Myeloblasts Under 20 Percent of Peripheral Blood White Cells

Preferred Label : Myeloblasts Under 20 Percent of Peripheral Blood White Cells;

NCIt synonyms : Myeloblasts Under 20% of Peripheral Blood White Cells; Myeloblasts Less than 20 Percent of Peripheral Blood White Cells;

NCIt definition : A semi-quantitative microscopic finding indicating less than 20 percent of the nucleated cells in a peripheral leukocyte sample are immature mononuclear cells of myeloid origin.;

Details

Origin ID

C36223;

UMLS CUI

C1334849;

Semantic type(s)
- Laboratory or Test Result [UMLS semantic type]
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- CTRP Biomarker Terminology [NCIt concept]
- CTRP Terminology [NCIt concept]
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- Adult Myelodysplastic Syndrome [NCIt concept]
- Alkylating Agent-Related Myelodysplastic Syndrome [NCIt concept]
- Childhood Myelodysplastic Syndrome [NCIt concept]
- Childhood Myelodysplastic Syndrome with Excess Blasts [NCIt concept]
- Childhood Myelodysplastic Syndrome with Low Blasts [NCIt concept]
- Childhood Myelodysplastic Syndrome with Low Blasts, Hypocellular [NCIt concept]
- Childhood Myelodysplastic Syndrome with Low Blasts, Not Otherwise Specified [NCIt concept]
- Epipodophyllotoxin-Related Myelodysplastic Syndrome [NCIt concept]
- Hereditary Myelodysplastic Syndrome [NCIt concept]
- Hypoplastic Myelodysplastic Syndrome [NCIt concept]
- Myelodysplastic Syndrome [NCIt concept]
- Myelodysplastic Syndrome Post Cytotoxic Therapy [NCIt concept]
- Myelodysplastic Syndrome with Biallelic TP53 Inactivation [NCIt concept]
- Myelodysplastic Syndrome with Biallelic TP53 Mutation [NCIt concept]
- Myelodysplastic Syndrome with Excess Blasts [NCIt concept]
- Myelodysplastic Syndrome with Excess Blasts and Fibrosis [NCIt concept]
- Myelodysplastic Syndrome with Excess Blasts-1 [NCIt concept]
- Myelodysplastic Syndrome with Genetic Abnormalities [NCIt concept]
- Myelodysplastic Syndrome with Low Blasts [NCIt concept]
- Myelodysplastic Syndrome with Monoallelic TP53 Mutation [NCIt concept]
- Myelodysplastic Syndrome with Mutated SF3B1 [NCIt concept]
- Myelodysplastic Syndrome with Mutated TP53 [NCIt concept]
- Myelodysplastic Syndrome with Ring Sideroblasts [NCIt concept]
- Myelodysplastic Syndrome with Ring Sideroblasts and Multilineage Dysplasia [NCIt concept]
- Myelodysplastic Syndrome with Ring Sideroblasts and Single Lineage Dysplasia [NCIt concept]
- Myelodysplastic Syndrome with Somatic Mutation [NCIt concept]
- Myelodysplastic Syndrome with TP53 Inactivation [NCIt concept]
- Myelodysplastic Syndrome with del(5q) [NCIt concept]
- Myelodysplastic Syndrome, Not Otherwise Specified [NCIt concept]
- Myelodysplastic Syndrome, Not Otherwise Specified with Multilineage Dysplasia [NCIt concept]
- Myelodysplastic Syndrome, Not Otherwise Specified with Single Lineage Dysplasia [NCIt concept]
- Myelodysplastic Syndrome, Unclassifiable [NCIt concept]
- Myelodysplastic Syndrome/Acute Myeloid Leukemia [NCIt concept]
- Myelodysplastic Syndrome/Acute Myeloid Leukemia with Mutated TP53 [NCIt concept]
- Myelodysplastic Syndrome/Acute Myeloid Leukemia with Myelodysplasia-Related Cytogenetic Abnormalities [NCIt concept]
- Myelodysplastic Syndrome/Acute Myeloid Leukemia with Myelodysplasia-Related Gene Mutations [NCIt concept]
- Myelodysplastic Syndrome/Acute Myeloid Leukemia, Not Otherwise Specified [NCIt concept]
- Recurrent Myelodysplastic Syndrome [NCIt concept]
- Refractory Anemia [NCIt concept]
- Refractory Cytopenia of Childhood [NCIt concept]
- Refractory Myelodysplastic Syndrome [NCIt concept]
- Refractory Neutropenia [NCIt concept]
- Refractory Thrombocytopenia [NCIt concept]
- SAMD9-Associated Hereditary Myelodysplastic Syndrome [NCIt concept]
- SAMD9L-Associated Hereditary Myelodysplastic Syndrome [NCIt concept]
- Secondary Myelodysplastic Syndrome [NCIt concept]
- de novo Myelodysplastic Syndrome [NCIt concept]

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