fetal akinesia Gene Set

Dataset GAD Gene-Disease Associations
Category disease or phenotype associations
Type disease
Description Decreases fetal activity associated with multiple joint contractures, facial anomalies and pulmonary hypoplasia. Ultrasound examination may reveal polyhydramnios, ankylosis, scalp edema, and decreased chest movements (reflecting pulmonary hypoplasia). (Human Phenotype Ontology, HP_0001989)
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Genes

1 genes associated with the disease fetal akinesia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

Symbol Name
RYR1 ryanodine receptor 1 (skeletal)