ORPHA:99143
OBSOLETE: Mandibulofacial dysostosis-lymphedema syndrome
inactive · referred to ORPHA:364526Primary bone dysplasia
- 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 Primary bone dysplasia
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Names in Orphadata languages
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | OBSOLETE: Mandibulofacial dysostosis-lymphedema syndrome | |
| fr | OBSOLETE : Syndrome de dysostose mandibulofaciale-lymphoedme | |
| de | OBSOLET: Mandibulo-faziale Dysostose - Lymphödem-Syndrom | |
| es | OBSOLETO: Disostosis mandibulofacial-síndrome de linfedema | |
| it | OBSOLETO: Disostosi mandibolofacciale - sindrome da linfedema | |
| nl | OBSOLEET: Mandibulofaciale dysostose - lymfoedeemsyndroom | |
| pt | OBSOLETO: Síndrome Disostose mandibulo-facial - linfedema | |
| pl | NIEAKTUALNE: Zespól dyzostoza zuchwowo-twarzowa - obrzek limfatyczny | |
| cs | NEAKTUÁLNÍ: Syndrom mandibulofaciální dysostózy a lymfedému | |
| uk | ЗАСТАРІЛО: Синдром щелепно-лицевого дизостозу-лімфедеми | |
| zh | 弃用：下颌面骨发育不全-淋巴水肿综合征 | |
| tr | Eski adı: Mandibulofasiyal dizostoz-lenfödem 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/99143
- This record as JSON: /data/d/99143.json