Which coagulation disorder is characterized by an autosomal dominant inheritance pattern and is caused by a mutation in the SERPINC1 gene?

A Hemophilia A
B Hemophilia B
C Antithrombin deficiency ✓
D Protein C deficiency

Explanation

Antithrombin deficiency is a coagulation disorder that is characterized by an autosomal dominant inheritance pattern and is caused by a mutation in the SERPINC1 gene, which codes for antithrombin.

Source

Orphanet Journal of Rare Diseases
Hematology Hematology: Coagulation Disorders Hematology: Coagulation Disorders Hard MEDICAL Confidence: medium