ORPHA:664787
Nicolau syndrome
Synonyms: Embolia cutis medicamentosa · Livedo-like dermatitis
- Type
- Clinical syndrome
- Group
- Disorder
- Inheritance
- Not applicable
- Status
- active
Orphadata ships no English definition for this code.
1
Names in Orphadata languages
10 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | Nicolau syndrome | Embolia cutis medicamentosa · Livedo-like dermatitis |
| fr | Syndrome de Nicolau | Dermite livédoïde de Nicolau · Embolie cutanée médicamenteuse |
| de | Nicolau-Syndrom | Embolia cutis medicamentosa · Livedo-artige Dermatitis |
| es | Síndrome de Nicolau | Dermatitis similar a livedo · Embolia cutis medicamentosa |
| it | Sindrome di Nicolau | Dermatite simil-livedo · Embolia cutis medicamentosa |
| nl | Syndroom van Nicolau | Embolia cutis medicamentosa · Livedo-achtige dermatitis |
| pt | Síndrome Nicolau | Dermatite livedo-like · Embolia cutis medicamentosa |
| pl | Syndrom Nicolaua | = en |
| cs | Nicolauův syndrom | = en |
| uk | Синдром Ніколау | Медикаментозна емболія шкірного покриву · Ліведоподібний дерматит |
2
Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| ICD-10 | T80.1 | NTBT | attributed | validated |
| MONDO | 0971103 | E | validated | |
| MONDO | 971103 | E | validated | |
| UMLS | C1142083 | E | validated | |
| MedDRA | 10058729 | 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:90077Other acquired skin disease
rare skin diseases
No children.
4
Genes
0 directOrphanet records no gene directly on this code.
5
Prevalence and incidence
2 records| Type | Class | Value | Area | Qualification | Validation | Source |
|---|---|---|---|---|---|---|
| Cases/families | 240 cases | Worldwide | Case(s) | Validated | 32679363[PMID] | |
| Point prevalence | <1 / 1 000 000 | — | Worldwide | Class only | Validated | 32679363[PMID]_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.
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/664787
- This record as JSON: /data/d/664787.json