×

Home work?

Keep your critical coding and billing tools with you no matter where you work.

Create your Find-A-Code account today!

subscribe

close

3B50.1 Congenital plasminogen activator inhibitor type 1 deficiency

International Classification of Diseases for Mortality and Morbidity Statistics, 11th Revision, v2024-01

Congenital plasminogen activator inhibitor type 1 (PAI-1) deficiency is a disorder that causes premature lysis of haemostatic clots and a moderate bleeding syndrome. Spontaneous bleeding is rarely observed, whereas moderate haemorrhages of the knees, elbows, nose and gingiva are usually triggered by mild trauma. However, menstrual bleeding may be severe and a prolonged bleeding after surgery is common. The PAI-1 deficiency may be qualitative or quantitative, total or partial.

synonyms

• Congenital plasminogen activator inhibitor type 1 deficiency
• Congenital PAI-1 - [plasminogen activator inhibitor type 1] deficiency

Thank you for choosing Find-A-Code, please Sign In to remove ads.