|Dataset||HPO Gene-Disease Associations|
|Category||disease or phenotype associations|
|Description||Apnea resulting from depression of the respiratory centers in the medulla oblongata. There is a lack of respiratory effort rather than obstruction of airflow. (Human Phenotype Ontology, HP_0002871)|
|Downloads & Tools|
6 genes associated with the central apnea phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.