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ICD10 code of Aspartylglycosaminuria and ICD9 code
What is the ICD10 code for Aspartylglycosaminuria? And the ICD9 code for Aspartylglycosaminuria?
The ICD-10 code for Aspartylglycosaminuria is E77.0. Aspartylglycosaminuria is a rare genetic disorder characterized by the deficiency of the enzyme aspartylglucosaminidase. This enzyme is responsible for breaking down certain complex molecules in the body. The ICD-9 code for this condition is 270.0. Aspartylglycosaminuria leads to the accumulation of certain substances in the body, causing various symptoms including intellectual disability, skeletal abnormalities, and coarse facial features.
Aspartylglycosaminuria is a rare genetic disorder that affects the metabolism of certain sugars and proteins in the body. The ICD-10 code for this condition is E77.0. This code falls under the category of "disorders of glycoprotein metabolism and other congenital disorders of glycosylation."
In the previous version of the International Classification of Diseases (ICD-9), the code for aspartylglycosaminuria was 277.5. This code was classified under "disorders of glycoprotein metabolism and other metabolic disorders."
Aspartylglycosaminuria is characterized by the deficiency of the enzyme aspartylglucosaminidase, leading to the accumulation of a specific substance called aspartylglucosamine in the body. This build-up can cause various symptoms including intellectual disability, skeletal abnormalities, impaired vision, and speech difficulties.
It is important to note that the provided information is purely for educational purposes and should not be used for medical diagnosis or treatment. If you suspect you or someone you know may have aspartylglycosaminuria, it is crucial to consult with a healthcare professional for proper evaluation and guidance.
In the previous version of the International Classification of Diseases (ICD-9), the code for aspartylglycosaminuria was 277.5. This code was classified under "disorders of glycoprotein metabolism and other metabolic disorders."
Aspartylglycosaminuria is characterized by the deficiency of the enzyme aspartylglucosaminidase, leading to the accumulation of a specific substance called aspartylglucosamine in the body. This build-up can cause various symptoms including intellectual disability, skeletal abnormalities, impaired vision, and speech difficulties.
It is important to note that the provided information is purely for educational purposes and should not be used for medical diagnosis or treatment. If you suspect you or someone you know may have aspartylglycosaminuria, it is crucial to consult with a healthcare professional for proper evaluation and guidance.
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