ORPHA:294925
Non-syndromic amelia
- Type
- Clinical group
- 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 | Non-syndromic amelia | |
| fr | Amélie non syndromique | |
| de | Amelie, nicht-syndromale | |
| es | Amelia no sindrómica | |
| it | Amelia non sindromica | |
| nl | Niet-syndromale amelie | |
| pt | Amelia não-sindrómica | |
| pl | Amelia niesyndromiczna | |
| cs | Amelie | |
| uk | Несиндромальна амелія | |
| zh | 缺肢 | |
| tr | Ameli |
2
Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| ICD-10 | Q73.0 | E | specific | validated |
| MONDO | 17419 | E | validated | |
| UMLS | C5925013 | E | validated | |
| MedDRA | 10001926 | 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.
7
Sources for this card
- Orphanet page: orpha.net/en/disease/detail/294925
- This record as JSON: /data/d/294925.json