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ICD-10-CM 2027

ICD-10 code for SCAD deficiency

E71.312

Short chain acyl CoA dehydrogenase deficiency

✓ Billable / specificCC — complication/comorbidity

From the official ICD-10-CM alphabetic index entry “Deficiency, deficient › SCAD (short chain acyl CoA dehydrogenase deficiency)”. Page updated September 29, 2026.

About coding SCAD deficiency

The ICD-10-CM code for SCAD deficiency is E71.312 (Short chain acyl CoA dehydrogenase deficiency).

Within E71.31 (disorders of fatty-acid oxidation), E71.312 is specifically for short chain acyl CoA dehydrogenase deficiency. Related codes cover long chain/very long chain acyl CoA dehydrogenase deficiency (E71.310), Medium chain acyl CoA dehydrogenase deficiency (E71.311), Glutaric aciduria type II (E71.313), muscle carnitine palmitoyltransferase deficiency (E71.314) and other disorders of fatty-acid oxidation (E71.318).

As a secondary diagnosis it is a CC (complication or comorbidity), which can move an inpatient stay into the "with CC" MS-DRG of its family, unless the principal diagnosis excludes it.

In MS-DRG v44.0, it is part of the grouping logic for DRG 642 (Inborn and Other Disorders of Metabolism, relative weight 1.3219), in MDC 10 (Endocrine, Nutritional and Metabolic Diseases and Disorders), as a principal or secondary diagnosis. The DRG a claim lands in depends on the principal diagnosis, procedures and any CC/MCC secondary diagnoses.

Common questions about SCAD deficiency ICD-10 codes

What is the ICD-10 code for SCAD deficiency?

E71.312 — Short chain acyl CoA dehydrogenase deficiency.

Is E71.312 billable?

Yes. E71.312 is a billable/specific ICD-10-CM code valid for FY2027 (October 1, 2026 – September 30, 2027).

Can E71.312 be used as a principal diagnosis?

Yes. The Medicare Code Editor doesn't restrict E71.312 as a principal diagnosis.

Is E71.312 a CC or MCC?

E71.312 is a CC (complication or comorbidity) under MS-DRG v44.0, unless excluded by the principal diagnosis.