chromosomes, human, pair 17

Preferred Label : chromosomes, human, pair 17;

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

MeSH synonym : chromosome 17;

Wikipedia link : https://en.wikipedia.org/wiki/Chromosomes, human, pair 17;

Details

Origin ID

D002886;

UMLS CUI

C0008659;

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 17 (cell structure) [SNOMED CT concept]
- Human Chromosome 17 [NCIt concept]
- chromosome pair 17 [SNOMED Notion]
- flotillin 2 [HGNC gene]
Record concept(s)
- chromosomes, human, pair 17 [MeSH concept]
Related MeSH Supplementary Concept(s)
- NF1 microdeletion syndrome [MeSH Supplementary Concept]
- chromosome 17 deletion [MeSH Supplementary Concept]
- chromosome 17 ring [MeSH Supplementary Concept]
- chromosome 17 trisomy [MeSH Supplementary Concept]
- chromosome 17, deletion 17q23 q24 [MeSH Supplementary Concept]
- chromosome 17, trisomy 17p [MeSH Supplementary Concept]
- chromosome 17, trisomy 17q22 [MeSH Supplementary Concept]
- chromosome 17q21.31 deletion syndrome [MeSH Supplementary Concept]
- hypertrichosis terminalis, generalized, with or without gingival hyperplasia [MeSH Supplementary Concept]
Semantic type(s)
- Cell Component [UMLS semantic type]
UMLS correspondences (same concept)
- Chromosome pair 17 [FMA entity]
- Chromosome pair 17 (cell structure) [SNOMED CT concept]
- Human Chromosome 17 [NCIt concept]
- chromosome pair 17 [SNOMED Notion]

Keyword's position in hierarchy(ies) :

Main resources

You can consult :

recommendations
documents concerning education
documents for patients