Disease

VEXAS Syndrome

About the Disease
Vexas Syndrome, also known as vexas, is related to neutrophilic dermatosis, acute febrile and plasma cell neoplasm. An important gene associated with Vexas Syndrome is UBA1 (Ubiquitin Like Modifier Activating Enzyme 1), and among its related pathways/superpathways is Parkinson's disease pathway. The drugs Mycophenolic acid and Cyclophosphamide have been mentioned in the context of this disorder. Affiliated tissues include bone marrow, myeloid and skin, and related phenotypes are pulmonary infiltrates and recurrent fever

Common Targets
UBA1

疾病靶点研报
VEXAS Syndrome

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

Other Diseases

Walker-Warburg Syndrome | Turner's Syndrome | Hairy Cell Leukemia | Fanconi Syndrome | Papillorenal Syndrome | Castleman Disease | Bethlem Myopathy | Nephropathy | Crohn's Disease | Oculocutaneous Albinism Type 1 | Polymicrogyria | Cold Agglutinin Disease | Evans Syndrome | Narcolepsy | Neuroblastoma | Spinocerebellar Ataxia Type 38 | Familial Advanced Sleep Phase Syndrome | Retinitis Pigmentosa 3 | Congenital Dyserythropoietic Anemia Type 1 | Glutaric Aciduria Type 1 | Leishmaniasis, Visceral | Basal Ganglia Cerebrovascular Disease | Autosomal Recessive Congenital Ichthyosis | Cerebellofaciodental Syndrome | Chronic Granulomatous Disease | Chronic Granulomatous Disease, X-linked | Birk-Barel Syndrome | Cantu Syndrome | Relapsing Polychondritis | Ectodermal Dysplasia | Mast Cell Leukemia | Blastomycosis | Majeed Syndrome | Myofibrillar Myopathy | Pierson Syndrome | Endocarditis | Fabry's Disease | Johanson-Blizzard Syndrome | Megaloblastic Anemia | Nemaline Myopathy 8 | Obesity | Keratoacanthoma | Epidermolytic Hyperkeratosis | Primary Progressive Aphasia | Hypertrophy | Hypersomnia | Osteoarthritis | Papilloma | 5-oxoprolinase Deficiency | Peroxisomal Disorder | Epidermodysplasia Verruciformis | Tatton-Brown-Rahman Syndrome | Coloboma | Hepatitis, Alcoholic | Chronic Thromboembolic Pulmonary Hypertension | Hypoparathyroidism | Methylmalonic Acidemia | Diabetes Type 1 | Menetrier Disease | Lissencephaly 2 | Glycogen Storage Disease Type 0 | Tyrosine Hydroxylase Deficiency | Pyruvate Decarboxylase Deficiency | Oculodentodigital Dysplasia | Stiff-man Syndrome | Anxiety Disorders | Moyamoya Disease | Ocular Albinism Type 1 | Wolfram Syndrome | Chordoid Glioma | Currarino Syndrome | Pseudo-pseudohypoparathyroidism | Presbyopia | Amish Infantile Epilepsy Syndrome | Macular Degeneration | Bacterial Meningitis | Pituitary Dwarfism | Proteus Syndrome | Lichen Planus | Retinal Dystrophy | Cramp Fasciculation Syndrome | Hyperkeratosis | Lateral Meningocele Syndrome | Stroke, Hemorrhagic | Hereditary Pyropoikilocytosis | Spastic Paraplegia Type 7 | Parapsoriasis | Cushing Syndrome | Pneumonia, Mycoplasma | Sarcoma | Myoclonus | Leukoencephalopathy, Progressive Multifocal | Isovaleric Acidemia | Neuromuscular Disorders | Atelosteogenesis Type 2 | Encephalitis, Tick-borne | Thymoma, Malignant | Spondyloperipheral Dysplasia | Obesity, Morbid | X-linked Sideroblastic Anemia | Homocystinuria | Stickler Syndrome | Varices | Split Hand-foot Malformation | Reticular Dysgenesis | Autoimmune Polyendocrine Syndrome | Krabbe Disease | Atopy | Frontometaphyseal Dysplasia | Hyperuricemia | Rhizomelic Chondrodysplasia Punctata | Hyperinsulinemia | Hyperuricemic Nephropathy, Familial Juvenile | Hypercholesterolemia | Epithelial-myoepithelial Carcinoma | Gangliosidosis, GM1 | Transient Bullous Dermolysis Of The Newborn | Duodenal Atresia | Craniosynostosis | Synovitis | Mitochondrial Encephalomyopathy | Hydronephrosis | Noonan Syndrome-like Disorder With Loose Anagen Hair | Achondrogenesis | Heart Failure | Hepatitis, Chronic | Jalili Syndrome | Cryptococcal Meningitis | Angioedema, Acquired | Stromal Corneal Dystrophy | Portal Vein Thrombosis | Takayasu's Arteritis | Learning Disability | Anorectal Fistula | Papilledema | Distal Myopathy | Large Granular Lymphocytic Leukemia | Roberts Syndrome | Neurodegeneration Due To Cerebral Folate Transport Deficiency | Hemorrhoids | Trigonocephaly | VACTERL/VATER Association | Amenorrhea | Microcephalic Osteodysplastic Primordial Dwarfism, Type II | Atrioventricular Septal Defect | Keratosis, Actinic | Nijmegen Breakage Syndrome | DICER1 Syndrome | Orotic Aciduria | Neurofibromatosis Type 1 | Kaposi Sarcoma | Hydrops Fetalis | Lymphoproliferative Disease, X-linked | Hemolytic Uremic Syndrome | Binge Eating Disorder | Osmotic Demyelination Syndrome | Tuberculous Meningitis | Sclerosteosis | Chromosome 8q21.11 Deletion Syndrome | Sporadic Hemiplegic Migraine | Glucagonoma | Hodgkin Lymphoma | Liddle Syndrome | Paroxysmal Kinesigenic Dyskinesia | Multifocal Motor Neuropathy | Renal-hepatic-pancreatic Dysplasia | Burn-McKeown Syndrome | Periodic Limb Movement Disorder | Basan Syndrome | Snyder-Robinson Syndrome | Cenani-Lenz Syndactyly Syndrome | Spinocerebellar Ataxia Type 10 | Becker Muscular Dystrophy | Hydrocephalus, Normal Pressure | Bronchiolitis | Myotonia | Dermatofibrosarcoma | Prediabetes | Corneal Dystrophy | Absence Epilepsy | Hypohidrotic Ectodermal Dysplasia, X-linked | Arthritis, Gouty | Congenital Diaphragmatic Hernia | Zellweger Syndrome | Familial Male-limited Precocious Puberty | Epidermolysis Bullosa Dystrophica | Bardet-Biedl Syndrome | Esophageal Motility Disorders | Hypoglycemia | Ebstein Anomaly | Leukodystrophies | Juvenile Xanthogranuloma | Impetigo | L-2-Hydroxyglutaric Aciduria | Eosinophilic Asthma | Spina Bifida | Esthesioneuroblastoma | Cardiomyopathy, Hypertrophic | Sclerosteosis 2 | Sclerosing Cholangitis | Cataract | Thrombophlebitis | Osteitis | Kidney Stones | Adult Polyglucosan Body Disease | Granular Corneal Dystrophy | Heimler Syndrome | Left Ventricular Noncompaction | Osteopetrosis | Blue Rubber Bleb Nevus Syndrome | Hemophilia | Peeling Skin Syndrome Type B | Pompe Disease | Benign Familial Pemphigus | Mountain Sickness | Best Macular Dystrophy | Apparent Mineralocorticoid Excess Syndrome | Neuroendocrine Cancer | Down Syndrome | Waardenburg Syndrome Type 2E | Nicotine Addiction | Hyperphenylalaninemia | Seminoma | Glycogen Storage Disease Type 1b | Glomerulonephritis | Retinal Degeneration | Granular Corneal Dystrophy Type 1 | Congenital Adrenal Hyperplasia 1 | Aneurysm, Thoracic Aortic | Lentigo | Renal Failure | Microcephalic Primordial Dwarfism | Ehlers-Danlos Syndrome | Glycogen Storage Disease Type 4 | Glutaric Aciduria Type 3 | Sickle Cell Anemia | Platyspondylic Lethal Skeletal Dysplasia, Torrance Type | Sickle Cell Disease | Blood Protein Disorders | Syphilis | Pleurisy | Eiken Syndrome | Osteogenesis Imperfecta Type IV | Congenital Sodium Diarrhea | Eclampsia | Usher Syndrome Type IIC | Neurotoxicity | POEMS Syndrome | Chronic Myelomonocytic Leukemia | Pseudohypoparathyroidism Type 1C | Infantile Neuroaxonal Dystrophy | Exfoliative Dermatitis | Greenberg Dysplasia | Twin-to-twin Transfusion Syndrome | Carotid Artery Disease | Liver Failure | Seizures-scoliosis-macrocephaly Syndrome | Optic Neuritis | Hypermetropia | Coronary Artery Disease | Sleep Disorder | Hyperbilirubinemia, Neonatal | Spinocerebellar Ataxia Type 42 | Meningioma | Sengers Syndrome | Diabetes | Beta-Propeller Protein-associated Neurodegeneration | Seizures | Mohr-Tranebjaerg Syndrome | Bicuspid Aortic Valve | Cancer, Bladder | Chudley-McCullough Syndrome | Hypertensive Nephropathy | Myositis | Hepatorenal Syndrome | Jawad Syndrome | Communication Disorders | Prune Belly Syndrome | Colitis, Collagenous | Cholangitis | Cystinosis | Pseudohypoparathyroidism Type 1B | Hemangioblastoma | Rickets | Pneumoconiosis | Conjunctivitis, Allergic | Spondylosis | Behavioral Variant Of Frontotemporal Dementia | Triphalangeal Thumb-polysyndactyly Syndrome | Ichthyosis, X-linked | Amyotrophic Lateral Sclerosis | Ocular Hypertension | Acrodermatitis Enteropathica | Astrocytoma | Avellino Corneal Dystrophy | Anodontia | Subcortical Band Heterotopia | Wagner Disease | Primary Carnitine Deficiency | Niemann-Pick Disease, Type B | Ectrodactyly | Goldenhar Syndrome | Osteonecrosis Of The Jaw | Thanatophoric Dysplasia Type 1 | Peripheral T-cell Lymphoma | Trichotillomania | Treacher Collins Syndrome | Duchenne Muscular Dystrophy | Porphyria | T-cell Chronic Lymphocytic Leukemia | Protein S Deficiency | Rhinitis | Primary Hyperoxaluria Type 3 | Primary Aldosteronism | Gastroenteritis | Nemaline Myopathy 10 | Distal Spinal Muscular Atrophy | Interstitial Lung Diseases | Potocki-Shaffer Syndrome | Spinal Cord Diseases | Phenylketonuria II | Hepatitis | Pulmonary Veno-occlusive Disease | CHARGE Syndrome | Acromicric Dysplasia | Uterine Leiomyoma | Celiac Disease | Charcot-Marie-Tooth Disease Type 4 | Hereditary Sensory And Autonomic Neuropathy | Mycosis Fungoides | Adenoid Cystic Carcinoma | Congenital Hereditary Endothelial Dystrophy Type I | Rhabdoid Tumor | Epidermolysis Bullosa Acquisita | Primary Pigmented Nodular Adrenocortical Disease | Cranioectodermal Dysplasia | Sarcosinemia | Gastritis | Double Outlet Right Ventricle | Intermittent Explosive Disorder | Carcinoma In Situ | Fibrosis | Inflammatory Bowel Disease | Barrett Esophagus | Schizencephaly | HUPRA Syndrome | Myosin Storage Myopathy | Retinal Coloboma | Craniometaphyseal Dysplasia | Cardiomyopathy, Restrictive | Spinocerebellar Ataxia Type 8 | Porphyria Cutanea Tarda | Ganglioglioma | Stargardt Disease | Pituitary Disorders | Diastrophic Dysplasia | Retinopathy, Diabetic | Multiple Sclerosis, Relapsing-remitting | Creatine Deficiency Syndrome | Malignant Peripheral Nerve Sheath Tumor | Adenoma, Pleomorphic | Mabry Syndrome | Lymphoma, Follicular | Intestinal Tuberculosis | Thyroid Dyshormonogenesis | Cervical Dystonia | Glycogen Storage Disease Type 0, Muscle | Infertility | Schizotypal Personality Disorder | Dystonia-parkinsonism, X-linked | Central Retinal Artery Occlusion | Rolandic Epilepsy | Familial Hyperaldosteronism | Dystonia Musculorum Deformans | Membranous Nephropathy | Keratosis, Seborrheic | Sarcoidosis | Gerstmann-Straussler-Scheinker Syndrome | Acquired Partial Lipodystrophy | Primary Lateral Sclerosis | Waardenburg Syndrome Type 4 | Hypophosphatemic Rickets, Autosomal Recessive, 1 | Bronchitis | Spinocerebellar Ataxia Type 5 | Hashimoto Thyroiditis | Hyperferritinemia-cataract Syndrome | Knobloch Syndrome | Iron Metabolism Disorders | Chronic Idiopathic Myelofibrosis | Common Cold | Neurodevelopmental Disorder With Central Hypotonia And Dysmorphic Facies | Lymphangioleiomyomatosis | Benign Familial Infantile Seizures | Hyperinsulinism-hyperammonemia Syndrome | Epidermolytic Palmoplantar Keratoderma | Mitochondrial DNA Depletion Syndrome | Guanidinoacetate Methyltransferase Deficiency | Kabuki Syndrome 2 | Pulverulent Zonular Cataract | Alagille Syndrome