del(12p13) - CISMeF

Preferred Label : del(12p13);

NCIt synonyms : del(12)(p13); del 12p13;

NCIt definition : A cytogenetic abnormality characterized by any loss of genetic material from the short arm of chromosome 12 within the band at 12p13.;

Details

Origin ID

C36429;

UMLS CUI

C2931806;

Semantic type(s)
- Cell or Molecular Dysfunction [UMLS semantic type]
UMLS correspondences (same concept)
- monosomy 12p13 [MeSH concept]
cytogenetic_abnormality_involves_chromosome
- Human Chromosome 12 [NCIt concept]
may_be_cytogenetic_abnormality_of_disease
- Recurrent T-Cell Prolymphocytic Leukemia [NCIt concept]
- Refractory T-Cell Prolymphocytic Leukemia [NCIt concept]
- Splenic Manifestation of T-Cell Prolymphocytic Leukemia [NCIt concept]
- T-Cell Prolymphocytic Leukemia [NCIt concept]
- T-Cell Prolymphocytic Leukemia Involving the Skin [NCIt concept]
- T-Cell Prolymphocytic Leukemia, Cerebriform Cell Variant [NCIt concept]
- T-Cell Prolymphocytic Leukemia, Small Cell Variant [NCIt concept]

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