Human Phenotype Ontology 
Grandparent Node:
expandAbnormal coronary artery morphology (HP:0006704)help
Grandparent Node:
expandArterial stenosis (HP:0100545)help
Grandparent Node:
expandAtherosclerosis (HP:0002621)help
Parent Node:
expandCoronary artery atherosclerosis (HP:0001677)help
..Starting node
..expandNonocclusive coronary artery atherosclerosis (HP:0012436)help
Term ID: 12436
Name: Nonocclusive coronary artery atherosclerosis
Synonym: Non-occlusive coronary artery disease; Non-occlusive coronary artery stenosis; Nonocclusive coronary artery disease; Nonocclusive coronary artery stenosis
Definition: Coronary disease that has not progressed to the point of causing significant occlusion (blockage) of the coronary arteries.
Comments:
Reference: HP:0012436
Genes and Diseases:
 
       Child Nodes:

 Sister Nodes: 
..expandPost-angioplasty coronary artery restenosis (HP:0004761) help
..expandPremature coronary artery atherosclerosis (HP:0005181) 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:0012436HP:0012436Nonocclusive coronary artery atherosclerosis0 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.