Human Phenotype Ontology 
Grandparent Node:
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Neoplasm of the central nervous system (HP:0100006)help
Parent Node:
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Neuronal/glioneuronal neoplasm of the central nervous system (HP:0025170)help
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Rosette-forming glioneuronal tumor (HP:0025171)help
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:
Reference: HP:0025171
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InputHPO IDHPO termDistanceGeneGene id entrezHGNC IDDiseaseIdDiseaseNameFrequencyOnsetHGMD variantsClinVar variants
 
HPO disease - gene - phenotype typical associations:
 
HPO disease - gene - phenotype less frequent non-typical associations:
HP:0025171HP:0025171Rosette-forming glioneuronal tumor0 CL E G H


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Human Phenotype Ontology(HPO) is developed by the Human Phenotype Ontology Consortium. The version used here is December 15 2022 release.