Peritonitis

About the Disease
Peritonitis, also known as retractile mesenteritis, is related to tuberculous peritonitis and appendicitis. An important gene associated with Peritonitis is TMEM67 (Transmembrane Protein 67), and among its related pathways/superpathways are Innate Immune System and ERK Signaling. The drugs Ertapenem and Dalbavancin have been mentioned in the context of this disorder. Affiliated tissues include small intestine, liver and colon, and related phenotypes are homeostasis/metabolism and nervous system

Common Targets
PPARG | CARM1 | Interleukin-1 (nonspecified subtype) | TRPV1 | G5743 | GPR18 | CCR2 | SOD2 | NEK7 | IL1B | G3569 | TREM2 | MIR210 | EPX | IL1RAP | LDHA | NLRP3 Inflammasome | BDKRB1 | G7124 | G114548 | CRBN | ALOX5 | CMKLR1 | G7099 | IL18 | MPO | RIPK2 | TFRC

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

Other Diseases

Congenital Hereditary Endothelial Dystrophy Type I | Obesity | Necrotizing Autoimmune Myopathy | Hemangioma | Microphthalmia, Syndromic 7 | Brugada Syndrome 1 | Hemosiderosis | Granular Corneal Dystrophy | Hyperuricemic Nephropathy, Familial Juvenile | DOCK8 Immunodeficiency Syndrome | Androgenic Alopecia | Schamberg Disease | Giant Cell Arteritis | DRESS Syndrome | Mosaic Variegated Aneuploidy Syndrome 2 | Aplasia Cutis Congenita | Progressive Encephalopathy-optic Atrophy Syndrome | Hereditary Xerocytosis | Fraser Syndrome | Charcot-Marie-Tooth Disease, Type 2C | Gingivitis | Lymphedema-distichiasis Syndrome | Cryoglobulinemia | Keratoacanthoma | Pancreatitis | Colorectal Adenoma | Vitamin A Deficiency | Aicardi-Goutieres Syndrome | Epithelial-myoepithelial Carcinoma | Galactosialidosis | Bullous Pemphigoid | Vasculitis | Non-proliferative Diabetic Retinopathy | Osteoporosis, Postmenopausal | MELAS Syndrome | X-linked Sideroblastic Anemia | Retinal Detachment | Hypomyelination With Atrophy Of Basal Ganglia And Cerebellum | Hypolipoproteinemia | Adams-Oliver Syndrome | Pontocerebellar Hypoplasia | Proopiomelanocortin Deficiency | Schizencephaly | Pure Red Cell Aplasia | Rotor Syndrome | Desmosterolosis | Hemangioblastoma | Multiple System Atrophy | Lichen Sclerosus | Heart Block | Papillorenal Syndrome | Cancer, Breast | Chromosome 17q21.31 Deletion Syndrome | Spondyloepimetaphyseal Dysplasia With Joint Laxity, Type 3 | Familial Retinal Arterial Macroaneurysm | Lennox-Gastaut Syndrome | Optic Neuropathy | Polyarteritis Nodosa | Methylmalonic Aciduria And Homocystinuria, CblC Type | Duodenal Atresia | Chronic Lymphocytic Leukemia | Japanese Encephalitis | Protein S Deficiency | Hypophosphatasia | Chronic Leukemia | Borjeson-Forssman-Lehmann Syndrome | Shprintzen-Goldberg Syndrome | Pancreatitis, Chronic | KBG Syndrome | Metachondromatosis | Microcephaly, Seizures, And Developmental Delay | Persistent Truncus Arteriosus | Meconium Ileus | Spinocerebellar Ataxia Type 23 | Eclampsia | Platyspondylic Lethal Skeletal Dysplasia, Torrance Type | Spinocerebellar Ataxia Type 20 | Hydrocephalus, Normal Pressure | Paraplegia | Panniculitis | Haim-Munk Syndrome | Long-chain 3-hydroxyacyl-coenzyme A Dehydrogenase Deficiency | Salla Disease | Dementia | Hypophosphatemic Rickets, Autosomal Recessive, 1 | Non-Hodgkin Lymphoma | Meleda Disease | ACTH-independent Macronodular Adrenal Hyperplasia | Retinopathy Of Prematurity | Primary Hyperoxaluria Type 1 | Cramp Fasciculation Syndrome | Cholestasis, Intrahepatic | Combined Malonic And Methylmalonic Acidemia | Gilbert Syndrome | Retinal Coloboma | Spitz Nevus | Nephrotic Syndrome Type 1 | Angioedema | Heroin Dependence | Pseudohypoparathyroidism Type 1C | Acute Motor Axonal Neuropathy | Meningioma | Neural Tube Defect | Ophthalmoplegia | Trichothiodystrophy | Spinocerebellar Ataxia Type 1 | Viral Meningitis | Microcephalic Osteodysplastic Primordial Dwarfism, Type II | Dubin-Johnson Syndrome | Cutaneous Mastocytosis | Lissencephaly 2 | Diabetes | Cervicitis | Large Granular Lymphocytic Leukemia | Mitochondrial DNA Depletion Syndrome | 3-hydroxyacyl-CoA Dehydrogenase Deficiency | Hypereosinophilic Syndrome | Hereditary Mixed Polyposis Syndrome | Diabetic Encephalopathy | Vitamin B12 Deficiency | Chorea | Familial Isolated Hyperparathyroidism | Spinocerebellar Ataxia Type 5 | HANAC Syndrome | Olmsted Syndrome | Hypophosphatemic Rickets With Hypercalciuria, Hereditary | Jacobsen Syndrome | Astrocytoma | Paronychia | Erythrokeratodermia Variabilis | Pityriasis Rubra Pilaris | Isovaleric Acidemia | Brachial Plexus Neuropathy | Spinocerebellar Ataxia | Congenital Stationary Night Blindness | Blastoma, Pleuropulmonary | Esophageal Adenocarcinoma | Fuchs Dystrophy | Cerebrotendinous Xanthomatosis | Spinocerebellar Ataxia Type 12 | Nemaline Myopathy 8 | Cardiac Sarcoidosis | Sick Sinus Syndrome | Rhinitis | Bipolar Disorder | Bacterial Meningitis | Epidermodysplasia Verruciformis | Currarino Syndrome | Gastroenteritis, Eosinophilic | Vaginitis | Primary Carnitine Deficiency | Dystonia Musculorum Deformans | Congenital Dyserythropoietic Anemia | Neurofibromatosis Type 2 | Sickle Cell Anemia | Antenatal Bartter Syndrome Type 1 | Multicystic Renal Dysplasia | Frank-ter Haar Syndrome | Multiple Hamartoma Syndrome | Osteogenesis Imperfecta | NDH Syndrome | Hereditary Folate Malabsorption | Hypoparathyroidism | Retinitis Pigmentosa 3 | Molybdenum Cofactor Deficiency | Familial Hypertrophic Cardiomyopathy | Hypertensive Nephropathy | Peyronie's Disease | Lipid Metabolism Disorders | Plasma Cell Dyscrasia | Hyperostosis | Intellectual Disability, Autosomal Dominant 5 | Macular Degeneration | Lymphomatoid Granulomatosis | Gaucher Disease | Papulopustular Rosacea | Open-angle Glaucoma | Reye Syndrome | Stuttering | Lactose Intolerance | Esophagitis, Eosinophilic | Arthrogryposis | Maternally Inherited Diabetes And Deafness | Hypertrophic Osteoarthropathy, Primary, Autosomal Recessive 2 | Lung Diseases | Cysticercosis | Primary Cutaneous Amyloidosis | Eiken Syndrome | Partington Syndrome | Fundus Albipunctatus | Relapsing Polychondritis | Herpes Genitalis | Pyloric Stenosis, Infantile Hypertrophic | Polymicrogyria | Rhabdomyosarcoma, Alveolar | Lattice Corneal Dystrophy | Succinic Semialdehyde Dehydrogenase Deficiency | Larsen Syndrome | Neuroblastoma | IgA Nephropathy | Osteonecrosis | ICF Syndrome | Rhabdomyosarcoma, Embryonal | Onchocerciasis | HUPRA Syndrome | Ependymoma | Neurofibromatosis-Noonan Syndrome | Sorsby Fundus Dystrophy | Acrocallosal Syndrome | Eosinophilia | Thanatophoric Dysplasia Type 1 | Spinal Muscular Atrophy With Progressive Myoclonic Epilepsy | Osteogenesis Imperfecta Type IV | Thalassemia | Hemochromatosis Type 2 | Angioedema, Hereditary | Pontocerebellar Hypoplasia Type 7 | Anuria | Chorioretinitis | Astrocytoma, Anaplastic | Familial Hemiplegic Migraine | Cancer, Lung | Glomerulonephritis | Vitelliform Macular Dystrophy | Leishmaniasis, Visceral | Fibromuscular Dysplasia | Chylomicron Retention Disease | Prune Belly Syndrome | Esophageal Motility Disorders | Hereditary Elliptocytosis | Acute Lymphocytic Leukemia | Congenital Diaphragmatic Hernia | Hereditary Sensory And Autonomic Neuropathy | Blepharitis | Acquired Partial Lipodystrophy | Niemann-Pick Disease, Type A | Teratozoospermia | Spondylolisthesis | Nestor-Guillermo Progeria Syndrome | Farber Disease | Gangliosidosis, GM1 | Meesmann Corneal Dystrophy | Aneurysm, Thoracic Aortic | Myelitis | Hyperlipidemia, Familial Combined | Congenital Stromal Corneal Dystrophy | Gastritis, Atrophic | Dwarfism | Hyperbilirubinemia | Trachoma | Lipid Storage Diseases | Light Chain Amyloidosis | Thyroiditis | Coronary Restenosis | Tendinitis | Xeroderma Pigmentosum | Cancer, Kidney | Hypermetropia | Hypoplastic Left Heart Syndrome | Limb Girdle Muscular Dystrophy | Polymyositis | Zimmermann-Laband Syndrome | Cold Agglutinin Disease | TARP Syndrome | Niemann-Pick Disease, Type C | Focal Facial Dermal Dysplasia | Conjunctivitis, Allergic | Mixed Connective Tissue Disease | Paraganglioma | Carcinoma, Merkel Cell | Dysgerminoma | Adenylosuccinate Lyase Deficiency | Congenital Sodium Diarrhea | Long QT Syndrome Type 1 | Neurocutaneous Syndromes | Muir-Torre Syndrome | Lamellar Ichthyosis | Hemorrhage | Empyema | Multicentric Carpotarsal Osteolysis Syndrome | Ehlers-Danlos Syndrome | Osteochondrosis | Charcot-Marie-Tooth Disease, Type 1A | Demyelinating Diseases | Hepatitis B, Chronic | Microtia | Cholecystitis | Early Infantile Epileptic Encephalopathy | Diastrophic Dysplasia | Cirrhosis | Benign Recurrent Intrahepatic Cholestasis 1 | Renpenning Syndrome | Coffin-Siris Syndrome | Pseudohermaphroditism | Hyperinsulinism-hyperammonemia Syndrome | Congenital Adrenal Hyperplasia | Persistent Fetal Circulation | Muckle-Wells Syndrome | Guttate Psoriasis | Hypersomnia | Centronuclear Myopathy | Nicotine Dependence | Carpal Tunnel Syndrome | Alagille Syndrome | Supravalvular Aortic Stenosis | Hypercholesterolemia, Familial | Splenomegaly | GATA2 Deficiency | Allergic Contact Dermatitis | Rickets | Charcot-Marie-Tooth Disease Type 2D | Priapism | Impetigo | Trichomegaly | Congenital Generalized Lipodystrophy | Hyperbilirubinemia, Neonatal | Arthropathy | Diffuse Intrinsic Pontine Glioma | Encephalitis, Tick-borne | Nance-Horan Syndrome | Seborrheic Dermatitis | Sarcoma | Neurofibroma, Plexiform | Exotropia | Hypertrophic Osteoarthropathy, Primary, Autosomal Recessive 1 | Kallmann Syndrome | Adenomyosis | Menetrier Disease | FG Syndrome | Myoclonus-dystonia Syndrome | Familial Digital Arthropathy-brachydactyly | Myasthenia | Fetal Akinesia Deformation Sequence | X-linked Myotubular Myopathy | Blastomycosis | Periventricular Nodular Heterotopia | Stickler Syndrome | Wolcott-Rallison Syndrome | Ganglioglioma | Fahr Disease | Cherubism | Menkes Disease | Multiple Sclerosis | Spinocerebellar Ataxia Type 13 | Vulvovaginitis | Zollinger-Ellison Syndrome | Epiphyseal Chondrodysplasia, Miura Type | Tetraplegia | Christianson Syndrome | Spondylocarpotarsal Synostosis Syndrome | Glutathione Synthetase Deficiency | Bainbridge-Ropers Syndrome | Renal Hypouricemia | Multiple Sclerosis, Secondary Progressive | Multisystemic Smooth Muscle Dysfunction Syndrome | Cavitary Optic Disc Anomalies | Alzheimer Disease, Late Onset | Adenoma, Pituitary | Torticollis | Ichthyosis Hystrix, Curth-Macklin Type | Hemophilia | Malignant Peripheral Nerve Sheath Tumor | Paget's Disease Of The Breast | Hypertension, Renal | Rhabdoid Tumor | Renal Oncocytoma | Loeys-Dietz Syndrome | Pulmonary Alveolar Microlithiasis | Protein C Deficiency | Thyroid Dysgenesis | Fibrillation, Atrial | Nail-Patella Syndrome | Papilloma | T-cell Chronic Lymphocytic Leukemia | Liddle Syndrome | Cholangitis | Crigler-Najjar Syndrome | Infertility | Myelomeningocele | Metaphyseal Chondrodysplasia, Schmid Type | Wagner Disease | Localized Scleroderma | Bicuspid Aortic Valve | Intracerebral Hemorrhage | Leukoencephalopathy, Progressive Multifocal | Mumps | Frontometaphyseal Dysplasia | Autoimmune Disease | Opisthorchiasis | Early Infantile Epileptic Encephalopathy 28 | Anorchia | Carcinoma, Transitional Cell | Spinal Muscular Atrophy Type 2 | Traboulsi Syndrome | Sclerocornea | 6-pyruvoyl-tetrahydropterin Synthase Deficiency | Epidermolysis Bullosa Simplex, Dowling-Meara Type | Apert Syndrome | Congenital Hemolytic Anemia | Thromboembolism