Imprinting Disorders

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.

Year introduced: 2024

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Do not include MeSH terms found below this term in the MeSH hierarchy.

Tree Number(s): C16.320.447

MeSH Unique ID: D000096803

Entry Terms:

• Disorder, Imprinting
• Imprinting Disorder
• Imprinting Diseases
• Disease, Imprinting
• Imprinting Disease
• Imprinting Syndromes
• Imprinting Syndrome
• Syndrome, Imprinting
• Genomic Imprinting Disorders
• Disorder, Genomic Imprinting
• Genomic Imprinting Disorder
• Imprinting Disorder, Genomic
• Genetic Imprinting Disorders
• Disorder, Genetic Imprinting
• Genetic Imprinting Disorder
• Imprinting Disorder, Genetic

Previous Indexing:

• Genomic Imprinting (2021-2023)

All MeSH Categories
Diseases Category
Congenital, Hereditary, and Neonatal Diseases and Abnormalities
Genetic Diseases, Inborn
Imprinting Disorders
Angelman Syndrome
Beckwith-Wiedemann Syndrome
Prader-Willi Syndrome
Silver-Russell Syndrome