Specific codes in ICD-10 are unique alphanumeric designations used to identify and categorize diseases, disorders, and conditions. They consist of 3-5 characters, including both letters and numbers, that provide a high level of detail and specificity.
| Language | Translation |
|---|---|
English
|
Hereditary factor IX deficiency |
French
|
Carence héréditaire en facteur IX |
| Level | Code | Title | |
|---|---|---|---|
| 1 | III | Diseases of the blood and blood-forming organs and certain disorders involving the immune mechanism | |
| 2 | D65-D69 | Coagulation defects, purpura and other haemorrhagic conditions | |
| 3 | D67 | Hereditary factor IX deficiency |
| Active Ingredient | Description | |
|---|---|---|
| Coagulation factor IX |
Factor IX is a single chain glycoprotein with a molecular mass of about 68,000 Dalton. It is a vitamin-K dependent coagulation factor and it is synthesised in the liver. Factor IX is activated by factor XIa in the intrinsic coagulation pathway and by the factor VII/tissue factor complex in the extrinsic pathway. Activated factor IX, in combination with activated factor VIII, activates factor X. |
