ORPHA:3450
Weissenbacher-Zweymuller syndrome
inactive · moved to ORPHA:166100Autosomal dominant otospondylomegaepiphyseal dysplasia
Synonyms: Pierre Robin sequence-fetal chondrodysplasia syndrome · Pierre Robin syndrome-fetal chondrodysplasia 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 Autosomal dominant otospondylomegaepiphyseal dysplasia
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Names in Orphadata languages
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | Weissenbacher-Zweymuller syndrome | Pierre Robin sequence-fetal chondrodysplasia syndrome · Pierre Robin syndrome-fetal chondrodysplasia syndrome |
| fr | Syndrome de Weissenbacher-Zweymuller | Syndrome de Pierre Robin-chondrodysplasie · Syndrome de séquence de Pierre Robin-chondrodysplasie |
| de | Weissenbacher-Zweymüller-Syndrom | Pierre Robin-Sequenz-fetale Chondrodysplasie-Syndrom · Pierre Robin-Syndrom-fetale Chondrodysplasie-Syndrom |
| es | Síndrome de Weissenbacher-Zweymuller | Síndrome de Pierre Robin-condrodisplasia fetal · Síndrome de secuencia de Pierre Robin-condrodisplasia fetal |
| it | Sindrome di Weissenbacher-Zweymuller | Displasia oto-spondilo-megaepifisaria eterozigote · OSMED, forma eterozigote · Sequenza di Pierre Robin - condrodisplasia fetale · Sindrome di Pierre Robin - condrodisplasia fetale |
| nl | Syndroom van Weissenbacher-Zweymuller | Pierre Robin sequentie - foetale chondrodysplasie-syndroom · Syndroom van Pierre Robin - foetale chondrodysplasie-syndroom |
| pt | Síndrome Weissenbacher-Zweymuller | Síndrome Pierre-Robin-condrodisplasia fetal · Síndrome de sequência Pierre-Robin-condrodisplasia fetal |
| pl | Zespół Weissenbachera i Zweymullera | Heterozygotyczna dysplazja uszno-kręgowo-nasadowa · Heterozygotyczna OSMED · Sekwencja Pierre'a i Robina - chondrodysplazja płodu · Zespół Pierre'a i Robina - chondrodysplazja płodu |
| cs | Weissenbacherův-Zweymullerův syndrom | Heterozygotní OSMED · Heterozygotní otospondylomegaepifyzeální dysplázie · Syndrom zahrnující Pierre Robinovu sekvenci a fetální chondrodysplázii · Syndrom zahrnující Pierre Robinův syndrom a fetální chondrodysplázii · Weissenbacher-Zweymullerův syndrom |
| uk | Синдром Вайсенбахера-Цвеймуллера | Синдром послідовності Пєра Робена - хондродисплазії плода · Синдром Пєра Робена - синдром хондродисплазії плода |
| zh | Weissenbacher-Zweymuller 综合征 | Pierre Robin序列征-胎儿软骨发育不全综合征 |
| tr | Weissenbacher-Zweymuller sendromu | Pierre Robin dizisi-fetal kondrodisplazi sendromu · Pierre Robin sendromu-fetal kondrodisplazi sendromu |
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Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| UMLS | C1848488 | E | validated | |
| GARD | 4351 | 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/3450
- This record as JSON: /data/d/3450.json