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Imprinting Disorders MeSH Descriptor Data 2024


MeSH Heading
Imprinting Disorders
Tree Number(s)
C16.320.447
Unique ID
D000096803
RDF Unique Identifier
http://id.nlm.nih.gov/mesh/D000096803
Scope Note
Disorders caused by transcriptional silencing of one parental gene allele (imprinted gene). Imprinted genes show genetic expression from only one parent of the gene pair through epigenetic processes with no change in the DNA sequence.
Entry Term(s)
Genetic Imprinting Disorders
Genomic Imprinting Disorders
Imprinting Diseases
Imprinting Syndromes
Previous Indexing
Genomic Imprinting (2021-2023)
Public MeSH Note
2024
History Note
2024
Date Established
2024/01/01
Date of Entry
2023/07/26
Revision Date
2023/06/01
Imprinting Disorders Preferred
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