ORPHA:307773
Autosomal dominant diffuse mutilating palmoplantar keratoderma
Synonyms: Autosomal dominant diffuse mutilating 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 | Autosomal dominant diffuse mutilating palmoplantar keratoderma | Autosomal dominant diffuse mutilating palmoplantar hyperkeratosis |
| fr | Kératodermie palmoplantaire diffuse mutilante autosomique dominante | Hyperkératose palmoplantaire diffuse mutilante autosomique dominante |
| de | Palmoplantarkeratose, diffuse mutilierende, autosomal-dominante | Palmoplantare Hyperkeratose, diffuse mutilierende, autosomal-dominante |
| es | Queratodermia palmoplantar mutilante difusa autosómica dominante | Hiperqueratosis palmoplantar mutilante difusa autosómica dominante |
| it | Cheratoderma palmoplantare mutilante diffuso autosomico dominante | Ipercheratosi palmoplantare mutilante diffusa autosomica dominante |
| nl | Autosomaal dominante diffuse mutilerende palmoplantaire keratodermie | Autosomaal dominante diffuse mutilerende palmoplantaire hyperkeratose |
| pt | Queratodermia palmoplantar mutilante difusa autossómica dominante | Hiperqueratose palmoplantar mutilante difusa autossómica dominante |
| pl | Autosomalny dominujący rozlany okaleczający rogowiec dłoniowo-podeszwowy | Autosomalna dominująca rozlana okaleczająca hiperkeratoza dłoniowo-podeszwowa |
| cs | Autozomálně dominantní difuzní mutilující palmoplantární keratoderma | Autozomálně dominantní difuzní mutilující palmoplantární hyperkeratóza |
| uk | Аутосомно-домінантна дифузна долонно-підошовна кератодермія, яка скалічує | Аутосомно-домінантний дифузний калічачий долонно-підошовний гіперкератоз |
| zh | 常染色体显性遗传弥漫性残毁性掌跖角化病 | 常染色体显性遗传弥漫性残毁性掌跖角化病 |
| tr | Otozomal dominant diffüz sakatlayıcı palmoplantar keratoderma | Otozomal baskın yaygın sakatlayıcı palmoplantar hiperkeratoz |
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Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| MONDO | 17670 | E | validated | |
| UMLS | C5679961 | 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:98352Autosomal dominant disease with diffuse palmoplantar keratoderma as a major feature
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/307773
- This record as JSON: /data/d/307773.json