Recurrent Aspiration Pneumonia Gene Set

Dataset	DisGeNET Gene-Disease Associations
Category	disease or phenotype associations
Type	disease
Description	Increased susceptibility to aspiration pneumonia, defined as pneumonia due to breathing in foreign material, as manifested by a medical history of repeated episodes of aspiration pneumonia. (Human Phenotype Ontology, HP_0002100)
External Link	https://www.disgenet.org/browser/0/1/0/C0747651
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Genes

11 genes associated with the disease Recurrent Aspiration Pneumonia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Symbol	Name
CSPP1	centrosome and spindle pole associated protein 1
EPM2A	epilepsy, progressive myoclonus type 2A, Lafora disease (laforin)
GBA	glucosidase, beta, acid
KDM6A	lysine (K)-specific demethylase 6A
KIAA0586	KIAA0586
KMT2D	lysine (K)-specific methyltransferase 2D
NFIX	nuclear factor I/X (CCAAT-binding transcription factor)
NHLRC1	NHL repeat containing E3 ubiquitin protein ligase 1
PIGN	phosphatidylinositol glycan anchor biosynthesis, class N
SLC25A24	solute carrier family 25 (mitochondrial carrier; phosphate carrier), member 24
SP110	SP110 nuclear body protein