ORPHA:295232
Congenital genu flexum
- Type
- Clinical subtype
- Group
- Subtype of disorder
- Status
- active
A rare congenital knee dislocation characterized by permanent knee flexion with limited extension. It can be unilateral or bilateral and may occur as an isolated malformation or be part of a syndrome (especially arthrogryposis multiplex congenita).
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Names in Orphadata languages
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | Congenital genu flexum | |
| fr | Genu flexum congénital | |
| de | Genu flexum, kongenital | |
| es | Genu flexum congénito | |
| it | Genu flexum congenito | |
| nl | Congenitale genu flexum | |
| pt | Genu flexum congénito | |
| pl | Wrodzony przykurcz zgięciowy w stawie kolanowym | |
| cs | Vrozené genu flexum | |
| uk | Вроджена гнучкість (genu flexum) | |
| zh | 先天性屈膝 | |
| tr | Doğumsal genu fleksum |
Definition in:
2
Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| ICD-10 | Q68.2 | NTBT | attributed | validated |
| ICD-11 | LB93.1 | E | specific | validated |
| MONDO | 0017561 | E | validated | |
| UMLS | C5681090 | 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
Preferential parent (Orphanet linearisation):
Parents in the classifications (1):
- ORPHA:295034Congenital knee dislocation
rare developmental anomalies during embryogenesis; rare genetic diseases
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/295232
- This record as JSON: /data/d/295232.json