Short answer · Medically reviewed summary · Last updated: 2023-07-10
Hereditary Thrombophilia due to Congenital Protein S Deficiency is a genetic condition characterized by a deficiency of protein S, a natural anticoagulant protein in the blood. This condition increases the risk of abnormal blood clot formation, leading to a higher likelihood of developing deep vein thrombosis or pulmonary embolism. In the International Classification of Diseases, Tenth Revision (ICD-10), the specific code for Hereditary Thrombophilia due to Congenital Protein S Deficiency is D68.51.
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ICD10 code of Hereditary Thrombophilia due to Congenital Protein S Deficiency and ICD9 code
ICD-10 and ICD-9 codes for Hereditary Thrombophilia due to Congenital Protein S Deficiency, with classification details for clinicians, coders and patients.
Hereditary Thrombophilia due to Congenital Protein S Deficiency is a genetic condition characterized by a deficiency of protein S, a natural anticoagulant protein in the blood. This condition increases the risk of abnormal blood clot formation, leading to a higher likelihood of developing deep vein thrombosis or pulmonary embolism.
In the International Classification of Diseases, Tenth Revision (ICD-10), the specific code for Hereditary Thrombophilia due to Congenital Protein S Deficiency is D68.51. The "D68" category is used for coagulation defects, purpura, and other hemorrhagic conditions, while the "51" subcategory is specifically assigned to Protein S deficiency. This code allows healthcare providers to accurately document and track cases of this particular condition.
In the previous version of the ICD, the Ninth Revision (ICD-9), the corresponding code for Hereditary Thrombophilia due to Congenital Protein S Deficiency is 289.81. The "289" category is used for diseases of blood and blood-forming organs, while the ".81" subcategory denotes other specified diseases of blood and blood-forming organs. This code enabled healthcare professionals to identify and classify cases of this condition before the implementation of ICD-10.
It is important to note that accurate coding is crucial for proper medical documentation, insurance claims, and statistical analysis. By using the appropriate ICD-10 code, healthcare providers can ensure accurate reporting of Hereditary Thrombophilia due to Congenital Protein S Deficiency, allowing for better understanding and management of this condition.
In the International Classification of Diseases, Tenth Revision (ICD-10), the specific code for Hereditary Thrombophilia due to Congenital Protein S Deficiency is D68.51. The "D68" category is used for coagulation defects, purpura, and other hemorrhagic conditions, while the "51" subcategory is specifically assigned to Protein S deficiency. This code allows healthcare providers to accurately document and track cases of this particular condition.
In the previous version of the ICD, the Ninth Revision (ICD-9), the corresponding code for Hereditary Thrombophilia due to Congenital Protein S Deficiency is 289.81. The "289" category is used for diseases of blood and blood-forming organs, while the ".81" subcategory denotes other specified diseases of blood and blood-forming organs. This code enabled healthcare professionals to identify and classify cases of this condition before the implementation of ICD-10.
It is important to note that accurate coding is crucial for proper medical documentation, insurance claims, and statistical analysis. By using the appropriate ICD-10 code, healthcare providers can ensure accurate reporting of Hereditary Thrombophilia due to Congenital Protein S Deficiency, allowing for better understanding and management of this condition.
Author: DiseaseMaps Editorial Team
Reviewed against authoritative medical sources (NIH GARD, Orphanet, OMIM)
Last updated: 2023-07-10
Medical disclaimer:
This information does not substitute professional medical advice. Always consult your doctor before making health decisions.
Source:
DiseaseMaps.org
