Antithrombin III Deficiency Gene Set

Dataset CTD Gene-Disease Associations
Category disease or phenotype associations
Type disease
Description An inherited blood coagulation disease characterized by the tendency to form clots in the veins. (Human Disease Ontology, DOID_3755)
External Link http://ctdbase.org/detail.go?type=disease&acc=MESH:D020152
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Genes

1 genes/proteins associated with the disease Antithrombin III Deficiency from the curated CTD Gene-Disease Associations dataset.

Symbol Name Standardized Value
SERPINC1 serpin peptidase inhibitor, clade C (antithrombin), member 1 2.88009