Term info
- ICD10CM:D61.0 (Orphanet:68383/ntbt)
- DOID:1342 (MONDO:equivalentTo)
- UMLS:C0702159 (MONDO:equivalentTo)
- Orphanet:68383 (MONDO:equivalentTo)
- SCTID:28975000 (MONDO:equivalentTo)
- UMLS:C0949116 (MONDO:equivalentTo)
- GARD:0006149 (MONDO:shared-umls-xref)
- ICD9:284.09 (MONDO:relatedTo)
- ICD9:284.0 (MONDO:i2s)
- MESH:D029502 (MONDO:equivalentTo)
disease_grouping, ordo_group_of_disorders
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://purl.obolibrary.org/obo/Orphanet_68383, http://identifiers.org/mesh/D029502, http://purl.bioontology.org/ontology/ICD10CM/D61.0, http://linkedlifedata.com/resource/umls/id/C0949116, http://linkedlifedata.com/resource/umls/id/C0702159
http://purl.obolibrary.org/obo/MONDO_0012197
constitutional aplastic anemia, hereditary aplastic anemia
rare constitutional aplastic anemia
congenital aplastic anemia, constitutional aplastic anaemia, hypoplastic anemia - familial, congenital hypoplastic anemia
MONDO:0001713