ORPHA:254411
Annular atrophic lichen planus
Synonyms: Annular atrophic LP
- Type
- Disease
- Group
- Disorder
- Age of onset
- Adult
- Status
- active
A rare variant of cutaneous lichen planus characterized by both annular and atrophic LP features in the same lesion.
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Names in Orphadata languages
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | Annular atrophic lichen planus | Annular atrophic LP |
| fr | Lichen plan annulaire atrophique | LP annulaire atrophique |
| de | Anulärer atrophischer Lichen planus | Atrophischer Lichen planus anularis |
| es | Liquen plano anular atrófico | |
| it | Lichen planus atrofico anulare | LP atrofico anulare |
| nl | Annulaire atrofische lichen planus | Annulaire atrofische LP · Ringvormige atrofische lichen planus |
| pt | Líquen plano atrófico anular | LP atrófico anular |
| pl | Liszaj płaski pierścieniowy zanikowy | LP pierścieniowy zanikowy |
| cs | Anulární atrofický lichen planus | Anulární atrofický LP |
| uk | Кільцеподібний атрофічний плескатий лишай | Кільцева атрофічна LP |
| zh | 环状萎缩性扁平苔藓 | 环状萎缩性LP |
| tr | Halka şeklindeki atrofik liken planus | Annular 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 | attributed | validated |
| MONDO | 0016771 | E | validated | |
| UMLS | C4304037 | E | validated | |
| GARD | 12676 | 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
2 records| Type | Class | Value | Area | Qualification | Validation | Source |
|---|---|---|---|---|---|---|
| Cases/families | 10 cases | Worldwide | Case(s) | Validated | [EXPERT] | |
| Point prevalence | <1 / 1 000 000 | — | Worldwide | Class only | 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/254411
- This record as JSON: /data/d/254411.json