Preferred Name |
myelodysplastic syndrome with single lineage dysplasia |
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Synonyms |
MDS-SLD refractory anemia RA MDS with single lineage dysplasia aregenerative anemia |
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Definitions |
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). 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. |
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ID |
http://purl.obolibrary.org/obo/MONDO_0005272 |
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comment |
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). |
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has_exact_synonym |
MDS-SLD refractory anemia RA MDS with single lineage dysplasia |
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has_related_synonym |
aregenerative anemia |
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IAO_0000233 | ||
label |
myelodysplastic syndrome with single lineage dysplasia |
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narrowMatch | ||
prefixIRI |
MONDO:0005272 |
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prefLabel |
myelodysplastic syndrome with single lineage dysplasia |
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textual definition |
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. |
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subClassOf |
Delete | Mapping To | Ontology | Source |
---|---|---|---|
http://purl.obolibrary.org/obo/MONDO_0005272 | MONDO | SAME_URI | |
http://purl.obolibrary.org/obo/MONDO_0005272 | MONDO | LOOM | |
http://purl.bioontology.org/ontology/MEDDRA/10088025 | MEDDRA | LOOM | |
http://purl.obolibrary.org/obo/NCIT_C82591 | BERO | LOOM |