ORPHA:238637
Megacystis-megaureter syndrome
Synonyms: Megaureter-megacystis syndrome
- Type
- Disease
- Group
- Disorder
- Age of onset
- Infancy, Neonatal
- Status
- active
Megacystic-megaureter syndrome is an urinary tract malformation characterized by the presence of a massive primary non-obstructive vesicoureteral reflux and a large capacity, smooth, thin walled bladder due to the continual recycling of refluxed urine. Recurrent urinary infections are commonly associated with this condition.
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Names in Orphadata languages
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | Megacystis-megaureter syndrome | Megaureter-megacystis syndrome |
| fr | Syndrome mégavessie-méga-uretères | Syndrome méga-uretères-mégavéssie |
| de | Megazystis-Megaureter-Syndrom | Megaureter-Megazystis-Syndrom |
| es | Síndrome megavejiga-megauréter | Síndrome megauréter-megavejiga |
| it | Sindrome megacisti-megauretere | Sindrome megauretere-megacisti |
| nl | Megacystis - mega-ureter-syndroom | Mega-ureter - megacystis-syndroom |
| pt | Síndrome megabexiga-megaureter | |
| pl | Zespół olbrzymiego pęcherza moczowego i moczowodów olbrzymich | Zespół moczowodów olbrzymich i olbrzymiego pęcherza moczowego |
| cs | Syndrom zahrnující megacystis a megaureter | Syndrom zahrnující megaureter a megacystis |
| uk | Синдром мегацистис-мегауретер | Синдром мегауретера-мегациститу |
| zh | 巨膀胱-巨输尿管综合征 | 巨输尿管-巨膀胱综合征 |
| tr | Megasitis-megaüreter sendromu | Megaüreter-megasist sendromu |
Definition in:
2
Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| ICD-10 | Q62.7 | NTBT | attributed | validated |
| ICD-11 | LB31.7 | E | specific | validated |
| MONDO | 0016548 | E | validated | |
| UMLS | C0431752 | 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:93546Non-syndromic renal or urinary tract malformation
rare developmental anomalies during embryogenesis; rare renal diseases; rare transplant-related disorders
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/238637
- This record as JSON: /data/d/238637.json