fetal akinesia Gene Set
| Dataset |
GAD Gene-Disease Associations
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| Category |
disease or phenotype associations
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| 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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| Similar Terms |
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| Downloads & Tools |
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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)
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