ORPHA:1409
Woolly hair-hypotrichosis-everted lower lip-outstanding ears syndrome
inactive · moved to ORPHA:170Woolly hair
Synonyms: Salamon syndrome
- Type
- Malformation syndrome
- Group
- Disorder
- Status
- inactive
- Flag
- Deprecated entity
This entity has been excluded from the Orphanet nomenclature of rare diseases and moved to Woolly hair
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Names in Orphadata languages
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | Woolly hair-hypotrichosis-everted lower lip-outstanding ears syndrome | Salamon syndrome |
| fr | Syndrome de cheveux laineux-hypotrichose-lèvres éversées-oreilles décollées | Syndrome de Salamon |
| de | Wollhaare-Hypotrichose-evertierte Unterlippe-abstehende Ohren-Syndrom | Salamon-Syndrom |
| es | Síndrome de cabello lanoso-hipotricosis-labio inferior evertido-orejas prominentes | Síndrome de Salamon |
| it | Sindrome capelli lanosi-ipotricosi-labbro inferiore rovesciato all'esterno-orecchie prominenti | Sindrome di Salamon |
| nl | Wollig haar - hypotrichose - eversie van onderlip - afstaande oren-syndroom | Syndroom van Salamon |
| pt | Síndrome cabelo encarapinhado-hipotricose-lábio inferior evertido-pavilhões auriculares descolados | Salamon |
| pl | Włosy wełniaste - hipotrichoza - wywinięta dolna warga - odstające uszy | Włosy wełniste - hipotrichoza - wywinięta dolna warga - odstające uszy · Zespół Salamona · Zespół wełnistych włosów, hipotrychozy, odwróconej dolnej wargi i wydatnych uszu |
| cs | Syndrom zahrnující vlněné vlasy, hypotrichózu, everzi spodního rtu a odstávající uši | Salamonův syndrom |
| uk | Синдром вовняного волосся-гіпотрихозу-вивернутої нижньої губи-стирчащих вух | Синдром Саламона · Синдром шерстяного волосяного покриву-гіпотрихозу-вивернутої нижньої губи-відстовбурчених вух |
| zh | 羊毛状发-毛发稀少-下唇外翻-外耳横突综合征 | 羊毛状发-少毛-下唇外翻-招风耳综合征 |
| tr | Kıllı saç-hipotrikoz-ters dönmüş alt dudak-dışa dönük kulak sendromu | Salamon sendromu · Kıllı saç-hipotrikoz-dışa dönük alt dudak-olağanüstü kulak sendromu |
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Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| OMIM | 278200 | E | validated | |
| MeSH | C536746 | E | validated | |
| UMLS | C0406718 | 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
Not placed in any Orphanet classification in this release.
No children.
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Genes
0 directOrphanet records no gene directly on this code.
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Prevalence and incidence
0 recordsNo prevalence record in this release.
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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/1409
- This record as JSON: /data/d/1409.json