ORPHA:2338
Isolated punctate palmoplantar keratoderma
Synonyms: Isolated punctate PPK · Isolated punctate palmoplantar hyperkeratosis
- Type
- Clinical group
- Group
- Group of disorders
- Inheritance
- Autosomal dominant
- 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 | Isolated punctate palmoplantar keratoderma | Isolated punctate PPK · Isolated punctate palmoplantar hyperkeratosis |
| fr | Kératodermie palmoplantaire ponctuée isolée | Hyperkératose palmoplantaire ponctuée isolée · Isolated punctate KPP · Isolated punctate PPK |
| de | Palmoplantarkeratose, isolierte punktierte | PPK, isolierte punktierte · Palmoplantarhyperkeratose, isolierte punktierte |
| es | Queratodermia palmoplantar punctata aislada | Hiperqueratosis palmoplantar punctata aislada · PPK punctata aislada |
| it | Cheratoderma palmoplantare puntato isolato | Ipercheratosi palmoplantare puntata isolata · PPK isolato puntato |
| nl | Geïsoleerde puntvormige palmoplantaire keratodermie | Geïsoleerde puntvormige PPK · Geïsoleerde puntvormige hyperkeratose van handpalm of voetzool · Geïsoleerde puntvormige keratodermie van handpalm of voetzool · Geïsoleerde puntvormige palmoplantaire hyperkeratose |
| pt | Queratodermia palmoplantar punctiforme isolada | Queratodermia palmoplantar punctiforme hereditária |
| pl | Rogowiec dłoni i stóp izolowany punktowy | Izolowana punktowa hiperkeratoza dłoni i stóp · Izolowany punktowy PPK |
| cs | Izolovaná keratoderma palmoplantaris punctata | Izolovaná PPK punctata · Izolovaná hyperkeratosis palmoplantaris punctata |
| uk | Ізольована точкова долонно-підошовна кератодермія | Ізольований точковий долонно-підошовний гіперкератоз · Ізольований пунктирний PPK |
| zh | 孤立型点状掌跖角皮病 | 孤立型点状掌跖角皮病 |
| tr | İzole noktalı palmoplantar keratoderma | İzole noktalı PPK · İzole noktalı palmoplantar hiperkeratoz |
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Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| MONDO | 16518 | E | validated | |
| UMLS | C5679617 | 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:307967Punctate palmoplantar keratoderma
rare genetic diseases; rare skin diseases
Children (5):
- ORPHA:307995Marginal papular palmoplantar keratoderma
- ORPHA:444138Peeling skin-leukonychia-acral punctate keratoses-cheilitis-knuckle pads syndrome
- ORPHA:737Porokeratosis plantaris palmaris et disseminata
- ORPHA:79501Punctate palmoplantar keratoderma type 1
- ORPHA:79502Punctate palmoplantar keratoderma type 2
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.
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Sources for this card
- Orphanet page: orpha.net/en/disease/detail/2338
- This record as JSON: /data/d/2338.json