ORPHA:399391
Osteochondrosis of genetic origin
- 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 | Osteochondrosis of genetic origin | |
| fr | Ostéochondrose d'origine génétique | |
| de | Osteochondrose, genetisch bedingte | |
| es | Osteocondrosis de origen genético | |
| it | Osteocondrosi di origine genetica | |
| nl | Osteochondrose van genetische oorsprong | |
| pt | Osteocondrose de origem genética | |
| pl | Osteochondroza pochodzenia genetycznego | |
| cs | Osteochondróza genetického původu | |
| uk | Генетично обумовлений остеохондроз | |
| zh | 遗传性骨软骨病 | |
| tr | Genetik kökenli osteokondroz |
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Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| MONDO | 18385 | E | validated | |
| UMLS | C5681168 | 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:399380Osteonecrosis of genetic origin
rare genetic diseases
Children (1):
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/399391
- This record as JSON: /data/d/399391.json