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) NOS (M35.9)
- certain conditions originating in the perinatal period (P00-P96)
- complications of pregnancy, childbirth and the puerperium (O00-O9A)
- congenital malformations, deformations and chromosomal abnormalities (Q00-Q99)
- endocrine, nutritional and metabolic diseases (E00-E88)
- human immunodeficiency virus [HIV] disease (B20)
- injury, poisoning and certain other consequences of external causes (S00-T88)
- neoplasms (C00-D49)
- symptoms, signs and abnormal clinical and laboratory findings, not elsewhere classified (R00-R94)
Also Known As / Clinical Terms
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
Frequently Asked Questions
What is ICD-10 code D67?
ICD-10-CM code D67 represents "Hereditary factor IX deficiency". It 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.
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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.