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• Conditions (81): Genetic and Rare Conditions, Autoimmune Hemolytic Anemia, Immune and Autoimmune, and 78 others Genetic and Rare Conditions, Autoimmune Hemolytic Anemia, Immune and Autoimmune, Warm Antibody AIHA, Hemolytic Anemia, Sjogren's Syndrome, Addison's Disease, Lupus, Evan's Syndrome, Rheumatoid Arthritis, AUTOIMMUNE HEMOLYTIC ANEMIA INVOLVING WARM REACTING ANTIBODY, Diseases and Conditions, Achalasia, Autoimmune Diseases, Agenesis of Corpus Callosum, Hirschsprung's Disease, Trimethylaminuria, PANDA Syndrome, Anencephaly, Dercum's Disease, Dandy Walker Syndrome, Fragile X Syndrome, Pachygyria, 1p36 Deletion Syndrome, Aarskog Syndrome, Legg-Calve-Perthes Disease, Ledderhose Disease, Behcet's Syndrome, Darier's Disease, Empty Sella Syndrome, Cri-du-Chat Syndrome, Cleidocranial Dysplasia, Fructose Intolerance, Kartagener Syndrome, Marfan syndrome, Menkes Kinky Hair Syndrome, Androgen Insensitivity Syndrome, Adie Syndrome, Angelman syndrome, Factor V Leiden, Williams Syndrome, Cushings Syndrome, Eosinophilic Gastroenteritis, Simpson-Golabi-Behmel Syndrome, Hydrocephalus, Friedreich's Ataxia, Ehlers-Danlos syndrome, Inflammatory Linear Verrucous Epidermal Nevus, Hashimoto's Encephalopathy, Adrenal Insufficiency, Acute Intermittent Porphyria, Post-Polio Syndrome, Idiopathic Edema, Cerebral Palsy, 9p Minus, CREST Syndrome, Pallister-Hall syndrome, Cystic Fibrosis, Autism / Autism Spectrum, Lissencephaly, Acromegaly, Epidermal Nevus, Complete Androgen Insensitivity Syndrome, Blood and Bone Marrow, Achondroplastic Dwarfism, Arnold-Chiari Malformation, Reiter Syndrome, Esophageal Atresia , Elephantiasis, Asperger's Syndrome, Langerhans Cell Histiocytosis, Klinefelter's Syndrome, Antiphospholipid Syndrome, Hailey-Hailey disease, Ellis-van Creveld syndrome, Susac syndrome, Brown-Sequard syndrome, Spina Bifida, Beal's syndrome, Joubert syndrome, Sturge-Weber syndrome [hide]
• Groups (26): Lupus, Scleroderma, Alopecia Areata, and 23 others Lupus, Scleroderma, Alopecia Areata, Achalasia, Rare 'Orphan' Disorders, PANDAS Syndrome, Hirschsprung's Disease, Agenesis of Corpus Callosum, Trimethylaminuria, Dercum's Disease, Addison's Disease, Anencephaly, Blepharophimosis, Dandy Walker Syndrome, Pachygyria, Ledderhose Disease, Fragile X Syndrome, Aarskog Syndrome, Legg-Calve-Perthes Disease, Microphthalmia, Darier's Disease, Cri-du-Chat Syndrome, Behcet's Syndrome, Empty Sella Syndrome, 1p36 Deletion Syndrome, Cleidocranial Dysplasia [hide]
• Symptoms (12): Blepharophimosis, Sweet Syndrome, Club Foot, and 9 others Blepharophimosis, Sweet Syndrome, Club Foot, Von Willebrand disease, Myasthenia Gravis, Scleroderma, Castleman's Disease, pyoderma gangrenosum, Tetralogy of Fallot, Reiter's Syndrome, Anemia, Hemolytic anemia direct Coombs positive [hide]
• Treatments (26): Cyclophosphamide 50 MG, GLOBULIN,IMMUNE (IV) 12 GM, Cyclophosphamide 50 MG Oral Tablet, and 23 others Cyclophosphamide 50 MG, GLOBULIN,IMMUNE (IV) 12 GM, Cyclophosphamide 50 MG Oral Tablet, CYCLOPHOSPHAMIDE 100 MG, Cyclophosphamide, Immunoglobulins, Intravenous, CYCLOPHOSPHAMIDE 200 MG, MULTIVITAMINS W/MINERALS TAB, MULTIVITAMINS/MINERALS TAB, MULTIVITAMINS/MINERALS,THERAPEUTIC CAP, MULTIVITAMINS W/MINERALS,THERAPEUTIC TAB, MULTIVITAMINS/MINERALS PRENATAL TAB, MULTIVITAMINS/FERROUS SO4 10MG/FLUORIDE 0.25MG/ML DROPS,ORAL, DAILY MULTIVITAMIN TAB, GERITOL COMPLETE TAB, GERITOL EXTEND TABS, MULTIVITAMINS/MINERALS/BONE MEAL TAB, Ferrous fumarate 250 MG / Folic Acid 1 MG Oral Tablet, Ferrous fumarate 200 MG Oral Tablet, GLOBULIN,IMMUNE (IV) 3 GM, GLOBULIN,IMMUNE (IV) 6 GM/VIL, CYCLOPHOSPHAMIDE 500 MG, Immunoglobulins, Intravenous 50 MG/ML Injectable Solution, Immunoglobulins 20000 MG Injectable Solution, Cyclophosphamide 25 MG, CYCLOPHOSPHAMIDE 1 GM/VIL [hide]

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