ORPHA:94059
Uremic pruritus
- Type
- Particular clinical situation in a disease or syndrome
- Group
- Disorder
- Inheritance
- Not applicable
- Age of onset
- Adolescent, Adult, Childhood, Elderly
- Status
- active
Orphadata ships no English definition for this code.
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Names in Orphadata languages
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | Uremic pruritus | |
| fr | Prurit urémique | |
| de | Pruritus, urämischer | |
| es | Prurito urémico | |
| it | Prurito uremico | |
| nl | Uremische pruritus | |
| pt | Prurido urémico | |
| pl | Świąd mocznicowy | |
| cs | Uremický pruritus | |
| uk | Уремічний свербіж | |
| zh | 尿毒症性皮肤瘙痒症 | |
| tr | Üremik kaşıntı |
2
Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| ICD-10 | L29.8 | NTBT | attributed | validated |
| ICD-11 | EC90.10 | E | specific | validated |
| UMLS | C1262019 | E | validated | |
| MedDRA | 10060875 | 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:90077Other acquired skin disease
rare skin diseases
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 | 1-5 / 10 000 | 35 / 100 000 | Europe | Value and class | Validated | European Medicines Agency 2010[OTHER] |
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
18 annotations · validated 2020-03-17| HPO | Term (as annotated by Orphanet) | Diagnostic |
|---|---|---|
| Very frequent (99-80%) | ||
| HP:0012622 | Chronic kidney disease | |
| HP:0000958 | Dry skin | |
| HP:0003138 | Increased blood urea nitrogen | |
| HP:0000989 | Pruritus | |
| Frequent (79-30%) | ||
| HP:0011112 | Abnormality of serum cytokine level | |
| HP:0011354 | Generalized abnormality of skin | |
| HP:0031901 | Increased serum mast cell beta-tryptase concentration | |
| HP:0031355 | Maintenance insomnia | |
| HP:0002360 | Sleep abnormality | |
| HP:0003774 | Stage 5 chronic kidney disease | |
| Occasional (29-5%) | ||
| HP:0000716 | Depression | |
| HP:0003072 | Hypercalcemia | |
| HP:0002918 | Hypermagnesemia | |
| HP:0011123 | Inflammatory abnormality of the skin | |
| HP:0100725 | Lichenification | |
| HP:0200034 | Papule | |
| HP:0001581 | Recurrent skin infections | |
| HP:0008732 | Renal hypophosphatemia | |
Run the differential on the 4 obligate / very frequent terms
Annotation source: 24402092[PMID]_29183013[PMID]_9585892[PMID]
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Sources for this card
- Orphanet page: orpha.net/en/disease/detail/94059
- This record as JSON: /data/d/94059.json