ORPHA:440701
Disorders of pentose/polyol metabolism
- 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 | Disorders of pentose/polyol metabolism | |
| fr | Trouble du métabolisme des pentoses/polyols | |
| de | Störung des Pentose/Polyol-Stoffwechels | |
| es | Trastornos del metabolismo de la pentosa/poliol | |
| it | Disturbi del metabolismo dei pentosi/polioli | |
| nl | Stoornissen van pentose/polyol-metabolisme | |
| pt | Doença do metabolismo da pentose/poliol | |
| pl | Zaburzenia metabolizmu pentozy/polioli | |
| cs | Poruchy metabolismu pentózy/polyolu | |
| uk | Порушення метаболізму пентози/поліолів | |
| zh | 戊糖/多元醇代谢紊乱 | |
| tr | Pentoz/poliol metabolizması bozuklukları |
2
Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| MONDO | 0018605 | E | validated | |
| MONDO | 18605 | E | validated | |
| UMLS | C5681188 | 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:79161Disorder of carbohydrate 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.
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Sources for this card
- Orphanet page: orpha.net/en/disease/detail/440701
- This record as JSON: /data/d/440701.json