Human Phenotype Ontology 
Grandparent Node:
expandAtherosclerosis (HP:0002621)help
Parent Node:
expandAtherosclerotic lesion (HP:0031678)help
..Starting node
..expandType I atherosclerotic lesion (HP:0031679)help
Term ID: 31679
Name: Type I atherosclerotic lesion
Synonym:
Definition: Type I lesions represent the very initial changes and are recognized as an increase in the number of intimal macrophages and the appearance of macrophages filled with lipid droplets (foam cells).
Comments:
Reference: HP:0031679
Genes and Diseases:
 
       Child Nodes:

 Sister Nodes: 
..expandType II atherosclerotic lesion (HP:0031680) 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:0031679HP:0031679Type I 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.