ORPHA:498491
Non-syndromic complete hemimelia
- 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 | Non-syndromic complete hemimelia | |
| fr | Hémimélie complète non syndromique | |
| de | Hemimelie, komplette, nicht-syndromale | |
| es | Hemimelia completa no sindrómica | |
| it | Emimelia completa non sindromica | |
| nl | Niet-syndromale volledige hemimelie | |
| pt | Hemimelia completa não-sindrómica | |
| pl | Całkowity niedorozwój kończyny | Niesyndromiczna całkowita hemimelia |
| cs | Kompletní hemimelie | |
| uk | Несиндромальна повна гемімелія | |
| zh | 完全性半肢畸形 | |
| tr | Tam hemimeli |
2
Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| MONDO | 0850030 | E | validated | |
| UMLS | C5925041 | 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:498461Non-syndromic terminal transverse limb defect
rare developmental anomalies during embryogenesis; rare genetic diseases; rare bone 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/498491
- This record as JSON: /data/d/498491.json