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loading...| Preferred Name | Pure Red Cell Aplasia | |
| Synonyms |
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|
| Definitions |
A disease characterized by normocytic, normochromic anemia, low hematocrit, reticulocytopenia, and selective erythroid hypoplasia. |
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| ID |
http://purl.obolibrary.org/obo/NCIT_C34974 |
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| ALT_DEFINITION |
A condition characterized by aplasia of the erythroid series only. The leukocytes and platelets are not affected. |
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| code |
C34974 |
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| Contributing_Source |
NICHD |
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| definition |
A disease characterized by normocytic, normochromic anemia, low hematocrit, reticulocytopenia, and selective erythroid hypoplasia. |
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| in_subset | ||
| label |
Pure Red Cell Aplasia |
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| Legacy Concept Name |
Pure_Red_Cell_Aplasia |
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| Preferred_Name |
Pure Red Cell Aplasia |
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| prefixIRI |
NCIT:C34974 |
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| prefLabel |
Pure Red Cell Aplasia |
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| Semantic_Type |
Disease or Syndrome |
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| UMLS_CUI |
C0034902 |
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| subClassOf |
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