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Chromosome 1q21.1 Deletion Syndrome, 1.35-Mb MeSH Supplementary Concept Data 2024


MeSH Supplementary
Chromosome 1q21.1 Deletion Syndrome, 1.35-Mb
Unique ID
C567291
RDF Unique Identifier
http://id.nlm.nih.gov/mesh/C567291
Entry Term(s)
1q21.1 Contiguous Gene Deletion
1q21.1 Deletion
1q21.1 Microdeletion
Chromosome 1q21.1 Deletion Syndrome
Registry Number
0
Heading Mapped to
*Abnormalities, Multiple
*Chromosome Deletion
Chromosomes, Human, Pair 1
*Megalencephaly
Frequency
21
Date of Entry
2012/11/05
Revision Date
2013/10/24
Chromosome 1q21.1 Deletion Syndrome, 1.35-Mb Preferred
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