raremaprare-disease reference indexOrphadata 2026-06-23 · HPO 2026-09-01
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.

1

Names in Orphadata languages

12 of 12 languages
LangNameSynonyms
enAtrophic lichen planusAtrophic LP
frLichen plan atrophiqueLP atrophique
deLichen planus atrophicansLP, atrophischer
esLiquen plano atrófico
itLichen planus atroficoLP atrofico
nlAtrofische lichen planusAtrofische LP
ptLíquen plano atróficoLP atrófico
plLiszaj płaski zanikowyLP zanikowy
csAtrofický lichen planusAtrofický LP
ukАтрофічний червоний плескатий лишайАтрофічна LP
zh萎缩性扁平苔藓萎缩性LP
trAtrofik liken planusAtrofik LP

Definition in:

2

Cross-references

qualifier = Orphanet mapping relation
SourceCodeQualifierICD relationValidation
ICD-10L43.8NTBTattributedvalidated
ICD-11EA91.YNTBTindexvalidated
MONDO0016773Evalidated
UMLSC0023647Evalidated
GARD12675Evalidated
MedDRA10056959Evalidated

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 (1):

No children.

4

Genes

0 direct

Orphanet records no gene directly on this code.

5

Prevalence and incidence

1 record
TypeClassValueAreaQualificationValidationSource
Point prevalenceUnknown—WorldwideClass onlyNot yet validatedORPHANET

Value is Orphadata's ValMoy: the mean estimate per 100 000 for prevalence and incidence, the number of cases or families for case reports.

6

HPO phenotypes

Orphanet has no HPO annotation for this code in this release.

7

Sources for this card