ORPHA:443192
Classic stiff person syndrome
Synonyms: Classic SPS · Classic stiff man syndrome · Classic SMS
- Type
- Clinical subtype
- Group
- Subtype of disorder
- Inheritance
- Not applicable
- Age of onset
- Adult
- Status
- active
Orphadata ships no English definition for this code.
1
Names in Orphadata languages
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | Classic stiff person syndrome | Classic SPS · Classic stiff man syndrome · Classic SMS |
| fr | Syndrome de la personne raide classique | Syndrome de l'homme raide classique |
| de | Stiff-person-Syndrom, klassisches | Klassisches SMS · Klassisches SPS · Stiff-Man-Syndrom, klassisches |
| es | Síndrome de la persona rígida clásico | SPS clásico |
| it | Sindrome della persona rigida classica | Sindrome classica dell'uomo rigido · SMS classica · SPS classica |
| nl | Klassiek 'stiff person'-syndroom | Klassiek 'stiff man'-syndroom · Klassiek SMS · Klassiek SPS |
| pt | Síndrome da pessoa rígida, clássica | SMS clássica · SPS clássica |
| pl | Klasyczny zespół sztywności uogólnionej | Klasyczny SPS |
| cs | Klasický syndrom ztuhlého těla | Klasický SPS |
| uk | Класичний синдром ригідної людини | Класичний SPS |
| zh | 经典僵人综合征 | 金典SPS |
| tr | Klasik katı kişi sendromu | Klasik SPS |
2
Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| OMIM | 184850 | NTBT | validated | |
| ICD-10 | G25.8 | NTBT | inclusion | validated |
| ICD-11 | 8E4A.0 | NTBT | index | validated |
| MONDO | 0018625 | E | validated | |
| UMLS | C5680058 | E | validated |
E exact · NTBT this ORPHAcode is narrower than the target · BTNT broader than the target · ND not decided.
3
Classification
Preferential parent (Orphanet linearisation):
Parents in the classifications (1):
- ORPHA:3198Stiff person spectrum disorder
rare neurological diseases; rare endocrine diseases
No children.
4
Genes
0 directOrphanet records no gene directly on this code.
5
Prevalence and incidence
1 record| Type | Class | Value | Area | Qualification | Validation | Source |
|---|---|---|---|---|---|---|
| Point prevalence | Unknown | — | Europe | Class only | Not yet validated | ORPHANET |
Value is Orphadata's ValMoy: the mean estimate per 100 000 for prevalence and incidence, the number of cases or families for case reports.
6
HPO phenotypes
Orphanet has no HPO annotation for this code in this release.
7
Sources for this card
- Orphanet page: orpha.net/en/disease/detail/443192
- This record as JSON: /data/d/443192.json