D67
BillableHereditary factor IX deficiency
Hereditary factor IX deficiency
Coding Notes
Inclusion Terms
Alternative clinical terms for this condition
- Christmas disease
- Factor IX deficiency (with functional defect)
- Hemophilia B
- Plasma thromboplastin component [PTC] deficiency
Excludes 2
Conditions not included here, but the patient may have both
- •autoimmune disease (systemic) NOSM35.9
- •certain conditions originating in the perinatal periodP00-P96
- •complications of pregnancy, childbirth and the puerperiumO9A)O00
- •congenital malformations, deformations and chromosomal abnormalitiesQ00-Q99
- •endocrine, nutritional and metabolic diseasesE00-E88
- •human immunodeficiency virus [HIV] diseaseB20
- •injury, poisoning and certain other consequences of external causesS00-T88
- •neoplasmsC00-D49
- •symptoms, signs and abnormal clinical and laboratory findings, not elsewhere classifiedR00-R94
ICD-11 Equivalents(1)
ICD-11 Equivalents
View full mappingCorresponding ICD-11 codes from the WHO crosswalk mapping
Also Known As / Clinical Terms(188)
SNOMED CT
- Christmas disease41788008
- Congenital factor IX deficiency41788008
- Haemophilia B41788008
- Hemophilia B41788008
- Hereditary factor IX deficiency disease41788008
- PTC deficiency disease41788008
- Sex-linked factor IX deficiency disease41788008
- Congenital factor IX deficiency variant234444001
- Congenital factor IX deficiency with inhibitor234445000
- Congenital factor IX deficiency without inhibitor426199009
- Haemophilia B with inhibitor438372000
- Hemophilia B with inhibitor438372000
- Hereditary factor IX deficiency disease with inhibitor438372000
- Haemophilia B without inhibitor438792009
- Hemophilia B without inhibitor438792009
- Hereditary factor IX deficiency disease without inhibitor438792009
- Severe haemophilia B with inhibitor440866009
- Severe hemophilia B with inhibitor440866009
- Severe hereditary factor IX deficiency disease with inhibitor440866009
- Moderate haemophilia B with inhibitor440867000
- Moderate hemophilia B with inhibitor440867000
- Moderate hereditary factor IX deficiency disease with inhibitor440867000
- Mild haemophilia B with inhibitor440868005
- Mild hemophilia B with inhibitor440868005
- Mild hereditary factor IX deficiency disease with inhibitor440868005
- Severe haemophilia B without inhibitor441190003
- Severe hemophilia B without inhibitor441190003
- Severe hereditary factor IX deficiency disease without inhibitor441190003
- Moderate haemophilia B without inhibitor441191004
- Moderate hemophilia B without inhibitor441191004
- Moderate hereditary factor IX deficiency disease without inhibitor441191004
- Mild haemophilia B without inhibitor441192006
- Mild hemophilia B without inhibitor441192006
- Mild hereditary factor IX deficiency disease without inhibitor441192006
- Factor IX deficiency767712006
- Severe hereditary factor IX deficiency disease with high response inhibitor1285661007
- Severe hereditary factor IX deficiency disease with low response inhibitor1285662000
- Moderate hereditary factor IX deficiency disease with high response inhibitor1285663005
- Moderate hereditary factor IX deficiency disease with low response inhibitor1285664004
- Mild hereditary factor IX deficiency disease with high response inhibitor1285665003
- Mild hereditary factor IX deficiency disease with low response inhibitor1285666002
- Mild haemophilia B1336091009
- Mild hemophilia B1336091009
- Mild hereditary factor IX deficiency disease1336091009
- Moderate haemophilia B1336092002
- Moderate hemophilia B1336092002
- Moderate hereditary factor IX deficiency disease1336092002
- Severe haemophilia B1336093007
- Severe hemophilia B1336093007
- Severe hereditary factor IX deficiency disease1336093007
- Factor 9 deficiency Leyden type1336117005
- Factor IX deficiency Leyden type1336117005
- Haemophilia B Leyden1336117005
- Hemophilia B Leyden1336117005
UMLS
- Bs, HemophiliaC0008533
- CHRISTMAS DISC0008533
- CHRISTMAS DISEASEC0008533
- Christmas DiseaseC0008533
- Christmas diseaseC0008533
- Christmas disease (Factor IX)C0008533
- Congenital factor IX deficiencyC0008533
- Congenital factor IX disorderC0008533
- DEFIC FACTOR IXC0008533
- Deficiencies, F9C0008533
- Deficiencies, Factor IXC0008533
- Deficiency, F9C0008533
- Deficiency, Factor IXC0008533
- Disease, ChristmasC0008533
- F9 DEFICIENCYC0008533
- F9 DeficienciesC0008533
- F9 DeficiencyC0008533
- FACTOR IX DEFICC0008533
- FACTOR IX DEFICIENCYC0008533
- Factor IX DeficienciesC0008533
- Factor IX DeficiencyC0008533
- Factor IX deficiencyC0008533
- Factor IX deficiency (disorder)C0008533
- HEMBC0008533
- HEMOPHILIA BC0008533
- HEMOPHILIA B LEYDENC0008533
- HEMOPHILIA B(M)C0008533
- Haemophilia BC0008533
- Haemophilia B (Factor IX)C0008533
- Haemophilia BsC0008533
- Hemophilia BC0008533
- Hemophilia B (Factor IX)C0008533
- Hemophilia B(M)C0008533
- Hemophilia BsC0008533
- Hemophilia Bs (M)C0008533
- Hereditary factor IX deficiencyC0008533
- Hereditary factor IX deficiency diseaseC0008533
- Hereditary factor IX deficiency disease (disorder)C0008533
- PLASMA THROMBOPLASTIN COMPONENT DEFICIENCYC0008533
- PTC deficiency diseaseC0008533
- Plasma Thromboplastin Component DeficiencyC0008533
- Plasma thromboplastin component [PTC] deficiencyC0008533
- Sex-linked factor IX deficiency diseaseC0008533
- b haemophiliaC0008533
- b hemophiliaC0008533
- christmas diseaseC0008533
- factor IX deficiencyC0008533
- factor ix deficiencyC0008533
- haemophilia bC0008533
- hemophilia BC0008533
- hemophilia bC0008533
- Factor IX deficiency (with functional defect)C2873784
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.