Preferred Label : chromosomes, human, pair 9;
MeSH definition : A specific pair of GROUP C CHROMSOMES of the human chromosome classification.;
MeSH synonym : chromosome 9;
Wikipedia link : https://en.wikipedia.org/wiki/Chromosomes, human, pair 9;
Origin ID : D002899;
UMLS CUI : C0008672;
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 C CHROMSOMES of the human chromosome classification.
https://www.has-sante.fr/jcms/p_3291595/fr/syndrome-de-kleefstra
2021
false
false
false
France
case management
heart defects, congenital
chromosomes, human, pair 9
intellectual disability
chromosome deletion
craniofacial abnormalities
intellectual disability
practice guideline
kleefstra syndrome
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http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=FR&Expert=99776
France
French
chromosome 9, trisomy mosaic
rare diseases
trisomy
mosaicism
chromosomes, human, pair 9
uniparental disomy
---
http://www.orpha.net/consor/cgi-bin/OC_Exp.php?Lng=FR&Expert=96183
2011
France
scientific and technical information
chromosomes, human, pair 9
uniparental disomy
purpura, thrombotic thrombocytopenic
chromosome 9, trisomy mosaic
---
http://www.orpha.net/consor/cgi-bin/OC_Exp.php?Lng=FR&Expert=96173
2011
France
scientific and technical information
chromosomes, human, pair 9
ring chromosomes
---
https://www.rarechromo.org/media/translations/Francais/9p%20Deletions%20French%20QFN.pdf
2007
United Kingdom
French
popular works
chromosome deletion
chromosomes, human, pair 9
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