{"orpha":715697,"name":"Infant-type hemispheric glioma ALK-altered","type":"Etiological subtype","group":"Subtype of disorder","status":"active","flags":[],"synonyms":[],"definition":null,"note":null,"url":"https://raremap.alftech.space/d/ORPHA-715697/","orphanet_url":"https://www.orpha.net/en/disease/detail/715697","names":{"fr":{"name":"Gliome hémisphérique infantile ALK-altéré"},"de":{"name":"Hemisphärisches Gliom vom infantilen Typ mit ALK-Alteration"},"es":{"name":"Glioma hemisférico de tipo infantil con alteración de ALK"},"it":{"name":"Glioma emisferico tipo infantile con alterazione di ALK"},"nl":{"name":"Infantiel hemisferisch glioom ALK-gewijzigd"},"pt":{"name":"Infant-type hemispheric glioma ALK-altered"},"pl":{"name":"Glejak półkulisty typu niemowlęcego ze zmianą ALK"},"cs":{"name":"Infant-type hemispheric glioma ALK-altered"}},"xrefs":[],"associations":[],"incoming_associations":[],"preferential_parent":{"orpha":250908,"name":"Rare neoplastic disease"},"parents":[{"orpha":695136,"name":"Infant-type hemispheric glioma","classifications":[181,202]}],"children":[],"genes":[{"symbol":"ALK","name":"ALK receptor tyrosine kinase","gene_type":"gene with protein product","association":"Part of a fusion gene in","status":"Assessed","source":"36910660[PMID]_37000961[PMID]_36996378[PMID]","hgnc":"427","ensembl":"ENSG00000171094","omim":"105590","loci":["2p23.2-p23.1"]}],"genes_via_subtypes":[],"inheritance":["Not applicable"],"onset":[],"prevalence":[],"phenotypes":null}