ORPHA:254827
Mitochondrial membrane transport 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.
1
Names in Orphadata languages
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | Mitochondrial membrane transport disorder | |
| fr | Anomalie de transport membranaire mitochondrial | |
| de | Mitochondriale Membrantransportstörung | |
| es | Trastorno en el transporte de la membrana mitocondrial | |
| it | Difetto del trasporto nelle membrane mitocondriali | |
| nl | Stoornis van mitochondriaal membraantransport | |
| pt | Doença do transporte membranar mitocondrial | |
| pl | Zaburzenie transportu przez błonę mitochondrialną | |
| cs | Porucha transportu mitochondriální membránou | |
| uk | Порушення мембранного транспорту мітохондрій | |
| zh | 线粒体膜转运障碍 | |
| tr | Mitokondriyal membran taşıma bozukluğu |
2
Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| ICD-11 | 5C53.3 | E | specific | validated |
| MONDO | 0016800 | E | validated | |
| MONDO | 16800 | E | validated | |
| UMLS | C5680718 | E | validated |
E exact · NTBT this ORPHAcode is narrower than the target · BTNT broader than the target · ND not decided.
3
Classification
Preferential parent (Orphanet linearisation):
Parents in the classifications (1):
- ORPHA:68380Mitochondrial disease
rare inborn errors of metabolism; rare genetic diseases
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.
7
Sources for this card
- Orphanet page: orpha.net/en/disease/detail/254827
- This record as JSON: /data/d/254827.json