Leishmaniasis, Visceral

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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Leber Hereditary Optic Neuropathy | Silver-Russell Syndrome | Porokeratosis | Charcot-Marie-Tooth Disease, Type 1A | Postpoliomyelitis Syndrome | Charcot-Marie-Tooth Disease Type 2D | Acanthosis Nigricans | Cholecystitis | AIDS Dementia Complex | Primary Torsion Dystonia | Coffin-Lowry Syndrome | Peters-plus Syndrome | Hyperparathyroidism | Sleep Apnea | Chronic Thromboembolic Pulmonary Hypertension | Large Granular Lymphocytic Leukemia | Erythematotelangiectatic Rosacea | Dwarfism | Gangliosidosis | Keratoacanthoma | Hidradenitis | Arteriovenous Malformations | Spastic Paraplegia Type 7 | Congenital Ichthyosiform Erythroderma | Combined Pituitary Hormone Deficiency | Acute Lymphocytic Leukemia | Partington Syndrome | Arterial Tortuosity Syndrome | Menetrier Disease | Urolithiasis | Stroke, Hemorrhagic | Dyslipidemia | Klippel-Feil Syndrome | Paraganglioma | Spinocerebellar Ataxia Type 7 | Noonan Syndrome-like Disorder With Loose Anagen Hair | Meconium Ileus | Hereditary Elliptocytosis 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Raine Syndrome | Paget's Disease Of The Breast | Fuchs Dystrophy | Chromosome 5q Deletion Syndrome | Congenital Tufting Enteropathy | Synpolydactyly | Uveitis, Anterior | Corneal Ulcer | Osteogenesis Imperfecta | Aspergillosis | Diastrophic Dysplasia | Protein S Deficiency | Congenital Stationary Night Blindness | Addison Disease | Turner's Syndrome | Costello Syndrome | Superficial Spreading Melanoma | Megacystis-microcolon-intestinal Hypoperistalsis Syndrome | Early Infantile Epileptic Encephalopathy 4 | Vasculitis | Pneumococcal Meningitis | Tumoral Calcinosis | LRBA Deficiency | Aldosterone Synthase Deficiency | Non-epidermolytic Palmoplantar Keratoderma | Multiple Sulfatase Deficiency | Charcot-Marie-Tooth Disease Type 4D | Parapsoriasis | Cerebrotendinous Xanthomatosis | Purpura | Hypotrichosis Simplex | Glioblastoma | Paternal Uniparental Disomy Of Chromosome 14 | C3 Glomerulonephritis | Vitreoretinal Degeneration, Snowflake Type | Oculocutaneous Albinism | 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Syndrome | Retinitis Pigmentosa | ICF Syndrome | Microvillus Inclusion Disease | Adult Polyglucosan Body Disease | Cerebellofaciodental Syndrome | Hereditary Multiple Exostoses | Hepatitis C, Chronic | Alagille Syndrome | Acute Chest Syndrome | Acquired Partial Lipodystrophy | Keratoconjunctivitis | Cerebral Amyloid Angiopathy | Saethre-Chotzen Syndrome | Epidermolysis Bullosa Simplex | Adrenal Insufficiency | Guttate Psoriasis | Erectile Dysfunction | Centronuclear Myopathy | Primary Erythromelalgia | Chronic Lymphocytic Leukemia | Epidermolysis Bullosa Simplex With Mottled Pigmentation | Stuttering | Wolfram Syndrome 2 | Aphasia | Globozoospermia | Avellino Corneal Dystrophy | Familial Hyperaldosteronism | Aplasia Cutis Congenita | Macrophagic Myofasciitis | Limb Girdle Muscular Dystrophy | Reticular Dysgenesis | Ataxia-hypogonadism-choroidal Dystrophy Syndrome | COACH Syndrome | Amish Infantile Epilepsy Syndrome | Cryopyrin-associated Periodic Syndromes | Joubert Syndrome | 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