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ICD10 code of Fucosidosis and ICD9 code

What is the ICD10 code for Fucosidosis? And the ICD9 code for Fucosidosis?

ICD9 and ICD10 codes of Fucosidosis

Fucosidosis is a rare genetic disorder characterized by the deficiency of the enzyme alpha-L-fucosidase. This leads to the accumulation of fucose-containing compounds in various tissues and organs. The ICD-10 code for Fucosidosis is E77.1. Unfortunately, there is no specific ICD-9 code for Fucosidosis as it was replaced by the ICD-10 coding system. It is important to consult a healthcare professional for accurate diagnosis and coding.


Fucosidosis is a rare genetic disorder that falls under the category of lysosomal storage diseases. It is characterized by a deficiency in the enzyme alpha-L-fucosidase, which leads to the accumulation of certain substances within cells, particularly in the brain and other organs. This condition is inherited in an autosomal recessive manner, meaning that both parents must carry the defective gene for a child to be affected.

In terms of medical coding, Fucosidosis is classified under the International Classification of Diseases, Tenth Revision (ICD-10). The specific ICD-10 code for Fucosidosis is E77.1. This code is used to identify and document the condition for medical billing, research, and statistical purposes.

In the previous revision, the International Classification of Diseases, Ninth Revision (ICD-9), the code for Fucosidosis was 271.8. However, it is important to note that the ICD-9 codes have been replaced by ICD-10 codes, which provide a more detailed and comprehensive classification system.

It is crucial for healthcare professionals to accurately assign the appropriate ICD-10 code for Fucosidosis when documenting a patient's medical records. This coding system ensures uniformity in healthcare data and facilitates communication among healthcare providers, researchers, and insurers.

In conclusion, the ICD-10 code for Fucosidosis is E77.1, while the previous ICD-9 code was 271.8. These codes enable healthcare professionals to accurately identify and document this rare genetic disorder for various medical purposes.
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