Short answer · Medically reviewed summary · Last updated: 2023-07-10
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.
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ICD10 code of Aspartylglycosaminuria and ICD9 code
ICD-10 and ICD-9 codes for Aspartylglycosaminuria, with classification details for clinicians, coders and patients.
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.
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
