ORPHA:1235
OBSOLETE: Ectodermal dysplasia-absent dermatoglyphs syndrome
inactive · referred to ORPHA:1658Absence of fingerprints-congenital milia syndrome
Synonyms: OBSOLETE: Basan syndrome
- Type
- Disease
- Group
- Disorder
- Status
- inactive
- Flag
- Obsolete entity
This entity has been obsoleted from the Orphanet nomenclature of rare diseases.<br/><br/>Instead, consider using Absence of fingerprints-congenital milia syndrome
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Names in Orphadata languages
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | OBSOLETE: Ectodermal dysplasia-absent dermatoglyphs syndrome | OBSOLETE: Basan syndrome |
| fr | OBSOLETE : Syndrome de Basan | OBSOLETE : Syndrome de dysplasie ectodermique-dermatoglyphes absents |
| de | OBSOLET: Basan-Syndrom | OBSOLET: Ektodermale Dysplasie mit fehlenden Dermatoglyphen |
| es | OBSOLETO: Síndrome de displasia ectodérmica-dermatoglifos ausentes | OBSOLETO: Síndrome de Basan |
| it | OBSOLETO: Sindrome displasia ectodermica-assenza dei dermatoglifi | OBSOLETO: Sindrome di Basan |
| nl | OBSOLEET: Ectodermale dysplasie - afwezige dermatoglyfen-syndroom | OBSOLEET: Syndroom van Basan |
| pt | OBSOLETO: Síndrome de displasia ectodérmica-dermatóglifos ausentes | |
| pl | NIEAKTUALNE: Dysplazja ektodermalna - brak dermatoglifów | NIEAKTUALNE: Zespół Basana |
| cs | NEAKTUÁLNÍ: Syndrom zahrnující ektodermální dysplázii a absenci dermatoglyfů | NEAKTUÁLNÍ: Basanův syndrom |
| uk | ЗАСТАРІЛО: Синдром ектодермальної дисплазії з відсутністю дерматогліфів | ЗАСТАРІЛО: Синдром Басана |
| zh | 弃用：真皮发育不良-皮纹缺乏综合征 | Basan综合征 |
| tr | Eski adı: Ektodermal displazi olmayan dermatoglif sendromu | Basan sendromu |
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Cross-references
qualifier = Orphanet mapping relationNo cross-references in this release.
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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/1235
- This record as JSON: /data/d/1235.json