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Chromosome 10q26 Deletion Syndrome
MeSH Supplementary Concept Data 2024
Details
Concepts
MeSH Supplementary
Chromosome 10q26 Deletion Syndrome
Unique ID
C567182
RDF Unique Identifier
http://id.nlm.nih.gov/mesh/C567182
Entry Term(s)
Terminal Chromosome 10q26 Deletion Syndrome
Registry Number
0
Heading Mapped to
*Chromosome Deletion
Chromosomes, Human, Pair 10
*Learning Disabilities
*Facies
Frequency
6
Date of Entry
2012/11/05
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Chromosome 10q26 Deletion Syndrome
Preferred
Concept UI
M0567482
Registry Number
0
Terms
Chromosome 10q26 Deletion Syndrome
Preferred Term
Term UI
T809910
Date
11/15/2011
LexicalTag
NON
ThesaurusID
OMIM (2013)
Terminal Chromosome 10q26 Deletion Syndrome
Term UI
T809911
Date
11/15/2011
LexicalTag
NON
ThesaurusID
OMIM (2013)
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