ORPHA:98356
Autosomal recessive isolated diffuse palmoplantar keratoderma
Synonyms: Autosomal recessive isolated diffuse palmoplantar hyperkeratosis
- Type
- Category
- Group
- Group of disorders
- Inheritance
- Autosomal recessive
- 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 recessive isolated diffuse palmoplantar keratoderma | Autosomal recessive isolated diffuse palmoplantar hyperkeratosis |
| fr | Kératodermie palmoplantaire diffuse isolée autosomique récessive | Hyperkératose palmoplantaire diffuse isolée autosomique récessive |
| de | Palmoplantarkeratose, autosomal-rezessive, isolierte diffuse | |
| es | Queratodermia palmoplantar difusa aislada autosómica recesiva | Hiperqueratosis palmoplantar difusa aislada autosómica recesiva |
| it | Cheratoderma palmoplantare diffuso isolato autosomico recessivo | Ipercheratosi palmoplantare diffusa isolata autosomica recessiva |
| nl | Autosomaal recessieve geïsoleerde diffuse palmoplantaire keratodermie | Autosomaal recessieve geïsoleerde diffuse palmoplantaire hyperkeratose |
| pt | Queratodermia palmoplantar difusa isolada autossómica recessiva | Hiperqueratose palmoplantar difusa isolada autossómica recessiva |
| pl | Autosomalny recesywny izolowany rozlany rogowiec dłoniowo-podeszwowy | Autosomalna recesywna izolowana rozlana hiperkeratoza dłoniowo-podeszwowa |
| cs | Autozomálně recesivní izolované difuzní palmoplantární keratoderma | Autozomálně recesivní izolovaná difuzní palmoplantární hyperkeratóza |
| uk | Аутосомно-рецесивна ізольована дифузна долонно-підошовна кератодермія | Аутосомно-рецесивний ізольований дифузний долонно-підошовний гіперкератоз |
| zh | 常染色体隐性遗传性孤立型弥漫性掌跖角化病 | 常染色体隐性遗传性孤立性弥漫性掌跖角化过度 |
| tr | Otozomal resesif izole difüz palmoplantar keratoderma | Otozomal Çekinik izole Yaygın palmoplantar hiperkeratoz |
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Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| UMLS | C5680346 | 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
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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/98356
- This record as JSON: /data/d/98356.json