ORPHA:438072
Disorder of keton body transport
- 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 | Disorder of keton body transport | |
| fr | Trouble du transport des corps cétoniques | |
| de | Ketonkörper-Transport-Störung | |
| es | Trastorno del transporte de cuerpos cetónicos | |
| it | Disturbo del trasporto dei corpi chetonici | |
| nl | Stoornis van transport van ketonlichamen | |
| pt | Transtonos do transporte do corpo de cetona | |
| pl | Zaburzenie transportu ciał ketonowych | |
| cs | Porucha transportu ketolátek | |
| uk | Порушення транспорту кетонових тіл | |
| zh | 酮体运输障碍 | |
| tr | Keton cisimciği taşıma bozukluğu |
2
Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| MONDO | 18579 | E | validated | |
| UMLS | C5681184 | 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:79174Disorder of fatty acid oxidation and ketone body metabolism
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/438072
- This record as JSON: /data/d/438072.json