diaphragmatic weakness Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description A decrease in the strength of the diaphragm. (Human Phenotype Ontology, HP_0009113)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0009113
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Genes

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

Symbol Name
BAG3 BCL2-associated athanogene 3
CPOX coproporphyrinogen oxidase
GAA glucosidase, alpha; acid
HMBS hydroxymethylbilane synthase
IGHMBP2 immunoglobulin mu binding protein 2
MEGF10 multiple EGF-like-domains 10
SLC52A3 solute carrier family 52 (riboflavin transporter), member 3
TRPV4 transient receptor potential cation channel, subfamily V, member 4
TTN titin