Disease

Dermatitis

About the Disease
Dermatitis, also known as eczema, is related to irritant dermatitis and dermatitis herpetiformis, and has symptoms including exanthema and pruritus. An important gene associated with Dermatitis is FLG (Filaggrin), and among its related pathways/superpathways are Innate Immune System and MIF Mediated Glucocorticoid Regulation. The drugs Salicylic acid and Titanium dioxide have been mentioned in the context of this disorder. Affiliated tissues include skin, breast and t cells, and related phenotypes are immune system and hematopoietic system

Common Targets
G595 | CCR10 | G29126 | Interleukin 17 (nonspecified subtype) | G3309 | PROC | IL36RN | G1026 | F2RL1 | Phosphodiesterase IV (PDE4) (nonspecified subtype) | Serine/Threonine Kinase (nonspecified subtype) | PDE4B | IKBKB | NR1H2 | FKBP1A | Interleukin-1 (nonspecified subtype) | CANX | PPARA | TYK2 | ALOX5AP | FLG | IL-10 Receptor | G1029 | TYR | TRPM8 | PPP3R2 | PPP3CC | TRAF6 | DYRK1A | ABCA1 | TNFSF10 | alpha-Adrenoceptor (nonspecified subtype) | IL-4 receptor | CCR2 | TRPV1 | G7124 | SYK | G6772 | PTPN1 | NTRK1 | Neurotrophic Tyrosine Kinase Receptor (TRK) (nonspecified subtype) | GSK3B | NR3C1 | TSLP | Mitogen-Activated Protein Kinase (nonspecified subtype) | Platelet-Derived Growth Factor Receptor (nonspecified subtype) | DSP | IL5 | G4193 | PTGDR2 | NFKBIL1 | VDR | beta-Adrenoceptor (nonspecified subtype) | IL1A | IL2 | Caspase (nonspecified subtype) | Serine protease (nonspecified subtype) | EPHA2 | IFNG | VCP | IL1RL2 | HRH1 | High affinity cAMP-specific 3',5'-cyclic phosphodiesterase 7 (nonspecified protein) | Cyclooxygenase (COX) (nonspecified subtype) | PPP3CB | NAMPT | CYSLTR2 | CLEC12B | PDE4A | PPP3R1 | Retinoid RXR receptor (nonspecified subtype) | APC | IL1B | TNIP1 | LTC4S | IL4 | KRR1 | JAK3 | ALOX5 | CALCR | G3569 | IL-13 receptor | JAK1 | CTNNB1 | Mitogen-activated protein kinase (JNK) (nonspecified subtype) | WNT2 | JAK2 | RIPK1 | S1PR1 | IL13 | PIK3CG | G3576 | DSG1 | HRH4 | TGFBR2 | SIK3 | DPYD | G6714 | Superoxide dismutase (SOD) (nonspecified subtype) | G6647 | G5133 | XBP1 | RIPK2 | PDE4D | HSP90B1 | Protein Phosphatase 2B | RORC

疾病靶点研报
Dermatitis

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

Other Diseases

Adenoma, Pituitary | Cri-du-chat Syndrome | Hyperthyroidism | Pontocerebellar Hypoplasia | Sepiapterin Reductase Deficiency | Haim-Munk Syndrome | Pyruvate Carboxylase Deficiency Disease | Branchiootorenal Syndrome | Hyperparathyroidism, Secondary | Loeys-Dietz Syndrome Type 4 | Ependymoma | Wolcott-Rallison Syndrome | Retinal Telangiectasia | Rubinstein-Taybi Syndrome | Mitochondrial DNA Depletion Syndrome, Myopathic Form | Progressive Encephalopathy-optic Atrophy Syndrome | Alpers Syndrome | Neuronal Ceroid Lipofuscinosis | REM Sleep Behavior Disorder | Micropenis | HIBCH Deficiency | Basal Cell Nevus Syndrome | Porphyria, Variegate | Episodic Ataxia | Hemimegalencephaly | Choroiditis | Primary Aldosteronism | Hypolipoproteinemia | Tricho-hepato-enteric Syndrome | Diamond-Blackfan Anemia | Chorea | Dengue Shock Syndrome | Adenylosuccinate Lyase Deficiency | Spinocerebellar Ataxia Type 3 | Neonatal Progeroid Syndrome | Amebiasis | Distal Spinal Muscular Atrophy | Osteoporosis-pseudoglioma Syndrome | Charcot-Marie-Tooth Disease, Type 1A | Hepatic Adenomatosis | Acrocallosal Syndrome | Esophageal Motility Disorders | Lymphoproliferative Disorders | Hypoparathyroidism | Exfoliative Dermatitis | Pyoderma Gangrenosum | Mitochondrial DNA Depletion Syndrome, Encephalomyopathic Form | Cone Dystrophy | Corneal Dystrophy And Perceptive Deafness | Nutrition Disorders | Cardiac Arrest | Japanese Encephalitis | Eosinophilic Asthma | Aarskog-Scott Syndrome | Wilson's Disease | Chitayat Syndrome | Cervicitis | Pulmonary Veno-occlusive Disease | Primary Hyperoxaluria Type 1 | Camptocormia | Open-angle Glaucoma | Fabry's Disease | Keratocystic Odontogenic Tumor | Congenital Nephrotic Syndrome | Retinitis | Amelanotic Melanoma | Asphyxia Neonatorum | Intracranial Hypertension | Hereditary Mixed Polyposis Syndrome | Spondyloarthritis | Hypotonia-cystinuria Syndrome | Carney Triad | D-2-Hydroxyglutaric Aciduria | Dystonia Musculorum Deformans | Mucolipidosis Type II | Congenital Primary Aphakia | Occipital Neuralgia | Cancer, Breast | Apraxia | Low Phospholipid Associated Cholelithiasis | Vitamin A Deficiency | Choriocarcinoma | Giant Cell Arteritis | VACTERL/VATER Association | Hyperparathyroidism-jaw Tumor Syndrome | Jawad Syndrome | Menetrier Disease | Antiphospholipid Syndrome | Alstrom Syndrome | Seminoma | Fibrosis | Microcephaly, Seizures, And Developmental Delay | Myoclonic Epilepsy With Ragged Red Fibers | Sarcomatoid Carcinoma Of The Lung | Neuromuscular Disorders | Smith-Kingsmore Syndrome | Generalized Epilepsy With Febrile Seizures Plus | Niemann-Pick Disease | Saul-Wilson Syndrome | Williams Syndrome | Mitochondrial Encephalomyopathy | Acute Chest Syndrome | Polyneuropathy | Ulcerative Colitis | Myhre Syndrome | Whipple's Disease | Adult Polyglucosan Body Disease | Ehlers-Danlos Syndrome | Hyperparathyroidism, Primary | Hamartoma | Renal Failure | Spinocerebellar Ataxia Type 15 | Vogt-Koyanagi-Harada Syndrome | Congenital Poikiloderma | Leukemia-lymphoma, Adult T-cell | Microcephaly | Anovulation | Pleomorphic Xanthoastrocytoma | Adenosine Deaminase Deficiency | Empyema | Persistent Mullerian Duct Syndrome | Pyelonephritis | Asthma | Hyperlipidemia Type V | Pompe Disease | Combined Malonic And Methylmalonic Acidemia | Leukocyte Adhesion Deficiency Type 1 | Cardiomyopathy, Peripartum | Cholelithiasis | Optic Neuritis | Neurogenic Bladder | Erectile Dysfunction | Anthrax | Common Cold | Trachoma | Papillon-Lefevre Syndrome | Beckwith-Wiedemann Syndrome | Spondylocarpotarsal Synostosis Syndrome | Microcephalic Osteodysplastic Primordial Dwarfism, Type I | Axenfeld-Rieger Syndrome | Usher Syndrome Type II | Hypomyelination With Atrophy Of Basal Ganglia And Cerebellum | Congenital Myopathy | Stroke | Idiopathic Pulmonary Fibrosis | Lymphopenia | Spinal Muscular Atrophy Type 3 | Renal Dysplasia | Alpha-1 Antitrypsin Deficiency | Lipoma | Antley-Bixler Syndrome | Seizures | Aicardi-Goutieres Syndrome | Brachial Plexus Neuropathy | Keratitis | Hypospadias | Polyomavirus Nephropathy | Facioscapulohumeral Muscular Dystrophy Type 1 | FG Syndrome | Craniofacial Dysostosis | Perry Syndrome | Roberts Syndrome | Lymphoma, B-cell | Auriculocondylar Syndrome | Carpenter Syndrome | Primary Familial Brain Calcification | Distal Myopathy | Hemangioma | Multiple Sulfatase Deficiency | Leiomyoma | Combined Deficiency Of Factor V And Factor VIII | Blastomycosis | Neurofibromatosis-Noonan Syndrome | Autoimmune Disease | Malaria, Cerebral | Mast Cell Leukemia | Raynaud Phenomenon | Subacute Sclerosing Panencephalitis | Familial Retinal Arterial Macroaneurysm | Speech Disorders | Hypertension, Pulmonary | Neurofibromatosis Type 1 | Oculodentodigital Dysplasia | Thrombocythemia, Essential | Myelitis | Neurodevelopmental Disorders | Otopalatodigital Syndrome Type 2 | Uremic Pruritus | Thymoma, Malignant | Primary Progressive Nonfluent Aphasia | Coronary Artery Disease | Pulmonary Tuberculosis | Hyperbilirubinemia, Neonatal | Veno-occlusive Disease | Ectopia Lentis, Isolated, Autosomal Recessive | Acromicric Dysplasia | Polycystic Liver | Pseudo-pseudohypoparathyroidism | Wolfram Syndrome | Waardenburg Syndrome Type 4A | Follicular Dendritic Cell Sarcoma | Cat Eye Syndrome | Spondyloperipheral Dysplasia | Proctitis | Alcoholism | Polycythemia Vera | Cyclic Vomiting Syndrome | Wiedemann-Steiner Syndrome | Primary Pigmented Nodular Adrenocortical Disease | Familial Digital Arthropathy-brachydactyly | Meniere's Disease | LMNA-related Congenital Muscular Dystrophy | Pearson Syndrome | Porokeratosis | Hyperinsulinemia | Major Depression | Tangier Disease | Transthyretin-related Amyloidosis | Arthropathy | Osteosclerosis | Pure Red Cell Aplasia | Shprintzen-Goldberg Syndrome | Muscle Wasting | Rhabdomyosarcoma, Embryonal | COACH Syndrome | Tay-Sachs Disease | Pseudohypoaldosteronism | Retinal Dystrophy | Hyperglycemia | Persistent Truncus Arteriosus | Spinal Cord Diseases | Pseudohypoparathyroidism Type 1B | Leprosy | Congenital Aniridia | Fascioliasis | Guanidinoacetate Methyltransferase Deficiency | Sporadic Hemiplegic Migraine | Lewy Body Dementia | Charcot-Marie-Tooth Disease Type 3 | Multiple Sclerosis, Primary Progressive | Trismus-pseudocamptodactyly Syndrome | Bursitis | Aldosteronism | Torticollis | Avian Influenza | Osteomalacia | Pfeiffer Syndrome | Huntington's Disease | Pupil Disorders | Stevens-Johnson Syndrome | Richter's Syndrome | MIRAGE Syndrome | Atelosteogenesis Type 1 | Mumps | Enhanced S-cone Syndrome | Familial Hypertrophic Cardiomyopathy | Interstitial Lung Diseases | Membranous Nephropathy | Meckel-Gruber Syndrome | Acquired Partial Lipodystrophy | Postaxial Polydactyly | Phosphoenolpyruvate Carboxykinase Deficiency, Cytosolic | Heavy Chain Disease | Albinism | Mabry Syndrome | Muckle-Wells Syndrome | Epidermolytic Ichthyosis, Annular | Hypoplastic Left Heart Syndrome | Pneumonia, Viral | Protein S Deficiency | Urethritis | Hypertension, Portal | C3 Glomerulopathy | Dysgerminoma | Nemaline Myopathy 8 | Botulism | Scapuloperoneal Myopathy, X-linked Dominant | Alveolar Capillary Dysplasia | Teratozoospermia | Carcinoma, Small Cell | Waldenstrom Macroglobulinemia | Goiter, Nodular | Language Disorders | Angelman Syndrome | Hypophosphatasia | Sleep Apnea, Obstructive | Glycogen Storage Disease Type 3 | Neural Tube Defect | Hypereosinophilic Syndrome | Seizures-scoliosis-macrocephaly Syndrome | Osteochondrosis | Keratoconjunctivitis | Spastic Paraplegia Type 7 | Dwarfism | Metachromatic Leukodystrophy | Erythematotelangiectatic Rosacea | Toxic Epidermal Necrolysis | Echinococcosis | Dominant Optic Atrophy | Corticobasal Syndrome | Tendinopathy | Tyrosine Hydroxylase Deficiency | X-linked Acrogigantism | Retinal Diseases | Hypercalcemia | Leukodystrophies | Polymicrogyria | Chorioretinitis | Glycogen Storage Disease Type 6 | Onchocerciasis | Diabetes | Pemphigus Foliaceus | Craniofrontonasal Syndrome | Progressive Familial Intrahepatic Cholestasis Type 2 | Frontometaphyseal Dysplasia | Obesity | Anxiety Disorders | CDKL5 Deficiency Disorder | Mesothelioma, Malignant | Nephropathy | Optic Neuropathy, Anterior Ischemic | Hereditary Hemorrhagic Telangiectasia Type 2 | Aneurysm, Abdominal Aortic | Multicentric Carpotarsal Osteolysis Syndrome | Cancer, Kidney | Inflammatory Joint Disease | Anterior Segment Dysgenesis | Silver-Russell Syndrome | Neuroma | Muscular Dystrophy | Oculocutaneous Albinism | Lipid Storage Diseases | IgA Nephropathy | Glaucoma | Johanson-Blizzard Syndrome | Ureteropelvic Junction Obstruction | Stuve-Wiedemann Syndrome | Angiomyolipoma | Multiple Hamartoma Syndrome | Schizencephaly | Wiskott-Aldrich Syndrome | Pregnancy, Ectopic | Hemophilia | Neurofibromatosis Type 2 | Thanatophoric Dysplasia | Xeroderma Pigmentosum Variant Type | Hepatoblastoma | Epidermolysis Bullosa Simplex With Mottled Pigmentation | Angioedema | Gaucher Disease | Syndactyly | Duodenal Atresia | Kaposiform Hemangioendothelioma | Leri-Weill Dyschondrosteosis | Glycogen Storage Disease Type 4 | Thrombotic Microangiopathy | Autosomal Recessive Spastic Paraplegia Type 35 | Vitelliform Macular Dystrophy | Hemochromatosis Type 2 | Schamberg Disease | Histoplasmosis | Benign Familial Pemphigus | Pemphigoid | Still Disease | Chloridorrhea, Congenital | Ocular Albinism Type 1 | Stuttering | Episodic Ataxia Type 1 | Thyroid Dyshormonogenesis | Holoprosencephaly | Autosomal Recessive Bestrophinopathy | Nephritis, Interstitial | Diabetic Neuropathy | GAPO Syndrome | Chromosome 9q34.3 Deletion Syndrome | Mevalonate Kinase Deficiency | Chronic Leukemia | Nijmegen Breakage Syndrome | Motor Neuron Diseases | Autosomal Recessive Spastic Paraplegia Type 75 | Joubert Syndrome 2 | Prolymphocytic Leukemia | Hyperlipidemia | Osteosarcoma | Nicotine Dependence | Cornelia De Lange Syndrome | Methemoglobinemia | Proopiomelanocortin Deficiency | Hypercholesterolemia, Familial | Ebstein Anomaly | Pyloric Stenosis, Infantile Hypertrophic | Poirier-Bienvenu Neurodevelopmental Syndrome | Juvenile Myelomonocytic Leukemia | Spinocerebellar Ataxia Type 14 | Neuroleptic Malignant Syndrome | Greenberg Dysplasia | Eczema | Pancreatitis, Chronic | Neuromyelitis Optica | Left Ventricular Noncompaction