Behcet's Disease

About the Disease
Behcet Syndrome, also known as behcet disease, is related to vogt-koyanagi-harada disease and spondyloarthropathy 1, and has symptoms including angina pectoris, chest pain and edema. An important gene associated with Behcet Syndrome is MEFV (MEFV Innate Immunity Regulator, Pyrin), and among its related pathways/superpathways are Innate Immune System and MIF Mediated Glucocorticoid Regulation. The drugs Fluocinolone acetonide and Pharmaceutical Solutions have been mentioned in the context of this disorder. Affiliated tissues include spinal cord, eye and skin, and related phenotypes are nausea and vomiting and arthritis

Common Targets
G5243 | LOC101927745 | IL23R | TNFSF4 | Phosphodiesterase (nonspecified subtype) | IL18 | CARD8 | HLA-C | TLR7 | LINC01147 | CPVL | SUGT1P4-STRA6LP-CCDC180 | G114548 | Protein Phosphatase 2B | JAK3 | PPIA | PVT1 | JAK1 | LINC01697 | MPO | HLA-DQB1 | PDE4D | AP1S3 | NFKB1 | G596 | CCDC26 | LOC107986649 | IFITM4P | CRBN | RUNX2 | LINC01950 | RORC | PTPN2 | LOC107986764 | G472 | GATD3 | TLR8 | LINC02511 | SLC9A2 | SORBS2 | LINC02656 | TSC1 | IL12B | JAK2 | ATG7 | IL1B | LOC105377499 | ETS2-AS1 | ITGAX | LINC02288 | LINC02270 | G6774 | WDR1 | IL1RN | Interleukin-1 (nonspecified subtype) | LRMDA | LOC105375523 | ERAP2 | PDE4B | LOC107987121 | G3569 | Phosphodiesterase IV (PDE4) (nonspecified subtype) | CYP2C19 | NRAD1 | DAP | LOC105370982 | IFI16 | SLC39A11 | TRAF5 | DNMT3A | BTK | VKORC1 | HOXB13 | DGUOK-AS1 | LOC105371006 | NRG1 | IL17RA | LINC02888 | NAGK | IL2RA | TGFB1 | IL-1 Receptor (nonspecified subtype) | DCDC2C | CLASP2 | CDK6 | TBX21 | PPP3R2 | HLA-DQA1 | JAKMIP1-DT | LOC105369325 | CARD9 | KLRC4 | SLC22A3 | IKBKG | ATG5 | LINC02964 | PIK3R4 | MRPL1 | MAP3K8 | IL12RB1 | NF-kappaB (NFkB) | LINC01121 | G7099 | TYK2 | NOP10 | AIM2 | PPID | PPP3CC | TNFSF13B | HLA-G | CSF1R | ADORA1 | UBASH3B | G5133 | ATG16L1 | PDGFRL | ADORA2B | LINC01484 | CD86 | TIRAP | CXCR1 | LACC1 | CAST | HLA-B | NOD2 | RNF175 | HLA-DQA2 | G29126 | LINC-PINT | LOC105375911 | REL | REL-DT | LOC105369568 | FOXP1 | G6772 | GIMAP1-GIMAP5 | UTS2 | LINC01019 | HLA-DRB1 | WAKMAR2 | ITGB2 | LINC01104 | SPATA13 | MIR182 | GPX1 | IL12RB2 | IL27 | CAVIN1 | NCOA5 | SOD2 | UBAC2 | SHISA9 | CD40 | LOC107984118 | CYP24A1 | TIMMDC1 | FKBP5 | AHNAK | ATG2A | LINC01399 | CCDC180 | LOC102724900 | ELMO1 | G581 | ADORA2A | RDUR | LOC105369735 | LOC105374364 | G3605 | F2 | SOCS3 | PSORS1C1 | LINC01194 | LINC02513 | ACHE | GPR19 | LINC02128 | PRG4 | TEX53 | CYP2R1 | NFIL3 | LINC00921 | Interferon alpha/beta Receptor (nonspecified subtype) | NTRK1 | NADSYN1 | LOC285626 | HLA-A | LINC01378 | TNFAIP3 | TLR2 | MS4A1 | LOC107984576 | DCX (DDB1-CUL4-X-box) E3 protein ligase complex | CHIA | LOC105371887 | CEP135 | G3630 | CCR1 | SLC37A1 | LINC02253 | IL1RAP | STAT4 | LINC02162 | G5970 | LINC01187 | LOC105376481 | CD80 | CLEC16A | MEFV | LOC105369850 | KLRC4-KLRK1 | G4318 | MMP2-AS1 | ERAP1 | BSN | IL12A-AS1 | PDCD1LG2 | LINC00578 | Janus Kinase (nonspecified subtype) | LOC107984903 | IL1A | MMP27 | CYP2C9 | PTPN22 | NOS3 | IRF8 | PON1 | LINC01475 | TNFSF15 | LINC02127 | PDE4A | LOC105376626 | IL2 | EGLN1 | PPP3CB | SPDEF | LINC03016 | MTUS1-DT | CXCR2 | TDRD7 | PPP3R1 | PRKCQ | HLA-DPB1 | LYN | DEFB1 | FUT2 | ITGAL | CPLX1 | TNIP1 | ATG10 | RUNX1 | Tubulin | MIR146A | ASTN2 | LOC107985935 | TLR9 | VDR | NOS2 | GATA3 | LOC101928516 | IFNG | HLA-DPB2 | LINC01725 | TRAF3IP2 | HLA-DRB6 | CTLA4 | MIF | LINC02405 | CCR5 | LOC105379031 | CYP27B1 | TNFRSF1A | LINC02864 | BSN-DT | MIR196A2 | LINC02126 | NLRP3 Inflammasome | G7124 | ATR | MICA | GLA | LINC02506 | IL6R | MTHFR | ULK1 | IL10 | IL4 | ULBP3 | FOXP3 | MIR6891 | MIR499A | LOC100506023 | METTL1 | RIPK2 | NCF1 | ETS1 | TRD-AS1

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

Other Diseases

Muckle-Wells Syndrome | Teratozoospermia | Camptocormia | Otosclerosis | Sezary Syndrome | Primary Cutaneous Amyloidosis | Prolidase Deficiency | Chediak-Higashi Syndrome | Papilloma | Schnyder Crystalline Corneal Dystrophy | Hypertensive Retinopathy | Leishmaniasis, Visceral | Anthrax | Hyperinsulinism-hyperammonemia Syndrome | Spondylolisthesis | Synpolydactyly | KBG Syndrome | Allergic Contact Dermatitis | Asthma | Spermatocele | Liddle Syndrome | Gastritis, Atrophic | Glaucoma | Waldenstrom Macroglobulinemia | Metabolic Syndrome | Mast Cell Leukemia | Keratocystic Odontogenic Tumor | Neurodevelopmental Disorder With Central Hypotonia And Dysmorphic Facies | Gigantism | Nail Disorder, Nonsyndromic Congenital | Hypogonadism | Spina Bifida | Carcinoid Syndrome | Sarcoma | Inflammatory Linear Verrucous Epidermal Nevus | Hyperparathyroidism-jaw Tumor Syndrome | Gnathodiaphyseal Dysplasia | Diverticulitis | Skin Papilloma | Glycogen Storage Disease Type 1b | Compartment Syndrome | Bronchitis | Personality Disorders | Hodgkin Lymphoma | Retinal Detachment | Glanzmann Thrombasthenia | Diabetes Mellitus, Transient Neonatal | Carcinoma In Situ | Combined Pituitary Hormone Deficiency | Neurogenic Bladder | Spinocerebellar Ataxia Type 28 | Oguchi Disease-2 | Lateral Meningocele Syndrome | Pityriasis Rubra Pilaris | Colitis, Microscopic | Congenital Hypofibrinogenemia | Sick Sinus Syndrome | Shock, Cardiogenic | Tatton-Brown-Rahman Syndrome | Parapsoriasis | Cornelia De Lange Syndrome | Canavan Disease | Conn Syndrome | Sialidosis | Charcot-Marie-Tooth Disease Type 4D | Prader-Willi Syndrome | Schizophrenia, Paranoid | Alexander Disease | Rash | Hereditary Sensory Neuropathy Type 1 | Apraxia | Thalassemia, Beta | Pantothenate Kinase-associated Neurodegeneration | Arteriosclerosis | Cluster Headache | Acute Motor Axonal Neuropathy | Hyperlipidemia, Familial Combined | T-cell Lymphoma, Subcutaneous Panniculitis-like | Carey-Fineman-Ziter Syndrome | Spondyloperipheral Dysplasia | Hartsfield Syndrome | Hyperekplexia | Thrombophilia | DiGeorge Syndrome | Cholelithiasis | Blue Rubber Bleb Nevus Syndrome | Charcot-Marie-Tooth Disease Type 4E | Glycogen Storage Disease Type 1a | Scleroderma, Diffuse | Sickle Cell Anemia | Yellow Fever | Encephalopathy | Lattice Corneal Dystrophy Type 1 | Dystonia-parkinsonism, X-linked | Congenital Poikiloderma | Pemphigus Foliaceus | Gout | Acromegaly | Lentigo | Best Macular Dystrophy | Papillon-Lefevre Syndrome | Metaphyseal Chondrodysplasia, Schmid Type | Waardenburg Syndrome | Ichthyosis | Colon Adenoma | Shwachman-Bodian-Diamond Syndrome | Facioscapulohumeral Muscular Dystrophy | Liebenberg Syndrome | Osteopathia Striata With Cranial Sclerosis | Christianson Syndrome | Sialoadenitis | CHOPS Syndrome | Biotinidase Deficiency | Hyperhomocysteinemia | Microvillus Inclusion Disease | Bartter Syndrome | Azoospermia | Spinocerebellar Ataxia Type 40 | Headache | Dermatitis Herpetiformis | Congenital Primary Aphakia | Myoclonic Epilepsy With Ragged Red Fibers | Basal Ganglia Cerebrovascular Disease | HANAC Syndrome | CREST Syndrome | Melnick-Needles Syndrome | Purpura, Thrombotic Thrombocytopenic | Kleine-Levin Syndrome | Focal Facial Dermal Dysplasia | Distal Myopathy | Low Phospholipid Associated Cholelithiasis | Lichen Planus | Huntington's Disease-like 2 | Gangliosidosis, GM1 | Basal Ganglia Disease, Biotin-responsive | Nicolaides-Baraitser Syndrome | Cyclic Vomiting Syndrome | Neuroblastoma | Stickler Syndrome | Granular Corneal Dystrophy Type 1 | Localized Scleroderma | Renal Medullary Carcinoma | Carcinoma, Transitional Cell | Meckel-Gruber Syndrome | Pleural Tuberculosis | Osteogenesis Imperfecta Type VI | Pure Autonomic Failure | Antisocial Personality Disorder | Triple A Syndrome | Neural Tube Defect | Osteomyelitis | Multiple System Atrophy | Sarcoidosis, Pulmonary | Fanconi Anemia | Epidermolysis Bullosa Simplex, Generalized | Takayasu's Arteritis | Aphasia | Hepatic Veno-occlusive Disease | Uveitis, Anterior | Diabetes Type 2 | Pulmonary Vein Stenosis | Bronchitis, Chronic | Kearns-Sayre Syndrome | Fukuyama Congenital Muscular Dystrophy | Chitayat Syndrome | Tuberculous Meningitis | Cerebellar Ataxia, Cayman Type | Neuroleptic Malignant Syndrome | Speech Disorders | Cryopyrin-associated Periodic Syndromes | Hidradenitis | Anodontia | Cystinuria | Insulin Resistance | Hypertensive Nephropathy | Sarcoma, Endometrial Stromal | Netherton Syndrome | Choriocarcinoma | Spinocerebellar Ataxia Type 27 | Patent Foramen Ovale | Familial Hypobetalipoproteinemia | Hepatoblastoma | Hypersensitivity Pneumonitis | Paget's Disease Of The Breast | Hypodontia | Very Long-chain Acyl-CoA Dehydrogenase Deficiency | Nephrotic Syndrome Type 1 | Hyperbilirubinemia | Strabismus | Panniculitis | Mitochondrial DNA Depletion Syndrome 13 | Hypertelorism | Ependymoma | GNE Myopathy | Krabbe Disease | Endometritis | Seborrheic Dermatitis | Pseudohypoaldosteronism | Renal Hypomagnesemia 3 | Ovarian Hyperstimulation Syndrome | Aneurysm, Thoracic Aortic | Silicosis | Cerebrotendinous Xanthomatosis | Anuria | Angioedema | Optic Nerve Diseases | Microcephaly | Pelizaeus-Merzbacher Disease | Waardenburg Syndrome Type 4A | Infantile Refsum Disease | Meningioma, Benign | Huntington's Disease | Twin-to-twin Transfusion Syndrome | Dermatofibrosarcoma | Uremic Pruritus | Meningioma | 3-methylcrotonyl-CoA Carboxylase Deficiency | Marfan Syndrome | Acrodermatitis | Premature Ejaculation | Gray Platelet Syndrome | Long QT Syndrome Type 3 | Polycystic Kidney, Autosomal Recessive | Acute Coronary Syndrome | Hypertension, Pulmonary | Chiari Malformation Type I | Periodic Limb Movement Disorder | Multisystemic Smooth Muscle Dysfunction Syndrome | Sporadic Inclusion Body Myositis | Hemochromatosis | Hypokalemic Periodic Paralysis | Unverricht-Lundborg Syndrome | Roberts Syndrome | POEMS Syndrome | Moyamoya Disease | Urea Cycle Disorder | Congenital Aniridia | Auriculocondylar Syndrome | Ocular Albinism Type 1 | Arthropathy | Noonan Syndrome-like Disorder With Loose Anagen Hair | Hypophosphatemic Rickets With Hypercalciuria, Hereditary | Tylosis With Esophageal Cancer | Subacute Sclerosing Panencephalitis | Metachromatic Leukodystrophy | Hemolytic Anemia | Inborn Errors Of Metabolism | Lassa Fever | Charcot-Marie-Tooth Disease Axonal Type 2N | Histoplasmosis | CDKL5 Deficiency Disorder | Achromatopsia | Chorea | Hypertrophic Osteoarthropathy, Primary, Autosomal Recessive 1 | Congenital Dyserythropoietic Anemia Type 1 | Pulmonary Tuberculosis | Corneal Dystrophy | Common Variable Immunodeficiency | Vestibular Disease | Bulimia Nervosa | Diffuse Mesangial Sclerosis | Vasculitis | Macrophagic Myofasciitis | Hepatitis, Autoimmune | Gliosarcoma | Lymphoproliferative Disease, X-linked | Sleep Apnea | 3-methylglutaconic Aciduria | Haim-Munk Syndrome | Myofibromatosis | Leukoencephalopathy, Progressive Multifocal | Pemphigus Vulgaris | Limb Girdle Muscular Dystrophy | Brooke-Spiegler Syndrome | Nestor-Guillermo Progeria Syndrome | Peyronie's Disease | C3 Glomerulonephritis | Bainbridge-Ropers Syndrome | Whipple's Disease | Marshall-Smith Syndrome | Chronic Mucocutaneous Candidiasis | Glycogen Storage Disease Type 0, Muscle | Juvenile Xanthogranuloma | Leukocyte Adhesion Deficiency Type 1 | Scleroderma | Infertility | Hyperinsulinemia | Coronary Heart Disease | Bartsocas-Papas Syndrome | B-cell Chronic Lymphocytic Leukemia | Scapuloperoneal Spinal Muscular Atrophy | Familial Hypertrophic Cardiomyopathy | Hypereosinophilic Syndrome | Myelodysplasia | Dystonia Musculorum Deformans | Dupuytren Disease | Melanocytic Nevus | Hemangioblastoma | Cholecystitis | Cold-induced Sweating Syndrome | Necrobiosis Lipoidica | Malaria | Cholesteryl Ester Storage Disease | Pericarditis | Keratoconus | Cardiac Sarcoidosis | Spinocerebellar Ataxia Type 6 | Congenital Muscular Dystrophy | Spondyloepimetaphyseal Dysplasia With Joint Laxity, Type 3 | Dyggve-Melchior-Clausen Disease | Diabetic Encephalopathy | Hypomyelination With Atrophy Of Basal Ganglia And Cerebellum | Pneumonia, Mycoplasma | Long QT Syndrome Type 2 | Dystonia | Crohn's Disease | Familial Digital Arthropathy-brachydactyly | Seminoma | Amyloidosis | Temtamy Preaxial Brachydactyly Syndrome | Hyperlipidemia Type V | Mountain Sickness | Stroke, Hemorrhagic | Progressive Familial Intrahepatic Cholestasis Type 1 | Peeling Skin Syndrome, Acral Type | Cat Eye Syndrome | Adenomyosis | Hashimoto Thyroiditis | Marinesco-Sjogren Syndrome | Idiopathic Multicentric Castleman Disease | Wieacker-Wolff Syndrome | Wolff-Parkinson-White Syndrome | Multicentric Carpotarsal Osteolysis Syndrome | Proteus Syndrome | Cardiac Arrest | Hemophilia | Vitiligo | Gaucher Disease | Intracranial Hypertension | Obsessive-compulsive Disorder | Rett Syndrome | Leukoplakia | Peritonitis | Beta-Propeller Protein-associated Neurodegeneration | Wolfram Syndrome | Polyarteritis Nodosa | WAGR Syndrome | Harlequin Ichthyosis | Osteochondroma | Cardiomyopathy, Restrictive | Fibrosarcoma | Leukemia-lymphoma, Adult T-cell | Coronary Restenosis | Avellino Corneal Dystrophy | Hypermethioninemia | Agoraphobia | H Syndrome | Glomerulonephritis, Membranous | Wagner Disease | Angiosarcoma Of The Breast | Porokeratosis | Esophageal Adenocarcinoma | Bicuspid Aortic Valve | Endometrial Hyperplasia | Mesial Temporal Lobe Epilepsy With Hippocampal Sclerosis | Adenosine Deaminase Deficiency | Polycythemia Vera | Chondroma | Anorchia | Pulmonary Alveolar Proteinosis | Corneal Neovascularization | Ameloblastic Carcinoma | Filariasis | Spinocerebellar Ataxia Type 3 | Blepharospasm | Hemoglobinopathies | Blau Syndrome | Chorioretinitis | Hereditary Spastic Paraplegia | Varices | Acute Chest Syndrome | IMAGe Syndrome | Fibrillation, Atrial | Actinomycetoma | Adenomatoid Tumor | Chylothorax, Congenital | Meningeal Melanocytoma | Alstrom Syndrome | Genitopatellar Syndrome | Nephrosclerosis | Amyotrophic Lateral Sclerosis, Juvenile | Osteosclerosis | Seasonal Mood Disorder | Sarcoidosis | Cysticercosis | Nephrocalcinosis | Pituitary Stalk Interruption Syndrome | Gastroschisis | Kaposi Sarcoma | Hyperuricemia