Human Phenotype Ontology 
Grandparent Node:
expandAbnormal coronary artery morphology (HP:0006704)help
Parent Node:
expandAbnormal coronary artery origin (HP:0011636)help
..Starting node
..expandCoronary ostial atresia (HP:0031626)help
Term ID: 31626
Name: Coronary ostial atresia
Synonym: Atresia of coronary ostium
Definition: Absence of the normal opening of a coronary ostium. There are normally two coronary ostia, which are site of origin of the main left or right main coronary artery and are located in the ascending aorta just above the aortic valve.
Comments:
Reference: HP:0031626
Genes and Diseases:
 
       Child Nodes:
........expandRight coronary artery ostial atresia (HP:0031637) help

 Sister Nodes: 
..expandAbsent left main coronary artery (HP:0031639) help
..expandAnomalous coronary artery arising from the opposite sinus (HP:0025503) help
..expandAnomalous origin of coronary artery from the pulmonary artery (HP:0011637) help
..expandAnomalous origin of the circumflex artery from the right sinus of Valsalva (HP:0025505) help
..expandSeparate origin of the left anterior descending and left circumflex artery (HP:0031536) help
..expandSingle coronary artery origin (HP:0011640) 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:0031626HP:0031626Coronary ostial atresia0 CL E G H
HP:0031626HP:0031637Right coronary artery ostial atresia1 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.