ORPHA:307141
Diffuse palmoplantar keratoderma
Synonyms: Diffuse PPK · Diffuse keratosis palmoplantaris · Diffuse palmoplantar hyperkeratosis
- Type
- Category
- Group
- Group of disorders
- Status
- active
This term does not characterize a disease but a group of diseases. To learn about the diseases included under this term, you can consult the classifications.
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Names in Orphadata languages
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | Diffuse palmoplantar keratoderma | Diffuse PPK · Diffuse keratosis palmoplantaris · Diffuse palmoplantar hyperkeratosis |
| fr | Kératodermie palmoplantaire diffuse | Hyperkératose palmoplantaire diffuse · KPP diffuse · PPK diffuse |
| de | Palmoplantarkeratose, diffuse | PPK, diffuse · Palmoplantare Hyperkeratose, diffuse |
| es | Queratodermia palmoplantar difusa | Hiperqueratosis palmoplantar difusa · PPK difusa · Queratosis palmoplantar difusa |
| it | Cheratoderma palmoplantare diffuso | Iperkeratosi palmoplantare diffusa · Keratosis palmoplantaris diffusa · PPK diffuso |
| nl | Diffuse palmoplantaire keratodermie | Diffuse PPK · Diffuse keratosis palmoplantaris · Diffuse palmoplantaire hyperkeratose |
| pt | Ceratodermia palmoplantar difusa | Hiperqueratose palmoplantar difusa |
| pl | Rozlany rogowiec dłoniowo-podeszwowy | Rozlana hiperkeratoza dłoniowo-podeszwowa · Rozlane rogowacenie dłoniowo-podeszwowe · Rozlany PPK |
| cs | Difuzní palmoplantární keratoderma | Difuzní PPK · Difuzní keratosis palmoplantaris · Difuzní palmoplantární hyperkeratóza |
| uk | Дифузна долонно-підошовна кератодермія | Дифузний кератоз долонь · Дифузний долонно-підошовний гіперкератоз · Дифузний PPK |
| zh | 弥漫性掌跖角化病 | 弥漫性掌跖角化病 |
| tr | Diffüz palmoplantar keratoderma | Yaygın PPK · Yaygın keratoz palmoplantaris · Yaygın palmoplantar hiperkeratoz |
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Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| ICD-11 | EC20.30 | E | specific | validated |
| MONDO | 0017666 | E | validated | |
| MONDO | 17666 | E | validated | |
| MeSH | D015776 | E | validated | |
| UMLS | C0022584 | 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:79357Hereditary palmoplantar keratoderma
rare genetic diseases; rare skin diseases
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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/307141
- This record as JSON: /data/d/307141.json