Congenital knee dislocation
- Type
- Morphological anomaly
- Group
- Disorder
- Status
- active
A rare congenital limb malformation characterized by either hyperextension of the knee greater than 0° associated with limited flexion (congenital genu recurvatum) or permanent knee flexion with limited extension (congenital genu flexum). It can be unilateral or bilateral and may occur as an isolated malformation, be associated with other orthopedic abnormalities (like developmental dysplasia of the hip or clubfoot), or be part of a syndrome (e. g. Larsen's syndrome, arthrogryposis multiplex congenita).
Names in Orphadata languages
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | Congenital knee dislocation | |
| fr | Luxation congénitale du genou | |
| de | Kniedislokation, kongenitale | |
| es | Luxación congénita de la rodilla | |
| it | Dislocazione congenita del ginocchio | |
| nl | Congenitale knieluxatie | |
| pt | Luxação congénita do joelho | |
| pl | Wrodzone zwichnięcie stawu kolanowego | |
| cs | Vrozená dislokace kolena | |
| uk | Вроджений вивих колінного суглоба | |
| zh | 先天性膝关节脱位 | |
| tr | Doğumsal diz çıkığı |
Definition in:
Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| ICD-10 | Q68.2 | NTBT | inclusion | validated |
| ICD-11 | LB93 | E | specific | validated |
| MONDO | 0017470 | E | validated | |
| UMLS | C0265669 | E | validated | |
| MedDRA | 10010520 | E | validated |
E exact · NTBT this ORPHAcode is narrower than the target · BTNT broader than the target · ND not decided.
Classification
Preferential parent (Orphanet linearisation):
Parents in the classifications (1):
- ORPHA:294951Congenital joint dislocations
rare developmental anomalies during embryogenesis; rare genetic diseases
Genes
0 directOrphanet records no gene directly on this code.
Prevalence and incidence
0 recordsNo prevalence record in this release.
HPO phenotypes
Orphanet has no HPO annotation for this code in this release.
Sources for this card
- Orphanet page: orpha.net/en/disease/detail/295034
- This record as JSON: /data/d/295034.json