Antithrombin III deficiency Gene Set

Dataset ClinVar Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description An inherited blood coagulation disease characterized by the tendency to form clots in the veins. (Human Disease Ontology, DOID_3755)
External Link http://www.omim.org/entry/613118
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Genes

1 genes associated with the Antithrombin III deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Symbol Name
SERPINC1 serpin peptidase inhibitor, clade C (antithrombin), member 1