D68.1 is the ICD-10 code for Hereditary factor XI deficiency. It is a four-character subcategory of D68 (Other coagulation defects), the most specific level in the WHO edition. It belongs to the block D65–D69 (Coagulation defects, purpura and other haemorrhagic conditions) in Chapter III, Diseases of the blood and blood-forming organs and certain disorders involving the immune mechanism.
- Code type
- Subcategory (4 characters)
- Chapter
- III · D50–D89
- Classification
- WHO ICD-10, 2019 version
What D68.1 includes
Conditions and terms that are coded here.
- Haemophilia C
- Plasma thromboplastin antecedent [PTA] deficiency
D68.1 in national editions
Countries report with their own edition of ICD-10. Most keep the WHO code and add more specific codes beneath it.
D68.1Arvelig mangel på koagulasjonsfaktor XI
DD681Arvelig faktor XI-mangel
D68.1Hyytymistekijä XI:n perinnöllinen puute
D68.1Hereditärer Faktor-XI-Mangel
D68.1Carence héréditaire en facteur XI
D68.1hereditaire factor XI-deficiëntie
D68.1Hereditary factor XI deficiency
Based on the World Health Organization’s International Statistical Classification of Diseases and Related Health Problems, 10th revision (ICD-10), 2019 version, and the national editions published by each country’s health authority. This page is a reference, not coding advice; follow your national coding rules when you report.
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