E72.22
Arginosuccinic aciduria
Approximate Synonyms
-
Argininosuccinate lyase deficiency
-
Deficiency, arginosuccinate lyase
Clinical Information
-
Autosomal recessive aminoacidopathy characterized by urinary excretion of argininosuccinic acid, due to a deficiency of argininosuccinate lyase, with hyperammonemia, argininosuccinicacidemia, and citrullinemia; clinical findings include mental retardation, seizures, ataxia, hepatomegaly, and friable hair.
Details
-
E72.22 is a billable/specific ICD-10-CM code that can be used to indicate a diagnosis for reimbursement purposes.
-
The 2023 edition of ICD-10-CM E72.22 became effective on October 1, 2022.
-
This is the American ICD-10-CM version of E72.22 – other international versions of ICD-10 E72.22 may differ.