Odonto-onycho-dermal Dysplasia

About the Disease
Odontoonychodermal Dysplasia, also known as odonto-onycho-dermal dysplasia, is related to tooth agenesis and tooth agenesis, selective, 4. An important gene associated with Odontoonychodermal Dysplasia is WNT10A (Wnt Family Member 10A). Affiliated tissues include skin and tongue, and related phenotypes are photophobia and dry skin

Common Targets
WNT10A

Note: If you'd like to get a target analysis report for Odonto-onycho-dermal Dysplasia, or if you are interested to learn how our AI-powered BDE-Chem can design therapeutic molecules to interact with the target(s) above against the disease of Odonto-onycho-dermal Dysplasia at a cost 90% lower than traditional approaches, please feel free to contact us at BD@silexon.ai.

Other Diseases

Perry Syndrome | Herpes Simplex Dermatitis | Donnai-Barrow Syndrome | Cryptococcal Meningitis | Ocular Albinism Type 1 | Thrombocytopenia | Macular Degeneration | Acute Lymphocytic Leukemia | Impetigo | Usher Syndrome Type IIC | Seasonal Mood Disorder | Prurigo Nodularis | Osteoporosis, Postmenopausal | Spondyloarthritis | Postpoliomyelitis Syndrome | 3-M Syndrome | Chediak-Higashi Syndrome | Congenital Diaphragmatic Hernia | Oligoasthenoteratozoospermia | Adenoma, Pituitary | Porokeratosis | Acromesomelic Dysplasia | Thyroid Hormone Resistance | Harlequin Ichthyosis | Fibrosis | Hypolipoproteinemia | Adrenoleukodystrophy, X-linked | Joubert Syndrome | Neurofibromatosis-Noonan Syndrome | Infantile Nephropathic Cystinosis | Spinocerebellar Ataxia Type 27 | Sarcoma | Diabetic Nephropathy | Hyperkalemic Periodic Paralysis | Primary Cutaneous Amyloidosis | ACTH-independent Macronodular Adrenal Hyperplasia | Glaucomatocyclitic Crisis | Oculocutaneous Albinism Type 1 | Hypokalemia | Esthesioneuroblastoma | Cutis Laxa | X-linked Myotubular Myopathy | Discoid Lupus Erythematosus | Renal Hypomagnesemia 3 | Schizoaffective Disorder | Albinism | Hemolytic Uremic Syndrome | Cellulitis | Glycogen Storage Disease Type 4 | Membranous Nephropathy | Blue Nevus | Coffin-Siris Syndrome | Myopathy | Lattice Corneal Dystrophy | Congenital Torticollis | Ocular Surface Squamous Neoplasia | Geleophysic Dysplasia | Lipodystrophy | Focal Segmental Glomerulosclerosis | Anemia | Deafness, Dystonia, And Cerebral Hypomyelination | Combined Pituitary Hormone Deficiency | Parkinsonism | Charcot-Marie-Tooth Disease, Type 2 | Chromosome 16p11.2 Deletion Syndrome | Fabry's Disease | Influenza | Pelvic Inflammatory Disease | Alveolar Capillary Dysplasia | Small Lymphocytic Lymphoma | Dementia | Vertebrobasilar Insufficiency | Alpha-thalassemia Myelodysplasia Syndrome | Arts Syndrome | Hemorrhagic Disorders | Polyarteritis Nodosa | Cerebral Cavernous Malformations | Osteitis | Osteopathia Striata With Cranial Sclerosis | Paraganglioma, Carotid Body | Larsen Syndrome | Multisystemic Smooth Muscle Dysfunction Syndrome | Hypotrichosis Simplex | Neurocysticercosis | Hepatitis B, Chronic | NDH Syndrome | Congenital Tufting Enteropathy | Glycogen Storage Disease Type 0 | Knobloch Syndrome | Heart Block | 5-oxoprolinase Deficiency | Muckle-Wells Syndrome | Retinal Vasculitis | Agranulocytosis | Hennekam Lymphangiectasia-lymphedema Syndrome | Multiple Sclerosis, Primary Progressive | Crohn's Disease | Hypogammaglobulinemia | Large Granular Lymphocytic Leukemia | Angioedema, Hereditary | Osteogenesis Imperfecta Type IV | Long QT Syndrome Type 2 | Rubeosis Iridis | Plasma Cell Dyscrasia | Herpes Genitalis | Cutaneous Lupus Erythematosus | Hypoproteinemia, Hypercatabolic | Macrophagic Myofasciitis | Xeroderma Pigmentosum Variant Type | Spinal Muscular Atrophy With Progressive Myoclonic Epilepsy | Guillain-Barre Syndrome | Shock, Cardiogenic | 3-methylglutaconic Aciduria Type I | Hyperhomocysteinemia | Familial Hypobetalipoproteinemia | Cataract | Pitt-Hopkins Syndrome | Long QT Syndrome Type 1 | Hydrops Fetalis | Sensory Neuropathy | Encephalopathy, Glycine | Mood Disorder | Meningioma, Benign | Hepatic Veno-occlusive Disease | Epidermolysis Bullosa Simplex, Dowling-Meara Type | Turner's Syndrome | Syncope | Tuberculosis | Polymicrogyria | Hemolytic Anemia | Meningitis | Nemaline Myopathy 10 | Blastoma, Pleuropulmonary | Hepatitis E | Pompe Disease | Mandibuloacral Dysplasia With Type A Lipodystrophy | Hereditary Xerocytosis | Antiphospholipid Syndrome | Recurrent Respiratory Papillomatosis | Anthrax | Mitochondrial DNA Depletion Syndrome, Myopathic Form | Proteus Syndrome | Papilloma | Autosomal Recessive Bestrophinopathy | Spondyloepiphyseal Dysplasia Tarda, X-linked | Senior-Loken Syndrome | Marfan Syndrome | Microcephaly, Seizures, And Developmental Delay | Coma | Ichthyosis, X-linked | Trichothiodystrophy | LEOPARD Syndrome | Neutrophilia | Chronic Inflammatory Demyelinating Polyneuropathy | Erdheim-Chester Disease | SAPHO Syndrome | Acute Leukemia | Neural Tube Defect | Osteoporosis | Hyperphenylalaninemia | Open-angle Glaucoma | Ureteropelvic Junction Obstruction | Beta-Propeller Protein-associated Neurodegeneration | Multiple System Atrophy | Hyperglycemia | Pulmonary Veno-occlusive Disease | Fucosidosis | Disseminated Superficial Actinic Porokeratosis | Tendinopathy | Proteasome-associated Autoinflammatory Syndrome 2 | Non-Hodgkin Lymphoma | Dengue Shock Syndrome | Saethre-Chotzen Syndrome | Hyperparathyroidism-jaw Tumor Syndrome | Hypotrichosis | Non-small Cell Lung Cancer | Thrombophilia | Spondylolisthesis | Chronic Leukemia | Neurocutaneous Syndromes | Dysgerminoma | Skin Fragility-woolly Hair Syndrome | Ventricular Septal Defect | Hypoplastic Left Heart Syndrome | Bipolar Disorder | Lafora Disease | Bronchitis | Congenital Nephrotic Syndrome | Allergic Contact Dermatitis | Venous Insufficiency | Generalized Epilepsy And Paroxysmal Dyskinesia | Epidermolysis Bullosa Acquisita | Megacystis-microcolon-intestinal Hypoperistalsis Syndrome | Zollinger-Ellison Syndrome | Shwachman-Bodian-Diamond Syndrome | Hypopigmentation | Pontocerebellar Hypoplasia | Anencephaly | Bone Giant Cell Tumor | Endophthalmitis | Hyperparathyroidism | Common Cold | Anxiety Disorders | Coronary Heart Disease | Carbonic Anhydrase VA Deficiency | Angioedema, Acquired | Cryopyrin-associated Periodic Syndromes | Achromatopsia | Heroin Dependence | Meier-Gorlin Syndrome | Cancer, Breast | Giant Cell Glioblastoma | Aplasia Cutis Congenita | Li-Fraumeni Syndrome | Microcephalic Osteodysplastic Primordial Dwarfism, Type I | Retinal Telangiectasia | Menetrier Disease | Compartment Syndrome | Poirier-Bienvenu Neurodevelopmental Syndrome | Danon Disease | Schuurs-Hoeijmakers Syndrome | Pneumothorax | Melanocytic Nevus | Neuroblastoma | Adenomyosis | Usher Syndrome | Whipple's Disease | Chondroma | Osteoporosis-pseudoglioma Syndrome | Syndactyly | Hypersensitivity Pneumonitis | Hereditary Multiple Exostoses | Epiphyseal Chondrodysplasia, Miura Type | Enhanced S-cone Syndrome | Apraxia | Glaucoma, Congenital | Cone Dystrophy | Lyme Disease | Renal Failure | Hypoparathyroidism | Multiple Hamartoma Syndrome | Gilbert Syndrome | Lymphoma, AIDS-related | Intestinal Pseudo-obstruction | Waardenburg Syndrome Type 4 | Robinow Syndrome | Hepatorenal Syndrome | Exocrine Pancreatic Insufficiency | Guttate Psoriasis | Lactose Intolerance | Renpenning Syndrome | Spinocerebellar Ataxia Type 20 | Myasthenia | Hemochromatosis Type 1 | CDKL5 Deficiency Disorder | Filariasis | Hereditary Inclusion Body Myopathy | Vitamin D Deficiency | Hemolytic Uremic Syndrome, Atypical | Dermatitis Herpetiformis | Parvovirus B19 Infection | Porphyria, Variegate | Non-Langerhans Cell Histiocytosis | Polycythemia Vera | Arteriovenous Malformations | Paronychia | Muscle Wasting | Uremic Pruritus | Hypercalcemia | Sandhoff Disease | Duane Retraction Syndrome | Cerebellofaciodental Syndrome | Eclampsia | Platelet Disorders | Ehlers-Danlos Syndrome With Progressive Kyphoscoliosis, Myopathy, And Hearing Loss | Fahr Disease | Common Variable Immunodeficiency | Congenital Heart Defects | Eating Disorder | Alpha-1 Antitrypsin Deficiency | Light Chain Amyloidosis | Non-proliferative Diabetic Retinopathy | Agoraphobia | Hypophosphatemic Rickets, Autosomal Recessive, 1 | Seborrheic Dermatitis | Pain | Chordoid Glioma | Chromosome 8q21.11 Deletion Syndrome | Proximal Symphalangism | 6-pyruvoyl-tetrahydropterin Synthase Deficiency | Eczema | N-acetylglutamate Synthase Deficiency | Congenital Myopathy | Micro Syndrome | Hyperthermia, Malignant | Chiari Malformation Type I | GLUT1 Deficiency Syndrome | Motor Neuron Diseases | Angiosarcoma Of The Breast | Norrie Disease | Mountain Sickness | Ophthalmia, Sympathetic | Anti-NMDA Receptor Encephalitis | Epithelial-myoepithelial Carcinoma | Hyperparathyroidism, Primary | Neurodegeneration Due To Cerebral Folate Transport Deficiency | Mitochondrial Encephalomyopathy | Central Retinal Artery Occlusion | Thrombocythemia, Essential | Pernicious Anemia | Bruck Syndrome | Chronic Granulomatous Disease, X-linked | Diabetes Insipidus, Nephrogenic | Thalassemia, Beta | Adrenomyeloneuropathy | Chorioretinitis | Spinocerebellar Ataxia Type 13 | ICF Syndrome | Canavan Disease | Spinocerebellar Ataxia Type 38 | Poikiloderma With Neutropenia | Urea Cycle Disorder | Gastroschisis | Carcinoid Tumor | Brachydactyly | Scapuloperoneal Spinal Muscular Atrophy | Hidradenitis Suppurativa | Veno-occlusive Disease | Pityriasis Rubra Pilaris | Autosomal Recessive Spastic Paraplegia Type 75 | Astrocytoma | Primary Biliary Cholangitis | Chronic Thromboembolic Pulmonary Hypertension | DEND Syndrome | Fetal Akinesia Deformation Sequence | Hepatic Adenomatosis | Encephalocele | Werner's Syndrome | Cyst | Dowling-Degos Disease | Palmoplantar Keratoderma | Leishmaniasis, Visceral | Xeroderma Pigmentosum | Melanoma | Malaria | Anuria | Kernicterus | Early Infantile Epileptic Encephalopathy 28 | Hereditary Pyropoikilocytosis | Pseudoachondroplasia | Amelogenesis Imperfecta | Spondylometaphyseal Dysplasia | Myositis, Focal | Ocular Hypertension | Antisynthetase Syndrome | Imerslund-Grasbeck Syndrome | Metabolic Diseases | Antenatal Bartter Syndrome Type 1 | Neovascular Glaucoma | Primary Carnitine Deficiency | Cholestasis, Intrahepatic | Kaposi Sarcoma | Spastic Paraplegia Type 7 | Calcium Pyrophosphate Deposition Disease | Rhabdomyosarcoma, Alveolar | Spinocerebellar Ataxia Type 12 | Wagner Disease | Patent Ductus Arteriosus | Methemoglobinemia Type IV | Communication Disorders | Lamellar Ichthyosis | Pseudohypoparathyroidism Type 2 | Weill-Marchesani Syndrome | Stargardt Disease | Toxic Epidermal Necrolysis | Chondrosarcoma | Spinocerebellar Ataxia Type 23 | Astigmatism | Angioimmunoblastic T-cell Lymphoma | Galactosemia | Clouston Hidrotic Ectodermal Dysplasia | Sulfite Oxidase Deficiency | Raine Syndrome | Erysipelas | Wiedemann-Steiner Syndrome | Netherton Syndrome | Trichuriasis | Adams-Oliver Syndrome | Juvenile Myelomonocytic Leukemia | Hypervalinemia | Glomerulonephritis, Membranous | Pituitary Stalk Interruption Syndrome | Pure Autonomic Failure | DiGeorge Syndrome | Aneurysm, Abdominal Aortic | Cutaneous T-cell Lymphoma | Gingivitis | Platyspondylic Lethal Skeletal Dysplasia, Torrance Type | Limb Girdle Muscular Dystrophy | Ectodermal Dysplasia