myelodysplastic syndrome with single lineage dysplasia
Go to external page http://purl.obolibrary.org/obo/MONDO_0005272
A myelodysplastic syndrome characterized by dysplasia seen in at least 10% of the early cells of 1 cell type (either red blood cells, white blood cells, or megakaryocytes) in the bone marrow. [ doi:10.5772/intechopen.82532 https://orcid.org/0000-0002-4142-7153 ]
Synonyms: refractory anaemia MDS with single lineage dysplasia MDS-SLD RA refractory anemia
Term information
- SCTID:1153345005 (MONDO:equivalentTo)
- NCIT:C82591 (MONDO:equivalentTo)
- ICDO:9980/3 (NCIT:C2872)
- MEDGEN:415300 (MONDO:equivalentTo)
- MedDRA:10038269 (Orphanet:98826/e)
- GARD:19585 (MONDO:GARD)
- EFO:0003802 (MONDO:equivalentTo)
- Orphanet:98826 (MONDO:equivalentTo)
- UMLS:C2826318 (MONDO:equivalentTo)
- ICD9:238.72 (MONDO:relatedTo)
- icd11.foundation:149518956 (https://orcid.org/0000-0001-5208-3432)
- NCIT:C2872 (MONDO:equivalentTo)
- MESH:D000753 (Orphanet:98826/e)
- SCTID:109996008 (MONDO:mondoIsBroaderThanSource)
ordo_disorder, gard_rare, otar, rare, nord_rare, orphanet_rare
This disease was reclassified by the World Health Organization (WHO) in 2016. It was referred to as refractory cytopenia with unilineage dysplasia (RCUD) in the previous classification system. It includes refractory anemia (unilineage erythroid dysplasia), refractory neutropenia (unilineage dysgranulopoiesis), and refractory thrombocytopenia (unilineage dysmegakaryocytopoiesis).
http://purl.obolibrary.org/obo/NCIT_C82591
http://www.orpha.net/ORDO/Orphanet_98826
http://purl.obolibrary.org/obo/NCIT_C2872
http://identifiers.org/medgen/415300
http://identifiers.org/mesh/D000753
http://linkedlifedata.com/resource/umls/id/C2826318
http://identifiers.org/snomedct/1153345005