E72.59
ICD-10-CMThis code signifies a group of rare, inherited metabolic disorders affecting the body's ability to process glycine, an amino acid. These conditions can lead to a buildup of glycine in the blood and other tissues, potentially causing neurological dysfunction and other systemic issues.
Apply this code for documented cases of glycine metabolism disorders that are not specifically classified elsewhere, such as nonketotic hyperglycinemia (glycine encephalopathy). This code is appropriate when the physician's documentation clearly identifies an "other" or unspecified disorder of glycine metabolism.
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