abnormality of the arachnoid mater Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description An abnormality of the Arachnoid mater. (Human Phenotype Ontology, HP_0100700)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0100700
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Genes

6 genes associated with the abnormality of the arachnoid mater phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
FGFR2 fibroblast growth factor receptor 2
GPSM2 G-protein signaling modulator 2
NRAS neuroblastoma RAS viral (v-ras) oncogene homolog
OFD1 oral-facial-digital syndrome 1
SHANK3 SH3 and multiple ankyrin repeat domains 3
XPNPEP3 X-prolyl aminopeptidase 3, mitochondrial