ORPHA:93389
Brachydactyly type A5
inactive · moved to ORPHA:93383Brachydactyly type B
- Type
- Malformation syndrome
- Group
- Disorder
- Status
- inactive
- Flag
- Deprecated entity
This entity has been excluded from the Orphanet nomenclature of rare diseases and moved to Brachydactyly type B
1
Names in Orphadata languages
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | Brachydactyly type A5 | |
| fr | Brachydactylie type A5 | |
| de | Brachydaktylie Typ A5 | |
| es | Braquidactilia tipo A5 | |
| it | Brachidattilia, tipo A5 | |
| nl | Brachydactylie type A5 | |
| pt | Braquidactilia tipo A5 | |
| pl | Brachydaktylia typu A5 | |
| cs | Brachydaktylie, typ A5 | |
| uk | Брахідактилія, тип А5 | |
| zh | 短指（趾）畸形A5型 | |
| tr | Brakidaktili tip A5 |
2
Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| UMLS | C1862138 | E | validated | |
| GARD | 982 | E | validated |
E exact · NTBT this ORPHAcode is narrower than the target · BTNT broader than the target · ND not decided.
3
Classification
Not placed in any Orphanet classification in this release.
No children.
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/93389
- This record as JSON: /data/d/93389.json