ORPHA:93423
Sulfation-related bone disorder
- 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 | Sulfation-related bone disorder | |
| fr | Maladie osseuse liée à la sulfatation | |
| de | Knochenkrankheit bei Sulfatierungsstörung | |
| es | Trastorno óseo asociado a la sulfatación | |
| it | Difetto osseo legato alla sulfazione | |
| nl | Sulfatatiegerelateerde botaandoening | |
| pt | Doença da sulfatação | |
| pl | Zaburzenia sulfatyzacji | |
| cs | Onemocnění kostí související se sulfatací | |
| uk | Розлади кісток, повязані з сульфатацією | |
| zh | 硫酸化相关骨病 | |
| tr | Sülfasyon-ilişkili kemik bozukluğu |
2
Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| UMLS | C5681607 | 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:364803Rare bone disease related to a common gene or pathway defect
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/93423
- This record as JSON: /data/d/93423.json