ORPHA:289098
Disorders of vitamin D 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.
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Names in Orphadata languages
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | Disorders of vitamin D metabolism | |
| fr | Troubles du métabolisme de la vitamine D | |
| de | Störung des Vitamin D-Stoffwechels | |
| es | Trastorno del metabolismo de la vitamina D | |
| it | Difetti del metabolismo della vitamina D | |
| nl | Stoornissen van vitamine D-metabolisme | |
| pt | Doenças do metabolismo da vitamina D | |
| pl | Zaburzenia metabolizmu witaminy D | |
| cs | Poruchy metabolismu vitaminu D | |
| uk | Порушення обміну вітаміну D | |
| zh | 维生素D代谢紊乱 | |
| tr | D vitamini metabolizması bozuklukları |
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Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| MONDO | 0017322 | E | validated | |
| MONDO | 17322 | E | validated | |
| UMLS | C5681017 | 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 (3):
- ORPHA:93447Primary bone dysplasia with defective bone mineralization
rare developmental anomalies during embryogenesis; rare genetic diseases; rare bone diseases - ORPHA:183634Rare genetic parathyroid disease and phosphocalcic metabolism disorder
rare genetic diseases - ORPHA:68415Rare parathyroid disease and phosphocalcic metabolism anomaly
rare endocrine diseases
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Genes
0 directOrphanet records no gene directly on this code.
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Prevalence and incidence
0 recordsNo prevalence record in this release.
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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/289098
- This record as JSON: /data/d/289098.json