potter's syndrome Gene Set

Dataset	DISEASES Text-mining Gene-Disease Association Evidence Scores
Category	disease or phenotype associations
Type	disease
Description	An oligohydramnios desribing the typical physical appearances of a fetus or neonate due to oligohydramnios experienced in the womb where there is a decrease in amniotic fluid volume sufficient to cause disruptions in morphogenesis of the fetus. (Human Disease Ontology, DOID_12594)
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Genes

10 genes co-occuring with the disease potter's syndrome in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

Symbol	Name	Standardized Value
HHLA1	HERV-H LTR-associating 1	2.19244
GRAP2	GRB2-related adaptor protein 2	1.26124
PLA2G10	phospholipase A2, group X	1.00035
LAX1	lymphocyte transmembrane adaptor 1	0.948269
PLA2G2A	phospholipase A2, group IIA (platelets, synovial fluid)	0.879833
GDNF	glial cell derived neurotrophic factor	0.59991
AFP	alpha-fetoprotein	0.58433
PLA2G1B	phospholipase A2, group IB (pancreas)	0.530768
RET	ret proto-oncogene	0.419892
SRC	SRC proto-oncogene, non-receptor tyrosine kinase	0.379626