| Preferred Name |
Acquired Pure Red Cell Aplasia |
| ID |
http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#C70548 |
| ALT_DEFINITION |
A disease characterized by normocytic, normochromic anemia, low hematocrit, reticulocytopenia, and selective erythroid hypoplasia. It can occur as a chronic or acute form; the former is predominantly seen in adults, and the latter in children. A rare disorder in which the bone marrow makes almost no red blood cells. It may be caused by infection or by certain drugs. Patients with this disorder may also have a thymoma (a tumor of the thymus) or an autoimmune condition such as lupus erythematosus or rheumatoid arthritis. |
| code |
C70548 |
| Concept_In_Subset | |
| Contributing_Source |
NICHD |
| DEFINITION |
A disease characterized by normocytic, normochromic anemia, low hematocrit, reticulocytopenia and selective erythroid hypoplasia. It can occur as a chronic or acute form; the former is predominantly seen in adults and the latter in children. Pathogenesis involves immune dysfunction with antibodies directed against erythroid precursor cells or erythropoietin, or due to T-cell mediated suppression of erythropoiesis. |
| FULL_SYN |
Acquired Pure Red Cell Aplasia acquired pure red cell aplasia |
| label |
Acquired Pure Red Cell Aplasia |
| Legacy Concept Name |
Acquired_Pure_Red_Cell_Aplasia |
| Preferred_Name |
Acquired Pure Red Cell Aplasia |
| prefixIRI |
Thesaurus:C70548 |
| prefLabel |
Acquired Pure Red Cell Aplasia |
| Semantic_Type |
Disease or Syndrome |
| UMLS_CUI |
C0340961 |
| subClassOf |
| Delete | Mapping To | Ontology | Source |
|---|---|---|---|
| http://purl.bmicc.cn/ontology/ICD11CN/3A61 | 《国际疾病分类》第11版中文版 / International Classification of Diseases, 11th Edition, China | LOOM |