Human Phenotype Ontology 
..Starting node
..expandOligodendroglioma (HP:0033681)help
Term ID: 33681
Name: Oligodendroglioma
Synonym:
Definition: Oligodendroglioma is a type of diffusely infiltrating glioma and constitutes approximately 5% of primary intracranial tumors. They often involve the cortical gray matter and are most commonly seen in the frontal lobes. OGs are generally low grade WHO grade II neoplasms that are slow-growing tumors and have a favorable treatment response when compared to other gliomas. Grade III anaplastic OG is a more malignant form of the tumor which portends a less favorable prognosis and may occur de novo or as degeneration from the lower grade OG.
Comments:
Reference: HP:0033681
Genes and Diseases:
 
       Child Nodes:

 Sister Nodes: 
InputHPO IDHPO termDistanceGeneGene id entrezHGNC IDDiseaseIdDiseaseNameFrequencyOnsetHGMD variantsClinVar variants
 
HPO disease - gene - phenotype typical associations:
 
HPO disease - gene - phenotype less frequent non-typical associations:
HP:0033681HP:0033681Oligodendroglioma0MLH1 CL E G H42927127OMIM:276300Mismatch repair cancer syndrome 11819


Genes (1) :MLH1

Diseases (1) :OMIM:276300
 

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