ORPHA:307995
Marginal papular palmoplantar keratoderma
Synonyms: Marginal papular 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.
1
Names in Orphadata languages
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | Marginal papular palmoplantar keratoderma | Marginal papular palmoplantar hyperkeratosis |
| fr | Kératodermie palmoplantaire papuleuse marginale | Hyperkératose palmoplantaire papuleuse marginale |
| de | Palmoplantarkeratose, marginale papulöse | Palmoplantare Hyperkeratose, marginale papulöse |
| es | Queratodermia palmoplantar papulosa marginal | Hiperqueratosis palmoplantar papulosa marginal |
| it | Cheratoderma palmoplantare papulare marginale | Ipercheratosi palmoplantare papulare marginale |
| nl | Marginale papuleuze palmoplantaire keratodermie | Marginale papuleuze palmoplantaire hyperkeratose |
| pt | Queratodermia palmoplantar papular marginal | Hiperqueratose palmoplantar papular marginal |
| pl | Rogowiec dłoniowo-podeszwowy brzeżny grudkowy | Hiperkertoza dłoniowo-podeszwowa brzeżna grudkowa |
| cs | Marginální papulární palmoplantární keratoderma | Marginální papulární palmoplantární hyperkeratóza |
| uk | Крайова папульозна долонно-підошовна кератодермія | Маргінальний папульозний долонно-підошовний гіперкератоз |
| zh | 边缘丘疹状掌跖角化病 | 边缘丘疹状掌跖角化病 |
| tr | Marjinal papüler palmoplantar keratoderma | Marjinal papüller palmoplantar hiperkeratoz |
2
Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| MONDO | 17676 | E | validated | |
| UMLS | C5679964 | 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:2338Isolated punctate palmoplantar keratoderma
rare genetic diseases; rare skin diseases
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.
7
Sources for this card
- Orphanet page: orpha.net/en/disease/detail/307995
- This record as JSON: /data/d/307995.json