Human Phenotype Ontology 
Grandparent Node:
expandArteriosclerosis (HP:0002634)help
Parent Node:
expandAtherosclerosis (HP:0002621)help
..Starting node
..expandThin-cap fibroatheroma (HP:0031012)help
Term ID: 31012
Name: Thin-cap fibroatheroma
Synonym: TCFA
Definition: Thin-cap fibroatheroma is characterized by a relatively large necrotic core with an overlying thin fibrous cap measuring less than 65 micrometers and typically containing numerous macrophages, and is considered to be the precursor lesion of plaque rupture which is the most common cause of coronary thrombosis.
Comments:
Reference: HP:0031012
Genes and Diseases:
 
       Child Nodes:

 Sister Nodes: 
..expandAccelerated atherosclerosis (HP:0004943) help
..expandAortic atherosclerotic lesion (HP:0012397) help
..expandAtherosclerotic lesion (HP:0031678) help
..expandCerebral artery atherosclerosis (HP:0007201) help
..expandCoronary artery atherosclerosis (HP:0001677) help
..expandFatty streak (HP:0031011) help
..expandFoam cells (HP:0003651) help
..expandPrecocious atherosclerosis (HP:0004416) 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:0031012HP:0031012Thin-cap fibroatheroma0 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.