ORPHA:79357
Hereditary palmoplantar keratoderma
Synonyms: Hereditary PPK · Hereditary keratosis palmoplantaris · Hereditary 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 | Hereditary palmoplantar keratoderma | Hereditary PPK · Hereditary keratosis palmoplantaris · Hereditary palmoplantar hyperkeratosis |
| fr | Kératodermie palmoplantaire héréditaire | Hypekératose palmoplantaire héréditaire · KPP héréditaire · PPK héréditaire |
| de | Palmoplantarkeratose, hereditäre | PPK, hereditäre · Palmoplantare Keratose, hereditäre |
| es | Queratodermia palmoplantar hereditaria | Hiperqueratosis palmoplantar hereditaria · PPK hereditaria · Queratosis palmoplantar hereditaria |
| it | Cheratoderma palmoplantare ereditario | Cheratosi palmoplantare ereditaria · Ipercheratosi palmoplantare ereditaria · PPK ereditario |
| nl | Erfelijke palmoplantaire keratodermie | Erfelijke PPK · Erfelijke hyperkeratose van handpalm of voetzool · Erfelijke keratodermie van handpalm of voetzool · Erfelijke keratosis palmoplantaris · Erfelijke palmoplantaire hyperkeratose |
| pt | Queratodermia palmoplantar hereditária | |
| pl | Dziedziczny rogowiec dłoni i stóp | Dziedziczna hiperkeratoza dłoni i stóp · Dziedziczny PPK · Dziedziczny rogowiec dłoniowo-podeszwowy |
| cs | Hereditární palmoplantární keratoderma | Hereditární PPK · Hereditární keratosis palmoplantaris · Hereditární palmoplantární hyperkeratóza |
| uk | Спадкова долонно-підошовна кератодермія | Спадковий кератоз долонь · Спадковий долонно-підошовний гіперкератоз · Спадковий PPK |
| zh | 遗传性掌跖角化病 | 遗传性掌跖角化过度 |
| tr | Kalıtsal palmoplantar keratoderma | Kalıtsal PPK · Kalıtsal keratoz palmoplantaris · Kalıtsal palmoplantar hiperkeratoz |
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Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| ICD-11 | EC20.3 | E | specific | validated |
| MONDO | 0019272 | E | validated | |
| MONDO | 19272 | E | validated | |
| UMLS | C0406757 | E | validated | |
| MedDRA | 10072537 | 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 (2):
- ORPHA:79353Epidermal disease
rare skin diseases - ORPHA:183426Genetic epidermal disorder
rare genetic 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/79357
- This record as JSON: /data/d/79357.json