DRESS Syndrome

About the Disease
Drug Reaction with Eosinophilia and Systemic Symptoms, also known as drug rash with eosinophilia and systemic symptoms, is related to hypereosinophilic syndrome and exanthem. The drugs Antibodies and Immunoglobulins, Intravenous have been mentioned in the context of this disorder. Affiliated tissues include skin, liver and t cells, and related phenotypes are fever and thyroiditis

Common Targets
HLA-B | HLA-A | EPHX1 | HLA-C

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

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Duodenal Atresia | Leigh Syndrome | Li-Fraumeni Syndrome | Venous Insufficiency | Peroxisomal Disorder | Hereditary Multiple Exostoses | Cushing Syndrome | Amyotrophic Lateral Sclerosis, Juvenile | Paraganglioma | Lyme Disease | Primrose Syndrome | Pfeiffer Syndrome | Astigmatism | Veno-occlusive Disease | Antenatal Bartter Syndrome Type 1 | Kohlschutter-Tonz Syndrome | Subacute Sclerosing Panencephalitis | Glaucoma | Prolactinoma | Cantu Syndrome | ICF Syndrome | Heavy Chain Disease | Osteogenesis Imperfecta Type IV | Cholesteryl Ester Storage Disease | Congenital Central Hypoventilation Syndrome | Aldosteronism | Spondylolisthesis | Bulimia Nervosa | Congenital Hypofibrinogenemia | Smith-Lemli-Opitz Syndrome | Multiple Sclerosis, Chronic Progressive | Skin Papilloma | Histoplasmosis | Salla Disease | Oculocutaneous Albinism Type 1 | Senior-Loken Syndrome | Osteosclerosis | Charcot-Marie-Tooth Disease Type 4B1 | Hemosiderosis | Nephrosclerosis | Fuchs Heterochromic Iridocyclitis | Malonyl-CoA Decarboxylase Deficiency | Congenital Dyserythropoietic Anemia Type 4 | Oligoastrocytoma | Neovascular Glaucoma | Trigonocephaly | Optic Nerve Hypoplasia, Bilateral | B-cell Chronic Lymphocytic Leukemia | Spinocerebellar Ataxia Type 17 | GATA2 Deficiency | Alopecia Areata | Proopiomelanocortin Deficiency | Pelizaeus-Merzbacher Disease | Aneurysm, Abdominal Aortic | Endometrial Hyperplasia | Migraine | Carcinoma, Signet Ring Cell | Pathological Gambling | Acute Chest Syndrome | Neurodevelopmental Disorder With Central Hypotonia And Dysmorphic Facies | Trichomegaly | Fibrodysplasia Ossificans Progressiva | Vitreoretinal Degeneration, Snowflake Type | Reticular Dysgenesis | Phosphoglycerate Dehydrogenase Deficiency | Cancer, Kidney | Encephalopathy, Ethylmalonic | Shprintzen-Goldberg Syndrome | Adenoid Cystic Carcinoma | Cystitis | Spinocerebellar Ataxia Type 28 | Epidermolytic Ichthyosis, Annular | Roberts Syndrome | Splenomegaly | Holoprosencephaly | Cryptococcal Meningitis | Mucormycosis | Hypokalemia | Meesmann Corneal Dystrophy | Meier-Gorlin Syndrome | Silver-Russell Syndrome | Iron Deficiency Anemia | Sulfite Oxidase Deficiency | Myopathy | Pontocerebellar Hypoplasia Type 7 | Meningioma | Genitopatellar Syndrome | Rhabdomyosarcoma, Alveolar | Multifocal Motor Neuropathy | Hemolytic Anemia | Graves Disease | Congenital Poikiloderma | Keratosis | Oguchi Disease-2 | Kallmann Syndrome | Huntington's Disease-like 2 | Hyperparathyroidism | Thin Basement Membrane Disease | Bainbridge-Ropers Syndrome | Osteopathia Striata With Cranial Sclerosis | Metanephric Adenoma | Hermansky-Pudlak Syndrome | Malignant Peripheral Nerve Sheath Tumor | Peyronie's Disease | Neuroma | Glaucoma, Congenital | Familial Hypobetalipoproteinemia | Mitochondrial Cytopathy | Panniculitis | Schindler Disease | Ischemia | Peritonitis | Cystinuria | Progressive Osseous Heteroplasia | Mitochondrial DNA Depletion Syndrome 13 | Echinococcosis | Swine Influenza | Headache | Xeroderma 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Dystrophy | Sandhoff Disease | Molybdenum Cofactor Deficiency | Cutaneous T-cell Lymphoma | Eosinophilia | Hereditary Spastic Paraplegia | Spinocerebellar Ataxia Type 2 | Rolandic Epilepsy | Multiple Epiphyseal Dysplasia | Hidradenitis | Sepiapterin Reductase Deficiency | Systemic Lupus Erythematosus | Chiari Malformation Type I | Cholecystitis | Lymphoproliferative Disorders | Sturge-Weber Syndrome | Bartsocas-Papas Syndrome | Hyperostosis | Familial Advanced Sleep Phase Syndrome | Mucolipidosis | Carbamoyl Phosphate Synthetase I Deficiency | Osteogenesis Imperfecta Type II | Schamberg Disease | Sertoli Cell-only Syndrome | Oculocutaneous Albinism | Ocular Albinism Type 1 | Wilson's Disease | Muscular Dystrophy | Macular Degeneration | Lymphoproliferative Disease, X-linked | Dystonia | Gaucher Disease | Epilepsy Of Infancy With Migrating Focal Seizures | Burn-McKeown Syndrome | Glycogen Storage Disease | Knobloch Syndrome | Proximal Symphalangism | Hypertension, Portal | 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Congenita | Hyperuricemic Nephropathy, Familial Juvenile | Globozoospermia | Schizoaffective Disorder | Juvenile Hyaline Fibromatosis | McKusick Type Metaphyseal Chondrodysplasia | GNE Myopathy | Acute Myeloid Leukemia | Leukoplakia, Oral | Pulverulent Zonular Cataract | Hypobetalipoproteinemias | Absence Epilepsy | Camurati-Engelmann Disease | Diamond-Blackfan Anemia | Bronchitis | Leukoencephalopathy, Progressive Multifocal | Hydrocephalus, Normal Pressure | Cerebellar Ataxia, Cayman Type | Dermatitis Herpetiformis | Blomstrand Osteochondrodysplasia | Peeling Skin Syndrome, Acral Type | Osteosarcoma | Mountain Sickness | Otopalatodigital Syndrome Type 2 | Viral Meningitis | Donnai-Barrow Syndrome | Gingivitis | Gray Platelet Syndrome | Inflammatory Linear Verrucous Epidermal Nevus | Pycnodysostosis | Familial Exudative Vitreoretinopathy | Keratoconus | Autoimmune Polyendocrine Syndrome | Crouzon Syndrome With Acanthosis Nigricans | Anthrax | Arthropathy | Primary Erythromelalgia | 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