Term ID: |
25171 |
Name: |
Rosette-forming glioneuronal tumor |
Synonym: |
Rosette-forming glioneuronal neoplasm; Rosette-forming glioneuronal tumor of the fourth ventricle; Rosette-forming glioneuronal tumour; Rosette-forming glioneuronal tumour of the fourth ventricle |
Definition: |
A tumor of the central nervous system that has components of both neurocytic and glial areas, whereby usually the glial component of the tumour predominates. Rossette-forming glioneuronal tumors (RGNT) have biphasic cytoarchitecture with two elements; neurocytic rosettes resembling Homer-Wright rosettes, and astrocytic component resembling a pilocytic astrocytoma. RGNTs are low-grade tumors that lack histopathological signs of malignancy. |
Comments: |
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Reference: |
HP:0025171 |
Genes and Diseases: | |
Child Nodes: |
Sister Nodes: |
Input | HPO ID | HPO term | Distance | Gene | Gene id entrez | HGNC ID | DiseaseId | DiseaseName | Frequency | Onset | HGMD variants | ClinVar variants |
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HPO disease - gene - phenotype typical associations: | HPO disease - gene - phenotype less frequent non-typical associations: | HP:0025171 | HP:0025171 | Rosette-forming glioneuronal tumor | 0 | CL E G H | | | | | | | | | | |
Genes (0) :
Diseases (0) : |
Human Phenotype Ontology(HPO) is developed by the Human Phenotype Ontology Consortium. The version used here is December 15 2022 release.
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