- Concept UI
- M000762635
- 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.
- Terms
-
Imprinting Disorders
Preferred Term
Term UI
T001132678
Date02/08/2023
LexicalTag
NON
ThesaurusID
NLM (2024)
-
Imprinting Diseases
Term UI
T001132681
Date02/08/2023
LexicalTag
NON
ThesaurusID
NLM (2024)
-
Imprinting Syndromes
Term UI
T001132682
Date02/08/2023
LexicalTag
NON
ThesaurusID
NLM (2024)
-
Genomic Imprinting Disorders
Term UI
T001132679
Date02/08/2023
LexicalTag
NON
ThesaurusID
NLM (2024)
-
Genetic Imprinting Disorders
Term UI
T001132680
Date02/08/2023
LexicalTag
NON
ThesaurusID
NLM (2024)