ORPHA:730226
Infant-type hemispheric glioma, fusion-negative
Synonyms: Infant-type hemispheric glioma, methylation-based fusion-negative
- Type
- Etiological subtype
- Group
- Subtype of disorder
- Inheritance
- Not applicable
- Status
- active
Orphadata ships no English definition for this code.
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Names in Orphadata languages
9 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | Infant-type hemispheric glioma, fusion-negative | Infant-type hemispheric glioma, methylation-based fusion-negative |
| fr | Gliome hémisphérique infantile, sans fusion | |
| de | Hemisphärisches Gliom vom infantilen Typ, Fusion-negativ | Hemisphärisches Gliom vom infantilen Typ, Fusion-negativ, mit eindeutiger DNA-Methylierungssignatur |
| es | Glioma hemisférico de tipo infantil con fusión negativa | Glioma hemisférico infantil basado en metilación con fusion negativa |
| it | Glioma emisferico tipo infantile, negativo per la fusione | Glioma emisferico di tipo infantile, negativo per la fusione basata sulla metilazione |
| nl | Infantiel glioom van hersenhelft, fusie-negatief | Infantiel type glioom van hersenhelft, methylatie-gebaseerd fusie-negatief |
| pt | Infant-type hemispheric glioma, fusion-negative | |
| pl | Infant-type hemispheric glioma, fusion-negative | = en |
| cs | Infant-type hemispheric glioma, fusion-negative | = en |
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Cross-references
qualifier = Orphanet mapping relationNo cross-references in this release.
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Classification
Preferential parent (Orphanet linearisation):
Parents in the classifications (1):
- ORPHA:695136Infant-type hemispheric glioma
rare neurological diseases; rare neoplastic diseases
No children.
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Genes
0 directOrphanet records no gene directly on this code.
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Prevalence and incidence
0 recordsNo prevalence record in this release.
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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/730226
- This record as JSON: /data/d/730226.json