Structured Summary
Abstract
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.
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Classification
Broader headings
Related Concepts
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MeSH Record
Synonyms
16 entry terms
- Genetic Imprinting Disorders
- Genomic Imprinting Disorders
- Imprinting Diseases
- Imprinting Syndromes
- Disease, Imprinting
- Disorder, Genetic Imprinting
- Disorder, Genomic Imprinting
- Disorder, Imprinting
- Genetic Imprinting Disorder
- Genomic Imprinting Disorder
- Imprinting Disease
- Imprinting Disorder
- Imprinting Disorder, Genetic
- Imprinting Disorder, Genomic
- Imprinting Syndrome
- Syndrome, Imprinting
MeSH Record
Aspects Covered
34 allowable subheadings
Indexed with the subheadings blood, cerebrospinal fluid, chemically induced, classification, complications, diagnosis, diagnostic imaging, diet therapy, drug therapy, economics, embryology, enzymology, epidemiology, ethnology, etiology, genetics, history, immunology, metabolism, microbiology, mortality, nursing, parasitology, pathology, physiopathology, prevention & control, psychology, radiotherapy, rehabilitation, surgery, therapy, urine, veterinary, virology.
MeSH Record
History Note
2024
MeSH Record
Previous Indexing
- Genomic Imprinting (2021-2023)
MeSH Hierarchy
Tree Number
AMA Style
References
- National Library of Medicine. Imprinting Disorders. Medical Subject Headings (MeSH). 2026. Unique ID D000096803. http://id.nlm.nih.gov/mesh/2026/D000096803
- Imprinting Disorders. In: Wikidata. https://www.wikidata.org/wiki/Q124335970