ORPHA:68341
Multiple congenital anomalies/dysmorphic syndrome
- 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 | Multiple congenital anomalies/dysmorphic syndrome | |
| fr | Anomalies congénitales multiples/syndrome dysmorphique | |
| de | Multiple kongenitale Anomalien/Dysmorphie-Syndrome | |
| es | Anomalías congénitas múltiples/síndrome dismórfico | |
| it | Sindrome dismorfica | |
| nl | Meervoudige congenitale anomalieën/dysmorfiesyndroom | |
| pt | Síndrome de anomalias congénitas múltiplas/dismorfia | |
| pl | Mnogie wady wrodzone/zespoł dysmorficzny | |
| cs | Syndromy zahrnující mnohočetné vrozené anomálie a dysmorfie | |
| uk | Множинні вроджені аномалії/дисморфічний синдром | |
| zh | 多重先天性异常/畸形综合征 | |
| tr | Çoklu doğumsal anomaliler/dismorfik sendrom |
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Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| MONDO | 0019042 | E | validated | |
| MONDO | 19042 | E | validated | |
| UMLS | C5681310 | 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
Preferential parent (Orphanet linearisation):
Parents in the classifications (1):
- ORPHA:93890Rare developmental defect during embryogenesis
rare developmental anomalies during embryogenesis
Codes that Orphanet moved or referred to this one:
- ORPHA:93472OBSOLETE: Dysmorphic syndrome associated with bone anomaly referred to · inactive
- ORPHA:98734OBSOLETE: Cardioskeletal syndrome referred to · inactive
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/68341
- This record as JSON: /data/d/68341.json