E74.09

Applicable To

• Andersen disease

• Hers disease

• Tauri disease

• Glycogen storage disease, types 0, IV, VI-XI

• Liver phosphorylase deficiency

• Muscle phosphofructokinase deficiency

Approximate Synonyms

• Glycogen storage disease type viii

• Glycogen storage disease, type 4

• Glycogen storage disease, type 6

• Glycogen storage disease, type 7

• Glycogen storage disease, type 8

• Glycogen storage disease, type 9

• Glycogen storage disease, type iv

• Glycogen storage disease, type ix

• Glycogen storage disease, type vi

• Glycogen storage disease, type vii

Clinical Information

• A hepatic glycogen storage disease in which there is an apparent deficiency of hepatic phosphorylase glycogen phosphorylase, liver form) activity.

• A rare inherited type of glycogen storage disease caused by deficiency of amylo-1,4-1,6 transglucosidase.

• An autosomal recessive glycogen storage disease in which there is deficient expression of 6-phosphofructose 1-kinase in muscle phosphofructokinase-1, muscle type) resulting in abnormal deposition of glycogen in muscle tissue. These patients have severe congenital muscular dystrophy and are exercise intolerant.

• An autosomal recessive metabolic disorder due to a deficiency in expression of glycogen branching enzyme 1 alpha-1,4-glucan-6-alpha-glucosyltransferase), resulting in an accumulation of abnormal glycogen with long outer branches. Clinical features are muscle hypotonia and cirrhosis. Death from liver disease usually occurs before age 2.

• Autosomal recessive glycogen storage disease in which there is deficient expression of 6-phosphofructose 1-kinase in muscle resulting in abnormal deposition of glycogen in muscle tissue; patients have severe congenital muscular dystrophy and are exercise intolerant.

• Autosomal recessive metabolic disorder due to a deficiency in expression of branching enzyme alpha-1,4-glucan-6-alpha-glucosyltransferase), resulting in an accumulation of abnormal glycogen with long outer branches; clinical features are muscle hypotonia and cirrhosis; death from liver disease usually occurs before age 2.

• Hepatic glycogen storage disease in which there is an apparent deficiency of hepatic phosphorylase activity.

Details

• E74.09 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 E74.09 became effective on October 1, 2022.

• This is the American ICD-10-CM version of E74.09 – other international versions of ICD-10 E74.09 may differ.