infant-type hemispheric glioma Disease Ontology Browser

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Disease Ontology Browser

infant-type hemispheric glioma (DOID:0081278)
Alliance: disease page
Alt IDs: NCI:C185471
Definition: A malignant astrocytoma that is characterized by receptor tyrosine kinase fusions in the NTRK family, ROS1, ALK, or MET genes, that arises in the cerebral hemisphere and occurs in early childhood.

Contributing Projects: Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO)
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