ICD-10 diagnosis code

D67 Hereditary factor IX deficiency

This page in Swedish

D67 is the ICD-10 code for Hereditary factor IX deficiency. It is a three-character category that is not subdivided further. 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
Category (3 characters)
Chapter
III · D50–D89
Classification
WHO ICD-10, 2019 version

What D67 includes

Conditions and terms that are coded here.

  • Christmas disease
  • Deficiency:
    • factor IX (with functional defect)
    • plasma thromboplastin component [PTC]
  • Haemophilia B

D67 in national editions

Countries report with their own edition of ICD-10. Most keep the WHO code and add more specific codes beneath it.

SwedenICD-10-SE

D67Ärftlig brist på faktor IX

  • D67.9Ärftlig brist på faktor IX
NorwayICD-10-NO

D67Arvelig mangel på koagulasjonsfaktor IX

DenmarkICD-10-DK

DD67Arvelig faktor IX-mangel

  • DD679Hæmofili B
FinlandICD-10-FI

D67Hyytymistekijä IX:n perinnöllinen puute

GermanyICD-10-GM

D67Hereditärer Faktor-IX-Mangel

FranceICD-10-FR

D67Carence héréditaire en facteur IX

NetherlandsICD-10-NL

D67hereditaire factor IX-deficiëntie

United StatesICD-10-CM

D67Hereditary factor IX 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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