ORPHA:276174
Idiopathic recurrent stupor
- Type
- Disease
- Group
- Disorder
- Inheritance
- Not applicable
- Age of onset
- Adult
- Status
- active
A rare neurologic disease characterized by unpredictable, transient and spontaneous unresponsiveness lasting from hours to days, with a frequency of three to seven attacks per year, in the absence of readily discernible toxic, metabolic or structural causes.
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Names in Orphadata languages
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | Idiopathic recurrent stupor | |
| fr | Stupeur récurrente idiopathique | Syndrome stuporeux récurrent idiopathique |
| de | Stupor, idiopathischer rekurrenter | |
| es | Estupor recurrente idiopático | |
| it | Stupor idiopatico ricorrente | |
| nl | Idiopathische recidiverende stupor | Idiopathische terugkerende stupor |
| pt | Estupor recorrente idiopático | |
| pl | Idiopatyczne otępienie nawracające | |
| cs | Idiopatický rekurentní stupor | |
| uk | Ідіопатичне рецидивуюче заціпеніння | |
| zh | 特发性反复木僵 | |
| tr | İdiyopatik tekrarlı uyuşukluk |
Definition in:
2
Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| ICD-10 | G93.8 | NTBT | attributed | validated |
| ICD-11 | 8E2Y | NTBT | index | validated |
| MONDO | 0017170 | E | validated | |
| UMLS | C4706562 | E | validated |
E exact · NTBT this ORPHAcode is narrower than the target · BTNT broader than the target · ND not decided.
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Classification
Preferential parent (Orphanet linearisation):
Parents in the classifications (1):
- ORPHA:98006Rare neurologic disease
rare neurological diseases
No children.
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Genes
0 directOrphanet records no gene directly on this code.
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Prevalence and incidence
1 record| Type | Class | Value | Area | Qualification | Validation | Source |
|---|---|---|---|---|---|---|
| Point prevalence | Unknown | — | Worldwide | 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.
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HPO phenotypes
Orphanet has no HPO annotation for this code in this release.
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Sources for this card
- Orphanet page: orpha.net/en/disease/detail/276174
- This record as JSON: /data/d/276174.json