Recurrent Genetic Abnormalities Present

Preferred Label : Recurrent Genetic Abnormalities Present;

NCIt definition : A laboratory test result indicating the presence of recurrent genetic abnormalities in cells.;

Details

Origin ID

C80329;

UMLS CUI

C2699018;

Semantic type(s)
- Finding [UMLS semantic type]
is_finding_of_disease
- Acute Leukemia of Ambiguous Lineage with BCL11B Rearrangement [NCIt concept]
- Acute Leukemia of Ambiguous Lineage with Defining Genetic Abnormalities [NCIt concept]
- Acute Myeloid Leukemia (Megakaryoblastic) with t(1;22)(p13.3;q13.1); RBM15-MKL1 [NCIt concept]
- Acute Myeloid Leukemia with BCOR-RARA [NCIt concept]
- Acute Myeloid Leukemia with BCR-ABL1 [NCIt concept]
- Acute Myeloid Leukemia with Biallelic CEBPA Mutation [NCIt concept]
- Acute Myeloid Leukemia with CEBPA Mutation [NCIt concept]
- Acute Myeloid Leukemia with FIP1L1-RARA [NCIt concept]
- Acute Myeloid Leukemia with FLT3/ITD Mutation [NCIt concept]
- Acute Myeloid Leukemia with FUS-ERG [NCIt concept]
- Acute Myeloid Leukemia with Germline CEBPA Mutation [NCIt concept]
- Acute Myeloid Leukemia with In-Frame bZIP CEBPA Mutation [NCIt concept]
- Acute Myeloid Leukemia with KAT6A-CREBBP [NCIt concept]
- Acute Myeloid Leukemia with KMT2A Rearrangement [NCIt concept]
- Acute Myeloid Leukemia with MECOM Rearrangement [NCIt concept]
- Acute Myeloid Leukemia with Monoallelic CEBPA Mutation [NCIt concept]
- Acute Myeloid Leukemia with NPM1 Mutation [NCIt concept]
- Acute Myeloid Leukemia with NPM1-MLF1 [NCIt concept]
- Acute Myeloid Leukemia with NUP98 Rearrangement [NCIt concept]
- Acute Myeloid Leukemia with Recurrent Genetic Abnormalities [NCIt concept]
- Acute Myeloid Leukemia with STAT3-RARA [NCIt concept]
- Acute Myeloid Leukemia with STAT5B-RARA [NCIt concept]
- Acute Myeloid Leukemia with TBL1XR1-RARA [NCIt concept]
- Acute Myeloid Leukemia with a Variant KMT2A Rearrangement [NCIt concept]
- Acute Myeloid Leukemia with a Variant MECOM Rearrangement [NCIt concept]
- Acute Myeloid Leukemia with a Variant RARA Rearrangement [NCIt concept]
- Acute Myeloid Leukemia with inv(16)(p13.1q22) or t(16;16)(p13.1;q22); CBFB-MYH11 [NCIt concept]
- Acute Myeloid Leukemia with inv(16)(p13.1q22); CBFB-MYH11 [NCIt concept]
- Acute Myeloid Leukemia with inv(3) (q21.3;q26.2); GATA2, MECOM [NCIt concept]
- Acute Myeloid Leukemia with inv(3)(q21.3;q26.2) or t(3;3)(q21.3;q26.2); GATA2, MECOM [NCIt concept]
- Acute Myeloid Leukemia with t(10;11)(p12.3;q23.3); MLLT10-KMT2A [NCIt concept]
- Acute Myeloid Leukemia with t(10;11)(q21.3;q23.3); TET1-KMT2A [NCIt concept]
- Acute Myeloid Leukemia with t(11;17)(q13;q21); NUMA1-RARA [NCIt concept]
- Acute Myeloid Leukemia with t(11;17)(q23;q21); ZBTB16-RARA [NCIt concept]
- Acute Myeloid Leukemia with t(11;19)(q23.3;p13.1); KMT2A-ELL [NCIt concept]
- Acute Myeloid Leukemia with t(11;19)(q23.3;p13.3); KMT2A-MLLT1 [NCIt concept]
- Acute Myeloid Leukemia with t(16;16)(p13.1;q22); CBFB-MYH11 [NCIt concept]
- Acute Myeloid Leukemia with t(1;17)(q42.3;q21.2); IRF2BP2-RARA [NCIt concept]
- Acute Myeloid Leukemia with t(3;12)(q26.2;p13.2); ETV6-MECOM [NCIt concept]
- Acute Myeloid Leukemia with t(3;21)(q26.2;q22.1); MECOM-RUNX1 [NCIt concept]
- Acute Myeloid Leukemia with t(3;3) (q21.3;q26.2); GATA2, MECOM [NCIt concept]
- Acute Myeloid Leukemia with t(3;8)(q26.2;q24); MYC, MECOM [NCIt concept]
- Acute Myeloid Leukemia with t(4;11)(q21.3;q23.3); AFF1-KMT2A [NCIt concept]
- Acute Myeloid Leukemia with t(5;17)(q35;q21); NPM1-RARA [NCIt concept]
- Acute Myeloid Leukemia with t(6;11)(q27;q23.3); MLLT4-KMT2A [NCIt concept]
- Acute Myeloid Leukemia with t(6;9)(p22.3;q34.1); DEK-NUP214 [NCIt concept]
- Acute Myeloid Leukemia with t(8;21)(q22; q22.1); RUNX1-RUNX1T1 [NCIt concept]
- Acute Myeloid Leukemia with t(9;11)(p21.3;q23.3); MLLT3-KMT2A [NCIt concept]
- Acute Promyelocytic Leukemia with t(15;17)(q24.1;q21.2); PML-RARA [NCIt concept]
- Adult Acute Myeloid Leukemia with Recurrent Genetic Abnormalities [NCIt concept]
- Adult Acute Myeloid Leukemia with inv(16)(p13.1q22); CBFB-MYH11 [NCIt concept]
- Adult Acute Myeloid Leukemia with t(16;16)(p13.1;q22); CBFB-MYH11 [NCIt concept]
- Adult Acute Myeloid Leukemia with t(8;21); (q22; q22.1); RUNX1-RUNX1T1 [NCIt concept]
- Adult Acute Myeloid Leukemia with t(9;11)(p21.3;q23.3); MLLT3-KMT2A [NCIt concept]
- Adult Acute Promyelocytic Leukemia with t(15;17)(q24.1;q21.2); PML-RARA [NCIt concept]
- Adult B Acute Lymphoblastic Leukemia with t(9;22)(q34.1;q11.2); BCR-ABL1 [NCIt concept]
- B Acute Lymphoblastic Leukemia with DUX4 Rearrangement [NCIt concept]
- B Acute Lymphoblastic Leukemia with ETV6-RUNX1-Like Features [NCIt concept]
- B Acute Lymphoblastic Leukemia with HLF Rearrangement [NCIt concept]
- B Acute Lymphoblastic Leukemia with IKZF1 N159Y Mutation [NCIt concept]
- B Acute Lymphoblastic Leukemia with Intrachromosomal Amplification of Chromosome 21 [NCIt concept]
- B Acute Lymphoblastic Leukemia with MEF2D Rearrangement [NCIt concept]
- B Acute Lymphoblastic Leukemia with MYC Rearrangement [NCIt concept]
- B Acute Lymphoblastic Leukemia with Mutated ZEB2 (p.H1038R) [NCIt concept]
- B Acute Lymphoblastic Leukemia with NUTM1 Rearrangement [NCIt concept]
- B Acute Lymphoblastic Leukemia with PAX5 Alteration [NCIt concept]
- B Acute Lymphoblastic Leukemia with PAX5 P80R Mutation [NCIt concept]
- B Acute Lymphoblastic Leukemia with Recurrent Genetic Abnormalities [NCIt concept]
- B Acute Lymphoblastic Leukemia with TCF3-HLF Rearrangement [NCIt concept]
- B Acute Lymphoblastic Leukemia with TCF4-HLF Rearrangement [NCIt concept]
- B Acute Lymphoblastic Leukemia with UBTF-ATXN7L3/PAN3, CDX2 (CDX2/UBTF) [NCIt concept]
- B Acute Lymphoblastic Leukemia with ZNF362 Rearrangement [NCIt concept]
- B Acute Lymphoblastic Leukemia with ZNF384 Rearrangement [NCIt concept]
- B Acute Lymphoblastic Leukemia with t(12;21)(p13.2;q22.1); ETV6-RUNX1 [NCIt concept]
- B Acute Lymphoblastic Leukemia with t(1;19)(q23;p13.3); TCF3-PBX1 [NCIt concept]
- B Acute Lymphoblastic Leukemia with t(4;11)(q21;23.3); KMT2A-AFF1 [NCIt concept]
- B Acute Lymphoblastic Leukemia with t(5;14)(q31.1;q32.3); IL3-IGH [NCIt concept]
- B Acute Lymphoblastic Leukemia with t(9;22)(q34.1;q11.2); BCR-ABL1 [NCIt concept]
- B Acute Lymphoblastic Leukemia with t(9;22)(q34.1;q11.2); BCR-ABL1 with Lymphoid Only Involvement [NCIt concept]
- B Acute Lymphoblastic Leukemia with t(9;22)(q34.1;q11.2); BCR-ABL1 with Multilineage Involvement [NCIt concept]
- B Acute Lymphoblastic Leukemia with t(v;11q23.3); KMT2A Rearranged [NCIt concept]
- B Acute Lymphoblastic Leukemia, BCR-ABL1-Like [NCIt concept]
- B Acute Lymphoblastic Leukemia, BCR-ABL1-Like [NCIt concept]
- B Acute Lymphoblastic Leukemia, BCR-ABL1-Like, ABL Class Rearranged [NCIt concept]
- B Acute Lymphoblastic Leukemia, BCR-ABL1-Like, ABL1 Rearranged [NCIt concept]
- B Acute Lymphoblastic Leukemia, BCR-ABL1-Like, JAK-STAT Activated [NCIt concept]
- B Acute Lymphoblastic Leukemia, BCR-ABL1-Like, Not Otherwise Specified [NCIt concept]
- B Lymphoblastic Leukemia/Lymphoma with ETV6-RUNX1-Like Features [NCIt concept]
- B Lymphoblastic Leukemia/Lymphoma with Intrachromosomal Amplification of Chromosome 21 [NCIt concept]
- B Lymphoblastic Leukemia/Lymphoma with MYC Rearrangement [NCIt concept]
- B Lymphoblastic Leukemia/Lymphoma with Recurrent Genetic Abnormalities [NCIt concept]
- B Lymphoblastic Leukemia/Lymphoma with TCF3-HLF Rearrangement [NCIt concept]
- B Lymphoblastic Leukemia/Lymphoma with t(12;21)(p13.2;q22.1); ETV6-RUNX1 [NCIt concept]
- B Lymphoblastic Leukemia/Lymphoma with t(1;19)(q23;p13.3); TCF3-PBX1 [NCIt concept]
- B Lymphoblastic Leukemia/Lymphoma with t(5;14)(q31.1;q32.3); IL3-IGH [NCIt concept]
- B Lymphoblastic Leukemia/Lymphoma with t(9;22)(q34.1;q11.2); BCR-ABL1 [NCIt concept]
- B Lymphoblastic Leukemia/Lymphoma with t(v;11q23.3); KMT2A Rearranged [NCIt concept]
- B Lymphoblastic Leukemia/Lymphoma, BCR-ABL1-Like [NCIt concept]
- Childhood Acute Megakaryoblastic Leukemia with NUP98-KDM5A [NCIt concept]
- Childhood Acute Myeloid Leukemia with NUP98 Rearrangement [NCIt concept]
- Childhood Acute Myeloid Leukemia with t(11;15)(p15;q35); NUP98-JARID1A [NCIt concept]
- Childhood Acute Myeloid Leukemia with t(5;11)(q35;p15); NUP98-NSD1 [NCIt concept]
- Childhood Acute Myeloid Leukemia with t(8;21); (q22; q22.1); RUNX1-RUNX1T1 [NCIt concept]
- Childhood Acute Myeloid Leukemia with t(9;11)(p21.3;q23.3); MLLT3-KMT2A [NCIt concept]
- Childhood Acute Promyelocytic Leukemia with t(15;17)(q24.1;q21.2); PML-RARA [NCIt concept]
- Childhood B Acute Lymphoblastic Leukemia with t(9;22)(q34.1;q11.2); BCR-ABL1 [NCIt concept]
- Core Binding Factor Acute Myeloid Leukemia [NCIt concept]
- Early T Precursor Acute Lymphoblastic Leukemia with BCL11B Rearrangement [NCIt concept]
- Hyperdiploid B Acute Lymphoblastic Leukemia [NCIt concept]
- Hyperdiploid B Lymphoblastic Leukemia/Lymphoma [NCIt concept]
- Hypodiploid B Acute Lymphoblastic Leukemia [NCIt concept]
- Hypodiploid B Lymphoblastic Leukemia/Lymphoma [NCIt concept]
- Low-Hypodiploid B Acute Lymphoblastic Leukemia [NCIt concept]
- Microgranular Acute Promyelocytic Leukemia [NCIt concept]
- Mixed Phenotype Acute Leukemia with BCR-ABL1 Fusion [NCIt concept]
- Mixed Phenotype Acute Leukemia with KMT2A Rearrangement [NCIt concept]
- Multiple Myeloma with CCND Family Translocation [NCIt concept]
- Multiple Myeloma with Hyperdiploidy [NCIt concept]
- Multiple Myeloma with MAF Family Translocation [NCIt concept]
- Multiple Myeloma with NSD2 Translocation [NCIt concept]
- Multiple Myeloma with Recurrent Genetic Abnormalities [NCIt concept]
- Multiple Myeloma with t(11;14)(q13;q32) [NCIt concept]
- Myelodysplastic Syndrome with Biallelic TP53 Inactivation [NCIt concept]
- Myelodysplastic Syndrome with Biallelic TP53 Mutation [NCIt concept]
- Myelodysplastic Syndrome with Genetic Abnormalities [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 Somatic Mutation [NCIt concept]
- Myelodysplastic Syndrome with TP53 Inactivation [NCIt concept]
- Myelodysplastic Syndrome with del(5q) [NCIt concept]
- Near-Haploid B Acute Lymphoblastic Leukemia [NCIt concept]
- Recurrent Acute Myeloid Leukemia with KMT2A Rearrangement [NCIt concept]
- Recurrent Acute Myeloid Leukemia with Recurrent Genetic Abnormalities [NCIt concept]
- Recurrent Acute Myeloid Leukemia with t(9;11)(p21.3;q23.3); MLLT3-KMT2A [NCIt concept]
- Recurrent Acute Promyelocytic Leukemia with t(15;17)(q24.1;q21.2); PML-RARA [NCIt concept]
- Recurrent B Acute Lymphoblastic Leukemia with t(9;22)(q34.1;q11.2); BCR-ABL1 [NCIt concept]
- Recurrent B Acute Lymphoblastic Leukemia, BCR-ABL1-Like [NCIt concept]
- Refractory B Acute Lymphoblastic Leukemia with t(9;22)(q34.1;q11.2); BCR-ABL1 [NCIt concept]
- Refractory B Acute Lymphoblastic Leukemia, BCR-ABL1-Like [NCIt concept]
- T Acute Lymphoblastic Leukemia with LMO1 Rearrangement [NCIt concept]
- T Acute Lymphoblastic Leukemia with LMO2 Rearrangement [NCIt concept]
- T Acute Lymphoblastic Leukemia with Recurrent Genetic Abnormalities [NCIt concept]
- T Acute Lymphoblastic Leukemia with SPI1 Rearrangement [NCIt concept]
- T Acute Lymphoblastic Leukemia with TAL1 Rearrangement [NCIt concept]
- T Acute Lymphoblastic Leukemia with TLX1 Rearrangement [NCIt concept]
- T Acute Lymphoblastic Leukemia with TLX3 Rearrangement [NCIt concept]
- T Acute Lymphoblastic Leukemia, HOXA Dysregulated [NCIt concept]
- Typical Acute Promyelocytic Leukemia [NCIt concept]
is_not_finding_of_disease
- Acute Myeloid Leukemia with ASXL1 Mutation [NCIt concept]
- Acute Myeloid Leukemia with BCOR Mutation [NCIt concept]
- Acute Myeloid Leukemia with Biallelic CEBPA Mutation [NCIt concept]
- Acute Myeloid Leukemia with CEBPA Mutation [NCIt concept]
- Acute Myeloid Leukemia with Complex Karyotype [NCIt concept]
- Acute Myeloid Leukemia with EZH2 Mutation [NCIt concept]
- Acute Myeloid Leukemia with FLT3/ITD Mutation [NCIt concept]
- Acute Myeloid Leukemia with Germline CEBPA Mutation [NCIt concept]
- Acute Myeloid Leukemia with Monoallelic CEBPA Mutation [NCIt concept]
- Acute Myeloid Leukemia with Multilineage Dysplasia [NCIt concept]
- Acute Myeloid Leukemia with Myelodysplasia-Related Cytogenetic Abnormalities [NCIt concept]
- Acute Myeloid Leukemia with Myelodysplasia-Related Gene Mutations [NCIt concept]
- Acute Myeloid Leukemia with NPM1 Mutation [NCIt concept]
- Acute Myeloid Leukemia with RUNX1 Mutation [NCIt concept]
- Acute Myeloid Leukemia with SF3B1 Mutation [NCIt concept]
- Acute Myeloid Leukemia with SRSF2 Mutation [NCIt concept]
- Acute Myeloid Leukemia with STAG2 Mutation [NCIt concept]
- Acute Myeloid Leukemia with Trisomy 8 [NCIt concept]
- Acute Myeloid Leukemia with U2AF1 Mutation [NCIt concept]
- Acute Myeloid Leukemia with ZRSR2 Mutation [NCIt concept]
- Acute Myeloid Leukemia with del(12p) [NCIt concept]
- Acute Myeloid Leukemia with del(17p) [NCIt concept]
- Acute Myeloid Leukemia with del(20q) [NCIt concept]
- Acute Myeloid Leukemia with del(5q) [NCIt concept]
- Acute Myeloid Leukemia with del(7q) [NCIt concept]
- Acute Myeloid Leukemia with i(17q) [NCIt concept]
- Acute Myeloid Leukemia with idic(X)(q13) [NCIt concept]
- Acute Myeloid Leukemia, Myelodysplasia-Related [NCIt concept]
- B Acute Lymphoblastic Leukemia, Not Otherwise Specified [NCIt concept]
- B Lymphoblastic Leukemia/Lymphoma, Not Otherwise Specified [NCIt concept]
- Multiple Myeloma, Not Otherwise Specified [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]
- Recurrent Acute Myeloid Leukemia with Multilineage Dysplasia [NCIt concept]
- Recurrent Acute Myeloid Leukemia, Myelodysplasia-Related [NCIt concept]
- Refractory Acute Myeloid Leukemia, Myelodysplasia-Related [NCIt concept]
- Refractory Anemia [NCIt concept]
- Refractory Neutropenia [NCIt concept]
- Refractory Thrombocytopenia [NCIt concept]

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