Localized lichen myxedematosus with mixed features of different subtypes
- Type
- Clinical subtype
- Group
- Subtype of disorder
- Age of onset
- Adult, Elderly
- Status
- active
Localized lichen myxedematosus (LM) with mixed features of different subtypes is a form of atypical lichen myxedematosus, characterized by mixed features of the 5 subtypes of localized LM which are: discrete papular LM, acral persistent papular mucinosis, self-healing papular mucinosis, papular mucinosis of infancy, and nodular LM.
Names in Orphadata languages
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | Localized lichen myxedematosus with mixed features of different subtypes | |
| fr | Lichen myxoedémateux localisé à présentation mixte | |
| de | Lichen myxoedematosus, lokalisierter, mit gemischten Eigenschaften der Subtypen | |
| es | Liquen mixedematoso localizado con rasgos mixtos de subtipos diferentes | |
| it | Lichen mixedematoso localizzato associato a diversi sottotipi | |
| nl | Gelokaliseerde lichen myxoedematosus met gemengde eigenschappen van verschillende subtypes | |
| pt | Líquen mixedematoso localizado com características de diferentes subtipos | |
| pl | Zlokalizowany liszaj śluzowaty z objawami mieszanymi w różnych podtypach | |
| cs | Lokalizovaný lichen myxedematosus se smíšenými prvky z jiných podtypů | |
| uk | Локалізований мікседематозний ліхен зі змішаними ознаками різних підтипів | |
| zh | 混合亚型局限性粘液水肿性苔癣 | |
| tr | Farklı alt tiplerin karma özellikleri ile seyreden lokalize liken miksödematozus |
Definition in:
Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| ICD-10 | L98.5 | NTBT | attributed | validated |
| ICD-11 | EB90.11 | NTBT | attributed | validated |
| MONDO | 0019583 | E | validated | |
| UMLS | C5681465 | E | validated |
E exact · NTBT this ORPHAcode is narrower than the target · BTNT broader than the target · ND not decided.
Classification
Preferential parent (Orphanet linearisation):
Parents in the classifications (1):
- ORPHA:86797Atypical lichen myxedematosus
rare skin diseases
No children.
Genes
0 directOrphanet records no gene directly on this code.
Prevalence and incidence
2 records| Type | Class | Value | Area | Qualification | Validation | Source |
|---|---|---|---|---|---|---|
| Cases/families | 10 cases | Worldwide | Case(s) | Validated | ORPHANET | |
| 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.
HPO phenotypes
Orphanet has no HPO annotation for this code in this release.
Sources for this card
- Orphanet page: orpha.net/en/disease/detail/90398
- This record as JSON: /data/d/90398.json