ORPHA:434809
Syndrome with woolly hair
- Type
- Category
- Group
- Group of disorders
- Age of onset
- Neonatal
- 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 | Syndrome with woolly hair | |
| fr | Syndrome avec cheveux laineux | |
| de | Syndrom mit Wollhaaren | |
| es | Síndrome con cabello lanoso | |
| it | Sindrome con capelli lanosi | |
| nl | Syndroom met wollig haar | |
| pt | Síndrome com cabelo lanoso | |
| pl | Zespół z włosami wełnistymi | |
| cs | Syndrom s vlněnými vlasy | |
| uk | Синдром з вовняним волоссям | |
| zh | 羊毛状发综合征 | |
| tr | Yünlü saçlı sendromu |
2
Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| MONDO | 18558 | E | validated | |
| UMLS | C0345427 | 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:79367Syndromic hair shaft abnormality
rare genetic diseases; 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/434809
- This record as JSON: /data/d/434809.json