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 DeCS Categories

C15 Hemic and Lymphatic Diseases .
C15.378 Hematologic Diseases .
C15.378.071 Anemia .
C15.378.071.085 Anemia, Aplastic .
C15.378.071.085.080 Anemia, Hypoplastic, Congenital .
C15.378. Anemia, Diamond-Blackfan .
C15.378. Fanconi Anemia .
C15.378.071.750 Red-Cell Aplasia, Pure .
C15.378.071.750.500 Anemia, Diamond-Blackfan .
C15.378.190 Bone Marrow Diseases .
C15.378.190.196 Anemia, Aplastic .
C15.378.190.196.080 Anemia, Hypoplastic, Congenital .
C15.378. Anemia, Diamond-Blackfan .
C15.378. Fanconi Anemia .
C16 Congenital, Hereditary, and Neonatal Diseases and Abnormalities .
C16.320 Genetic Diseases, Inborn .
C16.320.077 Anemia, Hypoplastic, Congenital .
C16.320.077.090 Anemia, Diamond-Blackfan .
C16.320.077.280 Fanconi Anemia .
C18 Nutritional and Metabolic Diseases .
C18.452 Metabolic Diseases .
C18.452.284 DNA Repair-Deficiency Disorders .
C18.452.284.280 Fanconi Anemia .
 Synonyms & Historicals
Anemia, Aplastic .
Aplastic Anemia .
Anemias, Aplastic .
Anemias, Hypoplastic .
Aplastic Anemias .
Hypoplastic Anemia .
Hypoplastic Anemias .
Anemia, Hypoplastic .
A form of anemia in which the bone marrow fails to produce adequate numbers of peripheral blood elements. .
Anemia, Hypoplastic, Congenital .
Anemia, Congenital Hypoplastic .
Anemias, Congenital Hypoplastic .
Congenital Hypoplastic Anemias .
Hypoplastic Anemias, Congenital .
Congenital Hypoplastic Anemia .
Hypoplastic Anemia, Congenital .
An inborn condition characterized by deficiencies of red cell precursors that sometimes also includes LEUKOPENIA and THROMBOCYTOPENIA. .
Fanconi Anemia .
Fanconi Hypoplastic Anemia .
Fanconi Pancytopenia .
Fanconi Panmyelopathy .
Fanconi's Anemia .
Anemia, Fanconi's .
Anemias, Fanconi .
Fanconi Anemias .
Anemia, Fanconi .
Congenital disorder affecting all bone marrow elements, resulting in ANEMIA; LEUKOPENIA; and THROMBOPENIA, and associated with cardiac, renal, and limb malformations as well as dermal pigmentary changes. Spontaneous CHROMOSOME BREAKAGE is a feature of this disease along with predisposition to LEUKEMIA. There are at least 7 complementation groups in Fanconi anemia: FANCA, FANCB, FANCC, FANCD1, FANCD2, FANCE, FANCF, FANCG, and FANCL. (from Online Mendelian Inheritance in Man,, August 20, 2004) .
Anemia, Diamond-Blackfan .
Anemia, Congenital Hypoplastic, Of Blackfan And Diamond .
Anemia, Diamond-Blackfan Type .
Blackfan Diamond Anemia .
Blackfan-Diamond Disease .
Blackfan-Diamond Syndrome .
Chronic Congenital Agenerative Anemia .
Congenital Erythroid Hypoplastic Anemia .
Congenital Hypoplastic Anemia of Blackfan and Diamond .
Congenital Pure Red Cell Anemia .
Congenital Pure Red Cell Aplasia .
Erythrogenesis Imperfecta .
Hypoplastic Congenital Anemia .
Inherited Erythroblastopenia .
Pure Hereditary Red Cell Aplasia .
Red Cell Aplasia, Pure, Hereditary .
Anemia, Blackfan Diamond .
Anemia, Diamond Blackfan .
Anemia, Diamond Blackfan Type .
Anemia, Hypoplastic Congenital .
Anemias, Hypoplastic Congenital .
Blackfan Diamond Disease .
Blackfan Diamond Syndrome .
Congenital Anemia, Hypoplastic .
Congenital Anemias, Hypoplastic .
Diamond Anemia, Blackfan .
Diamond Blackfan Anemia .
Diamond-Blackfan Type Anemia .
Disease, Blackfan-Diamond .
Erythroblastopenia, Inherited .
Erythroblastopenias, Inherited .
Erythrogenesis Imperfectas .
Hypoplastic Congenital Anemias .
Imperfecta, Erythrogenesis .
Imperfectas, Erythrogenesis .
Inherited Erythroblastopenias .
Diamond-Blackfan Anemia .
A rare congenital hypoplastic anemia that usually presents early in infancy. The disease is characterized by a moderate to severe macrocytic anemia, occasional neutropenia or thrombocytosis, a normocellular bone marrow with erythroid hypoplasia, and an increased risk of developing leukemia. (Curr Opin Hematol 2000 Mar;7(2):85-94) .