Mastitis
Mastitis
About the Disease
Mastitis, also known as inflammatory breast disease, is related to breast abscess and toxic shock syndrome, and has symptoms including signs and symptoms in breast An important gene associated with Mastitis is LTF (Lactotransferrin), and among its related pathways/superpathways are Innate Immune System and Akt Signaling. The drugs Betamethasone and Hydrocortisone have been mentioned in the context of this disorder. Affiliated tissues include breast, neutrophil and skin, and related phenotypes are liver/biliary system and endocrine/exocrine gland
Common Targets
Integrin alpha4beta7 (LPAM-1) receptor | G5743 | G367 | IL1B | G3569 | CYP19A1 | MSR1 | G7124 | TLR4/MD-2 complex

Note: If you'd like to get a target analysis report for Mastitis, 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 Mastitis at a cost 90% lower than traditional approaches, please feel free to contact us at BD@silexon.tech.
Other Diseases
Charcot-Marie-Tooth Disease Type 2T | Reflex Epilepsy | Frontometaphyseal Dysplasia | Hyperbilirubinemia | Schnitzler Syndrome | Spinal Muscular Atrophy With Progressive Myoclonic Epilepsy | McCune-Albright Syndrome | Atherosclerosis | Miyoshi Myopathy | Vitamin D Deficiency | Hyperinsulinism-hyperammonemia Syndrome | Aspergillosis | Glutaric Aciduria Type 1 | Ovarian Sex Cord-stromal Tumor | Pelizaeus-Merzbacher Disease | Crigler-Najjar Syndrome | Camurati-Engelmann Disease | Oculocutaneous Albinism Type 4 | Pulmonary Stenosis | Silicosis | Tendinitis | Familial Glucocorticoid Deficiency | Diarrhea | Keratoconjunctivitis | Sclerosteosis | Fanconi Anemia | Osteopetrosis | Multiple Epiphyseal Dysplasia | Alzheimer Disease, Late Onset | Cat Eye Syndrome | Gerodermia Osteodysplastica | Pyruvate Carboxylase Deficiency Disease | Hypokalemic Periodic Paralysis | Constipation | Pulmonary Vein Stenosis | Crimean-Congo Hemorrhagic Fever | Anuria | Bursitis | Williams Syndrome | Obesity | Pompe Disease | Pituitary Disorders | Stickler Syndrome | Behavioral Variant Of Frontotemporal Dementia | Lattice Corneal Dystrophy Type 1 | Asphyxia Neonatorum | CHOPS Syndrome | Arthritis, Psoriatic | Chronic Leukemia | Parkinson Disease 6, Autosomal Recessive Early-onset | Spinocerebellar Ataxia Type 10 | Osteoporosis | Neovascular Glaucoma | Necrobiosis Lipoidica | Withdrawal Syndrome | Cerebellofaciodental Syndrome | Hereditary Coproporphyria | Liver Diseases | Lymphoma | Non-Hodgkin Lymphoma | 3-hydroxy-3-methylglutaryl-CoA Synthase Deficiency | IMAGe Syndrome | Ichthyosis, X-linked | Parapsoriasis | Jacobsen Syndrome | Chronic Periodontitis | Prurigo Nodularis | Liver Failure | Pontocerebellar Hypoplasia | ACTH-independent Macronodular Adrenal Hyperplasia | Plasmacytoma | Common Cold | Potocki-Shaffer Syndrome | Melanoma | Blood Protein Disorders | Idiopathic Multicentric Castleman Disease | Liebenberg Syndrome | Osteosclerosis | Hidradenitis Suppurativa | Aromatic L-amino Acid Decarboxylase Deficiency | Juvenile Myelomonocytic Leukemia | Persistent Mullerian Duct Syndrome | Delayed Sleep Phase Syndrome | Corticobasal Syndrome | Wolff-Parkinson-White Syndrome | Localized Scleroderma | Trimethylaminuria | Hereditary Xerocytosis | Left Ventricular Noncompaction | Pulmonary Capillary Hemangiomatosis | Pseudohermaphroditism | Leukemia-lymphoma, Adult T-cell | Osteochondroma | Nephropathy | Progressive External Ophthalmoplegia | Infantile Nephropathic Cystinosis | Nemaline Myopathy 10 | Canavan Disease | Still Disease | Mumps | Dystonia-parkinsonism, X-linked | Syncope | Intestinal Obstruction | Kleine-Levin Syndrome | Gingivitis | Premature Ejaculation | Nicotine Dependence | Focal Dermal Hypoplasia | Multiple Sulfatase Deficiency | Corneal Dystrophy | Acrodysostosis | Hashimoto Thyroiditis | 3-hydroxy-3-methylglutaric Aciduria | Hodgkin Lymphoma | Paronychia | Cysticercosis | Cystinuria | Erectile Dysfunction | Primary Erythromelalgia | Central Retinal Artery Occlusion | Spinocerebellar Ataxia Type 42 | Orthostatic Intolerance | Myoclonus-dystonia Syndrome | Presbyopia | Hypothalamic Obesity | Diamond-Blackfan Anemia | Glioblastoma | Zollinger-Ellison Syndrome | Hepatorenal Syndrome | 3-M Syndrome | Gardner Syndrome | Creutzfeldt-Jakob Disease | Charcot-Marie-Tooth Disease Type 4 | Systemic Lupus Erythematosus | Fontaine Progeroid Syndrome | Charcot-Marie-Tooth Disease Type 2E | Hereditary Folate Malabsorption | Fibrodysplasia Ossificans Progressiva | Sporadic Hemiplegic Migraine | Encephalopathy, Glycine | Myofibrillar Myopathy | Chondroma | Cardiomyopathy, Restrictive | Familial Episodic Pain Syndrome | Arthritis | Wolman Disease | Diabetes Insipidus, Nephrogenic | Ectopia Lentis, Isolated, Autosomal Recessive | Primary Ovarian Insufficiency | Primary Hyperoxaluria | Glycogen Storage Disease Type 1b | Omenn Syndrome | Amyotrophic Lateral Sclerosis | Craniofacial Dysostosis | Uveitis, Anterior | Neuronal Ceroid Lipofuscinosis | Sporadic Inclusion Body Myositis | Creatine Deficiency Syndrome Due To AGAT Deficiency | Osteoarthritis | Rolandic Epilepsy | Dysplastic Nevus | Congenital Tufting Enteropathy | Low Phospholipid Associated Cholelithiasis | Erythema Multiforme | Carbonic Anhydrase VA Deficiency | Myelomeningocele | Haim-Munk Syndrome | Anterior Segment Dysgenesis | Neuroblastoma | Proteus Syndrome | Mucolipidosis Type II | Dupuytren Disease | Craniopharyngioma | Hypophosphatemic Rickets With Hypercalciuria, Hereditary | Esophageal Adenocarcinoma | Meningococcal Meningitis | Congenital Mirror Movements | Malnutrition | Thrombophlebitis | Rickets | Arts Syndrome | Autism | Schizencephaly | Dental Caries | Sertoli Cell-only Syndrome | Leri-Weill Dyschondrosteosis | Supravalvular Aortic Stenosis | Bietti Crystalline Dystrophy | Bacterial Meningitis | Dyskeratosis Congenita | Blepharospasm | Cancer, Lung | Choroideremia | T-cell Prolymphocytic Leukemia | Gangliosidosis, GM1 | Kabuki Syndrome 2 | Yellow Fever | Cervicitis | Hepatopulmonary Syndrome | Loeys-Dietz Syndrome | Carney-Stratakis Syndrome | Neurofibromatosis | Adenosine Deaminase Deficiency | Malaria | Spondylometaphyseal Dysplasia | Anorectal Fistula | Diabetic Encephalopathy | Ventricular Septal Defect | Avellino Corneal Dystrophy | Coffin-Siris Syndrome | Colorectal Adenoma | Hepatitis D | Cholestasis, Intrahepatic | Astrocytoma, Anaplastic | Meesmann Corneal Dystrophy | Lymphoma, Primary Cutaneous Anaplastic Large Cell | Hyperekplexia | Chronic Neutrophilic Leukemia | 3-methylglutaconic Aciduria | Carcinoma In Situ | GATA2 Deficiency | Graft-versus-host Disease | Immunoproliferative Disorders | Adenylosuccinate Lyase Deficiency | Early Infantile Epileptic Encephalopathy | Glycogen Storage Disease Type 4 | Saethre-Chotzen Syndrome | Meckel-Gruber Syndrome | Charcot-Marie-Tooth Disease Type 2D | Spondyloarthritis | Autosomal Recessive Congenital Ichthyosis | Renal Dysplasia | Oligodendroglioma | Porphyria | DiGeorge Syndrome | Sitosterolemia | Congenital Generalized Lipodystrophy | Esophageal Carcinoma | Hypertensive Retinopathy | Beare-Stevenson Syndrome | Insulin Resistance | Acrodermatitis | Chronic Granulomatous Disease, X-linked | Maple Syrup Urine Disease | Splenomegaly | Hyperparathyroidism, Primary | Pyruvate Kinase Deficiency | Cartilage Disorders | Renal Oncocytoma | Gnathodiaphyseal Dysplasia | Multiple Congenital Anomalies-hypotonia-seizures Syndrome 2 | Crohn's Disease | Coenzyme Q10 Deficiency | Hyperferritinemia-cataract Syndrome | Meconium Ileus | Angioedema | Ocular Albinism Type 1 | Hypereosinophilic Syndrome | Spinocerebellar Ataxia Type 3 | Primary Aldosteronism | Conduct Disorder | Panic Disorder | Paget's Disease Of The Breast | Aldosterone Synthase Deficiency | Androgen Insensitivity | Neuromyotonia | Anti-glomerular Basement Membrane Disease | Varicocele | Dyslipidemia | Sick Sinus Syndrome 1 | Panniculitis | Histoplasmosis | Mitochondrial Myopathy | Chylothorax, Congenital | Keratitis | Vestibular Disease | LRBA Deficiency | Ependymoma | Familial Retinal Arterial Macroaneurysm | Glioblastoma Multiforme | Hypotension, Orthostatic | Pelvic Inflammatory Disease | Pityriasis Rubra Pilaris | Antisynthetase Syndrome | Vertigo | Occipital Neuralgia | Blue Rubber Bleb Nevus Syndrome | Waardenburg Syndrome | Early Infantile Epileptic Encephalopathy 4 | Hypoglycemia | Isobutyryl-CoA Dehydrogenase Deficiency | Medium-chain Acyl-CoA Dehydrogenase Deficiency | Adrenomyeloneuropathy | Diabetes Insipidus, Neurogenic | Glucagonoma | Dominant Optic Atrophy | Ectodermal Dysplasia | Otopalatodigital Syndrome Type 2 | Erdheim-Chester Disease | Megaloblastic Anemia | Mycosis Fungoides | Glycogen Storage Disease Type 1a | Purpura | Hyperandrogenemia | Phenylketonuria | Neurodevelopmental Disorder With Central Hypotonia And Dysmorphic Facies | Wiskott-Aldrich Syndrome | Carcinoma, Small Cell | Episodic Ataxia Type 2 | Colitis | Alexander Disease | Glaucoma | Chromosome 16p11.2 Deletion Syndrome | Anthrax | Neonatal Progeroid Syndrome | Hemorrhage | Papilledema | Anorectal Malformations | Pitt-Hopkins Syndrome | Restless Legs Syndrome | Dwarfism | Macular Degeneration | Lymphoma, B-cell | Nasodigitoacoustic Syndrome | Chorea-acanthocytosis | Infantile Liver Failure Syndrome 1 | Cholecystitis | Optic Atrophy 2 | Neurogenic Bladder | Bainbridge-Ropers Syndrome | Chronic Myelomonocytic Leukemia | Bethlem Myopathy | Bardet-Biedl Syndrome | Glycogen Storage Disease Type 1 | Trachoma | Parkinson's Disease | Charcot-Marie-Tooth Disease Type 4D | McLeod Syndrome | Familial Hypobetalipoproteinemia | Kernicterus | Hypobetalipoproteinemias | Heroin Dependence | Ophthalmoplegia | Protein C Deficiency | Anorchia | Hyperlipidemia Type V | Congenital Dyserythropoietic Anemia Type 1 | Pseudomyxoma Peritonei | Antenatal Bartter Syndrome Type 1 | Gestational Trophoblastic Disease | Spinal Cord Diseases | Acquired Partial Lipodystrophy | Heimler Syndrome | Anorexia Nervosa | Achondrogenesis | Wolfram Syndrome 2 | Lathosterolosis | Pituitary Stalk Interruption Syndrome | Personality Disorders | Oculocutaneous Albinism Type 1 | Periodontitis | Meningococcal Infections | Seizures | Amenorrhea | Mitochondrial DNA Depletion Syndrome, Hepatocerebral Form | GAPO Syndrome | Renal-hepatic-pancreatic Dysplasia | Hemophagocytic Lymphohistiocytosis | Biotinidase Deficiency | Glutaric Aciduria Type 3 | Spondylocostal Dysostosis | Robinow Syndrome | Long QT Syndrome Type 1 | Macular Corneal Dystrophy Type 1 | Polyomavirus Nephropathy | Triphalangeal Thumb-polysyndactyly Syndrome | Hypophosphatemic Rickets, Autosomal Recessive, 1 | X-linked Charcot-Marie-Tooth Disease | Fucosidosis | Multiple Hamartoma Syndrome | Alopecia Areata | Lissencephaly 2 | 3-hydroxyacyl-CoA Dehydrogenase Deficiency | Bartter Syndrome | Primary Progressive Nonfluent Aphasia | Tinea Versicolor | Neuroendocrine Cancer | Joubert Syndrome 2 | Chitayat Syndrome | Pemphigoid | Amyloidosis | Chordoma | Hydrocephalus, Normal Pressure | Peripheral T-cell Lymphoma | Enterocolitis, Necrotizing | Pulmonary Alveolar Microlithiasis | Intestinal Pseudo-obstruction | Acute Lymphocytic Leukemia | Malonyl-CoA Decarboxylase Deficiency | Familial Partial Lipodystrophy