ORPHA:86923
Hereditary palmoplantar keratoderma, Gamborg-Nielsen type
inactive · moved to ORPHA:87503Mal de Meleda
Synonyms: Hereditary palmoplantar hyperkeratosis, Gamborg-Nielsen type · PPK, Gamborg-Nielsen type
- Type
- Disease
- Group
- Disorder
- Status
- inactive
- Flag
- Deprecated entity
This entity has been excluded from the Orphanet nomenclature of rare diseases and moved to Mal de Meleda
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Names in Orphadata languages
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | Hereditary palmoplantar keratoderma, Gamborg-Nielsen type | Hereditary palmoplantar hyperkeratosis, Gamborg-Nielsen type · PPK, Gamborg-Nielsen type |
| fr | Kératodermie palmoplantaire héréditaire type Gamborg-Nielsen | Hyperkératose palmoplantaire héréditaire type Gamborg-Nielsen · KPP type Gamborg-Nielsen · PPK type Gamborg-Nielsen |
| de | Palmoplantarkeratose, hereditäre, Typ Gamborg-Nielsen | PPK, Typ Gamborg-Nielsen · Palmoplantarkeratose, diffuse, rezessiver Typ Norbotten |
| es | Queratodermia palmoplantar hereditaria tipo Gamborg-Nielsen | Hiperqueratosis palmoplantar hereditaria tipo Gamborg-Nielsen · PPK tipo Gamborg-Nielsen |
| it | Cheratoderma palmoplantare ereditario, tipo Gamborg-Nielsen | Ipercheratosi palmoplantare ereditaria, tipo Gamborg-Nielsen · PPK, tipo Gamborg-Nielsen |
| nl | Hereditaire palmoplantaire keratodermie, Gamborg-Nielsen-type | Erfelijke palmoplantaire hyperkeratose, Gamborg-Nielsen-type · PPK, Gamborg-Nielsen-type |
| pt | Queratodermia palmoplantar hereditária, tipo Gamborg-Nielsen | |
| pl | Dziedziczny rogowiec dłoniowo-podeszwowy typu Gamborga i Nielsena | Dziedziczna hiperkeratoza dłoniowo-podeszwowa typu Gamborga i Nielsena · PPK, typ Gamborga i Nielsena |
| cs | Hereditární palmoplantární keratoderma, Gamborgův-Nielsenův typ | Dědičná palmoplantární hyperkeratóza, Gamborgův-Nielsenův typ · PPK, Gamborgův-Nielsenův typ · Hereditární palmoplantární keratoderma, Gamborg-Nielsenův typ · Dědičná palmoplantární hyperkeratóza, Gamborg-Nielsenův typ |
| uk | Спадкова долонно-підошовна кератодермія, тип Гамборга-Нільсена | Спадковий долонно-підошовний гіперкератоз, тип Гамборга-Нільсена · PPK, тип Гамборга-Нільсена |
| zh | 遗传性掌跖角化病，Gamborg-Nielsen型 | 遗传性掌跖角化过度，Gamborg-Nielsen型 |
| tr | Kalıtsal palmoplantar keratoderma, Gamborg-Nielsen tipi | PPK, Gamborg-Nielsen türü · Kalıtsal palmoplantar hiperkeratoz, Gamborg-Nielsen tipi |
Definition in:
2
Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| MONDO | 0009489 | E | validated | |
| UMLS | C4273986 | 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
Not placed in any Orphanet classification in this release.
No children.
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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/86923
- This record as JSON: /data/d/86923.json