ORPHA:97361
Renal hypoplasia, unilateral
- Type
- Clinical subtype
- Group
- Subtype of disorder
- Inheritance
- Not applicable
- Age of onset
- All ages
- Status
- active
A form of renal hypoplasia characterized by unilateral abnormally small kidneys with reduced number of nephrons. Patients are usually asymptomatic however some patients may present with hypertension and urinary tract infections. Risk of renal failure in childhood is minimal.
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Names in Orphadata languages
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | Renal hypoplasia, unilateral | |
| fr | Hypoplasie rénale unilatérale | |
| de | Nierenhypoplasie, unilaterale | |
| es | Hipoplasia renal unilateral | |
| it | Ipoplasia renale unilaterale | |
| nl | Unilaterale renale hypoplasie | |
| pt | Hipoplasia renal, unilateral | |
| pl | Hipoplazja nerki, jednostronna | |
| cs | Renální hypoplázie, jednostranná | |
| uk | Гіпоплазія нирок, одностороння | |
| zh | 单侧肾发育不全 | |
| tr | Renal hipoplazi, unilateral |
Definition in:
2
Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| ICD-10 | Q60.3 | E | specific | validated |
| ICD-11 | LB30.0Y | NTBT | index | validated |
| MONDO | 0019979 | E | validated | |
| UMLS | C0431691 | 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:93101Renal hypoplasia
rare developmental anomalies during embryogenesis; rare genetic diseases; 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
1 record| Type | Class | Value | Area | Qualification | Validation | Source |
|---|---|---|---|---|---|---|
| Point prevalence | Unknown | — | Worldwide | Class only | Validated | [EXPERT] |
Value is Orphadata's ValMoy: the mean estimate per 100 000 for prevalence and incidence, the number of cases or families for case reports.
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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/97361
- This record as JSON: /data/d/97361.json