Autoimmune Hemolytic Anemia

About the Disease
Anemia, Autoimmune Hemolytic, also known as autoimmune hemolytic anemia, is related to evans' syndrome and splenic marginal zone lymphoma. An important gene associated with Anemia, Autoimmune Hemolytic is TLR8 (Toll Like Receptor 8), and among its related pathways/superpathways are Class I MHC mediated antigen processing and presentation and Innate Immune System. The drugs Tacrolimus and Calcineurin Inhibitors have been mentioned in the context of this disorder. Affiliated tissues include t cells, bone marrow and heart, and related phenotypes are muscle weakness and fatigue

Common Targets
DNASE1L3 | C1S | IFNB1 | PIK3CD | LTA | PSMB9 | FCGRT | CD38 | CD200 | Immunoproteasome | Complement Complex | KMT2D | C3 | G7124 | PSMB8 | DOCK8 | SERPING1 | MPO

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Larsen Syndrome | Pompe Disease | Glutaric Aciduria Type 1 | DRESS Syndrome | Primary Torsion Dystonia | Congenital Hemolytic Anemia | Sclerocornea | TARP Syndrome | Chronic Beryllium Disease | Lipid Storage Myopathy | Veno-occlusive Disease | Autoimmune Polyendocrinopathy Syndrome Type I | Currarino Syndrome | Gnathodiaphyseal Dysplasia | Glioblastoma | Glycogen Storage Disease Type 5 | Hereditary Spastic Paraplegia | Menkes Disease | Alagille Syndrome | Liver Failure | Maternally Inherited Diabetes And Deafness | Hereditary Pyropoikilocytosis | Dysequilibrium Syndrome | Leigh Syndrome | Mucolipidosis | Basan Syndrome | Homocystinuria | Aneurysm, Thoracic Aortic | Congenital Stationary Night Blindness | Progressive Familial Intrahepatic Cholestasis Type 1 | Chudley-McCullough Syndrome | Restrictive Dermopathy | Palmoplantar Keratoderma | Bullous Pemphigoid | Spinal Muscular Atrophy | Leber Hereditary Optic Neuropathy | Alpha-thalassemia Myelodysplasia Syndrome | Dyslexia | 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Neurofibromatosis Type 2 | Trachoma | Muscular Dystrophy | Mast Cell Leukemia | Kallmann Syndrome | Sepiapterin Reductase Deficiency | Progressive External Ophthalmoplegia | Pituitary Stalk Interruption Syndrome | Hypertension | Klippel-Feil Syndrome | HELLP Syndrome | Malnutrition | Osteopathia Striata With Cranial Sclerosis | Growth Hormone Excess | Hyperhomocysteinemia | Castleman Disease | Parvovirus B19 Infection | Cyclic Vomiting Syndrome | Ocular Hypertension | Cerebellar Ataxia, Cayman Type | Choreoathetosis, Hypothyroidism, And Neonatal Respiratory Distress | Sarcoma | Neurofibroma | Gastrointestinal Disorders | Tuberculous Meningitis | Sialidosis Type I | Porphyria Cutanea Tarda | Diabetes Type 1 | Dengue Shock Syndrome | Diarrhea | Alpha-mannosidosis | Benign Familial Infantile Seizures | Glaucomatocyclitic Crisis | Coffin-Siris Syndrome | Pitt-Hopkins Syndrome | Motion Sickness | Scabies | Primary Progressive Aphasia | Pouchitis | Keratitis-ichthyosis-deafness Syndrome | 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