ORPHA:715701
Infant-type hemispheric glioma ROS1-altered
- 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 ROS1-altered | |
| fr | Gliome hémisphérique infantile ROS1-altéré | |
| de | Hemisphärisches Gliom vom infantilen Typ mit ROS1-Alteration | |
| es | Glioma hemisférico de tipo infantil con alteración de ROS1 | |
| it | Glioma emisferico tipo infantile con alterazione di ROS1 | |
| nl | Infantiel hemisferisch glioom ROS1-gewijzigd | |
| pt | Infant-type hemispheric glioma ROS1-altered | |
| pl | Glejak półkulisty typu niemowlęcego ze zmianą ROS1 | |
| cs | Infant-type hemispheric glioma ROS1-altered |
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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
1 direct| Gene | Association | Status | HGNC | Ensembl | OMIM | Locus | Name | Source of validation |
|---|---|---|---|---|---|---|---|---|
| ROS1 | Part of a fusion gene in | Assessed | HGNC:10261 | ENSG00000047936 | 165020 | 6q22.1 | ROS proto-oncogene 1, receptor tyrosine kinase | 36316040[PMID]_35404193[PMID] |
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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/715701
- This record as JSON: /data/d/715701.json