Preferred Label : Imprinting Disorders;
MeSH definition : 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.;
MeSH synonym : Disorder, Imprinting; Imprinting Disorder; Genetic Imprinting Disorders; Disorder, Genetic Imprinting; Genetic Imprinting Disorder; Imprinting Disorder, Genetic; Genomic Imprinting Disorders; Disorder, Genomic Imprinting; Genomic Imprinting Disorder; Imprinting Disorder, Genomic; Imprinting Diseases; Disease, Imprinting; Imprinting Disease; Imprinting Syndromes; Imprinting Syndrome; Syndrome, Imprinting;
Origin ID : D000096803;
- Allowable qualifiers
- Record concept(s)
- Related MeSH Supplementary Concept(s)
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.