Glutaric aciduria type II
Billable / specific
E71.313 is a billable, specific ICD-10-CM code that can be used to indicate a diagnosis for reimbursement purposes in FY2027.
Inclusion terms
Applicable to
- Glutaric aciduria type II A
- Glutaric aciduria type II B
- Glutaric aciduria type II C
Includes (from E71)
- Note: All neoplasms, whether functionally active or not, are classified in Chapter 2. Appropriate codes in this chapter (i.e. E05.8, E07.0, E16-E31, E34.-) may be used as additional codes to indicate either functional activity by neoplasms and ectopic endocrine tissue or hyperfunction and hypofunction of endocrine glands associated with neoplasms and other conditions classified elsewhere.
Excludes1
Not coded here — never report together with this code.
- glutaric aciduria (type 1) NOS (E72.3)
- peroxisomal disorders (E71.5) (from E71.3)
- Refsum's disease (G60.1) (from E71.3)
- Schilder's disease (G37.0) (from E71.3)
- transitory endocrine and metabolic disorders specific to newborn (P70-P74) (from E71)
- androgen insensitivity syndrome (E34.5-) (from E71)
- congenital adrenal hyperplasia (E25.0) (from E71)
- hemolytic anemias attributable to enzyme disorders (D55.-) (from E71)
- Marfan syndrome (Q87.4-) (from E71)
- 5-alpha-reductase deficiency (E29.1) (from E71)
Excludes2
Not included here — may be reported together when both conditions exist.
Also known as
- Glutaric aciduria type II A
- Glutaric aciduria type II B
- Glutaric aciduria type II C
- Aciduria, glutaric, type II
Parent code
- E71.31Disorders of fatty-acid oxidationHeader
Related codes
- E71.310Long chain/very long chain acyl CoA dehydrogenase deficiencyBillable
- E71.311Medium chain acyl CoA dehydrogenase deficiencyBillable
- E71.312Short chain acyl CoA dehydrogenase deficiencyBillable
- E71.314Muscle carnitine palmitoyltransferase deficiencyBillable
- E71.318Other disorders of fatty-acid oxidationBillable