elevated amniotic fluid alpha-fetoprotein Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description An elevation of alpha-feto protein measured in the amniotic fluid. (Human Phenotype Ontology, HP_0004639)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0004639
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Genes

2 genes associated with the elevated amniotic fluid alpha-fetoprotein phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
MKS1 Meckel syndrome, type 1
OCRL oculocerebrorenal syndrome of Lowe