Tracheal Disorders

About the Disease
Tracheal Disease, also known as tracheal diseases, is related to tracheitis and tracheomalacia, and has symptoms including coughing and snoring. An important gene associated with Tracheal Disease is ADAMTSL2 (ADAMTS Like 2), and among its related pathways/superpathways are Embryonic and Induced Pluripotent Stem Cells and Lineage-specific Markers and TGF-beta receptor signaling in skeletal dysplasias. The drugs Dexamethasone acetate and Dexamethasone have been mentioned in the context of this disorder. Affiliated tissues include trachea, lung and heart, and related phenotypes are homeostasis/metabolism and growth/size/body region

Common Targets
ADCY2

Note: If you'd like to get a target analysis report for Tracheal Disorders, 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 Tracheal Disorders at a cost 90% lower than traditional approaches, please feel free to contact us at BD@silexon.ai.

Other Diseases

Congenital Dyserythropoietic Anemia | Hyperinsulinemic Hypoglycemia | Bronchiolitis | Cardiomyopathy, Peripartum | Thrombophlebitis | Angioimmunoblastic T-cell Lymphoma | Cavitary Optic Disc Anomalies | Blepharoconjunctivitis | Urofacial Syndrome | Rotor Syndrome | Cancer, Brain | Coma | Nephroblastoma | Allergic Contact Dermatitis | Ovarian Sex Cord-stromal Tumor | VEXAS Syndrome | Rhabdomyosarcoma | Occipital Neuralgia | Coloboma | Glycogen Storage Disease Type 1b | Spinocerebellar Ataxia Type 23 | Hemangioma | Enhanced S-cone Syndrome | Renal Oncocytoma | Urticaria | Kleine-Levin Syndrome | Skin Carcinoma | 17-beta-hydroxysteroid Dehydrogenase X Deficiency | Strabismus | Bleeding Disorder Due To CalDAG-GEFI Deficiency | Hereditary Coproporphyria | Oligoasthenoteratozoospermia | Ocular Albinism Type 1 | Saethre-Chotzen Syndrome | Atelosteogenesis Type 2 | Cat Eye Syndrome | Hyperammonemia | Cheilitis | Methemoglobinemia Type IV | Intellectual Disability, Autosomal Dominant 5 | Diabetic Macular Edema | Adenoma, Villous | Unverricht-Lundborg Syndrome | Eosinophilic Asthma | Connective Tissue Disorders | Calcium Pyrophosphate Deposition Disease | Cystitis | Netherton Syndrome | Hereditary Hemorrhagic Telangiectasia | Glycogen Storage Disease Type 4 | Polymicrogyria | Portal Vein Thrombosis | Cabezas Syndrome | Becker Muscular Dystrophy | Colitis, Lymphocytic | Creatine Deficiency Syndrome Due To AGAT Deficiency | Multiple Hamartoma Syndrome | Sitosterolemia | Rubinstein-Taybi Syndrome | Cyst | Hyperinsulinism-hyperammonemia Syndrome | Infectious Diarrhea | Spina Bifida | Epidermolysis Bullosa Dystrophica | Epithelioid Hemangioma | Hypobetalipoproteinemias | Ovarian Hyperstimulation Syndrome | Pyoderma Gangrenosum | Acute Chest Syndrome | Pouchitis | Spinocerebellar Ataxia Type 14 | Spinocerebellar Ataxia Type 31 | Proctitis | Bronchitis | Pseudo-pseudohypoparathyroidism | Charcot-Marie-Tooth Disease, Type 2A | Behavioral Variant Of Frontotemporal Dementia | Hepatitis, Alcoholic | Melanocytic Nevus | Mevalonate Kinase Deficiency | Goiter | Thalassemia, Beta | Pierre Robin Syndrome | Hypophosphatasia | Fatty Aldehyde Dehydrogenase Deficiency | Mitochondrial DNA Depletion Syndrome, Encephalomyopathic Form | Mohr-Tranebjaerg Syndrome | Familial Glucocorticoid Deficiency | Anorectal Malformations | Generalized Epilepsy And Paroxysmal Dyskinesia | Chromosome 17q21.31 Deletion Syndrome | Hyperphosphatasia With Intellectual Disability Syndrome 4 | Familial Exudative Vitreoretinopathy | Fabry's Disease | Lipid Metabolism Disorders | Oculocutaneous Albinism | Skin Fragility-woolly Hair Syndrome | Spinocerebellar Ataxia Type 15 | Depression | Esophagitis | Diverticulitis | Pituitary Dwarfism | Eating Disorder | Osteosclerosis | Alpha-mannosidosis | Micro Syndrome | 3-methylglutaconic Aciduria | 3-hydroxy-3-methylglutaryl-CoA Synthase Deficiency | Hypercalciuria | REM Sleep Behavior Disorder | SAPHO Syndrome | Hypodontia | Prurigo Nodularis | Schistosomiasis Mansoni | Chronic Thromboembolic Pulmonary Hypertension | Fukuyama Congenital Muscular Dystrophy | Hypercholesterolemia, Familial | Congenital Heart Defects | Endometritis | Motor Neuron Diseases | Sturge-Weber Syndrome | Primary Progressive Nonfluent Aphasia | Neurofibromatosis-Noonan Syndrome | Homocystinuria | Guillain-Barre Syndrome | Delirium | Hypertelorism | Common Cold | Metabolic Diseases | Keratoacanthoma | Prediabetes | Opisthorchiasis | Neuromyotonia | Medium-chain Acyl-CoA Dehydrogenase Deficiency | Juvenile Myelomonocytic Leukemia | Osteoporosis, Postmenopausal | Adenoid Cystic Carcinoma | Tinea | Fibronectin Glomerulopathy | Congenital Hereditary Endothelial Dystrophy Type I | Primary Carnitine Deficiency | Pancreatitis | Tularemia | Kohlschutter-Tonz Syndrome | Anencephaly | Cholelithiasis | Ureteropelvic Junction Obstruction | Sarcoidosis, Pulmonary | Carcinoma, Transitional Cell | Peyronie's Disease | Keratitis-ichthyosis-deafness Syndrome | NDH Syndrome | Ectrodactyly | Pterygium | Rhabdomyosarcoma, Embryonal | Conn Syndrome | Low Phospholipid Associated Cholelithiasis | Episodic Ataxia Type 2 | Familial Hypobetalipoproteinemia | Ehlers-Danlos Syndrome With Progressive Kyphoscoliosis, Myopathy, And Hearing Loss | Acute Generalized Exanthematous Pustulosis | Autoimmune Polyendocrine Syndrome | Osteomalacia | Platyspondylic Lethal Skeletal Dysplasia, Torrance Type | Congenital Disorders Of Glycosylation | Lymphedema-distichiasis Syndrome | Hemophilia | Ellis-Van Creveld Syndrome | Corneal Neovascularization | Urea Cycle Disorder | Cluster Headache | Blepharitis | Cenani-Lenz Syndactyly Syndrome | Sarcoma, Endometrial Stromal | Spinal And Bulbar Muscular Atrophy | TARP Syndrome | Dyslipidemia | Congenital Myasthenic Syndrome | Atopic Dermatitis | 3C Syndrome | Autoimmune Polyendocrinopathy Syndrome Type I | Retinal Detachment | DOCK8 Immunodeficiency Syndrome | Presbycusis | Atelosteogenesis Type 1 | Osteopathia Striata With Cranial Sclerosis | Primary Pigmented Nodular Adrenocortical Disease | Pulmonary Tuberculosis | Lymphoma, Follicular | Multiple Sclerosis, Primary Progressive | Ocular Hypertension | Cri-du-chat Syndrome | Mitochondrial Cytopathy | Sickle Cell Anemia | Aneurysm, Abdominal Aortic | Osteoporosis | Lichen Planus | Pure Autonomic Failure | Wolfram Syndrome | Klippel-Feil Syndrome | Spinal Muscular Atrophy Type 3 | Rheumatic Heart Disease | Apert Syndrome | Galactosialidosis | Glomerulonephritis, Membranous | Bare Lymphocyte Syndrome | Lymphangioleiomyomatosis | Familial Dysautonomia | Uremia | Influenza | Sporadic Hemiplegic Migraine | Epidermal Nevus Syndrome | Hypercholesterolemia | Meningioma | Harlequin Ichthyosis | Ichthyosis | Partington Syndrome | Kashin-Beck Disease | Hereditary Elliptocytosis | Emery-Dreifuss Muscular Dystrophy | Bainbridge-Ropers Syndrome | Mastitis | Dentinogenesis Imperfecta | Carey-Fineman-Ziter Syndrome | Myositis, Focal | Alpers Syndrome | Congenital Primary Aphakia | IgA Deficiency | Agammaglobulinemia | Cardiospondylocarpofacial Syndrome | Anti-NMDA Receptor Encephalitis | Thin Basement Membrane Disease | Early Infantile Epileptic Encephalopathy 28 | Fowler's Syndrome | Amebiasis | Amenorrhea | Paracoccidioidomycosis | Phenylketonuria II | Glycogen Storage Disease Type 1 | Mitochondrial DNA Depletion Syndrome, Hepatocerebral Form | Marshall-Smith Syndrome | Ectopia Lentis, Isolated, Autosomal Recessive | Hypertrophic Osteoarthropathy, Primary, Autosomal Recessive 2 | Spondylosis | Stroke, Ischemic | Fundus Albipunctatus | Echinococcosis | Combined Malonic And Methylmalonic Acidemia | Cholangitis | Still Disease | Microcephalic Osteodysplastic Primordial Dwarfism, Type II | Neurocutaneous Melanocytosis | Neurofibroma, Plexiform | Carney Triad | Porokeratosis | Melanoma, Uveal | Retinal Diseases | Lymphoma, Primary Cutaneous Anaplastic Large Cell | Fraser Syndrome | Myelitis, Transverse | Torticollis | Trichorhinophalangeal Syndrome | Chondrodysplasia Punctata | Mannosidase Deficiency Diseases | Osmotic Demyelination Syndrome | Goldenhar Syndrome | Gerstmann-Straussler-Scheinker Syndrome | Sleep Disorder | Von Willebrand Disease | Congenital Hemolytic Anemia | Hernia, Inguinal | Astrocytoma | Juvenile Hyaline Fibromatosis | Multiple System Atrophy | Anthrax | Congenital Disorders Of Glycosylation Type II | Auriculocondylar Syndrome | 3-hydroxyacyl-CoA Dehydrogenase Deficiency | Autoimmune Hemolytic Anemia | Amyotrophic Lateral Sclerosis | Periventricular Leukomalacia | Liebenberg Syndrome | Esophageal Adenocarcinoma | Leukoplakia, Oral | Myoclonic Atonic Epilepsy | Leukodystrophies | Pompe Disease | Hydrops Fetalis | Schwartz-Jampel-Aberfeld Syndrome | Hypoalbuminemia | Nasodigitoacoustic Syndrome | Common Variable Immunodeficiency | Craniometaphyseal Dysplasia | Non-Langerhans Cell Histiocytosis | Fontaine Progeroid Syndrome | Spondyloepiphyseal Dysplasia Tarda, X-linked | Hypokalemia | Okihiro Syndrome | Prune Belly Syndrome | Spinocerebellar Ataxia Type 42 | Tyrosinemia | Intracerebral Hemorrhage | Danon Disease | DNA Ligase IV Deficiency | Persistent Hyperplastic Primary Vitreous | Optic Atrophy 2 | Hypertension, Pulmonary | Dowling-Degos Disease | Multifocal Motor Neuropathy | Krabbe Disease | Microphthalmia | Progressive Osseous Heteroplasia | Palmoplantar Keratoderma | Joubert Syndrome | Basal Ganglia Disease | Hypopituitarism | Hyperparathyroidism-jaw Tumor Syndrome | Keratosis, Actinic | Clouston Hidrotic Ectodermal Dysplasia | Thyroid Dyshormonogenesis | Language Disorders | Loeys-Dietz Syndrome Type 4 | Hereditary Spastic Paraplegia | Traboulsi Syndrome | Hyperandrogenemia | Amelanotic Melanoma | Usher Syndrome | Primary Torsion Dystonia | Papilledema | Charcot-Marie-Tooth Disease, Type 2 | Primary Erythromelalgia | Pseudoexfoliation Syndrome | Oligoastrocytoma | Snyder-Robinson Syndrome | Chorea | Thyroid Dysgenesis | Lafora Disease | Aplastic Anemia | Leiomyosarcoma | Conduct Disorder | Angiosarcoma Of The Breast | Combined Deficiency Of Factor V And Factor VIII | Transcobalamin Deficiency | Lassa Fever | Histoplasmosis | Glioblastoma Multiforme | Trigonocephaly | Spinocerebellar Ataxia Type 13 | Diabetes Gestational | Tuberculosis | Absence Epilepsy | Sclerosteosis | Malaria | Centronuclear Myopathy | Chronic Leukemia | Vitelliform Macular Dystrophy | Argininosuccinic Aciduria | Meningococcal Infections | Milk Allergy | Spermatocele | Thrombophilia | Congenital Sodium Diarrhea | Poikiloderma With Neutropenia | Cardiac Arrest | Loeys-Dietz Syndrome | Spinocerebellar Ataxia Type 5 | Nager Acrofacial Dysostosis | IMAGe Syndrome | Cherubism | Ulcerative Colitis | Achromatopsia | Stroke | Focal Segmental Glomerulosclerosis | Neuroma | Transthyretin-related Amyloidosis | Benign Hereditary Chorea | Dyslexia | Peripheral Neuropathy | Majeed Syndrome | Inborn Errors Of Metabolism | CHOPS Syndrome | Kernicterus | Esophageal Carcinoma | Sclerosteosis 2 | Leukocyte Adhesion Deficiency | Maple Syrup Urine Disease | Diabetes Type 1 | Hypospadias | Arteriovenous Malformations | Asphyxia Neonatorum | Orotic Aciduria | Aphasia | Diastrophic Dysplasia | Scapuloperoneal Myopathy, X-linked Dominant | Compartment Syndrome | Hypotonia-cystinuria Syndrome | Hemimegalencephaly | Bursitis | Axenfeld-Rieger Syndrome | Pierson Syndrome