obstructive sleep apnea Gene Set

Dataset	HPO Gene-Disease Associations
Category	disease or phenotype associations
Type	phenotype
Description	A sleep apnea that is characterized by repeated collapse and obstruction of the upper airway during sleep, which results in reduced airflow (hypopnea) or complete airflow cessation (apnea), oxygen desaturation, and arousals from sleep. (Human Disease Ontology, DOID_0050848)
External Link	http://compbio.charite.de/hpoweb/showterm?id=HP:0002870
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Genes

9 genes associated with the obstructive sleep apnea phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol	Name
AHDC1	AT hook, DNA binding motif, containing 1
CREBBP	CREB binding protein
DNA2	DNA replication helicase/nuclease 2
HRAS	Harvey rat sarcoma viral oncogene homolog
IDS	iduronate 2-sulfatase
IDUA	iduronidase, alpha-L-
NFIX	nuclear factor I/X (CCAAT-binding transcription factor)
SKI	SKI proto-oncogene
TRPV4	transient receptor potential cation channel, subfamily V, member 4