ORPHA:93395
Ballard syndrome
inactive · moved to ORPHA:93387Brachydactyly type E
Synonyms: Brachydactyly, combined B and E types · Pitt-Williams brachydactyly
- 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 E
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Names in Orphadata languages
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | Ballard syndrome | Brachydactyly, combined B and E types · Pitt-Williams brachydactyly |
| fr | Syndrome de Ballard | Brachydactylie de Pitt-Williams · Brachydactylie types B et E combinées |
| de | Ballard-Syndrom | Brachydaktylie Typ B und E kombiniert · Pitt-Williams-Brachydaktylie |
| es | Síndrome de Ballard | Braquidactilia tipo B y C combinadas |
| it | Sindrome di Ballard | Brachidattilia di Pitt-Williams · Brachidattilia, tipi B ed E combinati |
| nl | Syndroom van Ballard | Brachydactylie type B en E gecombineerd · Brachydactylie van Pitt-Williams |
| pt | Síndrome de Ballard | |
| pl | Zespół Ballarda | Brachydaktylia mieszane typy B i E · Brachydaktylia Pitta i Williamsa |
| cs | Syndrom Ballardových | Kombinovaná brachydaktylie, typy B a E · Pittové-Williamsova brachydaktylie · Pitt-Williamsova brachydaktylie |
| uk | Синдром Балларда | Брахідактилія, комбіновані типи B і E · Брахідактилія Пітта-Вільямса |
| zh | Ballard 综合征 | 短指(趾)畸形,B和D融合型 |
| tr | Ballard sendromu | Pitt-Williams brakidaktili · Brakidaktili, kombine B ve E tipleri |
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Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| OMIM | 112440 | E | validated | |
| UMLS | C1862163 | 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
Not placed in any Orphanet classification in this release.
No children.
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Genes
0 directOrphanet records no gene directly on this code.
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Prevalence and incidence
0 recordsNo prevalence record in this release.
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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/93395
- This record as JSON: /data/d/93395.json