D82.2Immunodeficiency with short-limbed stature

D82.2 is the ICD-10-CM diagnosis code for immunodeficiency with short-limbed stature. It belongs to category D82 (immunodeficiency associated with other major defects), block D80-D89 (certain disorders involving the immune mechanism) and chapter 3 (diseases of the blood and blood-forming organs and certain disorders involving the immune mechanism). It is billable, so it can be reported on its own for dates of service from October 1, 2026 through September 30, 2027.

Within D82 (immunodeficiency associated with other major defects), D82.2 is specifically for immunodeficiency with short-limbed stature. Related codes cover Wiskott-Aldrich syndrome (D82.0), Di George's syndrome (D82.1), immunodeficiency following hereditary defective response to Epstein-Barr virus (D82.3), Hyperimmunoglobulin E [IgE] syndrome (D82.4), immunodeficiency associated with other specified major defects (D82.8) and immunodeficiency associated with major defect, unspecified (D82.9).

It is not a CC or MCC, so as a secondary diagnosis it doesn't change the MS-DRG severity level.

In MS-DRG v44.0, it is part of the grouping logic for DRG 814 (Reticuloendothelial and Immunity Disorders with MCC, relative weight 2.0729), DRG 815 (Reticuloendothelial and Immunity Disorders with CC, relative weight 1.0444) and DRG 816 (Reticuloendothelial and Immunity Disorders without CC/MCC, relative weight 0.7381), in MDC 16 (Diseases and Disorders of the Blood and Blood Forming Organs and Immunological 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.

It has been part of ICD-10-CM since the code set took effect on October 1, 2015 and hasn't changed since.

Before ICD-10, this condition was coded in ICD-9-CM as 279.8 (other specified disorders involving the immune mechanism).