ORPHA:402007
Lichen myxedematosus
- Type
- Clinical group
- Group
- Group of disorders
- Age of onset
- Adult, Infancy
- Status
- active
This term does not characterize a disease but a group of diseases. To learn about the diseases included under this term, you can consult the classifications.
1
Names in Orphadata languages
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | Lichen myxedematosus | |
| fr | Lichen myxoedémateux | |
| de | Lichen myxödematosus | |
| es | Liquen mixedematoso | |
| it | Lichen mixedematoso | |
| nl | Lichen myxoedematosus | |
| pt | Líquen mixedematoso | |
| pl | Liszaj śluzowaty | |
| cs | Lichen myxedematosus | |
| uk | Лишай мікседематозний (Lichen myxedematosus) | |
| zh | 黏液水肿性苔藓 | |
| tr | Liken miksödem |
2
Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| ICD-11 | EB90.1 | NTBT | attributed | validated |
| MONDO | 0018432 | E | validated | |
| MONDO | 18432 | E | validated | |
| UMLS | C5848049 | E | validated | |
| MedDRA | 10055046 | 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:79381Other dermis disorder
rare skin diseases
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/402007
- This record as JSON: /data/d/402007.json