ORPHA:726832
Radiation-induced Moyamoya syndrome
Synonyms: RIMMS
- Type
- Disease
- Group
- Disorder
- Inheritance
- Not applicable
- Age of onset
- Adolescent, Childhood
- Status
- active
Orphadata ships no English definition for this code.
1
Names in Orphadata languages
9 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | Radiation-induced Moyamoya syndrome | RIMMS |
| fr | Syndrome de Moyamoya induit par radiation | = en |
| de | Strahleninduziertes Moyamoya-Syndrom | = en |
| es | Síndrome de Moyamoya inducido por radiación | = en |
| it | Malattia di moyamoya indotta dalle radiazioni | = en |
| nl | Moyamoya-syndroom door straling | = en |
| pt | Radiation-induced Moyamoya syndrome | |
| pl | Radiation-induced Moyamoya syndrome | = en |
| cs | Radiation-induced Moyamoya syndrome | = en |
2
Cross-references
qualifier = Orphanet mapping relationNo cross-references in this release.
3
Classification
Preferential parent (Orphanet linearisation):
Parents in the classifications (2):
- ORPHA:477768Moyamoya angiopathy
rare neurological diseases - ORPHA:521132Radiation-induced disorder
rare disorders due to toxic effects
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 | — | Worldwide | Class only | 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/726832
- This record as JSON: /data/d/726832.json