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Chromosome 16p13.3 Deletion Syndrome MeSH Supplementary Concept Data 2025


MeSH Supplementary
Chromosome 16p13.3 Deletion Syndrome
Unique ID
C566433
RDF Unique Identifier
http://id.nlm.nih.gov/mesh/C566433
Entry Term(s)
RSTS, Severe
Rubinstein-Taybi Syndrome, Severe
Registry Numbers
0
Heading Mapped to
Chromosomes, Human, Pair 16
*Rubinstein-Taybi Syndrome
Frequency
2
Date of Entry
2012/11/05
Revision Date
1955/01/01
Chromosome 16p13.3 Deletion Syndrome Preferred
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