ORPHA:453
IBIDS syndrome
inactive · moved to ORPHA:33364Trichothiodystrophy
Synonyms: Tay syndrome · Trichothiodystrophy type E · Trichothiodystrophy with congenital ichthyosis
- Type
- Disease
- Group
- Disorder
- Status
- inactive
- Flag
- Deprecated entity
This entity has been excluded from the Orphanet nomenclature of rare diseases and moved to Trichothiodystrophy
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Names in Orphadata languages
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | IBIDS syndrome | Tay syndrome · Trichothiodystrophy type E · Trichothiodystrophy with congenital ichthyosis |
| fr | Syndrome IBIDS | Ichtyose avec trichothiodystrophie · Syndrome de Tay · Trichothiodystrophie type E |
| de | IBIDS-Syndrom | Tay-Syndrom · Trichothiodystrophie Typ E · Trichothiodystrophie mit kongenitaler Ichthyose |
| es | Síndrome IBIDS | |
| it | Sindrome IBIDS | Sindrome di Tay · Tricotiodistrofia con ittiosi congenita · Tricotiodistrofia, tipo E |
| nl | IBIDS-syndroom | Taysyndroom · Trichothiodystrofie met congenitale ichthyosis · Trichothiodystrofie type E |
| pt | Síndrome IBIDS | Síndrome Tay · Tricotiodistrofia tipo E · Tricotiodistrofia-ictiose congénita |
| pl | Zespół IBIDS | Trichotiodystrofia typu E · Trichotiodystrofia z rybią łuską wrodzoną · Zespół Tay'a |
| cs | IBIDS syndrom | Trichothiodystrofie, typ E · Trichothiodystrofie s vrozenou ichtyózou · Tayův syndrom |
| uk | Синдром IBIDS | Синдром Тея · Трихотіодистрофія типу Е · Трихотіодистрофія з вродженим іхтіозом |
| zh | IBIDS综合征 | 毛发低硫营养不良伴先天性鱼鳞病 |
| tr | IBIDS sendromu | Tay sendromu · Trikotiyodistrofi tip E · Doğumsal iktiyozlu trikotiyodistrofi |
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Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| UMLS | C1866505 | 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/453
- This record as JSON: /data/d/453.json