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)
- 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
