ORPHA:228285
Acquired cutis laxa
Synonyms: Cutis laxa acquisita
- Type
- Disease
- Group
- Disorder
- Inheritance
- Not applicable
- Age of onset
- Adolescent, Adult, Childhood, Elderly, Infancy
- Status
- active
A rare disorder of the connective tissue characterized by skin inflammation inducing elastolysis, leading to sudden, progressive fine skin wrinkling, and variable systemic involvement.
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Names in Orphadata languages
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | Acquired cutis laxa | Cutis laxa acquisita |
| fr | Cutis laxa acquise | = en |
| de | Cutis laxa, erworbene | = en |
| es | Cutis laxa adquirido | = en |
| it | Cutis laxa acquisita | |
| nl | Verworven cutis laxa | = en |
| pt | Cutis laxa adquirida | |
| pl | Skóra wiotka nabyta | = en |
| cs | Získaná cutis laxa | = en |
| uk | Набута cutis laxa | = en |
| zh | 获得性皮肤松弛 | 获得性皮肤松弛 |
| tr | Edinsel cutis laxa | Kutis laksa akuisita |
Definition in:
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Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| ICD-10 | L98.8 | NTBT | attributed | validated |
| ICD-11 | EE41.0 | NTBT | index | validated |
| MONDO | 0016446 | E | validated | |
| UMLS | C0406549 | 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):
No children.
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Genes
0 directOrphanet records no gene directly on this code.
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Prevalence and incidence
2 records| Type | Class | Value | Area | Qualification | Validation | Source |
|---|---|---|---|---|---|---|
| Cases/families | 110 cases | Worldwide | Case(s) | Validated | 38924070[PMID] | |
| Point prevalence | Unknown | — | Worldwide | Class only | Not yet validated | ORPHANET |
Value is Orphadata's ValMoy: the mean estimate per 100 000 for prevalence and incidence, the number of cases or families for case reports.
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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/228285
- This record as JSON: /data/d/228285.json