ORPHA:328269
OBSOLETE: Rare bone disease with limb reduction defect
inactive · referred to ORPHA:294955Syndrome with limb reduction defects
Synonyms: OBSOLETE: Rare bone disease with limb hypoplasia
- Type
- Category
- Group
- Group of disorders
- Status
- inactive
- Flag
- Obsolete entity
This entity has been obsoleted from the Orphanet nomenclature of rare diseases.<br/><br/>This term does not characterize a disease but a group of diseases. To learn about the diseases included under this term, you can consult the classifications.<br/><br/>Instead, consider using Syndrome with limb reduction defects
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Names in Orphadata languages
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | OBSOLETE: Rare bone disease with limb reduction defect | OBSOLETE: Rare bone disease with limb hypoplasia |
| fr | OBSOLETE : Maladie osseuse rare avec anomalie réductionnelle des membres | |
| de | OBSOLET: Seltene Knochenkrankheit mit Gliedmaßen-Reduktionsdefekt | OBSOLET: Seltene Knochenkrankheit mit assoziierter Hypoplasie der Gliedmaßen |
| es | OBSOLETO: Enfermedad ósea rara con un defecto de reducción de extremidades | OBSOLETO: Enfermedad ósea rara con hipoplasia de extremidades |
| it | OBSOLETO: Malattia scheletrica rara con difetto da riduzione degli arti | OBSOLETO: Malattia scheletrica rara con ipoplasia degli arti |
| nl | OBSOLEET: Zeldzame botziekte met reductiedefect van ledemaat | OBSOLEET: Zeldzame botziekte met hypoplasie van ledemaat |
| pt | OBSOLETO: Doença óssea rara com defeito de redução do membro | |
| pl | NIEAKTUALNE: Rzadka choroba kosci ze skróceniem konczyn | NIEAKTUALNE: Rzadka choroba kości z hipoplazją kończyn |
| cs | NEAKTUÁLNÍ: Vzácné onemocnění kostí s defektem redukce končetiny | = en |
| uk | ЗАСТАРІЛО: Рідкісне захворювання кісток з дефектом редукції кінцівок | ЗАСТАРІЛО: Рідкісне захворювання кісток з гіпоплазією кінцівок |
| zh | 弃用：罕见骨病伴肢体减少缺陷 | 罕见骨病伴肢体发育不全 |
| tr | Eski adı: Ekstremite redüksiyon defekti ile seyreden nadir kemik hastalığı | Ekstremite hipoplazi ile seyreden nadir kemik hastalığı |
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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/328269
- This record as JSON: /data/d/328269.json