Paracoccidioidomycosis
Paracoccidioidomycosis
About the Disease
Paracoccidioidomycosis, also known as mucocutaneous-lymphangitic paracoccidioidomycosis, is related to histoplasmosis and cryptococcosis. An important gene associated with Paracoccidioidomycosis is IL10 (Interleukin 10), and among its related pathways/superpathways are Innate Immune System and ERK Signaling. Affiliated tissues include mucosa, lymph nodes and bone, and related phenotypes are no effect and no effect
Common Targets
IL4
Note: If you'd like to get a target analysis report for Paracoccidioidomycosis, 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 Paracoccidioidomycosis at a cost 90% lower than traditional approaches, please feel free to contact us at BD@silexon.ai.
Other Diseases
Gastroenteritis | Asplenia | Hyperacusis | Mitochondrial Cytopathy | Familial Dysautonomia | Panic Disorder | Ichthyosis Bullosa Of Siemens | Myoclonus | Fibrosis | McKusick Type Metaphyseal Chondrodysplasia | Alpha-mannosidosis | Pyelonephritis | Urticaria | Diabetes Insipidus, Nephrogenic | Osteogenesis Imperfecta Type II | Gitelman Syndrome | Renal Medullary Carcinoma | Lennox-Gastaut Syndrome | Polycythemia | Infantile Spasm | Spinocerebellar Ataxia Type 1 | Azoospermia | Niemann-Pick Disease, Type C | Antley-Bixler Syndrome | Open-angle Glaucoma | Neurocysticercosis | Tatton-Brown-Rahman Syndrome | Ataxia-hypogonadism-choroidal Dystrophy Syndrome | Dystrophy, Cone-rod | Microvillus Inclusion Disease | Keratitis-ichthyosis-deafness Syndrome | Autism Spectrum Disorders | Spasticity | Pulmonary Tuberculosis | Beta-Propeller Protein-associated Neurodegeneration | NGLY1 Deficiency | Brachial Plexus Neuropathy | Choreoathetosis, Hypothyroidism, And Neonatal Respiratory Distress | Intestinal Tuberculosis | Congenital Muscular Dystrophy | Pancytopenia | Pituitary Stalk Interruption Syndrome | Nemaline Myopathy | Renal Tubular Acidosis | Intestinal Pseudo-obstruction | Camptocormia | D-2-Hydroxyglutaric Aciduria | Liver Failure | Syndactyly | Pneumonia, Viral | Otitis Externa | Christianson Syndrome | Chronic Leukemia | Heart Septal Defects | Short-chain Acyl-CoA Dehydrogenase Deficiency | Neurofibromatosis Type 2 | Micropenis | Spinocerebellar Ataxia Type 6 | Pseudohypoparathyroidism Type 1B | Extramammary Paget's Disease | Kidney Stones | Premature Ejaculation | Von Willebrand Disease | Lichen Planus | Teratozoospermia | Multiple System Atrophy | Autoimmune Hemolytic Anemia | Lymphedema-distichiasis Syndrome | Bulimia Nervosa | Lipoma | Megalencephaly | Bronchitis | Hydronephrosis | Osteogenesis Imperfecta Type III | Poirier-Bienvenu Neurodevelopmental Syndrome | Cholestasis, Intrahepatic | Polyomavirus Nephropathy | Hypertension | SAPHO Syndrome | Branchiootorenal Syndrome | Pfeiffer Syndrome | Hypertension, Renovascular | Congenital Tufting Enteropathy | Cutaneous Mastocytosis | Thrombotic Microangiopathy | Traboulsi Syndrome | Binge Eating Disorder | Presbyopia | Osteosarcoma | Robinow Syndrome | Glycogen Storage Disease Type 1 | Poikiloderma With Neutropenia | Goldenhar Syndrome | Pierpont Syndrome | Stuve-Wiedemann Syndrome | Gigantism | Papilledema | Nanophthalmos | Coffin-Siris Syndrome | Dysmorphophobia | Hyperlipidemia Type V | Chronic Inflammatory Demyelinating Polyneuropathy | Orotic Aciduria | Warsaw Breakage Syndrome | Encephalitis | Actinomycetoma | Neuropathy | Renal Hypomagnesemia 3 | Chromosome 5q Deletion Syndrome | Myelitis, Transverse | Heart Failure | 3-hydroxy-3-methylglutaric Aciduria | Melanoma, Uveal | Anencephaly | Lathosterolosis | Bardet-Biedl Syndrome | Varicocele | Silicosis | Cancer, Bladder | Acute Motor Axonal Neuropathy | Benign Hereditary Chorea | Spondyloperipheral Dysplasia | Schnyder Crystalline Corneal Dystrophy | Geleophysic Dysplasia | Colitis | Prolactinoma | Urolithiasis | Wolman Disease | Hepatitis D | Arteriosclerosis | Osteosclerosis | Takotsubo Cardiomyopathy | Neutrophilia | Hypothyroidism | Zimmermann-Laband Syndrome | Hypopituitarism | Isovaleric Acidemia | Spinal Cord Diseases | Schwartz-Jampel-Aberfeld Syndrome | Tangier Disease | Eczema | Sclerosing Cholangitis | Hydrocephalus, Normal Pressure | Multiple Congenital Anomalies-hypotonia-seizures Syndrome 2 | Hypercholesterolemia | Intermittent Claudication | Milk Allergy | Tyrosinemia Type 2 | Progressive Familial Intrahepatic Cholestasis Type 3 | Bronchitis, Chronic | Pulmonary Veno-occlusive Disease | Birt-Hogg-Dube Syndrome | Cartilage Disorders | Sarcoma, Endometrial Stromal | Hyperthyroidism | Citrullinemia | Congenital Nephrotic Syndrome | Optic Nerve Diseases | Brugada Syndrome 1 | Neutropenia | Congenital Dyserythropoietic Anemia Type 4 | Feingold Syndrome | Roberts Syndrome | Antithrombin III Deficiency | Periventricular Nodular Heterotopia | Vici Syndrome | Scapuloperoneal Spinal Muscular Atrophy | Leukoplakia, Oral | Diastrophic Dysplasia | Cole-Carpenter Syndrome | Episodic Ataxia Type 1 | Nager Acrofacial Dysostosis | Eosinophilia | Spondyloepiphyseal Dysplasia Tarda, X-linked | Postpoliomyelitis Syndrome | Chromosome 8q21.11 Deletion Syndrome | MIRAGE Syndrome | Personality Disorders | Very Long-chain Acyl-CoA Dehydrogenase Deficiency | Von Hippel-Lindau Disease | Osteogenesis Imperfecta Type VI | Sarcosinemia | Infantile Liver Failure Syndrome 1 | Microtia | Exfoliative Dermatitis | Schnitzler Syndrome | Esophageal Adenocarcinoma | Hydrops Fetalis | Ghosal Syndrome | Tracheal Disorders | Neuroectodermal Tumors, Primitive | Trachoma | LRBA Deficiency | Aneurysm, Thoracic Aortic | Esophagitis, Eosinophilic | Premenstrual Syndrome | Epidermolysis Bullosa Simplex, Localized | Anosmia, Congenital | Venous Insufficiency | Coronary Artery Disease | Central Pain Syndrome | Primrose Syndrome | Trichothiodystrophy | Stickler Syndrome | Neurofibromatosis Type 1 | Juvenile Hyaline Fibromatosis | Osteomyelitis | Congenital Heart Block | Pancreatitis | Cholesteryl Ester Storage Disease | Greig Cephalopolysyndactyly Syndrome | Esophagitis | Pyloric Stenosis, Infantile Hypertrophic | Snyder-Robinson Syndrome | Erythematotelangiectatic Rosacea | Gardner Syndrome | Ulcerative Colitis | Ollier Disease | Hypophosphatasia | Neuroblastoma | Non-small Cell Lung Cancer | Graft-versus-host Disease | Thyroid Dysgenesis | Leukodystrophies | Turner's Syndrome | Sensory Ataxic Neuropathy, Dysarthria, And Ophthalmoparesis | Sponastrime Dysplasia | Megacystis-microcolon-intestinal Hypoperistalsis Syndrome | Hartsfield Syndrome | Meniere's Disease | Norrie Disease | Familial Isolated Hyperparathyroidism | Spinocerebellar Ataxia Type 15 | Paget's Disease Of The Breast | Patent Foramen Ovale | Dupuytren Disease | Epidermolysis Bullosa Simplex, Generalized | Goiter | Transient Bullous Dermolysis Of The Newborn | Hypertension, Renal | Carcinoma In Situ | Oligospermia | Withdrawal Syndrome | Leprosy | Presbycusis | Progressive Familial Intrahepatic Cholestasis Type 1 | Behcet's Disease | Hypersensitivity | Angelman Syndrome | Tendinitis | Osteopetrosis | Priapism | Usher Syndrome | Cranial Nerve Disease | Sotos Syndrome | Cushing Syndrome | Arthritis, Reactive | Hypertelorism | Dermatitis | Chondrosarcoma | Scabies | Basal Cell Nevus Syndrome | Lesch-Nyhan Syndrome | Rhabdomyosarcoma, Embryonal | Antiphospholipid Syndrome | Oculocutaneous Albinism Type 4 | Rash | Speech Disorders | Hypopigmentation | T-cell Lymphoma, Subcutaneous Panniculitis-like | Tenosynovial Giant Cell Tumor | Sporadic Inclusion Body Myositis | Acrodermatitis Enteropathica | Charcot-Marie-Tooth Disease, Type 2A | Torticollis | Lymphangioma | Hypotrichosis Simplex | Heterotaxy | Episodic Ataxia | Keratoconus | Nicotine Dependence | Anorexia Nervosa | Periventricular Leukomalacia | Charcot-Marie-Tooth Disease | Cerebral Amyloid Angiopathy | Encephalopathy, Hepatic | Learning Disability | Language Disorders | Aldosteronism | Non-epidermolytic Palmoplantar Keratoderma | Retinal Coloboma | Carcinoma, Merkel Cell | Pityriasis Rubra Pilaris | Homocystinuria | Chronic Kidney Disease | T-cell Prolymphocytic Leukemia | Bone Marrow Necrosis | Epilepsy Of Infancy With Migrating Focal Seizures | Mannosidase Deficiency Diseases | Erythropoietic Protoporphyria | Waardenburg Syndrome Type 2E | Acrodysostosis | Maple Syrup Urine Disease | Histiocytic Sarcoma | Cornelia De Lange Syndrome | Hypertensive Retinopathy | Amebiasis | Multiple Mitochondrial Dysfunctions Syndrome Type 1 | Myoclonus-dystonia Syndrome | Impulse Control Disorder | Miyoshi Myopathy | Bruck Syndrome | Nicotine Addiction | Nephrotic Syndrome | Rett Syndrome | Hyperparathyroidism, Secondary | Autosomal Recessive Spastic Paraplegia Type 54 | Donnai-Barrow Syndrome | Spinocerebellar Ataxia Type 10 | Megaloblastic Anemia | Multiple Hamartoma Syndrome | Granuloma Annulare | Glycogen Storage Disease Type 5 | Hennekam Lymphangiectasia-lymphedema Syndrome | Waardenburg Syndrome | Clouston Hidrotic Ectodermal Dysplasia | Multiple Sclerosis, Secondary Progressive | Antenatal Bartter Syndrome Type 1 | Epidermolysis Bullosa Simplex, Dowling-Meara Type | Hermansky-Pudlak Syndrome | Esophageal Carcinoma | Hypokalemia | Diffuse Palmoplantar Keratoderma | Methylmalonic Acidemia | Vaginitis | Thanatophoric Dysplasia | Familial Cerebral Amyloid Angiopathy | Carpenter Syndrome | Allan-Herndon-Dudley Syndrome | Cancer, Colon | Seborrheic Dermatitis | Multiple Sclerosis, Relapsing-remitting | Meier-Gorlin Syndrome | Vitamin K Deficiency | COACH Syndrome | Glaucoma | Gilbert Syndrome | Tinea Versicolor | Acute Anterior Uveitis | Raine Syndrome | Gastritis, Atrophic | Spinocerebellar Ataxia Type 5 | Hyperparathyroidism | Cancer, Lung | Platelet Disorders | Spondylo-ocular Syndrome | Blau Syndrome | Thrombophilia | Bacterial Meningitis | Spinal Muscular Atrophy Type 3 | Otitis Media | Crohn's Disease | Cheilitis | Retinopathy Of Prematurity | Mucolipidosis Type II | Cluster Headache | Cystitis, Interstitial | Large Granular Lymphocytic Leukemia | Sialidosis Type I | Hypertensive Nephropathy | Gastroenteritis, Eosinophilic | Fibromyalgia | Glycogen Storage Disease Type 6 | Richter's Syndrome | Wolfram Syndrome 2 | Phenylketonuria | Galactosialidosis | 3-methylglutaconic Aciduria | Schamberg Disease | Pterygium | Cervicitis | Fragile X Syndrome | Anuria | Sleep Apnea, Obstructive | Myoclonic Epilepsy With Ragged Red Fibers | Endocarditis | Schwannomatosis | Alopecia Areata | Dengue Hemorrhagic Fever | Spinocerebellar Ataxia Type 23 | Oculopharyngeal Muscular Dystrophy | X-linked Acrogigantism | Aldosterone Deficiency | Situs Inversus | Kabuki Syndrome 2 | Nephrocalcinosis | Anal Fissure | Spinocerebellar Ataxia Type 38 | Lung Diseases | Spondylocostal Dysostosis