ORPHA:93455
Patellar dysostosis
- 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 | Patellar dysostosis | |
| fr | Dysostose rotulienne | |
| de | Dysostose, patellare | |
| es | Disostosis patelar | |
| it | Disostosi patellare | |
| nl | Patellaire dysostose | |
| pt | Disostose rotuliana | |
| pl | Dyzostoza rzepki | |
| cs | Dysostózy čéšky | Patelární dysostózy |
| uk | Дизостоз колінної чашечки | |
| zh | 髌骨发育不全 | |
| tr | Patellar disostoz |
2
Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| UMLS | C5681590 | 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 (2):
- ORPHA:364559Dysostosis
rare developmental anomalies during embryogenesis; rare bone diseases - ORPHA:404568Dysostosis of genetic origin
rare genetic diseases
Codes that Orphanet moved or referred to this one:
- ORPHA:1428OBSOLETE: Familial chondromalacia patellae referred to · inactive
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/93455
- This record as JSON: /data/d/93455.json