ORPHA:98349
Autosomal dominant isolated diffuse palmoplantar keratoderma
Synonyms: Autosomal dominant isolated diffuse palmoplantar hyperkeratosis
- Type
- Category
- 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 isolated diffuse palmoplantar keratoderma | Autosomal dominant isolated diffuse palmoplantar hyperkeratosis |
| fr | Kératodermie palmoplantaire diffuse isolée autosomique dominante | Hyperkératose palmoplantaire diffuse isolée autosomique dominante |
| de | Palmoplantarkeratose, autosomal-dominante, isolierte diffuse | |
| es | Queratodermia palmoplantar difusa aislada autosómica dominante | Hiperqueratosis palmoplantar difusa aislada autosómica dominante |
| it | Cheratoderma palmoplantare diffuso isolato autosomico dominante | Ipercheratosi palmoplantare diffusa isolata autosomica dominante |
| nl | Autosomaal dominante geïsoleerde diffuse palmoplantaire keratodermie | Autosomaal dominante geïsoleerde diffuse palmoplantaire hyperkeratose |
| pt | Queratodermia palmoplantar difusa autossómica dominante isolada | Hiperqueratose palmoplantar difusa autossómica dominante isolada |
| pl | Autosomalny dominujący izolowany rozlany rogowiec dłoniowo-podeszwowy | Autosomalna dominująca izolowana rozlana hiperkeratoza dłoniowo-podeszwowa |
| cs | Autozomálně dominantní izolované difuzní palmoplantární keratoderma | Autozomálně dominantní izolovaná difuzní palmoplantární hyperkeratóza |
| uk | Аутосомно-домінантна ізольована дифузна долонно-підошовна кератодермія | Аутосомно-домінантний ізольований дифузний долонно-підошовний гіперкератоз |
| zh | 常染色体显性遗传性孤立型弥漫性掌跖角化病 | 常染色体显性遗传性孤立性弥漫性掌跖角化过度 |
| tr | Otozomal dominant izole diffüz palmoplantar keratoderma | Otozomal dominant izole yaygın palmoplantar hiperkeratoz |
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Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| UMLS | C5680349 | 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:307148Isolated diffuse palmoplantar keratoderma
rare genetic diseases; rare skin diseases
Children (5):
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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/98349
- This record as JSON: /data/d/98349.json