ORPHA:656071
Atrophic papulosis
Synonyms: Degos disease · Köhlmeier-Degos disease
- Type
- Disease
- Group
- Disorder
- Inheritance
- Not applicable
- Age of onset
- Adult
- Status
- active
Orphadata ships no English definition for this code.
1
Names in Orphadata languages
10 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | Atrophic papulosis | Degos disease · Köhlmeier-Degos disease |
| fr | Papulose atrophiante | Maladie de Degos · Maladie de Köhlmeier-Degos |
| de | Köhlmeier-Degos-Krankheit | Atrophische Papulose · Degos-Syndrom · Papulosis maligna atrophicans |
| es | Papulosis atrófica | Enfermedad de Degos · Enfermedad de Köhlmeier-Degos |
| it | Papulosi atrofica | Malattia di Degos · Malattia di Köhlmeier-Degos |
| nl | Atrofische papulose | Papulosis atrophicans · Ziekte van Degos · Ziekte van Köhlmeier-Degos |
| pt | Papulose atrófica | Doença Degos · Doença Köhlmeier-Degos |
| pl | Grudkowatość zanikowa | = en |
| cs | Atrofická papulóza | = en |
| uk | Атрофічний папульоз | Хвороба Дегоса · Хвороба Кельмейера-Дегоса |
2
Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| ICD-10 | I77.8 | NTBT | index | validated |
| ICD-11 | EF5Y | NTBT | attributed | validated |
| MONDO | 0958110 | E | validated | |
| MONDO | 958110 | 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 (2):
- ORPHA:183478Genetic skin vascular disorder
rare genetic diseases - ORPHA:79379Skin vascular disease
rare skin diseases
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 | 200 cases | Worldwide | Case(s) | Validated | 36353773[PMID] | |
| Point prevalence | <1 / 1 000 000 | — | Worldwide | Class only | Validated | 36353773[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/656071
- This record as JSON: /data/d/656071.json