccharidosis VI (Maroteaux-Lamy syndrome) Mucopolysaccharidosis VII (Sly syndrome) Multicentric lymphoma Multifocal retinal dysplasia (no skeletal deformities) Multifocal retinal dysplasia with skeletal abnormalities (Oculo-skeletal dysplasia) Multifocal bullous retinopathy Multifocal retinopathy Multiple endocine diseases Multiple epiphyseal dysplasia Multiple ocular defects Muscular dystrophy Muscle hypertonicity Musladin-Leuke Syndrome Myasthenia gravis Myoclonus epilepsy Myopathy Myopathy and neuropathy Myopia Myotonia Myotonic dystrophy Myotonic myopathy Narcolepsy Nasal dermatitis Nasal parakeratosis Necrosis of femoral head (Legg-Calve-Perthe disease) Necrotizing encephalitis Necrotizing meningoencephalomyelitis Nemaline rod myopathy Neonatal encephalopathy with seizures Neoplasia - cutaneous melanoma Neoplasia - glioma Neoplasia - haemangioma & haemangiosarcoma Neoplasia - histiocytosis Neoplasia - mammary carcinoma Neoplasia - Mammary tumours Neoplasia - mast cell tumour Neoplasia - oral melanoma Neoplasia - osteosarcoma Neoplasia - soft tissue sarcoma Neoplasia - squamous cell carcinoma Neoplasia, various Nephropathy (juvenile) Nervousness Neural Tube Defect Neuroaxonal dystrophy (NAD) Neurodegeneration Neurogenic muscular atrophy Neuronal abiotrophy Neuronal ceroid lipofuscinosis Neuronal vacuolation Neutrophil defect Niemann-Pick disease Type A/B Niemann-Pick disease Type C Non-Hodgkin's lymphoma Nonspherocytic hemolysis Ocular dermoid cysts Ocular melanosis Oculo-skeletal dysplasia, drd1 Oculo-skeletal dysplasia, drd2 Oculo-skeletal-heamatological syndrome Oligodendroglial dystrophy Oligodontia Onychodystrophy Optic nerve hypoplasia Osmotic fragility Osteoarthrosis Osteochondrodysplasia Osteochondromatosis Osteochondrosis dissecans, shoulder Osteochondrosis dissecans, shoulder & stifle joints Osteochondrosis of lateral trochlear ridge Osteogenesis imperfecta Otitis externa Overshot jaw Oxalate nephropathy Palmoplantar hyperkeratosis Pancreatic acinar atrophy Pancreatitis Panniculitis Pannus Paroxysmal dystonic choreoathetosis Paroxysmal seizures Patent ductus arteriosus Patellar luxation Pectus excavatum Pectinate ligament dyplasia Pelger-Huet anomaly Pemphigus foliaceus Pericardial mesothelioma Peripheral (femoral) artery occlusive disease Peripheral neuropathy Perivasculitis Persistent hyaloid remnants Persistent hyperplastic primary vitreous (PHPV) Persistent hyperplastic primary vitreous (PHPV)/Persistent hyperplastica tunica vasculosa lentis (PHTVL) Persistent hyperplastic tunic vasculosa lentis (PHTVL) Persistent Mullerian duct syndrome (PMDS) Persistent pupillary membranes Persistent right aortic arch Persistent scratching Pharmacogenetic abnormalities Pigmentary glaucoma Pituitary dependent hyperadrenocorticism Pituitary dwarfism (combined pituitary hormone deficiency) Platelet mediated bleeding disorder (Scott's syndrome) Platelet storage pool defect (with cyclic neutropenia) Pneumocystis pneumonia Polioencephalomyelopathy Polycystic kidney and liver disease Polycystic kidney disease Polydactyly Polydactyly and skeletal and soft tissue abnormalities Polydactyly and skeletal malformations Polyglucosan body disease Polyneuropathy Polyradiculoneuritis Pompe disease Portosystemic shunt Primary familial hyperphosphatasemia Primary glaucoma Primary hyperoxaluria type 1 Primary hypertension Primary open angle glaucoma Primary orthostatic tremor Primary sensory neuropathy Progressive axonopathy Progressive hereditary nephritis Progressive paralysis and dementia (Alexander Disease) Progressive Retinal Atrophy Progressive Retinal Atrophy - cone rod dystrophy Progressive Retinal Atrophy – early retinal degeneration (erd) Progressive Retinal Atrophy of late onset Progressive Retinal Atrophy – photoreceptor dysplasia (pd) Progressive Retinal Atrophy- probably as rod-cone dystrophy type 1 (rcd1) Progressive Retinal Atrophy – progressive rod cone degeneration (prcd) Progressive Retinal Atrophy – rod-cone dystrophy type 2 (rcd2) Progressive Retinal Atrophy – rod-cone dystrophy type 3 (rcd3) Progressive Retinal Atrophy – X-linked progressive retinal atrophy Progressive Retinal Atrophy (retinal pigment epithelium dystrophy) Progressive Rod Cone Degeneration Protein losing enteropathy (PLE) Protein losing nephropathy (PLN) Pseudoachondroplasia Psychomotor retardation Pulmonary fibrosis Pulmonary hypertension Pulmonary Oedema Pulmonic stenosis Pyoderma (skin infections) Pyometra Pyruvate kinase deficiency Quadriplegia Rage Syndrome Renal amyloidosis Renal calculi Renal cystadenocarcinoma and nodular dermatofibrosis Renal dysplasia Renal vasculopathy Respiratory distress syndrome Retinal dysplasia Retinal dysplasia (multifocal, mrd) Retinal dysplasia/degeneration - ceroid lipofuscinosis Retinal Ganglion cell distribution Retinal pigment epithelium dystrophy Rhinitis Sacral osteochondrosis Sandhoff disease Sanfilippo syndrome Sarcoma Schisis Scott's syndrome Sebaceous adenitis Sebacious gland hyperplasia Seborrhoea Seborrhoea (primary) See-saw nystagmus Seizures: malonic acidurea Selective intestinal cobalamin malabsorption Sensorial deafness Sensorineural deafness Sensory axonopathy Severe combined immunodeficiency (SCID) Shaking pup Shar Pei Fever Sick sinus syndrome Siezures (partial) Skin and hair abnormalities Sly syndrome Sodium thiopentane sensitivity Solid intraocular xanthogranuloma Spectrin Deficiency Spherocytosis Spina bifida Spinal cerebellar degeneration Spinal muscular atrophy Spinocerebellar ataxia Spondyloarthrosis Spondylo-epithelial dysplasia Spondylolithesis Spongiform degeneration Spontaneous chronic corneal epithelial defects (SCCED) Spontaneous hypertension Sry –ve sex reversal Stenosis of the bundle of His Stiff Skin Syndrome Stomatocytosis Stomatocytosis with chondrodysplasia Stomatocytosis with hypertrophic gastritis Subacute necrotizing encephalopathy Subaortic stenosis Sudden Acquired Retinal Degeneration Syndrome Sudden death syndrome Superficial stromal keratitis Symmetrical Lupoid Onychodystrophy Syringomelia Syringohydromelia Systemic lupus erythematosis Tail chasing Tapetal degeneration Taurine deficiency Tay-Sachs disease T-cell non-Hodgkin's lymphoma Telangiectasia Tetralogy of Falot Thiopurine-S-Methyltransferase deficiency Thrombocytopenia Thrombopathy Thrombopathy: delta storage pool defect Thyroiditis Tied tongue Tracheal collapse Trapped neutrophil syndrome Tremor syndrome: central axonopathy Tricuspid (right atrio-ventricular) valve dysplasia Tubular transport dysfunction “Fanconi’s syndrome” Type 1 von Willebrand disease Type 2 von Willebrand disease Type 3 von Willebrand disease Urate urolithiasis Urinary incontinence Uroliths (cystine) Uroliths (struvite, oxalate, other) Uveodermatological syndrome Vasculitis Ventricular arrhythmia Ventricular septal defect Vitiligo Vitreous degeneration von Gierke disease von Willebrand's disease (Type I) von Willebrand's disease (Type II) von Willebrand's disease (Type III) Vogt-Koyanagi-Harada syndrome Westie Lung Disease White matter spongy degeneration Wobbler syndrome Xanthinuria X-linked myopathy: muscular dystrophy X-Linked Progressive Retinal Atrophy XLPRA1 X-linked Progressive Retinal Atrophy XLPRA2 X-linked severe combined immunodeficiency Zinc responsive dermatosis   

 

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