ORPHA:238654
Congenital primary megaureter, nonrefluxing and unobstructed form
- Type
- Clinical subtype
- Group
- Subtype of disorder
- Inheritance
- Unknown
- Age of onset
- Infancy, Neonatal
- Status
- active
This disease is described under Congenital primary megaureter
1
Names in Orphadata languages
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | Congenital primary megaureter, nonrefluxing and unobstructed form | |
| fr | Méga-uretère primitif congénital nonobstructif sans reflux | |
| de | Megaureter, kongenitaler primärer, nicht refluxierende und nicht obstruktive Formen | |
| es | Megauréter primitivo congénito no obstructivo sin reflujo | |
| it | Megauretere primitivo congenito, forma non ostruttiva e senza reflusso | |
| nl | Congenitale primaire mega-ureter, niet-refluerende en niet-obstructieve vorm | |
| pt | Megaureter primário congénito, forma sem refluxo e sem obstrução | |
| pl | Wrodzony moczowód olbrzymi, postać nierefluksowa i nieprzeszkodowa | |
| cs | Vrozený primární megaureter, nerefluktující a neobstrukční forma | |
| uk | Вроджений первинний мегауретер, без рефлюксу та безперешкодна форма | |
| zh | 无回流无阻塞性先天性原发性巨输尿管 | |
| tr | Doğumsal primer megaüreter, reflü ve tıkalı olmayan formu |
2
Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| ICD-10 | Q62.2 | NTBT | attributed | validated |
| ICD-11 | LB31.1 | NTBT | index | validated |
| MONDO | 0016552 | E | validated | |
| UMLS | C5680934 | 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:617Congenital primary megaureter
rare developmental anomalies during embryogenesis; rare genetic diseases; rare urogenital diseases; rare renal diseases; rare transplant-related disorders
No children.
4
Genes
0 directOrphanet records no gene directly on this code.
5
Prevalence and incidence
1 record| Type | Class | Value | Area | Qualification | Validation | Source |
|---|---|---|---|---|---|---|
| Point prevalence | Unknown | — | Worldwide | Class only | Not yet validated | ORPHANET |
Value is Orphadata's ValMoy: the mean estimate per 100 000 for prevalence and incidence, the number of cases or families for case reports.
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/238654
- This record as JSON: /data/d/238654.json