| Dataset | GAD Gene-Disease Associations |
| Category | disease or phenotype associations |
| Type | disease |
| 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) |
| Similar Terms | |
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2 genes associated with the disease oligohydramnios in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
