central apnea Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
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)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0002871
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6 genes associated with the central apnea phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
AHI1 Abelson helper integration site 1
CEP290 centrosomal protein 290kDa
INPP5E inositol polyphosphate-5-phosphatase, 72 kDa
PSAP prosaposin
TECPR2 tectonin beta-propeller repeat containing 2
TMEM216 transmembrane protein 216