Congenital urachal anomaly
- Type
- Category
- Group
- Group of disorders
- Age of onset
- Antenatal, Neonatal
- Status
- active
Congenital urachal anomaly (CUA) describes a group of urachal remnants, found more frequently in males than females, that result from incomplete closure of the urachus (an embryological remnant of the allantois) during prenatal development, and that are usually asymptomatic (and found as an incidental finding on a radiological study) but can also present with umbilical discharge (in patent urachus or urachal sinus), infraumblical mass and pain, or with complications such as obstruction and infection. CUAs include patent urachus, urachal sinus, urachal cyst and urachal diverticulum.
Names in Orphadata languages
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | Congenital urachal anomaly | |
| fr | Anomalie congénitale de l'ouraque | |
| de | Urachus-Anomalie, kongenitale | |
| es | Anomalía congénita uracal | |
| it | Anomalia congenita dell'uraco | |
| nl | Congenitale urachale anomalie | Congenitale anomalie van urachus |
| pt | Anomalia congénita uracal | |
| pl | Wrodzona wada moczownika | |
| cs | Vrozené anomálie urachu | |
| uk | Вроджена аномалія сечоводу | |
| zh | 先天性脐尿管异常 | |
| tr | Doğumsal urakal anomali |
Definition in:
Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| MONDO | 0018565 | E | validated | |
| MONDO | 18565 | E | validated | |
| UMLS | C1739100 | E | validated |
E exact · NTBT this ORPHAcode is narrower than the target · BTNT broader than the target · ND not decided.
Classification
Preferential parent (Orphanet linearisation):
Parents in the classifications (2):
- ORPHA:93546Non-syndromic renal or urinary tract malformation
rare developmental anomalies during embryogenesis; rare renal diseases; rare transplant-related disorders - ORPHA:182124Non-syndromic urogenital tract malformation of male and female
rare developmental anomalies during embryogenesis; rare urogenital diseases; rare transplant-related disorders
Genes
0 directOrphanet records no gene directly on this code.
Prevalence and incidence
0 recordsNo prevalence record in this release.
HPO phenotypes
Orphanet has no HPO annotation for this code in this release.
Sources for this card
- Orphanet page: orpha.net/en/disease/detail/435743
- This record as JSON: /data/d/435743.json