ORPHA:93176
Unilateral congenital megacalycosis
- Type
- Clinical subtype
- Group
- Subtype of disorder
- Status
- active
Orphadata ships no English definition for this code.
1
Names in Orphadata languages
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | Unilateral congenital megacalycosis | |
| fr | Mégacalicose congénitale unilatérale | |
| de | Megakalikose, kongenitale, unilaterale | |
| es | Megacalicosis congénita unilateral | |
| it | Megacalicosi congenita unilaterale | |
| nl | Unilaterale congenitale megacalycose | |
| pt | Megacalicose congénita unilateral | |
| pl | Jednostronne wrodzone poszerzenie kielichów nerki | |
| cs | Vrozená jednostranná dilatace renálních kalichů | |
| uk | Односторонній вроджений мегакалікоз | |
| zh | 单侧先天性巨肾盏 | |
| tr | Tek taraflı Doğumsal megakalikoz |
2
Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| ICD-10 | Q63.8 | NTBT | attributed | validated |
| ICD-11 | LB31.Y | NTBT | index | validated |
| MONDO | 0019646 | E | validated | |
| UMLS | C5681456 | 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:93109Congenital megacalycosis
rare developmental anomalies during embryogenesis; rare renal diseases; rare transplant-related disorders
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/93176
- This record as JSON: /data/d/93176.json