{placental abruption} Gene Set
| Dataset |
OMIM Gene-Disease Associations
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| Category |
disease or phenotype associations
|
| Type |
phenotype |
| Description |
A placenta disease that is characterized by separation of the placental lining from the uterus of the mother. (Human Disease Ontology, DOID_9667)
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| Similar Terms |
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| Downloads & Tools |
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Genes
1 genes associated with the {placental abruption} phenotype from the curated OMIM Gene-Disease Associations dataset.
| Symbol |
Name |
|
NOS3
|
nitric oxide synthase 3 (endothelial cell)
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