Human Phenotype Ontology 
Grandparent Node:
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Abnormal glial cell morphology (HP:0100705)help
Parent Node:
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Gliosis (HP:0002171)help
..Starting node
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Myelin-dependent gliosis (HP:0006990)help
Term ID: 6990
Name: Myelin-dependent gliosis
Synonym:
Definition: A type of gliosis that occurs in the vicinity of injured neurons.
Comments:
Reference: HP:0006990
Genes and Diseases:
 
       Child Nodes:

 Sister Nodes: 
..expandBasal ganglia gliosis (HP:0006999) help
..expandCerebellar gliosis (HP:0012698) help
..expandHypothalamic gliosis (HP:0025037) help
..expandSubstantia nigra gliosis (HP:0011960) help
InputHPO IDHPO termDistanceGeneGene id entrezHGNC IDDiseaseIdDiseaseNameFrequencyOnsetHGMD variantsClinVar variants
 
HPO disease - gene - phenotype typical associations:
 
HPO disease - gene - phenotype less frequent non-typical associations:
HP:0006990HP:0006990Myelin-dependent gliosis0 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.