Imprinting Disorders

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;

Détails

Origin ID

D000096803;

UMLS CUI

C5816793;

Allowable qualifiers
- blood [MeSH Qualifier]
- cerebrospinal fluid [MeSH Qualifier]
- chemically induced [MeSH Qualifier]
- classification [MeSH Qualifier]
- complications [MeSH Qualifier]
- diagnosis [MeSH Qualifier]
- diagnostic imaging [MeSH Qualifier]
- diet therapy [MeSH Qualifier]
- drug therapy [MeSH Qualifier]
- economics [MeSH Qualifier]
- embryology [MeSH Qualifier]
- enzymology [MeSH Qualifier]
- epidemiology [MeSH Qualifier]
- ethnology [MeSH Qualifier]
- etiology [MeSH Qualifier]
- genetics [MeSH Qualifier]
- history [MeSH Qualifier]
- immunology [MeSH Qualifier]
- metabolism [MeSH Qualifier]
- microbiology [MeSH Qualifier]
- mortality [MeSH Qualifier]
- nursing [MeSH Qualifier]
- parasitology [MeSH Qualifier]
- pathology [MeSH Qualifier]
- physiopathology [MeSH Qualifier]
- prevention and control [MeSH Qualifier]
- psychology [MeSH Qualifier]
- radiotherapy [MeSH Qualifier]
- rehabilitation [MeSH Qualifier]
- surgery [MeSH Qualifier]
- therapy [MeSH Qualifier]
- urine [MeSH Qualifier]
- veterinary [MeSH Qualifier]
- virology [MeSH Qualifier]
Record concept(s)
- Imprinting Disorders [MeSH concept]
Related MeSH Supplementary Concept(s)
- 6q24-Related transient neonatal diabetes mellitus [MeSH Supplementary Concept]
- Schaaf-Yang syndrome [MeSH Supplementary Concept]
- Temple syndrome [MeSH Supplementary Concept]
- uniparental disomy, paternal, chromosome 14 [MeSH Supplementary Concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]

Position du mot-clé dans l'(les) arborescence(s) :

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