myICD10.com Logo
congenital afibrinogenemia

Wikipedia Summary

Congenital afibrinogenemia is a rare, genetically inherited blood fibrinogen disorder in which the blood does not clot normally due to the lack of fibrinogen, a blood protein necessary for coagulation. This disorder is autosomal recessive, meaning that two unaffected parents can have a child with the disorder...
Related Codes (10)
Code
Description
Billable
Details
O45.01Premature separation of placenta with afibrinogenemia
O45.011Premature separation of placenta with afibrinogenemia, first trimester
O45.012Premature separation of placenta with afibrinogenemia, second trimester
O45.013Premature separation of placenta with afibrinogenemia, third trimester
O45.019Premature separation of placenta with afibrinogenemia, unspecified trimester
O46.01Antepartum hemorrhage with afibrinogenemia
O46.011Antepartum hemorrhage with afibrinogenemia, first trimester
O46.012Antepartum hemorrhage with afibrinogenemia, second trimester
O46.013Antepartum hemorrhage with afibrinogenemia, third trimester
O46.019Antepartum hemorrhage with afibrinogenemia, unspecified trimester

Rows per page

Page 1 of 1