ORPHA:254449
Atrophic lichen planus
Synonyms: Atrophic LP
- Type
- Disease
- Group
- Disorder
- Age of onset
- All ages
- Status
- active
A rare variant of cutaneous lichen planus characterized by the development of pale papules or plaques with an atrophic center.
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Names in Orphadata languages
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | Atrophic lichen planus | Atrophic LP |
| fr | Lichen plan atrophique | LP atrophique |
| de | Lichen planus atrophicans | LP, atrophischer |
| es | Liquen plano atrófico | |
| it | Lichen planus atrofico | LP atrofico |
| nl | Atrofische lichen planus | Atrofische LP |
| pt | Líquen plano atrófico | LP atrófico |
| pl | Liszaj płaski zanikowy | LP zanikowy |
| cs | Atrofický lichen planus | Atrofický LP |
| uk | Атрофічний червоний плескатий лишай | Атрофічна LP |
| zh | 萎缩性扁平苔藓 | 萎缩性LP |
| tr | Atrofik liken planus | Atrofik LP |
Definition in:
2
Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| ICD-10 | L43.8 | NTBT | attributed | validated |
| ICD-11 | EA91.Y | NTBT | index | validated |
| MONDO | 0016773 | E | validated | |
| UMLS | C0023647 | E | validated | |
| GARD | 12675 | E | validated | |
| MedDRA | 10056959 | 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:254370Rare cutaneous lichen planus
rare skin diseases
No children.
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Genes
0 directOrphanet records no gene directly on this code.
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Prevalence and incidence
1 record| Type | Class | Value | Area | Qualification | Validation | Source |
|---|---|---|---|---|---|---|
| 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/254449
- This record as JSON: /data/d/254449.json