ORPHA:254834
Mitochondrial protein import disorder
- Type
- Category
- Group
- Group of disorders
- Status
- active
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.
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Names in Orphadata languages
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | Mitochondrial protein import disorder | |
| fr | Anomalie d'import des protéines mitochondriales | |
| de | Störungen der mitochondrialen Proteinimports | |
| es | Trastorno de la importación de proteínas mitocondriales | |
| it | Difetto dell'importo delle proteine mitocondriali | |
| nl | Stoornis van mitochondriale eiwitimport | |
| pt | Doença da importação protéica mitocondrial | |
| pl | Zaburzenie mitochondrialnego importu białek | |
| cs | Porucha proteinového importu mitochondrií | |
| uk | Порушення імпорту мітохондріального білка | |
| zh | 线粒体蛋白质转入障碍 | |
| tr | Mitokondriyal protein import bozukluğu |
2
Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| ICD-11 | 5C53.31 | E | specific | validated |
| MONDO | 0016802 | E | validated | |
| MONDO | 16802 | E | validated | |
| UMLS | C5680717 | E | validated |
E exact · NTBT this ORPHAcode is narrower than the target · BTNT broader than the target · ND not decided.
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Classification
Preferential parent (Orphanet linearisation):
Parents in the classifications (1):
- ORPHA:254827Mitochondrial membrane transport disorder
rare inborn errors of metabolism; rare genetic diseases
Children (1):
4
Genes
0 directOrphanet records no gene directly on this code.
5
Prevalence and incidence
0 recordsNo prevalence record in this release.
6
HPO phenotypes
Orphanet has no HPO annotation for this code in this release.
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Sources for this card
- Orphanet page: orpha.net/en/disease/detail/254834
- This record as JSON: /data/d/254834.json