ORPHA:97368
Drug-related renal tubular dysgenesis
- Type
- Etiological subtype
- Group
- Subtype of disorder
- Inheritance
- Not applicable
- Status
- active
This disease is described under Renal tubular dysgenesis
1
Names in Orphadata languages
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | Drug-related renal tubular dysgenesis | |
| fr | Dysgénésie tubulaire rénale d'origine médicamenteuse | |
| de | Dysgenesie, renale tubuläre, Medikamenten-induzierte | |
| es | Disgenesia tubular renal asociada a fármacos | |
| it | Disgenesia dei tubuli renali farmaco-correlata | |
| nl | Medicatiegerelateerde renale tubulaire dysgenesie | |
| pt | Disgenesia tubular renal relacionada com fármacos | |
| pl | Dysgenezja kanalików nerkowych związana z lekami | |
| cs | Poléková renální tubulární dysgeneze | |
| uk | Дисгенезія ниркових канальців, повязана з медикаментозним лікуванням | |
| zh | 药物相关性肾小管发育不全 | |
| tr | İlaç-ilişkili renal tübüler disgenezi |
2
Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| ICD-10 | Q63.8 | NTBT | attributed | validated |
| ICD-11 | LB30.3 | NTBT | index | validated |
| MONDO | 0019985 | E | validated | |
| UMLS | C5438798 | 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:3033Renal tubular dysgenesis
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/97368
- This record as JSON: /data/d/97368.json