ORPHA:647916
Conjoined twins
Synonyms: Siamese twins
- Type
- Malformation syndrome
- Group
- Disorder
- Inheritance
- Not applicable
- Status
- active
Orphadata ships no English definition for this code.
1
Names in Orphadata languages
10 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | Conjoined twins | Siamese twins |
| fr | Jumeaux siamois | Jumeaux conjoints · Siamois |
| de | Siamesische Zwillinge | |
| es | Gemelos unidos | Gemelos siameses |
| it | Gemelli congiunti | Gemelli siamesi |
| nl | Dubbelmonstrum | Siamese tweeling |
| pt | Gémeos unidos | Gémeos siameses |
| pl | Bliźnięta syjamskie | = en |
| cs | Siamská dvojčata | = en |
| uk | Зрощені двійнята | Сіамські близнюки |
2
Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| ICD-10 | Q89.4 | E | specific | validated |
| ICD-11 | LD2G | E | specific | validated |
| MONDO | 0958083 | E | validated | |
| MONDO | 958083 | E | validated | |
| MeSH | D014428 | E | validated | |
| UMLS | C0041428 | E | validated | |
| MedDRA | 10010688 | 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:93890Rare developmental defect during embryogenesis
rare developmental anomalies during embryogenesis
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/647916
- This record as JSON: /data/d/647916.json