ORPHA:498
Keratosis pilaris atrophicans
- Type
- Clinical group
- Group
- Group of disorders
- 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 | Keratosis pilaris atrophicans | |
| fr | Kératose pilaire rouge et atrophiante | |
| de | Keratosis pilaris rubra atrophicans | Keratosis pilaris atrophicans |
| es | Queratosis pilosa roja y atrofiante | |
| it | Cheratosi pilifera e atrofizzante | |
| nl | Keratosis pilaris atrophicans | |
| pt | Queratose pilaris atrófica | |
| pl | Rogowacenie mieszkowe zanikowe | |
| cs | Keratosis pilaris atrophicans | |
| uk | Атрофічний волосяний кератоз | |
| zh | 萎缩性毛发角化病 | |
| tr | Keratoz pilaris atrofikans |
2
Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| ICD-11 | ED56 | NTBT | index | validated |
| MONDO | 0018855 | E | validated | |
| MONDO | 18855 | E | validated | |
| MedDRA | 10083835 | 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 (2):
- ORPHA:79359Other epidermal disorder
rare skin diseases - ORPHA:79360Other genetic epidermal disease
rare genetic 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.
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Sources for this card
- Orphanet page: orpha.net/en/disease/detail/498
- This record as JSON: /data/d/498.json