|Dataset||ClinVar Gene-Phenotype Associations|
|Category||disease or phenotype associations|
|Description||An inherited blood coagulation disease characterized by the tendency to form clots in the veins. (Human Disease Ontology, DOID_3755)|
|Downloads & Tools|
1 genes associated with the Antithrombin III deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
|SERPINC1||serpin peptidase inhibitor, clade C (antithrombin), member 1|