inv(16)(p13.1;q22)

Preferred Label : inv(16)(p13.1;q22);

NCIt synonyms : inv(16)(p13q22); inv(16)(p13;q22); inv 16 p13 q22; inv(16)(p13.1q22.1); inv(16)(p13.1;q22.1); inv(16)(p13.1q22);

NCIt definition : A chromosomal inversion that involves chromosome 16. It is associated with the development of acute myeloid leukemia CBFB-MYH11, acute myelomonocytic leukemia with abnormal eosinophils, and granulocytic sarcoma.;

Détails

Origin ID

C36373;

UMLS CUI

C3897145;

Semantic type(s)
- Cell or Molecular Dysfunction [UMLS semantic type]
concept_is_in_subset
- AML Authorized Value Terminology [NCIt concept]
- AML Minimal Residual Disease Table [NCIt concept]
- AML Molecular Analysis Table [NCIt concept]
- CTRP Biomarker Terminology [NCIt concept]
- CTRP Molecular Genetic Biomarker Terminology [NCIt concept]
- CTRP Terminology [NCIt concept]
cytogenetic_abnormality_involves_chromosome
- Human Chromosome 16 [NCIt concept]
is_cytogenetic_abnormality_of_disease
- Acute Myeloid Leukemia with inv(16)(p13.1q22); CBFB-MYH11 [NCIt concept]
- Adult Acute Myeloid Leukemia with inv(16)(p13.1q22); CBFB-MYH11 [NCIt concept]
may_be_cytogenetic_abnormality_of_disease
- Blastic Granulocytic Sarcoma [NCIt concept]
- Core Binding Factor Acute Myeloid Leukemia [NCIt concept]
- Differentiated Granulocytic Sarcoma [NCIt concept]
- Granulocytic Sarcoma [NCIt concept]
- Immature Granulocytic Sarcoma [NCIt concept]
- Mediastinal Granulocytic Sarcoma [NCIt concept]
molecular_abnormality_involves_gene
- CBFB Gene [NCIt concept]
- CBFB/MYH11 Fusion Gene [NCIt concept]
- MYH11 Gene [NCIt concept]

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