Condition: Oligohydramnios


rs867410737 in ATP5F1D gene and Oligohydramnios PMID 29478781 2018 Biallelic Mutations in ATP5F1D, which Encodes a Subunit of ATP Synthase, Cause a Metabolic Disorder.

rs1057519389 in EBF3 gene and Oligohydramnios PMID 28017372 2017 A Syndromic Neurodevelopmental Disorder Caused by De Novo Variants in EBF3.