ORPHA:309836
Disorder of mineral absorption 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 mineral absorption and transport | |
| fr | Anomalie de l'absorption et du transport des minéraux | |
| de | Mineralstoffabsorptionsstörungen | Mineralstofftransportstörungen |
| es | Trastornos de absorción y transporte de minerales | |
| it | Difetto del trasporto e dell'assorbimento dei minerali | |
| nl | Stoornis van mineraalabsorptie en transport | |
| pt | Alteração de absorção mineral e transporte | |
| pl | Zaburzenia wchłaniania i transportu minerałów | |
| cs | Poruchy absorpce a transportu minerálů | |
| uk | Порушення всмоктування та транспортування мінералів | |
| zh | 矿物质吸收-运输障碍 | |
| tr | Mineral emilim ve taşınım bozuklukluğu |
2
Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| ICD-11 | 5C64 | E | specific | validated |
| MONDO | 0017761 | E | validated | |
| MONDO | 17761 | E | validated | |
| UMLS | C5681035 | 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:309824Disorder of metabolite 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/309836
- This record as JSON: /data/d/309836.json