ORPHA:90394
Discrete papular lichen myxedematosus
- Type
- Disease
- Group
- Disorder
- Status
- active
Discrete papular lichen myxedematosus is a rare chronic, slowly progressive form of localized lichen myxedematosus characterized by the development of a few to multiple small symmetrical skin-coloured mucinous papules on the limbs and trunk.
1
Names in Orphadata languages
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | Discrete papular lichen myxedematosus | |
| fr | Lichen myxoedémateux discret | |
| de | Lichen myxoedematosus, diskreter papulöser | |
| es | Liquen mixedematoso papular discreto | |
| it | Lichen mixedematoso papuloso, forma discreta | |
| nl | Discrete papulaire lichen myxoedematosus | |
| pt | Líquen mixedematoso papular, discreto | |
| pl | Liszaj śluzowaty dyskretna odmiana grudkowa | |
| cs | Diskrétní papulární myxedematózní lichen | |
| uk | Дискретний папульозний лишай мікседематозний | |
| zh | 散发性丘疹性粘液水肿性苔癣 | |
| tr | Ayrık papüler liken miksödemöz |
Definition in:
2
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 | 0019579 | E | validated | |
| UMLS | C4273967 | E | validated |
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):
- ORPHA:86795Localized lichen myxedematosus
rare skin diseases
No children.
4
Genes
0 directOrphanet records no gene directly on this code.
5
Prevalence and incidence
0 recordsNo prevalence record in this release.
6
HPO phenotypes
Orphanet has no HPO annotation for this code in this release.
7
Sources for this card
- Orphanet page: orpha.net/en/disease/detail/90394
- This record as JSON: /data/d/90394.json