AutoICD API

D66

Billable

Hereditary factor VIII deficiency

Hereditary factor VIII deficiency

Status

Billable / Specific

Block

D65-D69

ICD-11 Mapping

1 equivalent

Coding Notes

Inclusion Terms

Alternative clinical terms for this condition

  • Classical hemophilia
  • Deficiency factor VIII (with functional defect)
  • Hemophilia NOS
  • Hemophilia A

Excludes 1

Codes that cannot be used together with this code (mutual exclusion)

Excludes 2

Conditions not included here, but the patient may have both

ICD-11 Equivalents(1)

ICD-11 Equivalents

View full mapping

Corresponding ICD-11 codes from the WHO crosswalk mapping

3B10.ZHereditary factor VIII deficiency, unspecifiedequivalentPrimary
Also Known As / Clinical Terms(265)

SNOMED CT

UMLS

Clinical Terms

  • Hemophilic arthropathy of left hip
  • Severe hereditary factor VIII deficiency disease with high response inhibitor
  • Disorder of joint of right elbow due to hemophilia
  • HEMOPHILIA, CLASSIC
  • Collodion baby
  • Severe hereditary factor VIII deficiency disease without inhibitor
  • Hereditary combined coagulation factor deficiency
  • Congenital factor VIII disorder
  • hemophilia a
  • Deficiency factor VIII (with functional defect)
  • Mild haemophilia A
  • Severe haemophilia A
  • Moderate hemophilia A without inhibitor
  • Moderate hemophilia A with inhibitor
  • AHG deficiency disease
  • Mild hereditary factor VIII deficiency disease with low response inhibitor
  • Hemophilic arthropathy of bilateral shoulders
  • Hereditary factor VIII deficiency disease without inhibitor
  • Disorder of bilateral hip joints due to hemophilia
  • Haemophilia A
  • Moderate hereditary factor VIII deficiency disease with high response inhibitor
  • Congenital factor VIII deficiency disease
  • Factor V deficiency
  • Hemophilic arthropathy of left knee
  • HEMA
  • Hemophilia (disorder)
  • Haemophilia NOS
  • Disorder of joint of left wrist due to hemophilia
  • Hemophilic arthropathy of both elbows
  • Hereditary factor VIII deficiency disease
  • Mild hemophilia A
  • Disorder of bilateral knee joints due to hemophilia
  • Severe hemophilia A with inhibitor
  • Hemophilic arthropathy of left wrist
  • Haemophilia
  • Hemophilic arthropathy of left ankle
  • Classical hemophilia
  • Hemophilia As
  • Congenital factor VIII deficiency
  • Disorder of joint of left hip due to hemophilia
  • Factor VIII deficiency
  • Mild haemophilia A with inhibitor
  • Mild hemophilia A without inhibitor
  • Severe hereditary factor VIII deficiency disease with low response inhibitor
  • Factor V and factor VIII combined deficiency
  • Hemophilic arthropathy of bilateral elbows
  • Moderate hemophilia A
  • Congenital Hemophilia As
  • Combined deficiency of factor V and factor VIII
  • Mild hereditary factor VIII deficiency disease with inhibitor
  • factor viii hemophilia
  • Congenital Hemophilia A
  • Hemophilia A (Factor VIII)
  • Haemophilia A (Factor VIII)
  • Haemophilia A with inhibitor
  • Hemophilic arthropathy of right shoulder
  • Severe haemophilia A without inhibitor
  • Hereditary factor VIII deficiency disease with inhibitor
  • Disorder of bilateral elbow joints due to hemophilia
  • Disorder of joint of right ankle due to hemophilia
  • Mild hereditary factor VIII deficiency disease with high response inhibitor
  • Moderate hereditary factor VIII deficiency disease with low response inhibitor
  • Classical haemophilia
  • Hemophilia
  • Mild hereditary factor VIII deficiency disease
  • Severe hemophilia A
  • Disorder of joint of left knee due to hemophilia
  • Moderate haemophilia A
  • Hemophilic arthropathy of bilateral knees
  • Classic Hemophilias
  • Hemophilic arthropathy of both knees
  • Familial multiple coagulation factor deficiency
  • Hemophilic arthropathy of bilateral hips
  • Disorder of joint of left ankle due to hemophilia
  • Hemophilic arthropathy of both wrists
  • Hemophilias, Classic
  • Hemophilic arthropathy of right ankle
  • Moderate haemophilia A without inhibitor
  • Moderate haemophilia A with inhibitor
  • hemophilias
  • Hereditary factor VIII deficiency disease (disorder)
  • Lamellar ichthyosis
  • Severe hereditary factor VIII deficiency disease with inhibitor
  • Disorder of bilateral shoulder joints due to hemophilia
  • Mild haemophilia A without inhibitor
  • Haemophilia A without inhibitor
  • Hemophilic arthropathy of both shoulders
  • Hemophilia A with inhibitor
  • Hemophilic arthropathy of right elbow
  • Hemophilic arthropathy of bilateral wrists
  • Severe hereditary factor VIII deficiency disease
  • Hemophilia A without inhibitor
  • Disorder of joint of right hip due to hemophilia
  • Moderate hereditary factor VIII deficiency disease without inhibitor
  • Disorder of joint of left shoulder due to hemophilia
  • Hemophilic arthropathy of both hips
  • Disorder of bilateral ankle joints due to hemophilia
  • Disorder of bilateral wrist joints due to hemophilia
  • Sex-linked factor VIII deficiency
  • Mild hereditary factor VIII deficiency disease without inhibitor
  • Hemophilic arthropathy of bilateral ankles
  • hemophilia disorder
  • Multiple sclerosis, ichthyosis, factor VIII deficiency syndrome
  • Severe haemophilia A with inhibitor
  • Hemophilic arthropathy of right knee
  • Disorder of joint of right wrist due to hemophilia
  • Hemophilic arthropathy of left shoulder
  • Hemophilia A, Congenital
  • Moderate hereditary factor VIII deficiency disease with inhibitor
  • Disorder of joint of right shoulder due to hemophilia
  • Hemophilic arthropathy of both ankles
  • Disorder of joint of right knee due to hemophilia
  • Mild hemophilia A with inhibitor
  • Hemophilia As, Congenital
  • Disorder of joint of left elbow due to hemophilia
  • Hemophilic arthropathy of right hip
  • Hemophilic arthropathy of left elbow
  • Severe hemophilia A without inhibitor
  • Hemophilic arthropathy of right wrist
  • Classic Hemophilia
  • Hemophilia NOS
  • Moderate hereditary factor VIII deficiency disease
Frequently Asked Questions
What is the ICD-10 code for hereditary factor viii deficiency?

The ICD-10-CM code for hereditary factor viii deficiency is D66. The full clinical description is "Hereditary factor VIII deficiency". D66 is a billable/specific code that can be used on insurance claims and medical billing.

What does ICD-10 code D66 mean?

ICD-10-CM code D66 represents “Hereditary factor VIII 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 D66 a billable code?

Yes, D66 is a billable/specific ICD-10-CM code and can be used to indicate a diagnosis on a medical claim.

What chapter is D66 in?

D66 is in Chapter 3: Diseases of the Blood and Blood-Forming Organs (codes D50-D89).

What codes cannot be used with D66?

D66 has Excludes1 notes indicating codes that cannot be used together with it, including: factor VIII deficiency with vascular defect (D68.0-).

What SNOMED CT codes does D66 map to?

D66 maps to 43 SNOMED CT concepts: 28293008, 205550003, 715559004, 911781000124102, 911771000124100, and 38 more. SNOMED CT is a clinical terminology used in electronic health records.

What are the UMLS CUIs for D66?

D66 is linked to 3 UMLS Concept Unique Identifiers: C0019069, C2873783, C0684275. The UMLS (Unified Medical Language System) integrates multiple biomedical vocabularies maintained by the U.S. National Library of Medicine.

How does D66 relate to ICF functioning codes?

ICF (International Classification of Functioning, Disability and Health) codes describe how conditions like hereditary factor viii 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 D66?

D66 maps to the ICD-11 code: 3B10.Z (Hereditary factor VIII 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.