Human Phenotype Ontology 
Grandparent Node:
expandAtherosclerosis (HP:0002621)help
Parent Node:
expandAtherosclerotic lesion (HP:0031678)help
..Starting node
..expandType V atherosclerotic lesion (HP:0031682)help
Term ID: 31682
Name: Type V atherosclerotic lesion
Synonym:
Definition: Type V lesions are defined as lesions in which prominent new fibrous connective tissue has formed. When the new tissue is part of a lesion with a lipid core (type IV), this type of morphology may be referred to as fibroatheroma or type Va lesion. A type V lesion in which the lipid core and other parts of the lesion are calcified may be referred to as type Vb. A type V lesion in which a lipid core is absent and lipid in general is minimal may be referred to as type Vc. With these lesions, arteries are variously narrowed, generally more than with type IV. Importantly, as with type IV lesions, type V lesions may develop fissures, hematoma, and/or thrombus (type VI lesion), and for this reason too they are clinically relevant.
Comments:
Reference: HP:0031682
Genes and Diseases:
 
       Child Nodes:

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