Human Chromosome 10

Preferred Label : Human Chromosome 10;

NCIt related terms : chr10; Chromosome 10;

NCIt definition : The designation for each member of the tenth largest human autosomal chromosome pair. Chromosome 10 spans about 135 million base pairs and represents between 4 and 4.5% of the total DNA in normal diploid cells.;

Details

Origin ID

C13205;

UMLS CUI

C0008652;

Anatomic structure is physical part of
- Chromatin [NCIt concept]
Automatic exact mappings (from CISMeF team)
- chromosomes, human, pair 10 [MeSH Descriptor]
- chromosomes, human, pair 10 [MeSH concept]
Contains anatomical structure(s)
- 10p [NCIt concept]
- 10q [NCIt concept]
Semantic type(s)
- Cell Component [UMLS semantic type]
UMLS correspondences (same concept)
- Chromosome pair 10 [FMA entity]
- Chromosome pair 10 (cell structure) [SNOMED CT concept]
- chromosome pair 10 [SNOMED Notion]
- chromosomes, human, pair 10 [MeSH concept]
- chromosomes, human, pair 10 [MeSH Descriptor]
chromosome_involved_in_cytogenetic_abnormality
- ABI1 Gene Rearrangement [NCIt concept]
- Concurrent Gain of Chromosome 7 and Loss of Chromosome 10 [NCIt concept]
- FGFR2 Gene Rearrangement [NCIt concept]
- FGFR2 Gene Translocation [NCIt concept]
- Gain of Chromosome 10 [NCIt concept]
- Gain of Chromosome 10p [NCIt concept]
- Gain of Chromosome 10q [NCIt concept]
- KIF5B Gene Rearrangement [NCIt concept]
- Loss of Chromosome 10 [NCIt concept]
- Loss of Chromosome 10p [NCIt concept]
- Loss of Chromosome 10q [NCIt concept]
- MLLT10 Gene Rearrangement [NCIt concept]
- Monosomy 10 [NCIt concept]
- NFKB2 Gene Rearrangement [NCIt concept]
- NUTM2A Gene Rearrangement [NCIt concept]
- OGA (MGEA5) Gene Rearrangement [NCIt concept]
- PTEN Gene Deletion [NCIt concept]
- Polysomy 10 [NCIt concept]
- RET Gene Translocation [NCIt concept]
- RET/PTC Rearrangement [NCIt concept]
- Rearrangement of 10p12.3 [NCIt concept]
- Simultaneous Trisomies of Chromosomes 4 and 10 [NCIt concept]
- Simultaneous Trisomies of Chromosomes 4, 10, and 17 [NCIt concept]
- TET1 Gene Rearrangement [NCIt concept]
- TLX1 Gene Rearrangement [NCIt concept]
- Trisomy 10 [NCIt concept]
- del(10q23) [NCIt concept]
- del(10q23)/PTEN Gene Locus Deletion [NCIt concept]
- del(10q24-qter) [NCIt concept]
- del(10q24q25) [NCIt concept]
- del(10q25-26) [NCIt concept]
- t(10;11)(p11.2;q23) [NCIt concept]
- t(10;11)(p11;q23) [NCIt concept]
- t(10;11)(p12.1;q23.3) [NCIt concept]
- t(10;11)(p12.3;q23.3) [NCIt concept]
- t(10;11)(p12;q23) [NCIt concept]
- t(10;11)(q21.3;q23.3) [NCIt concept]
- t(10;14)(q24;q11) [NCIt concept]
- t(10;17)(q22;p13) [NCIt concept]
- t(10;19)(q26;q13) [NCIt concept]
- t(1;10)(p22-31;q24-25) [NCIt concept]
- t(1;10)(p22;q24) [NCIt concept]
- t(7;10)(q34;q24) [NCIt concept]
- t(X;10)(p11;q23) [NCIt concept]
chromosome_mapped_to_disease
- 10p13-p14 Deletion Syndrome [NCIt concept]
- Dysplastic Cerebellar Gangliocytoma [NCIt concept]
concept_is_in_subset
- CTDC Value Terminology [NCIt concept]
- CTRP Biomarker Terminology [NCIt concept]
- CTRP Molecular Genetic Biomarker Terminology [NCIt concept]
- CTRP Terminology [NCIt concept]
- GDC Terminology [NCIt concept]
- GDC Value Terminology [NCIt concept]

Keyword's position in hierarchy(ies) :

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