ORPHA:309845
Disorder of zinc metabolism and 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 zinc metabolism and transport | |
| fr | Anomalie du métabolisme et du transport du zinc | |
| de | Zink-Stoffwechselstörung | |
| es | Trastornos del metabolismo del cinc | |
| it | Difetto del metabolismo dello zinco | |
| nl | Stoornis van zinkmetabolisme | |
| pt | Alteração do metabolismo do zinco | |
| pl | Zaburzenia metabolizmu cynku | |
| cs | Poruchy metabolismu zinku | |
| uk | Порушення метаболізму та транспорту цинку | |
| zh | 锌代谢与转运障碍 | |
| tr | Çinko metabolizması ve taşınım bozuklukluğu |
2
Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| ICD-10 | E83.2 | E | specific | validated |
| MONDO | 0017764 | E | validated | |
| MONDO | 17764 | E | validated | |
| UMLS | C0268085 | E | validated | |
| MedDRA | 10086140 | 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:309836Disorder of mineral absorption and transport
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/309845
- This record as JSON: /data/d/309845.json