ORPHA:1088
OBSOLETE: Short stature-heart defect-craniofacial anomalies syndrome
inactive · referred to ORPHA:102283Multiple congenital anomalies/dysmorphic syndrome-intellectual disability
Synonyms: OBSOLETE: Rommen-Mueller-Sybert 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 Multiple congenital anomalies/dysmorphic syndrome-intellectual disability
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Names in Orphadata languages
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | OBSOLETE: Short stature-heart defect-craniofacial anomalies syndrome | OBSOLETE: Rommen-Mueller-Sybert syndrome |
| fr | OBSOLETE : Syndrome d'anomalies craniofaciales multiples-cardiopathie-retard de croissance | OBSOLETE : Syndrome de Rommen-Mueller-Sybert |
| de | OBSOLET: Kleinwuchs-Herzfehler-kraniofaziale Anomalien-Syndrom | OBSOLET: Rommen-Mueller-Sybert-Syndrom |
| es | OBSOLETO: Síndrome de talla baja-cardiopatía-anomalías craneofaciales | OBSOLETO: Síndrome de Rommen-Mueller-Sybert |
| it | OBSOLETO: Sindrome bassa statura-cardiopatia-anomalie craniofacciali | OBSOLETO: Sindrome di Rommen-Mueller-Sybert |
| nl | OBSOLEET: Kleine gestalte - hartdefect - craniofaciale anomalieën-syndroom | OBSOLEET: Syndroom van Rommen-Mueller-Sybert |
| pt | OBSOLETO: Síndrome de baixa estatura-defeito cardíaco-anomalias crânio-faciais | |
| pl | NIEAKTUALNE: Zespól niskiego wzrostu, wady serca i anomalii czaszkowo-twarzowej | NIEAKTUALNE: Zespół Rommena, Muellera i Syberta |
| cs | NEAKTUÁLNÍ: Syndrom zahrnující malý vzrůst, srdeční defekt a kraniofaciální anomálie | NEAKTUÁLNÍ: Rommenův-Muellerův-Sybertův syndrom · NEAKTUÁLNÍ: Rommen-Mueller-Sybertův syndrom |
| uk | Синдром низького зросту - серцевої вади - черепно-лицьових аномалій | ЗАСТАРІЛО: Синдром Роммена-Мюллера-Сіберта |
| zh | 废弃：身材矮小-心脏缺陷-颅面畸形综合征 | Rommen-Mueller-Sybert综合征 |
| tr | Eski adı: Kısa boy-kalp defekti-kraniyofasiyal anomaliler sendromu | Rommen-Mueller-Sybert 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/1088
- This record as JSON: /data/d/1088.json