True congenital shoulder dislocation
- Type
- Morphological anomaly
- Group
- Disorder
- Status
- active
A rare congenital limb malformation characterized by true congenital dislocation of the shoulder, developing in utero. It can be unilateral or bilateral and is usually associated with other abnormalities of the shoulder girdle, such as in the glenoid, the humeral head, the joint capsule, and the scapula. In addition, it may be accompanied by other malformations, like developmental hip dysplasia or cardiac malformation.
Names in Orphadata languages
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | True congenital shoulder dislocation | |
| fr | Luxation congénitale vraie de l'épaule | |
| de | Schulterdislokation, kongenitale | |
| es | Luxación congénita verdadera del hombro | |
| it | Dislocazione congenita vera della spalla | |
| nl | Echte congenitale schouderluxatie | |
| pt | Luxação congénita do ombro | |
| pl | Prawdziwe wrodzone przemieszczenie ramienia | |
| cs | Vrozená dislokace ramene | |
| uk | Дійсний вроджений вивих плеча | |
| zh | 真性先天性肩关节脱位 | |
| tr | Gerçek doğumsal omuz çıkığı |
Definition in:
Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| ICD-10 | Q68.8 | NTBT | inclusion | validated |
| ICD-11 | LB91 | E | specific | validated |
| MONDO | 17468 | E | validated | |
| UMLS | C5886734 | 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
No children.
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/295030
- This record as JSON: /data/d/295030.json