Preferred Label : chromosomes, human, pair 21;
MeSH definition : A specific pair of GROUP G CHROMOSOMES of the human chromosome classification.;
MeSH synonym : chromosome 21;
Wikipedia link : https://en.wikipedia.org/wiki/Chromosome 21;
Origin ID : D002891;
UMLS CUI : C0008664;
Allowable qualifiers
Automatic exact mappings (from CISMeF team)
Record concept(s)
Related MeSH Supplementary Concept(s)
Semantic type(s)
UMLS correspondences (same concept)
A specific pair of GROUP G CHROMOSOMES of the human chromosome classification.
https://alzheimer.ca/sites/default/files/files/national/other-dementias/down_syndrome_f.pdf
2016
false
true
false
Canada
alzheimer disease
alzheimer disease
chromosomes, human, pair 21
scientific and technical information
down syndrome
alzheimer disease
---
http://www.orpha.net/consor/cgi-bin/OC_Exp.php?Lng=FR&Expert=574
2012
false
France
French
scientific and technical information
monosomy
chromosomes, human, pair 21
chromosome 21 monosomy
---
http://www.orpha.net/consor/cgi-bin/OC_Exp.php?Lng=FR&Expert=96195
2011
France
scientific and technical information
chromosome 21, uniparental disomy of
uniparental disomy
chromosomes, human, pair 21
patulin
Chromosome 21, uniparental disomy of
---
http://www.orpha.net/consor/cgi-bin/OC_Exp.php?Lng=FR&Expert=96187
2011
France
scientific and technical information
chromosomes, human, pair 21
purpura, thrombotic thrombocytopenic
chromosome 21, uniparental disomy of
uniparental disomy
Chromosome 21, uniparental disomy of
---