ORPHA:295067
OBSOLETE: Femoral agenesis/hypoplasia, bilateral
inactive · referred to ORPHA:1987Isolated femoral agenesis/hypoplasia
Synonyms: OBSOLETE: Femoral intercalary meromelia, bilateral
- Type
- Clinical subtype
- Group
- Subtype of disorder
- Status
- inactive
- Flag
- Obsolete entity
This entity has been obsoleted from the Orphanet nomenclature of rare diseases.<br/><br/>Instead, consider using Isolated femoral agenesis/hypoplasia
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Names in Orphadata languages
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | OBSOLETE: Femoral agenesis/hypoplasia, bilateral | OBSOLETE: Femoral intercalary meromelia, bilateral |
| fr | OBSOLETE : Agénésie/hypoplasie bilatérale du fémur | OBSOLETE : Agénésie/hypoplasie bilatérale fémorale · OBSOLETE : Méromélie intercalaire bilatérale du fémur · OBSOLETE : Méromélie intercalaire bilatérale fémorale |
| de | OBSOLET: Femuragenesie/-hypoplasie, bilateral | OBSOLET: Femorale interkalare Meromelie, bilateral |
| es | OBSOLETO: Agenesia/hipoplasia femoral bilateral | OBSOLETO: Meromelia intercalar femoral bilateral |
| it | OBSOLETO: Agenesia/ipoplasia del femore, bilaterale | OBSOLETO: Meromelia intercalare del femore, bilaterale |
| nl | OBSOLEET: Femorale agenesie/hypoplasie, bilateraal | OBSOLEET: Femorale intercalaire meromelie, bilateraal |
| pt | OBSOLETO: Agenesia/hipoplasia femoral, bilateral | OBSOLETO: Meromelia intercalar femoral, bilateral |
| pl | NIEAKTUALNE: Agenezja/hipoplazja kosci udowej, obustronna | = en |
| cs | NEAKTUÁLNÍ: Oboustranná ageneze/hypoplázie femuru | NEAKTUÁLNÍ: Oboustranná interkalární meromelie femuru |
| uk | ЗАСТАРІЛО: Агенезія/гіпоплазія стегнової кістки, двостороння | ЗАСТАРІЛО: Стегнова інтеркалярна меромелія, двобічна |
| zh | 弃用:双侧股骨发育不全/发育不良 | 双侧股骨骨干残肢畸形 |
| tr | Eski adı: Femoral agenezi / hipoplazi, bilateral | Femoral interkalar meromeli, bilateral |
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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/295067
- This record as JSON: /data/d/295067.json