| Descriptor English: | Imprinting Disorders | ||||||
| Descriptor Spanish: |
Trastornos de Impronta
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| Descriptor Portuguese: | Transtornos da Impressão Genômica | ||||||
| Descriptor French: | Without translation | ||||||
| Entry term(s): |
Disease, Imprinting Disorder, Genetic Imprinting Disorder, Genomic Imprinting Disorder, Imprinting Genetic Imprinting Disorder Genetic Imprinting Disorders Genomic Imprinting Disorder Genomic Imprinting Disorders Imprinting Disease Imprinting Diseases Imprinting Disorder Imprinting Disorder, Genetic Imprinting Disorder, Genomic Imprinting Syndrome Imprinting Syndromes Syndrome, Imprinting |
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| Tree number(s): |
C16.320.447 |
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| RDF Unique Identifier: | https://id.nlm.nih.gov/mesh/D000096803 | ||||||
| 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. |
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| Allowable Qualifiers: |
BL blood CF cerebrospinal fluid CI chemically induced CL classification CO complications DG diagnostic imaging DH diet therapy DI diagnosis DT drug therapy EC economics EH ethnology EM embryology EN enzymology EP epidemiology ET etiology GE genetics HI history IM immunology ME metabolism MI microbiology MO mortality NU nursing PA pathology PC prevention & control PP physiopathology PS parasitology PX psychology RH rehabilitation RT radiotherapy SU surgery TH therapy UR urine VE veterinary VI virology |
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| Previous Indexing: |
Genomic Imprinting (2021-2023) |
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| Public MeSH Note: | 2024 |
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| History Note: | 2024 |
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| DeCS ID: | 60520 | ||||||
| Unique ID: | D000096803 | ||||||
| Documents indexed in the Virtual Health Library (VHL): | Click here to access the VHL documents | ||||||
| Date Established: | 2024/01/01 | ||||||
| Date of Entry: | 2023/07/26 | ||||||
| Revision Date: | 2023/06/01 |
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Imprinting Disorders
- Preferred
| 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. |
| Preferred term | Imprinting Disorders |
| Entry term(s) |
Disease, Imprinting Disorder, Genetic Imprinting Disorder, Genomic Imprinting Disorder, Imprinting Genetic Imprinting Disorder Genetic Imprinting Disorders Genomic Imprinting Disorder Genomic Imprinting Disorders Imprinting Disease Imprinting Diseases Imprinting Disorder Imprinting Disorder, Genetic Imprinting Disorder, Genomic Imprinting Syndrome Imprinting Syndromes Syndrome, Imprinting |
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