chromosomes, human, pair 1

Preferred Label : chromosomes, human, pair 1;

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

MeSH synonym : chromosome 1;

Wikipedia link : https://en.wikipedia.org/wiki/Chromosomes, human, pair 1;

Details

Origin ID

D002878;

UMLS CUI

C0008651;

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 1 (cell structure) [SNOMED CT concept]
- Human Chromosome 1 [NCIt concept]
- chromosome pair 1 [SNOMED Notion]
Record concept(s)
- chromosomes, human, pair 1 [MeSH concept]
Related MeSH Supplementary Concept(s)
- chromosome 1 ring [MeSH Supplementary Concept]
- chromosome 1, deletion q21 q25 [MeSH Supplementary Concept]
- chromosome 1, duplication 1p21 p32 [MeSH Supplementary Concept]
- chromosome 1, monosomy 1p [MeSH Supplementary Concept]
- chromosome 1, monosomy 1p22 p13 [MeSH Supplementary Concept]
- chromosome 1, monosomy 1p31 p22 [MeSH Supplementary Concept]
- chromosome 1, monosomy 1p32 [MeSH Supplementary Concept]
- chromosome 1, monosomy 1p34 p32 [MeSH Supplementary Concept]
- chromosome 1, monosomy 1q25 q32 [MeSH Supplementary Concept]
- chromosome 1, monosomy 1q32 q42 [MeSH Supplementary Concept]
- chromosome 1, monosomy 1q4 [MeSH Supplementary Concept]
- chromosome 1, q42 11 q42 12 duplication [MeSH Supplementary Concept]
- chromosome 1, trisomy 1q32 qter [MeSH Supplementary Concept]
- chromosome 1, trisomy 1q42 qter [MeSH Supplementary Concept]
- chromosome 1, uniparental disomy 1q12 q21 [MeSH Supplementary Concept]
- chromosome 1p36 deletion syndrome [MeSH Supplementary Concept]
- chromosome 1q, duplication 1q12 q21 [MeSH Supplementary Concept]
- chromosome 1q21.1 deletion syndrome, 1.35-Mb [MeSH Supplementary Concept]
- chromosome 1q21.1 duplication syndrome [MeSH Supplementary Concept]
- chromosome 1q43-Q44 deletion syndrome [MeSH Supplementary Concept]
- holoprosencephaly 10 [MeSH Supplementary Concept]
Semantic type(s)
- Cell Component [UMLS semantic type]
UMLS correspondences (same concept)
- Chromosome pair 1 [FMA entity]
- Chromosome pair 1 (cell structure) [SNOMED CT concept]
- Human Chromosome 1 [NCIt concept]
- chromosome pair 1 [SNOMED Notion]

Keyword's position in hierarchy(ies) :

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