| General Information | |||
|---|---|---|---|
| Term | myxoid glioneuronal tumor | ID (Ontology) | DOID:0081285 (Human Disease) |
| Definition | A central nervous system benign neoplasm that is characterized by a dinucleotide mutation at codon 385 of the PDGFR gene. It usually occurs in the septum pellucidum but has also been described in the corpus callosum and periventricular white matter of the lateral ventricle. It is composed of oligodendrocyte-like cells in a prominent myxoid stroma. | ||
| Also Known As | "Myxoid glioneuronal tumour" | ||
| Comment | |||
| Links to External Ontologies | |||
| DO.org | |||
| Annotations | |||
| Records annotated with this term OR any of its CHILD TERMS | |||
Full annotation statements including this term (annotations to child terms are NOT included), and relevant FlyBase records
|
|||
|
No relevant statements available
|
|||
|
||||||
nervous system benign neoplasm__ central nervous system disease__| central nervous system benign neoplasm |__myxoid glioneuronal tumor |
| Spanning Tree View Settings | |||
|---|---|---|---|
| Parents/Children View Depth |
|||
Relationships
|
|||
| Is a | central nervous system benign neoplasm | ||
| Part of | |||
Synonyms & Secondary IDs
|
|||
| Synonyms | |||
|
|||
| Secondary IDs | |||
|
|
|||
External Crossreferences & Linkouts
|
|||
|
ICDO:9509/1 NCI:C179229 |
|||