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| Term | pure red-cell aplasia | ID (Ontology) | DOID:1340 (Human Disease) |
| Definition | A congenital hypoplastic anemia that is characterized by a normocytic normochromic anemia with severe reticulocytopenia and marked reduction or absence of erythroid precursors from the bone marrow. | ||
| Also Known As | "primary red cell aplasia" ; "pure red cell aplasia" ; "Red cell hypoplasia" | ||
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Full annotation statements including this term (annotations to child terms are NOT included), and relevant FlyBase records
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physical disorder__ aplastic anemia____| congenital hypoplastic anemia |__pure red-cell aplasia 25 rec. |__Diamond-Blackfan anemia 25 rec. |__Diamond-Blackfan anemia 1 2 rec. |__Diamond-Blackfan anemia 2 |__Diamond-blackfan anemia 3 1 rec. |__Diamond-Blackfan anemia 4 1 rec. |__Diamond-Blackfan anemia 5 1 rec. |__Diamond-Blackfan anemia 6 1 rec. |__Diamond-Blackfan anemia 7 1 rec. |__Diamond-Blackfan anemia 8 1 rec. |__Diamond-Blackfan anemia 9 2 rec. |__Diamond-Blackfan anemia 10 1 rec. |__Diamond-Blackfan anemia 11 1 rec. |__Diamond-Blackfan anemia 12 1 rec. |__Diamond-Blackfan anemia 13 1 rec. |__Diamond-Blackfan anemia 14 with mandibulofacial dysostosis 1 rec. |__Diamond-Blackfan anemia 15 with mandibulofacial dysostosis 3 rec. |__Diamond-Blackfan anemia 16 1 rec. |__Diamond-Blackfan anemia 17 1 rec. |__Diamond-Blackfan anemia 18 1 rec. |__Diamond-Blackfan anemia 19 1 rec. |__Diamond-Blackfan anemia 20 2 rec. |
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| Is a | congenital hypoplastic anemia | ||
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External Crossreferences & Linkouts
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GARD:7504 MESH:D012010 NCI:C34974 SNOMEDCT_US_2023_03_01:191252000 UMLS_CUI:C0034902 |
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