Term info
database cross reference
- GARD:0007504 (MONDO:equivalentTo)
- DOID:1340 (MONDO:equivalentTo)
- MESH:D012010 (MONDO:equivalentTo)
- UMLS:C0034902 (NCIT:C34974)
- ICD9:284.81 (MONDO:relatedTo)
- NCIT:C34974 (MONDO:equivalentTo)
- SCTID:50715003 (MONDO:equivalentTo)
definition
A disease characterized by normocytic, normochromic anemia, low hematocrit, reticulocytopenia, and selective erythroid hypoplasia.
exactMatch
http://identifiers.org/mesh/D012010, http://identifiers.org/snomedct/50715003, http://linkedlifedata.com/resource/umls/id/C0034902, http://purl.obolibrary.org/obo/NCIT_C34974, http://purl.obolibrary.org/obo/DOID_1340
excluded subClassOf
http://purl.obolibrary.org/obo/MONDO_0012197
has exact synonym
red cell hypoplasia, primary red cell aplasia, PRCA, pure red cell aplasia
id
MONDO:0001705