An inborn condition characterized by deficiencies of red cell precursors that sometimes also includes leukopenia and thrombocytopenia. [ MESH:D029502 ]
Synonyms: constitutional aplastic anaemia hereditary aplastic anaemia hereditary aplastic anemia constitutional aplastic anemia
Term information
- SCTID:28975000 (MONDO:equivalentTo)
- GARD:18889 (Orphanet:68383)
- ICD9:284.0 (MONDO:i2s)
- DOID:1342 (MONDO:equivalentTo)
- ICD10CM:D61.0 (Orphanet:68383/ntbt)
- Orphanet:68383 (MONDO:equivalentTo)
- MESH:D029502 (MONDO:equivalentTo)
- ICD9:284.09 (MONDO:relatedTo)
gard_rare, disease_grouping, rare, nord_rare, orphanet_rare, ordo_group_of_disorders
In DO this is classified as idiopathic; however, ORDO classifies idiopathic as acquired which leads to an inconsistency
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://purl.bioontology.org/ontology/ICD10CM/D61.0
hypoplastic anaemia - familial
congenital aplastic anemia
hypoplastic anemia - familial
congenital aplastic anaemia
congenital hypoplastic anemia
congenital hypoplastic anaemia