An inborn condition characterized by deficiencies of red cell precursors that sometimes also includes leukopenia and thrombocytopenia. [ MESH:D029502 ]
Term information
- ICD9:284.0 (i2s)
- MESH:D029502 (MONDO:equivalentTo)
- ICD10:D61.01 (DOID:1342)
- UMLS:C0702159 (MONDO:equivalentTo)
- UMLS:C0949116 (MONDO:equivalentTo)
- DOID:1342 (MONDO:equivalentTo)
- ICD9:284.09 (i2s)
- SCTID:28975000 (MONDO:equivalentTo)
- Orphanet:68383 (MONDO:equivalentTo)
- GARD:0006149 (shared-umls-xref)
- ICD10:D61.0 (Orphanet:68383)
ordo_group_of_disorders
http://identifiers.org/snomedct/154808006
http://identifiers.org/snomedct/191242004
http://identifiers.org/snomedct/188588001
http://identifiers.org/snomedct/267523003
http://identifiers.org/snomedct/191235004
http://identifiers.org/snomedct/191236003
In DO this is classified as idiopathic; however, ORDO classifies idiopathic as acquired which leads to an inconsistency
An inborn condition characterized by deficiencies of red cell precursors that sometimes also includes leukopenia and thrombocytopenia.
http://identifiers.org/snomedct/28975000
http://purl.obolibrary.org/obo/DOID_1342
http://identifiers.org/mesh/D029502
http://www.orpha.net/ORDO/Orphanet_68383
http://linkedlifedata.com/resource/umls/id/C0949116
http://linkedlifedata.com/resource/umls/id/C0702159
hereditary aplastic anemia
constitutional aplastic anemia
congenital hypoplastic anemia
congenital aplastic anemia
constitutional aplastic anaemia
hypoplastic anemia - familial