ORPHA:2454
OBSOLETE: Familial intestinal malrotation-facial anomalies syndrome
inactive · referred to ORPHA:508410Familial intestinal malrotation
Synonyms: OBSOLETE: Stalker-Chitayat syndrome
- Type
- Malformation syndrome
- Group
- Disorder
- Status
- inactive
- Flag
- Obsolete entity
This entity has been obsoleted from the Orphanet nomenclature of rare diseases.<br/><br/>Instead, consider using Familial intestinal malrotation
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Names in Orphadata languages
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | OBSOLETE: Familial intestinal malrotation-facial anomalies syndrome | OBSOLETE: Stalker-Chitayat syndrome |
| fr | OBSOLETE : Syndrome familial de malrotation intestinale-dysmorphie | OBSOLETE : Syndrome de Stalker-Chitayat |
| de | OBSOLET: Familiäre syndromale intestinale Malrotation mit Gesichtsanomalien | OBSOLET: Stalker-Chitayat-Syndrom |
| es | OBSOLETO: Síndrome familiar de malrotación intestinal-anomalías faciales | OBSOLETO: Síndrome de Stalker-Chitayat |
| it | OBSOLETO: Sindrome malrotazione intestinale familiare-anomalie facciali | OBSOLETO: Sindrome di Stalker-Chitayat |
| nl | OBSOLEET: Familiaal intestinale malrotatie - faciale anomalieën-syndroom | OBSOLEET: Syndroom van Stalker-Chitayat |
| pt | OBSOLETO: Síndrome de malrotação intestinal-anomalias faciais familiar | OBSOLETO: Síndrome Stalker-Chitayat |
| pl | NIEAKTUALNE: Rodzinna malrotacja jelit - wady twarzy | NIEAKTUALNE: Zespół Stalkera i Chitayata |
| cs | NEAKTUÁLNÍ: Syndrom zahrnující familiární intestinální malrotaci a obličejové anomálie | NEAKTUÁLNÍ: Stalkerův-Chitayatův syndrom · NEAKTUÁLNÍ: Stalker-Chitayatův syndrom |
| uk | ЗАСТАРІЛО: Сімейний синдром кишкової мальротації-лицевих аномалій | ЗАСТАРІЛО: Синдром Сталкера-Читаята |
| zh | 弃用:家族遗传性肠道转位异常-面部异常综合征 | Stalker-Chitayat综合征 |
| tr | Eski adı: ailesel bağırsak malrotasyonu-yüz anomalileri sendromu | Stalker-Chitayat 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/2454
- This record as JSON: /data/d/2454.json