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ICD10 code of Infantile Myofibromatosis and ICD9 code
What is the ICD10 code for Infantile Myofibromatosis? And the ICD9 code for Infantile Myofibromatosis?
The ICD-10 code for Infantile Myofibromatosis is D48.1. This code is used to classify and document this rare benign tumor that occurs in infants and young children. In the previous ICD-9 system, the corresponding code for Infantile Myofibromatosis was 8821. These codes are essential for accurate medical record keeping and billing purposes.
Infantile myofibromatosis is a rare disorder characterized by the development of benign tumors in the soft tissues of infants. The International Classification of Diseases, Tenth Revision (ICD-10) provides a specific code to classify this condition, which is D48.9. This code falls under the category of "Neoplasms of uncertain behavior, unspecified."
On the other hand, the International Classification of Diseases, Ninth Revision (ICD-9) is an older coding system that has been replaced by ICD-10. However, for historical reference, the ICD-9 code for infantile myofibromatosis is 216.8. This code represents "Benign neoplasm of skin of other and unspecified sites."
Infantile myofibromatosis is a condition that primarily affects children under the age of two, with tumors commonly appearing on the skin, muscles, bones, or internal organs. The tumors can vary in size and number, and their growth can lead to various symptoms depending on their location. While the cause of this condition is unknown, some cases have been associated with genetic mutations.
It is important to note that the information provided above is for educational purposes only and should not be used for diagnostic or medical purposes. If you suspect that you or someone you know may have infantile myofibromatosis, it is crucial to consult a healthcare professional for an accurate diagnosis and appropriate management.
On the other hand, the International Classification of Diseases, Ninth Revision (ICD-9) is an older coding system that has been replaced by ICD-10. However, for historical reference, the ICD-9 code for infantile myofibromatosis is 216.8. This code represents "Benign neoplasm of skin of other and unspecified sites."
Infantile myofibromatosis is a condition that primarily affects children under the age of two, with tumors commonly appearing on the skin, muscles, bones, or internal organs. The tumors can vary in size and number, and their growth can lead to various symptoms depending on their location. While the cause of this condition is unknown, some cases have been associated with genetic mutations.
It is important to note that the information provided above is for educational purposes only and should not be used for diagnostic or medical purposes. If you suspect that you or someone you know may have infantile myofibromatosis, it is crucial to consult a healthcare professional for an accurate diagnosis and appropriate management.
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