Preferred Label : Infant-Type Hemispheric Glioma;
NCIt definition : A high-grade cellular astrocytoma that arises in the cerebral hemisphere and occurs
in early childhood. It is characterized by receptor tyrosine kinase fusions in the
NTRK family, ROS1, ALK, or MET genes. It includes the following subtypes: infant-type
hemispheric glioma, NTRK-altered, infant-type hemispheric glioma, ROS1-altered, infant-type
hemispheric glioma, ALK-altered, and infant-type hemispheric glioma, MET-altered.;
Neoplastic status : Malignant;
NCI Metathesaurus CUI : CL1773773;
Origin ID : C185471;
UMLS CUI : C5669919;
Currated CISMeF NLP mapping
Disease may have findings
Excludes anatomical site(s)
Has associated anatomic sites
Semantic type(s)
UMLS correspondences (same concept)
disease_excludes_finding
disease_has_abnormal_cell
disease_has_finding
disease_has_grade
disease_has_normal_cell_origin
disease_has_normal_tissue_origin
disease_has_primary_anatomic_site