Isolated sternocostoclavicular hyperostosis
Synonyms: Isolated SCCH
- Type
- Disease
- Group
- Disorder
- Status
- active
Isolated sternocostoclavicular hyperostosis is a rare rheumatologic disease characterized by predominantly bilateral, chronic, sterile inflammation and progressive sclerosis and hyperostosis of the sternocostoclavicular joint, with adjacent soft tissue ossification, in the absence of other joint involvement. It presents as recurrent episodes of pain, edema and/or erythema of the sternoclavicular region. Palmoplantar pustulosis may be additionally observed in some cases.
Names in Orphadata languages
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | Isolated sternocostoclavicular hyperostosis | Isolated SCCH |
| fr | Hyperostose sterno-costo-claviculaire isolée | |
| de | Hyperostose, isolierte sternokostoklavikuläre | SCCH, isolierte |
| es | Hiperostosis esternocostoclavicular aislada | SCCH aislado |
| it | Iperostosi isolata sterno-costo-clavicolare | |
| nl | Geïsoleerde sternocostoclaviculaire hyperostose | Geïsoleerde SCCH |
| pt | Hiperostose esternocostoclavicular isolada | |
| pl | Izolowana hiperostoza mostkowo-żebrowo-obojczykowa | = en |
| cs | Izolovaná sternokostoklavikulární hyperostóza | Syndrom SAPHO |
| uk | Ізольований грудинно-реберно-ключичний гіперостоз | Ізольований SCCH |
| zh | 孤立性胸肋锁骨肥厚症 | 孤立性SCCH |
| tr | İzole sternokostoklaviküler hiperostoz | İzole SCCH |
Definition in:
Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| ICD-10 | M85.8 | NTBT | attributed | validated |
| MONDO | 0044355 | E | validated | |
| UMLS | C4707796 | 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:182231Rare rheumatologic disease
rare systemic and rheumatological 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/178311
- This record as JSON: /data/d/178311.json