D68.52
BillableProthrombin gene mutation
Prothrombin gene mutation
Coding Notes
Excludes 1
Codes that cannot be used together with this code (mutual exclusion)
- abnormal coagulation profile NOS (R79.1)
- antiphospholipid syndrome (D68.61)
- lupus anticoagulant (D68.62)
- secondary activated protein C resistance (D68.69)
- secondary antiphospholipid antibody syndrome (D68.69)
- secondary lupus anticoagulant with hypercoagulable state (D68.69)
- secondary systemic lupus erythematosus [SLE] inhibitor with hypercoagulable state (D68.69)
- systemic lupus erythematosus [SLE] inhibitor finding without diagnosis (R76.0)
- systemic lupus erythematosus [SLE] inhibitor with hemorrhagic disorder (D68.312)
- thrombotic thrombocytopenic purpura (M31.19)
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
Frequently Asked Questions
What is the ICD-10 code for prothrombin gene mutation?
The ICD-10-CM code for prothrombin gene mutation is D68.52. The full clinical description is "Prothrombin gene mutation". D68.52 is a billable/specific code that can be used on insurance claims and medical billing.
What does ICD-10 code D68.52 mean?
ICD-10-CM code D68.52 represents "Prothrombin gene mutation". 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 D68.52 a billable code?
Yes, D68.52 is a billable/specific ICD-10-CM code and can be used to indicate a diagnosis on a medical claim.
What chapter is D68.52 in?
D68.52 is in Chapter 3: Diseases of the Blood and Blood-Forming Organs (codes D50-D89).
What codes cannot be used with D68.52?
D68.52 has Excludes1 notes indicating codes that cannot be used together with it, including: abnormal coagulation profile NOS (R79.1); antiphospholipid syndrome (D68.61); lupus anticoagulant (D68.62); and 7 more.
What SNOMED CT codes does D68.52 map to?
D68.52 maps to 3 SNOMED CT concepts: 441421001, 441420000, 440989002. SNOMED CT is a clinical terminology used in electronic health records.
What are the UMLS CUIs for D68.52?
D68.52 is linked to 1 UMLS Concept Unique Identifier: C1260403. 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.