chromosomes, human, pair 2

Preferred Label : chromosomes, human, pair 2;

MeSH definition : A specific pair of human chromosomes in group A (CHROMOSOMES, HUMAN, 1-3) of the human chromosome classification.;

MeSH synonym : chromosome 2;

Wikipedia link : https://en.wikipedia.org/wiki/Chromosomes, human, pair 2;

Details

Origin ID

D002889;

UMLS CUI

C0008662;

Allowable qualifiers
- chemistry [MeSH Qualifier]
- classification [MeSH Qualifier]
- drug effects [MeSH Qualifier]
- enzymology [MeSH Qualifier]
- genetics [MeSH Qualifier]
- immunology [MeSH Qualifier]
- metabolism [MeSH Qualifier]
- microbiology [MeSH Qualifier]
- parasitology [MeSH Qualifier]
- physiology [MeSH Qualifier]
- radiation effects [MeSH Qualifier]
- ultrastructure [MeSH Qualifier]
- virology [MeSH Qualifier]
Automatic exact mappings (from CISMeF team)
- Chromosome pair 2 (cell structure) [SNOMED CT concept]
- Human Chromosome 2 [NCIt concept]
- chromosome pair 2 [SNOMED Notion]
Record concept(s)
- chromosomes, human, pair 2 [MeSH concept]
Related MeSH Supplementary Concept(s)
- chromosome 2, monosomy 2p22 [MeSH Supplementary Concept]
- chromosome 2, monosomy 2pter p24 [MeSH Supplementary Concept]
- chromosome 2, monosomy 2q [MeSH Supplementary Concept]
- chromosome 2, monosomy 2q24 [MeSH Supplementary Concept]
- chromosome 2, trisomy 2p [MeSH Supplementary Concept]
- chromosome 2, trisomy 2p13 p21 [MeSH Supplementary Concept]
- chromosome 2, trisomy 2pter p24 [MeSH Supplementary Concept]
- chromosome 2, trisomy 2q [MeSH Supplementary Concept]
- chromosome 2, trisomy 2q37 [MeSH Supplementary Concept]
- chromosome 2p16.1-P15 deletion syndrome [MeSH Supplementary Concept]
- chromosome 2q31.2 deletion syndrome [MeSH Supplementary Concept]
- chromosome 2q32-Q33 deletion syndrome [MeSH Supplementary Concept]
- chromosome 2q37 deletion syndrome [MeSH Supplementary Concept]
- uniparental disomy of chromosome 2 [MeSH Supplementary Concept]
Semantic type(s)
- Cell Component [UMLS semantic type]
UMLS correspondences (same concept)
- Chromosome pair 2 [FMA entity]
- Chromosome pair 2 (cell structure) [SNOMED CT concept]
- Human Chromosome 2 [NCIt concept]
- chromosome pair 2 [SNOMED Notion]

Keyword's position in hierarchy(ies) :

Main resources

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