ORPHA:715697
Infant-type hemispheric glioma ALK-altered
- Type
- Etiological subtype
- Group
- Subtype of disorder
- Inheritance
- Not applicable
- Status
- active
Orphadata ships no English definition for this code.
1
Names in Orphadata languages
9 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | Infant-type hemispheric glioma ALK-altered | |
| fr | Gliome hémisphérique infantile ALK-altéré | |
| de | Hemisphärisches Gliom vom infantilen Typ mit ALK-Alteration | |
| es | Glioma hemisférico de tipo infantil con alteración de ALK | |
| it | Glioma emisferico tipo infantile con alterazione di ALK | |
| nl | Infantiel hemisferisch glioom ALK-gewijzigd | |
| pt | Infant-type hemispheric glioma ALK-altered | |
| pl | Glejak półkulisty typu niemowlęcego ze zmianą ALK | |
| cs | Infant-type hemispheric glioma ALK-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.
4
Genes
1 direct| Gene | Association | Status | HGNC | Ensembl | OMIM | Locus | Name | Source of validation |
|---|---|---|---|---|---|---|---|---|
| ALK | Part of a fusion gene in | Assessed | HGNC:427 | ENSG00000171094 | 105590 | 2p23.2-p23.1 | ALK receptor tyrosine kinase | 36910660[PMID]_37000961[PMID]_36996378[PMID] |
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Prevalence and incidence
0 recordsNo prevalence record in this release.
6
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/715697
- This record as JSON: /data/d/715697.json