D68.1
BillableHereditary factor XI deficiency
Hereditary factor XI deficiency
Coding Notes
Inclusion Terms
Alternative clinical terms for this condition
- Hemophilia C
- Plasma thromboplastin antecedent [PTA] deficiency
- Rosenthal's disease
Excludes 1
Codes that cannot be used together with this code (mutual exclusion)
- abnormal coagulation profile NOS (R79.1)
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)
- coagulation defects complicating abortion or ectopic or molar pregnancy (O00-O07, O08.1)
- coagulation defects complicating pregnancy, childbirth and the puerperium (O45.0, O46.0, O67.0, O72.3)
Also Known As / Clinical Terms
SNOMED CT
- Factor XI deficiency, type II33169001
- Factor XI deficiency, type III45963004
- Congenital factor XI deficiency disease49762007
- Haemophilia C49762007
- Hemophilia C49762007
- Hereditary factor XI deficiency disease49762007
- PTA deficiency49762007
- Plasma thromboplastin antecedent deficiency49762007
- Rosenthal's disease49762007
- Thromboplastin antecedent deficiency49762007
- Factor XI deficiency, type I88540000
- Factor XI deficiency767713001
UMLS
- Congenital factor XI deficiencyC0015523
- Congenital factor XI deficiency diseaseC0015523
- DEFIC FACTOR XIC0015523
- Deficiencies, Factor 11C0015523
- Deficiencies, Factor ElevenC0015523
- Deficiencies, Factor XIC0015523
- Deficiency, Factor 11C0015523
- Deficiency, Factor ElevenC0015523
- Deficiency, Factor XIC0015523
- F11 DEFICIENCYC0015523
- F11 deficiencyC0015523
- FACTOR XI DEFICC0015523
- FACTOR XI DEFICIENCYC0015523
- Factor 11 DeficienciesC0015523
- Factor 11 DeficiencyC0015523
- Factor 11 deficiencyC0015523
- Factor Eleven DeficienciesC0015523
- Factor Eleven DeficiencyC0015523
- Factor XI DeficienciesC0015523
- Factor XI DeficiencyC0015523
- Factor XI deficiencyC0015523
- Haemophilia CC0015523
- Haemophilia C (Factor XI)C0015523
- Hemophilia CC0015523
- Hemophilia C (Factor XI)C0015523
- Hereditary Factor XI DeficiencyC0015523
- Hereditary Factor XI Deficiency DiseaseC0015523
- Hereditary factor XI deficiencyC0015523
- Hereditary factor XI deficiency diseaseC0015523
- Hereditary factor XI deficiency disease (disorder)C0015523
- PLASMA THROMBOPLASTIN ANTECEDENT DEFICIENCYC0015523
- PTA DEFICIENCYC0015523
- PTA deficiencyC0015523
- Plasma Thromboplastin Antecedent DeficiencyC0015523
- Plasma thromboplastin antecedent [PTA] deficiencyC0015523
- Plasma thromboplastin antecedent deficiencyC0015523
- ROSENTHAL SYNDROMEC0015523
- Rosenthal SyndromeC0015523
- Rosenthal SyndromesC0015523
- Rosenthal factor deficiencyC0015523
- Rosenthal syndromeC0015523
- Rosenthal's SyndromeC0015523
- Rosenthal's SyndromesC0015523
- Rosenthal's diseaseC0015523
- Rosenthals SyndromeC0015523
- Syndrome, RosenthalC0015523
- Syndrome, Rosenthal'sC0015523
- Thromboplastin antecedent deficiencyC0015523
- c hemophiliaC0015523
- factor xi deficiencyC0015523
- haemophilia cC0015523
- hemophilia cC0015523
- rosenthal syndromeC0015523
Frequently Asked Questions
What is the ICD-10 code for hereditary factor xi deficiency?
The ICD-10-CM code for hereditary factor xi deficiency is D68.1. The full clinical description is "Hereditary factor XI deficiency". D68.1 is a billable/specific code that can be used on insurance claims and medical billing.
What does ICD-10 code D68.1 mean?
ICD-10-CM code D68.1 represents "Hereditary factor XI 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 D68.1 a billable code?
Yes, D68.1 is a billable/specific ICD-10-CM code and can be used to indicate a diagnosis on a medical claim.
What chapter is D68.1 in?
D68.1 is in Chapter 3: Diseases of the Blood and Blood-Forming Organs (codes D50-D89).
What codes cannot be used with D68.1?
D68.1 has Excludes1 notes indicating codes that cannot be used together with it, including: abnormal coagulation profile NOS (R79.1).
What SNOMED CT codes does D68.1 map to?
D68.1 maps to 5 SNOMED CT concepts: 49762007, 767713001, 88540000, 33169001, 45963004. SNOMED CT is a clinical terminology used in electronic health records.
What are the UMLS CUIs for D68.1?
D68.1 is linked to 1 UMLS Concept Unique Identifier: C0015523. 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.