chromosomes, human, pair 22

Preferred Label : chromosomes, human, pair 22;

MeSH definition : A specific pair of GROUP G CHROMOSOMES of the human chromosome classification.;

MeSH synonym : chromosome 22;

Wikipedia link : https://en.wikipedia.org/wiki/Chromosomes, human, pair 22;

Details

Origin ID

D002892;

UMLS CUI

C0008665;

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 22 (cell structure) [SNOMED CT concept]
- Human Chromosome 22 [NCIt concept]
- chromosome pair 22 [SNOMED Notion]
Record concept(s)
- chromosomes, human, pair 22 [MeSH concept]
Related MeSH Supplementary Concept(s)
- Schmid-Fraccaro syndrome [MeSH Supplementary Concept]
- chromosome 22 ring [MeSH Supplementary Concept]
- chromosome 22, microdeletion 22 q11 [MeSH Supplementary Concept]
- chromosome 22, monosome mosaic [MeSH Supplementary Concept]
- chromosome 22, trisomy [MeSH Supplementary Concept]
- chromosome 22, trisomy q11 q13 [MeSH Supplementary Concept]
- chromosome 22q11.2 deletion syndrome, distal [MeSH Supplementary Concept]
- chromosome 22q11.2 microduplication syndrome [MeSH Supplementary Concept]
- telomeric 22q13 monosomy syndrome [MeSH Supplementary Concept]
- trisomy 22 mosaicism syndrome [MeSH Supplementary Concept]
See also
- philadelphia chromosome [MeSH Descriptor]
Semantic type(s)
- Cell Component [UMLS semantic type]
UMLS correspondences (same concept)
- Chromosome pair 22 [FMA entity]
- Chromosome pair 22 (cell structure) [SNOMED CT concept]
- Human Chromosome 22 [NCIt concept]
- chromosome pair 22 [SNOMED Notion]

Keyword's position in hierarchy(ies) :

Main resources

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