OBSOLETE: Mitochondrial disorder due to a transcription or a translation defect of mitochondrial DNA
inactive · referred to ORPHA:35696Mitochondrial disorder due to a defect in mitochondrial protein synthesis
Synonyms: OBSOLETE: Mitochondrial disorder due to a transcription or a translation defect of mtDNA
- Type
- Category
- Group
- Group of disorders
- Status
- inactive
- Flag
- Obsolete entity
This entity has been obsoleted from the Orphanet nomenclature of rare diseases.<br/><br/>This term does not characterize a disease but a group of diseases. To learn about the diseases included under this term, you can consult the classifications.<br/><br/>Instead, consider using Mitochondrial disorder due to a defect in mitochondrial protein synthesis
Names in Orphadata languages
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | OBSOLETE: Mitochondrial disorder due to a transcription or a translation defect of mitochondrial DNA | OBSOLETE: Mitochondrial disorder due to a transcription or a translation defect of mtDNA |
| fr | OBSOLETE : Anomalie mitochondriale par défaut de transcription ou traduction de l'ADN mitochondrial | OBSOLETE : Anomalie mitochondriale par défaut de transcription ou traduction de l'ADNmt |
| de | OBSOLET: Mitochondriopathie durch Transkriptions- oder Translationsdefekt der mitochondrialen DNA | OBSOLET: Mitochondriopathie durch Transkriptions- oder Translationsdefekt der mtDNA |
| es | OBSOLETO: Trastorno mitocondrial por un defecto de transcripción o traducción del ADN mitocondrial | OBSOLETO: Trastorno mitocondrial por un defecto de transcripción o traducción del ADNmt |
| it | OBSOLETO: Malattia mitocondriale da difetto della trascrizione o della traduzione del DNA mitocondriale | OBSOLETO: Malattia mitocondriale da difetto della trascrizione o della traduzione del mtDNA |
| nl | OBSOLEET: Mitochondriale aandoening door transcriptie- of translatiedefect van mitochondriaal DNA | OBSOLEET: Mitochondriale aandoening door transcriptie- of translatiedefect van mtDNA |
| pt | OBSOLETO: Doença mitocondrial devido a uma transcrição ou um defeito de tradução do DNA mitocondrial | |
| pl | NIEAKTUALNE: Zaburzenia mitochondrialne z powodu defektu transkrypcji lub translacji mitochondrialnego DNA | NIEAKTUALNE: Zaburzenia mitochondrialne z powodu defektu transkrypcji lub translacji mtDNA |
| cs | NEAKTUÁLNÍ: Mitochondriální porucha způsobená poruchou transkripce nebo translace mitochondriální DNA | NEAKTUÁLNÍ: Mitochondriální porucha způsobená poruchou transkripce nebo translace mtDNA |
| uk | ЗАСТАРІЛО: Мітохондріальний розлад внаслідок дефекту транскрипції або трансляції мітохондріальної ДНК. | ЗАСТАРІЛО: Мітохондріальний розлад внаслідок дефекту транскрипції або трансляції мтДНК. |
| zh | 弃用：由于呼吸链复合体的组装或成熟缺陷所致线粒体紊乱 | 线粒体DNA组装或成熟缺陷所致线粒体紊乱 |
| tr | Eski adı: Mitokondriyal DNA'nın transkripsiyon veya translasyon defektine bağlı mitokondriyal bozukluk | MtDNA'nın bir transkripsiyon veya translasyon defektine bağlı mitokondriyal bozukluk |
Cross-references
qualifier = Orphanet mapping relationNo cross-references in this release.
Classification
Not placed in any Orphanet classification in this release.
No children.
Genes
0 directOrphanet records no gene directly on this code.
Prevalence and incidence
0 recordsNo prevalence record in this release.
HPO phenotypes
Orphanet has no HPO annotation for this code in this release.
Sources for this card
- Orphanet page: orpha.net/en/disease/detail/309139
- This record as JSON: /data/d/309139.json