Medial condensing osteitis of the clavicle
Synonyms: Osteitis condensans of the clavicle
- Type
- Disease
- Group
- Disorder
- Inheritance
- Not applicable
- Age of onset
- Adolescent, Adult, Childhood
- Status
- active
A rare bone disease characterized by benign, usually unilateral, sclerosis of the inferomedial third of the clavicle. Patients present with localized swelling and persistent pain. Typical radiographic findings are expansion of the medial end of the clavicle with increased radio-density and signs of bone remodeling.
Names in Orphadata languages
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | Medial condensing osteitis of the clavicle | Osteitis condensans of the clavicle |
| fr | Ostéite condensante médiane de la clavicule | |
| de | Kondensierende Ostitis der medialen Klavikula | |
| es | Osteítis condensante medial de la clavícula | Osteítis condensante de la clavícula |
| it | Osteite condensante della parte mediana della clavicola | |
| nl | Mediale condenserende osteïtis van clavicula | Mediale condenserende osteïtis van sleutelbeen · Osteitis condensans van clavicula |
| pt | Osteíte condensante da clavícula medial | |
| pl | Pośrodkowe kondensujące zapalenie obojczyka | Kondensujące zapalenie obojczyka |
| cs | Mediální kondenzující osteitida klavikuly | = en |
| uk | Медіальний конденсаційний остеїт ключиці | Ущільнений остеїт ключиці |
| zh | 锁骨内侧压缩性骨炎 | 锁骨致密性骨炎 |
| tr | Klavikulanın medial yoğunlaşan osteiti | Klavikulanın osteit kondansanları |
Definition in:
Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| ICD-10 | M85.3 | NTBT | attributed | validated |
| ICD-11 | LB72.Y | NTBT | index | validated |
| MONDO | 0018929 | E | validated | |
| UMLS | C5396729 | E | validated | |
| GARD | 10910 | 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:399319Osteochondrosis
rare systemic and rheumatological diseases; rare bone diseases
No children.
Genes
0 directOrphanet records no gene directly on this code.
Prevalence and incidence
2 records| Type | Class | Value | Area | Qualification | Validation | Source |
|---|---|---|---|---|---|---|
| Cases/families | 58 cases | Worldwide | Case(s) | Validated | 27622150[PMID] | |
| Point prevalence | <1 / 1 000 000 | — | Worldwide | Class only | Validated | ORPHANET_27622150[PMID] |
Value is Orphadata's ValMoy: the mean estimate per 100 000 for prevalence and incidence, the number of cases or families for case reports.
HPO phenotypes
5 annotations · validated 2019-05-27| HPO | Term (as annotated by Orphanet) | Diagnostic |
|---|---|---|
| Frequent (79-30%) | ||
| HP:0000889 | Abnormality of the clavicle | |
| HP:0010657 | Patchy reduction of bone mineral density | |
| HP:0030834 | Shoulder pain | |
| Occasional (29-5%) | ||
| HP:0011227 | Elevated circulating C-reactive protein concentration | |
| HP:0006467 | Limited shoulder movement | |
Annotation source: 15329764[PMID]_25272551[PMID]_27622150[PMID]
Sources for this card
- Orphanet page: orpha.net/en/disease/detail/57196
- This record as JSON: /data/d/57196.json