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

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Other Diseases

Acute Lymphocytic Leukemia | Prader-Willi Syndrome | Craniopharyngioma | Osteoarthritis | Tenosynovial Giant Cell Tumor | Influenza | Transcobalamin Deficiency | Peripheral Neuropathy | Krabbe Disease | Macular Corneal Dystrophy | Glioblastoma | Spastic Paraplegia Type 7 | POEMS Syndrome | Herpes Simplex Dermatitis | Vitiligo | Pemphigus Vulgaris | Congenital Bile Acid Synthesis Defect | Mitochondrial DNA Depletion Syndrome, Encephalomyopathic Form | Speech Disorders | Skin Fragility-woolly Hair Syndrome | Heterotaxy | Diabetic Nephropathy | Crohn's Disease | Diffuse Idiopathic Pulmonary Neuroendocrine Cell Hyperplasia | Craniometaphyseal Dysplasia | Jacobsen Syndrome | Cousin Syndrome | Low Phospholipid Associated Cholelithiasis | Lipid Metabolism Disorders | Aromatic L-amino Acid Decarboxylase Deficiency | Roberts Syndrome | Schistosomiasis | Chronic Beryllium Disease | Spermatocele | Adenoid Cystic Carcinoma | Primary Carnitine Deficiency | Contact Dermatitis | Systemic Lupus Erythematosus | Shock, Cardiogenic | 6-pyruvoyl-tetrahydropterin Synthase Deficiency | Retinopathy, Diabetic | Intestinal Pseudo-obstruction | Cutaneous Mastocytosis | Episodic Ataxia Type 2 | B-cell Prolymphocytic Leukemia | Keratocystic Odontogenic Tumor | Burn-McKeown Syndrome | Hemangioblastoma | Myelodysplasia | Myoclonus | Neovascular Glaucoma | Melanoma, Uveal | Posterior Polar Cataract | Mitochondrial DNA Depletion Syndrome, Hepatocerebral Form | Charcot-Marie-Tooth Disease Type 2D | Vitamin B12 Deficiency | Inflammatory Myopathy | Hereditary Multiple Exostoses | Essential Fructosuria | Focal Cortical Dysplasia Type 2 | Yellow Fever | Birt-Hogg-Dube Syndrome | Gangliosidosis | Mast Cell Leukemia | CHARGE Syndrome | Congenital Dyserythropoietic Anemia | Pompe Disease | Pseudomyxoma Peritonei | Meningeal Melanocytoma | Focal Dermal Hypoplasia | Multiple Congenital Anomalies-hypotonia-seizures Syndrome 2 | Ovarian Hyperstimulation Syndrome | Brugada Syndrome 1 | Myofibromatosis | Behavioral Variant Of Frontotemporal Dementia | Spondylosis | Alopecia Areata | Hereditary Inclusion Body Myopathy | Multiple System Atrophy | Stuttering | Chanarin-Dorfman Syndrome | Pyoderma Gangrenosum | Angina Pectoris | Citrullinemia | Cervicitis | Ataxia-ocular Apraxia 2 | Myopia | 3-M Syndrome | Spitz Nevus | Dyslexia | Kashin-Beck Disease | Neuroleptic Malignant Syndrome | Psoriasis | Hypercholesterolemia, Familial | Sleep Apnea, Central | Malignant Fibrous Histiocytoma | Homocystinuria | Sotos Syndrome | Takenouchi-Kosaki Syndrome | C3 Glomerulopathy | Sorsby Fundus Dystrophy | Brenner Tumor | Vitamin A Deficiency | Microcephalic Osteodysplastic Primordial Dwarfism, Type II | Usher Syndrome | Hypohidrotic Ectodermal Dysplasia | Erythematotelangiectatic Rosacea | Sleep Apnea, Obstructive | Tylosis With Esophageal Cancer | Eczema | Keratoconjunctivitis | Nail Disorder, Nonsyndromic Congenital | Distal Myopathy 2 | Galloway-Mowat Syndrome | Adenocarcinoma | Acute Leukemia | McKusick Type Metaphyseal Chondrodysplasia | Hyperparathyroidism | Phosphoglycerate Dehydrogenase Deficiency | Saul-Wilson Syndrome | Endocarditis | Retinal Vasculitis | Arthritis, Psoriatic | Mucolipidosis Type III | Thromboembolism | Neutrophilia | Prurigo Nodularis | Heart Failure | Glanzmann Thrombasthenia | Sporadic Hemiplegic Migraine | Chromosome 5q Deletion Syndrome | Colitis | Phosphoenolpyruvate Carboxykinase Deficiency, Cytosolic | Nicotine Addiction | Glycogen Storage Disease Type 1b | Blau Syndrome | Congenital Hereditary Endothelial Dystrophy Type II | Pelvic Inflammatory Disease | Trismus-pseudocamptodactyly Syndrome | Cholelithiasis | Primary Progressive Aphasia | CREST Syndrome | Macular Degeneration | Papillon-Lefevre Syndrome | Encephalitis, Tick-borne | Chediak-Higashi Syndrome | Anal Fissure | Bernard-Soulier Syndrome | Erythema Nodosum | Long QT Syndrome Type 2 | Li-Fraumeni Syndrome | Bardet-Biedl Syndrome | Wiedemann-Steiner Syndrome | Arthritis | Amyloidosis | 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Erythrokeratodermia Variabilis | Liver Failure | Zygomycosis | Liver Failure, Acute Infantile | Bone Giant Cell Tumor | Esophageal Carcinoma | Waardenburg Syndrome Type 4A | Carcinoid Syndrome | DiGeorge Syndrome | Spinocerebellar Ataxia Type 5 | Tumoral Calcinosis | Wieacker-Wolff Syndrome | Transient Bullous Dermolysis Of The Newborn | Lymphoma, B-cell | Small Lymphocytic Lymphoma | Hypersomnia | Autonomic Nervous System Disorders | Acromesomelic Dysplasia | Chronic Leukemia | Left Ventricular Noncompaction | Thyrotoxic Periodic Paralysis | Autonomic Neuropathy | Metabolic Syndrome | Fuchs Dystrophy | Headache | Menkes Disease | Cryopyrin-associated Periodic Syndromes | Peeling Skin Syndrome Type B | Situs Inversus | Schizencephaly | Wagner Disease | Kleine-Levin Syndrome | Oculocutaneous Albinism Type 1 | Hypoplastic Left Heart Syndrome | Vici Syndrome | Neuronal Ceroid Lipofuscinosis | Meesmann Corneal Dystrophy | Ornithine Transcarbamylase Deficiency | Retinal Dystrophy | Purpura 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