ORPHA:37559
Acquired kinky hair syndrome
- Type
- Disease
- Group
- Disorder
- Status
- active
A rare hair disorder characterized by the appearance of lustreless, curly, frizzy, and coarse hair generally during adolescence predominantly in the frontal, temporal, and vertex regions of the scalp. Eyelashes, as well as growth and pigmentation of the hair, may also be affected.
1
Names in Orphadata languages
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | Acquired kinky hair syndrome | |
| fr | Syndrome kinky hair acquis | |
| de | Kinky-hair-Syndrom, erworbenes | APKH · Erworbenes progredientes Kräuseln der Haare |
| es | Síndrome del cabello ensortijado adquirido | |
| it | Sindrome dei capelli crespi, forma acquisita | |
| nl | Verworven kroeshaarsyndroom | |
| pt | Síndrome do cabelo impenteável adquirido | |
| pl | Nabyty zespół kręconych włosów | |
| cs | Získaný syndrom neučesatelných vlasů | |
| uk | Синдром набутого кучерявого волосся | |
| zh | 获得性卷发综合征 | |
| tr | Edinsel karışık saç sendromu |
Definition in:
2
Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| ICD-10 | L67.8 | NTBT | attributed | validated |
| ICD-11 | ED73.Y | NTBT | attributed | validated |
| MONDO | 0018302 | E | validated | |
| UMLS | C0263486 | 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
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/37559
- This record as JSON: /data/d/37559.json