Human Phenotype Ontology 
Grandparent Node:
expandAtherosclerosis (HP:0002621)help
Parent Node:
expandAtherosclerotic lesion (HP:0031678)help
..Starting node
..expandType II atherosclerotic lesion (HP:0031680)help
Term ID: 31680
Name: Type II atherosclerotic lesion
Synonym:
Definition: Type II atherosclerotic lesions include the fatty streak lesion, the first grossly visible lesion, and are characterized by layers of macrophage foam cells and lipid droplets within intimal smooth muscle cells and minimal coarse-grained particles and heterogeneous droplets of extracellular lipid.
Comments:
Reference: HP:0031680
Genes and Diseases:
 
       Child Nodes:

 Sister Nodes: 
..expandType I atherosclerotic lesion (HP:0031679) help
..expandType III atherosclerotic lesion (HP:0031681) help
..expandType IV atherosclerotic lesion (HP:0002635) help
..expandType V atherosclerotic lesion (HP:0031682) help
..expandType VI atherosclerotic lesion (HP:0031683) 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:0031680HP:0031680Type II atherosclerotic lesion0 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.