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Chromosome 17 deletion MeSH Supplementary Concept Data 2025


MeSH Supplementary
Chromosome 17 deletion
Unique ID
C538045
RDF Unique Identifier
http://id.nlm.nih.gov/mesh/C538045
Entry Term(s)
17p- Syndrome
Chromosome 17p Deletion Syndrome
Deletion 17p Syndrome
Interstitial deletion 17p
Partial Monosomy 17p
Registry Numbers
0
Heading Mapped to
*Chromosome Deletion
Chromosomes, Human, Pair 17
*Smith-Magenis Syndrome
Frequency
80
Note
See SMITH-MAGENIS SYNDROME. OMIM: 182290
Date of Entry
2010/08/25
Revision Date
2015/08/18
Chromosome 17 deletion Preferred
17p- Syndrome Narrower
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