Disease

Visceral Leishmaniasis

About the Disease
Visceral Leishmaniasis, also known as leishmaniasis, visceral, is related to leishmaniasis and cutaneous leishmaniasis. An important gene associated with Visceral Leishmaniasis is KAZA1 (Kala-Azar (Visceral Leishmaniasis), Susceptibility To), and among its related pathways/superpathways are Innate Immune System and ERK Signaling. The drugs Miconazole and Clotrimazole have been mentioned in the context of this disorder. Affiliated tissues include bone marrow, spleen and bone, and related phenotypes are homeostasis/metabolism and immune system

Common Targets
IL4 | IL10 | FCN2 | IL2RB | G7124 | IL12B | FAM120B | IL1B | G3569 | LTA | IL12RB1 | Protein Tyrosine Phosphatase (PTP) (nonspecified subtype) | HLA-DRB1 | CCL1 | CCL16 | CDK12/Cyclin K | DLL1 | AGMO | CXCR2 | SLC11A1 | FAS | TLR9 | CDK12

疾病靶点研报
Visceral Leishmaniasis

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

Other Diseases

Tardive Dyskinesia | Herpes Simplex Dermatitis | Chronic Mucocutaneous Candidiasis | Methemoglobinemia | Cri-du-chat Syndrome | Schnitzler Syndrome | Graves Disease | Pyelonephritis | Malignant Fibrous Histiocytoma | Epidermolysis Bullosa Simplex | Keratopathy | Bleeding Disorder Due To CalDAG-GEFI Deficiency | Intracranial Hypertension | Progressive Myoclonic Epilepsy | Nasodigitoacoustic Syndrome | Hyperinsulinism-hyperammonemia Syndrome | MELAS Syndrome | Werner's Syndrome | Paraganglioma, Carotid Body | Retinal Dystrophy | Leiomyoma | Spondyloarthritis | Narcolepsy | Chondrosarcoma | Esophagitis, Eosinophilic | Hyperandrogenemia | Juvenile Myelomonocytic Leukemia | X-linked Myotubular Myopathy | Bartter Syndrome | Open-angle Glaucoma | Diabetes Type 1 | Vogt-Koyanagi-Harada Syndrome | GATA2 Deficiency | Amyotrophic Lateral Sclerosis | Intracerebral Hemorrhage | Eccrine Porocarcinoma | Cancer, Breast | Spondylocostal Dysostosis | Liddle Syndrome | Erectile Dysfunction | Orthostatic Intolerance | Sulfite Oxidase Deficiency | Infantile Refsum Disease | Spinocerebellar Ataxia Type 23 | Early Infantile Epileptic Encephalopathy 4 | Nephritis, Interstitial | Pregnancy, Ectopic | Hypohidrotic Ectodermal Dysplasia | Neurocutaneous Syndromes | Spina Bifida | Mucolipidosis | Arthritis, Psoriatic | Sturge-Weber Syndrome | Pseudohypoparathyroidism Type 1B | Pure Autonomic Failure | Autoimmune Disease | Nemaline Myopathy | Actinomycetoma | Adrenomyeloneuropathy | Localized Scleroderma | Lichen Planus | Meckel-Gruber Syndrome | Diabetes | Autosomal Recessive Bestrophinopathy | Whipple's Disease | Kaposi Sarcoma | Dent Disease | Ornithine Transcarbamylase Deficiency | Adams-Oliver Syndrome | Aplasia Cutis Congenita | Choroiditis | Hemosiderosis | Myasthenia Gravis | Scapuloperoneal Myopathy, X-linked Dominant | Tetraplegia | Progressive External Ophthalmoplegia | Tay-Sachs Disease | Cervicitis | Alopecia Areata | Retinitis Pigmentosa 3 | Aldosterone Synthase Deficiency | Rubeosis Iridis | Wolfram Syndrome | Pyruvate Carboxylase Deficiency Disease | Blepharitis | Pseudoachondroplasia | Vaginitis | Teratozoospermia | Ataxia-hypogonadism-choroidal Dystrophy Syndrome | Colitis, Collagenous | Myelomeningocele | Trigonocephaly | Hypophosphatemic Rickets, Autosomal Recessive, 1 | Pituitary Dwarfism | Osteogenesis Imperfecta Type I | Meningioma, Benign | Overactive Bladder | Chondromyxoid Fibroma | Optic Neuritis | Multiple Sclerosis | McKusick Type Metaphyseal Chondrodysplasia | Osteogenesis Imperfecta Type III | Asthma, Exercise-induced | Granular Corneal Dystrophy Type 1 | Epicondylitis | CHOPS Syndrome | Charcot-Marie-Tooth Disease Type 2D | Lyme Disease | Ileitis | Behavioral Variant Of Frontotemporal Dementia | Polycystic Ovary Syndrome | Schizoaffective Disorder | Tonsillitis | Waardenburg Syndrome | Ichthyosis Bullosa Of Siemens | Twin-to-twin Transfusion Syndrome | Sarcoma, Ewing | Japanese Encephalitis | Hydrops Fetalis | Hemophagocytic Lymphohistiocytosis | Neuromuscular Disorders | Chylomicron Retention Disease | Ichthyosis | Anosmia, Congenital | Congenital Disorders Of Glycosylation Type II | Renal Failure | Spastic Paraplegia Type 7 | Congenital Heart Defects | Richter's Syndrome | Strabismus | Nager Acrofacial Dysostosis | Disseminated Intravascular Coagulation | Tinea Versicolor | Varices | Adrenal Insufficiency | 17-beta-hydroxysteroid Dehydrogenase X Deficiency | Dysfibrinogenemia | Bronchiolitis | Prune Belly Syndrome | Aneurysm, Abdominal Aortic | Glutaric Aciduria Type 3 | Pre-eclampsia | Microcephaly, Seizures, And Developmental Delay | Hepatitis D | Coffin-Siris Syndrome | Primary Aldosteronism | Myelofibrosis | Non-proliferative Diabetic Retinopathy | Sitosterolemia | Hypertension, Renovascular | Hypobetalipoproteinemias | Congenital Bilateral Absence Of Vas Deferens | Giant Cell Glioblastoma | Stevens-Johnson Syndrome | Hypotrichosis | Epidermolysis Bullosa Dystrophica | Polycystic Kidney, Autosomal Dominant | Astrocytoma, Anaplastic | Gangliosidosis | Rhizomelic Chondrodysplasia Punctata | Coma | Chondroma | Bietti Crystalline Dystrophy | T-cell Chronic Lymphocytic Leukemia | Swine Influenza | Progressive Osseous Heteroplasia | Glycogen Storage Disease Type 0, Muscle | Neurodermatitis | Neurofibroma | Central Retinal Artery Occlusion | Xeroderma Pigmentosum Variant Type | Retinoblastoma | Asphyxia Neonatorum | Systemic Lupus Erythematosus | Hydrolethalus Syndrome | Desbuquois Syndrome | Disseminated Superficial Actinic Porokeratosis | Myopathy | Crisponi Syndrome | Cerebral Amyloid Angiopathy | Alzheimer Disease, Late Onset | Hypocalcemia | Neurocysticercosis | Familial Partial Lipodystrophy | Cystitis, Interstitial | Fontaine Progeroid Syndrome | Aicardi-Goutieres Syndrome | Celiac Disease | Carbonic Anhydrase VA Deficiency | Congenital Stromal Corneal Dystrophy | Spinocerebellar Ataxia Type 1 | Retinal Dystrophy, Early-onset Severe | Charcot-Marie-Tooth Disease Type 3 | Reticular Dysgenesis | Congenital Generalized Lipodystrophy | Osteitis | Measles | Knobloch Syndrome | Glycogen Storage Disease | Waldenstrom Macroglobulinemia | Pemphigus | Dementia | Bicuspid Aortic Valve | Spinocerebellar Ataxia Type 38 | Metabolic Syndrome | Arthritis, Reactive | Congenital Dysfibrinogenemia | Congenital Primary Aphakia | Optic Atrophy 2 | Tularemia | Medium-chain Acyl-CoA Dehydrogenase Deficiency | ACTH-independent Macronodular Adrenal Hyperplasia | Metachromatic Leukodystrophy | Zygomycosis | Urea Cycle Disorder | Retinoschisis | Autism | Pneumoconiosis | VACTERL/VATER Association | Primary Sclerosing Cholangitis | Desmosterolosis | Osteogenesis Imperfecta Type IV | Alazami Syndrome | Acquired Partial Lipodystrophy | Waardenburg Syndrome Type 2A | Heroin Dependence | COACH Syndrome | Seasonal Mood Disorder | Cryptococcal Meningitis | Goldenhar Syndrome | Myotonia | Rotor Syndrome | Hodgkin Lymphoma | Spasticity | Vascular Cognitive Impairment | Hartsfield Syndrome | Cartilage Disorders | Cheilitis | Multicentric Carpotarsal Osteolysis Syndrome | Martsolf Syndrome | Pituitary Stalk Interruption Syndrome | Congenital Mirror Movements | Glycogen Storage Disease Type 1b | Peritonitis | Granuloma Annulare | Leri-Weill Dyschondrosteosis | Congenital Dyserythropoietic Anemia | Hemorrhage | Jalili Syndrome | Hyperphenylalaninemia | Diabetes Insipidus | Shwachman-Bodian-Diamond Syndrome | Primary Hyperoxaluria Type 1 | Esthesioneuroblastoma | Hypertrophy | Mitochondrial DNA Depletion Syndrome, Encephalomyopathic Form | X-linked Creatine Transporter Deficiency | Endophthalmitis | Glanzmann Thrombasthenia | Saul-Wilson Syndrome | Herpes Genitalis | Thin Basement Membrane Disease | Stromal Corneal Dystrophy | Combined Pituitary Hormone Deficiency | Bartsocas-Papas Syndrome | Leishmaniasis, Cutaneous | Autoimmune Hemolytic Anemia | NGLY1 Deficiency | Pancytopenia | Rhinitis | Adenoma, Pleomorphic | Gangliosidosis, GM1 | Fanconi Syndrome | Crohn's Disease | Hypothyroidism | Peripheral Neuropathy | Harlequin Ichthyosis | Fuchs Dystrophy | Adenoma, Pituitary | Multiple Sulfatase Deficiency | Pleomorphic Xanthoastrocytoma | Lattice Corneal Dystrophy Type 1 | Familial Mediterranean Fever | Cushing Syndrome | Krabbe Disease | Hyperphosphatasia With Intellectual Disability Syndrome 4 | Synovitis | Lymphoma | Distal Spinal Muscular Atrophy | Epidermolytic Hyperkeratosis | Familial Hyperaldosteronism | Neuromyelitis Optica | Amyotrophic Lateral Sclerosis-parkinsonism-dementia Complex | Crouzon Syndrome With Acanthosis Nigricans | Hereditary Pyropoikilocytosis | Muckle-Wells Syndrome | Aplastic Anemia | Choriocarcinoma | Incontinentia Pigmenti | Fanconi Anemia | Rhabdomyosarcoma | Facioscapulohumeral Muscular Dystrophy | Infantile Liver Failure Syndrome 1 | Kearns-Sayre Syndrome | Paraplegia | Camurati-Engelmann Disease | Congenital Nystagmus | Tenosynovial Giant Cell Tumor | Holt-Oram Syndrome | Renal Hypouricemia | Glycogen Storage Disease Type 9 | Mabry Syndrome | Silver-Russell Syndrome | Pyruvate Decarboxylase Deficiency | Sleep Apnea, Central | Pulmonary Stenosis | Phosphoenolpyruvate Carboxykinase Deficiency, Cytosolic | Neuroma | Congenital Stationary Night Blindness | Angioimmunoblastic T-cell Lymphoma | Idiopathic Multicentric Castleman Disease | Scoliosis | Sweet Syndrome | Klippel-Feil Syndrome | Thyroiditis | Antisocial Personality Disorder | Autosomal Recessive Spastic Paraplegia Type 35 | Chronic Leukemia | Genitopatellar Syndrome | Congenital Diaphragmatic Hernia | Double Outlet Right Ventricle | Woodhouse-Sakati Syndrome | Megacystis-microcolon-intestinal Hypoperistalsis Syndrome | Achondrogenesis | Haim-Munk Syndrome | Erythematotelangiectatic Rosacea | Uremia | Carney Triad | Stroke, Ischemic | Neonatal Progeroid Syndrome | Anthrax | Platyspondylic Lethal Skeletal Dysplasia, Torrance Type | Currarino Syndrome | Supravalvular Aortic Stenosis | Keratitis-ichthyosis-deafness Syndrome | Acne Vulgaris | Infectious Diarrhea | Inflammatory Joint Disease | Mumps | Bardet-Biedl Syndrome | Colitis, Lymphocytic | Phenylketonuria II | Joubert Syndrome | Acute Lymphocytic Leukemia | Branchiootorenal Syndrome | Angioedema, Hereditary | Menetrier Disease | CEDNIK Syndrome | Hereditary Mixed Polyposis Syndrome | Huntington's Disease-like 2 | Gnathodiaphyseal Dysplasia | Myocardial Infarction | IMAGe Syndrome | Osteonecrosis | Aspergillosis | High Molecular Weight Kininogen Deficiency | Borderline Personality Disorder | Familial Exudative Vitreoretinopathy | Anxiety Disorders | Dentinogenesis Imperfecta | Takayasu's Arteritis | Congenital Hemolytic Anemia | Erdheim-Chester Disease | Alopecia | Pterygium | Steel Syndrome | Subacute Sclerosing Panencephalitis | Nicotine Addiction | Waardenburg Syndrome Type 2 | Hyperinsulinemic Hypoglycemia | 3-hydroxyacyl-CoA Dehydrogenase Deficiency | Aceruloplasminemia | Spondylo-ocular Syndrome | Hyperammonemia | Tylosis With Esophageal Cancer | PASLI Disease | Raine Syndrome | Epidermolysis Bullosa Simplex, Dowling-Meara Type | Spinal Muscular Atrophy | Pompe Disease | Ehlers-Danlos Syndrome | Dermatomyositis | Periodic Limb Movement Disorder | Wiedemann-Steiner Syndrome | Basan Syndrome | Diabetic Nephropathy | Oculocutaneous Albinism Type 1 | Microcephalic Osteodysplastic Primordial Dwarfism, Type I | Alpers Syndrome | Non-small Cell Lung Cancer