oligohydramnios Gene Set

Dataset GeneRIF Biological Term Annotations
Category structural or functional annotations
Type biological term
Description A placenta disease that is characterized by a deficiency of amniotic fluid sometimes resulting in an embryonic defect through adherence between embryo and amnion. (Human Disease Ontology, DOID_12215)
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Genes

5 genes co-occuring with the biological term oligohydramnios in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.

Symbol Name
AQP1 aquaporin 1 (Colton blood group)
AQP3 aquaporin 3 (Gill blood group)
EDN1 endothelin 1
HLA-G major histocompatibility complex, class I, G
NPPB natriuretic peptide B