ORPHA:79385
Unclassified genetic skin disorder
- Type
- Category
- Group
- Group of disorders
- 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 | Unclassified genetic skin disorder | |
| fr | Maladie génétique non classifiée de la peau | |
| de | Hautkrankheit, genetisch bedingte, sonstige | |
| es | Enfermedad de la piel de origen genético no clasificada | |
| it | Malattia genetica della cute non classificata | |
| nl | Niet-geclassificeerde genetische aandoening van huid | |
| pt | Doença dermatológica, genética, outra | |
| pl | Niesklasyfikowany choroby skóry pochodzenia genetycznego | |
| cs | Neklasifikované geneticky podmíněné nemoci kůže | |
| uk | Некласифіковане генетично обумовлене захворювання шкіри | |
| zh | 未分类的遗传性皮肤疾病 | |
| tr | Sınıflandırılmamış genetik cilt bozukluğu |
2
Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| MONDO | 19299 | E | validated | |
| UMLS | C5681473 | E | validated |
E exact · NTBT this ORPHAcode is narrower than the target · BTNT broader than the target · ND not decided.
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Classification
Preferential parent (Orphanet linearisation):
Parents in the classifications (2):
- ORPHA:68346Rare genetic skin disease
rare genetic diseases - ORPHA:89826Rare skin disease
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.
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Sources for this card
- Orphanet page: orpha.net/en/disease/detail/79385
- This record as JSON: /data/d/79385.json