AutoICD API

D67

Billable

Hereditary factor IX deficiency

Hereditary factor IX deficiency

Status

Billable / Specific

Block

D65-D69

ICD-11 Mapping

1 equivalent

Coding Notes

ICD-11 Equivalents(1)

ICD-11 Equivalents

View full mapping

Corresponding ICD-11 codes from the WHO crosswalk mapping

Also Known As / Clinical Terms(188)

SNOMED CT

UMLS

Clinical Terms

  • Christmas Disease
  • HEMOPHILIA B
  • Factor IX deficiency Leyden type
  • Disease, Christmas
  • Moderate hereditary factor IX deficiency disease
  • FACTOR IX DEFICIENCY
  • Moderate hemophilia B without inhibitor
  • Christmas disease (Factor IX)
  • F9 Deficiency
  • Moderate hereditary factor IX deficiency disease with low response inhibitor
  • Severe hereditary factor IX deficiency disease
  • F9 Deficiencies
  • DEFIC FACTOR IX
  • Mild hereditary factor IX deficiency disease with inhibitor
  • Hereditary factor IX deficiency disease (disorder)
  • Haemophilia B without inhibitor
  • Moderate haemophilia B with inhibitor
  • Hemophilia Bs (M)
  • Mild hemophilia B
  • Factor IX deficiency (with functional defect)
  • Mild hereditary factor IX deficiency disease
  • Haemophilia B (Factor IX)
  • Plasma thromboplastin component [PTC] deficiency
  • Deficiencies, F9
  • PTC deficiency disease
  • Haemophilia Bs
  • Haemophilia B with inhibitor
  • Hemophilia B without inhibitor
  • Moderate haemophilia B without inhibitor
  • Hemophilia B with inhibitor
  • Moderate hereditary factor IX deficiency disease with inhibitor
  • Bs, Hemophilia
  • Severe haemophilia B with inhibitor
  • Deficiency, Factor IX
  • Severe hemophilia B
  • Severe hereditary factor IX deficiency disease with inhibitor
  • Severe hemophilia B with inhibitor
  • Mild hereditary factor IX deficiency disease with high response inhibitor
  • Hemophilia B(M)
  • Mild hereditary factor IX deficiency disease with low response inhibitor
  • b haemophilia
  • Mild hereditary factor IX deficiency disease without inhibitor
  • Moderate hemophilia B with inhibitor
  • Mild haemophilia B without inhibitor
  • Moderate hemophilia B
  • Hereditary factor IX deficiency disease without inhibitor
  • PLASMA THROMBOPLASTIN COMPONENT DEFICIENCY
  • FACTOR IX DEFIC
  • Mild hemophilia B without inhibitor
  • Haemophilia B
  • Factor IX Deficiencies
  • Factor IX deficiency (disorder)
  • Moderate hereditary factor IX deficiency disease without inhibitor
  • CHRISTMAS DIS
  • Congenital factor IX deficiency
  • Severe hemophilia B without inhibitor
  • Mild hemophilia B with inhibitor
  • Congenital factor IX deficiency variant
  • Congenital factor IX disorder
  • Factor 9 deficiency Leyden type
  • b hemophilia
  • Moderate haemophilia B
  • HEMB
  • Sex-linked factor IX deficiency disease
  • Severe haemophilia B without inhibitor
  • Hereditary factor IX deficiency disease with inhibitor
  • Congenital factor IX deficiency with inhibitor
  • Severe hereditary factor IX deficiency disease with high response inhibitor
  • HEMOPHILIA B LEYDEN
  • Moderate hereditary factor IX deficiency disease with high response inhibitor
  • Congenital factor IX deficiency without inhibitor
  • Severe hereditary factor IX deficiency disease without inhibitor
  • Hemophilia Bs
  • Deficiencies, Factor IX
  • Hemophilia B (Factor IX)
  • Haemophilia B Leyden
  • Severe hereditary factor IX deficiency disease with low response inhibitor
  • Hereditary factor IX deficiency disease
  • Mild haemophilia B with inhibitor
  • Severe haemophilia B
  • Mild haemophilia B
  • Deficiency, F9
Frequently Asked Questions
What is the ICD-10 code for hereditary factor ix deficiency?

The ICD-10-CM code for hereditary factor ix deficiency is D67. The full clinical description is "Hereditary factor IX deficiency". D67 is a billable/specific code that can be used on insurance claims and medical billing.

What does ICD-10 code D67 mean?

ICD-10-CM code D67 represents “Hereditary factor IX deficiency”. It is classified under Chapter 3: Diseases of the Blood and Blood-Forming Organs and is a billable/specific code that can be used on a claim.

Is D67 a billable code?

Yes, D67 is a billable/specific ICD-10-CM code and can be used to indicate a diagnosis on a medical claim.

What chapter is D67 in?

D67 is in Chapter 3: Diseases of the Blood and Blood-Forming Organs (codes D50-D89).

What SNOMED CT codes does D67 map to?

D67 maps to 23 SNOMED CT concepts: 41788008, 234444001, 234445000, 426199009, 1336117005, and 18 more. SNOMED CT is a clinical terminology used in electronic health records.

What are the UMLS CUIs for D67?

D67 is linked to 2 UMLS Concept Unique Identifiers: C0008533, C2873784. The UMLS (Unified Medical Language System) integrates multiple biomedical vocabularies maintained by the U.S. National Library of Medicine.

How does D67 relate to ICF functioning codes?

ICF (International Classification of Functioning, Disability and Health) codes describe how conditions like hereditary factor ix deficiency affect a person's functioning — body functions, activities, participation, and environmental factors. AutoICD provides ICF Core Sets for 12+ conditions and can map clinical text to ICF categories automatically. Browse the ICF directory to explore functioning codes.

What is the ICD-11 equivalent of D67?

D67 maps to the ICD-11 code: 3B11.Z (Hereditary factor IX deficiency, unspecified).

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Includes SNOMED Clinical Terms® (SNOMED CT®) used by permission of SNOMED International. Includes content from the UMLS Metathesaurus, courtesy of the U.S. National Library of Medicine.