| Metadata | |
|---|---|
| ID | DOID:0081278 |
| Name | infant-type hemispheric glioma |
| 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. https://pubmed.ncbi.nlm.nih.gov/35404193/, https://pubmed.ncbi.nlm.nih.gov/36315913/, https://pubmed.ncbi.nlm.nih.gov/36316040/ |
| Xrefs |
ICDO:9385/3 |
| Subsets |
DO_childhood_cancer_slim NCIthesaurus |
| Parent Relationships | |
| Subclass Logical Relationships |
existence starts during some Infantile onset disease has location some cerebral hemisphere |