Monosomy 10 - CISMeF

Preferred Label : Monosomy 10;

NCIt definition : A chromosomal abnormality characterized by the absence of one of the copies of chromosome 10.;

Details

Origin ID

C36468;

UMLS CUI

C1513476;

Semantic type(s)
- Cell or Molecular Dysfunction [UMLS semantic type]
cytogenetic_abnormality_involves_chromosome
- Human Chromosome 10 [NCIt concept]
may_be_cytogenetic_abnormality_of_disease
- Adult Astroblastoma, MN1-Altered [NCIt concept]
- Anaplastic Astroblastoma, MN1-Altered [NCIt concept]
- Astroblastoma, MN1-Altered [NCIt concept]
- Childhood Astroblastoma, MN1-Altered [NCIt concept]

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