cerebrovascular disease, occlusive Gene Set

Dataset OMIM Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
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Genes

1 genes associated with the cerebrovascular disease, occlusive phenotype from the curated OMIM Gene-Disease Associations dataset.

Symbol Name
SERPINA3 serpin peptidase inhibitor, clade A (alpha-1 antiproteinase, antitrypsin), member 3