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.