Category · FY2027
D82 Immunodeficiency associated with other major defects
- Header · not billable
D82 is not billable. The category heads 7 billable codes in FY2027: the 7 codes directly below it.
Index → code
Where it sits
- Chapter 3 Diseases of the blood and blood-forming organs and certain disorders involving the immune mechanism (D50-D89)
- D80-D89 Certain disorders involving the immune mechanism (D80-D89)
- D82 Immunodeficiency associated with other major defects
- Billable codes
- 7
- Subdivisions
- 7
- CC / MCC codes
- 2 / 0
- HCC V28 codes
- 2
- New FY2027
- 0
- Index entries
- 29
Codes in D82
- D82.0Wiskott-Aldrich syndromeBillableCC115
Inclusion terms 1
Inclusion terms
- Immunodeficiency with thrombocytopenia and eczema
- D82.1Di George's syndromeBillableCC115
Inclusion terms 3
Inclusion terms
- Pharyngeal pouch syndrome
- Thymic alymphoplasia
- Thymic aplasia or hypoplasia with immunodeficiency
- D82.2Immunodeficiency with short-limbed statureBillable
- D82.3Immunodeficiency following hereditary defective response to Epstein-Barr virusBillable
Inclusion terms 1
Inclusion terms
- X-linked lymphoproliferative disease
- D82.4Hyperimmunoglobulin E [IgE] syndromeBillable
- D82.8Immunodeficiency associated with other specified major defectsBillable
- D82.9Immunodeficiency associated with major defect, unspecifiedBillable
CC/MCC: as a secondary diagnosis, unless the principal diagnosis is on the code’s PDX exclusion list (MS-DRG v44 Appendix C; list on the code card).
Instructions
At D82
Excludes1
- ataxia telangiectasia [Louis-Bar] (G11.3) G11.3
Notes that also apply
Block D80-D89 instructions (Includes 3, Excludes1 2, Excludes2 1): printed on the block page.
Chapter 3 instructions (Excludes2 9): printed on the chapter 3 page.
Index entries
- Aldrich (-Wiskott) syndrome (eczema-thrombocytopenia) → D82.0
- Wiskott-Aldrich syndrome → D82.0
- Alymphoplasia, thymic → D82.1
- Di George's syndrome → D82.1
- DiGeorge's syndrome (thymic hypoplasia) → D82.1
- Pharyngeal pouch syndrome → D82.1
- Lymphoproliferation, X-linked disease → D82.3
- Syndrome›Aldrich (-Wiskott) → D82.0
- Syndrome›eczema-thrombocytopenia → D82.0
- Syndrome›familial eczema-thrombocytopenia (Wiskott-Aldrich) → D82.0
- Syndrome›Wiskott-Aldrich → D82.0
- Alymphocytosis›thymic (with immunodeficiency) → D82.1
- Aplasia›parathyroid-thymic → D82.1
- Aplasia›thymic, with immunodeficiency → D82.1
- Dysplasia›thymic, with immunodeficiency → D82.1
- Hypoplasia, hypoplastic›thymic, with immunodeficiency → D82.1
- Syndrome›di George's → D82.1
- Syndrome›pharyngeal pouch → D82.1
- Short, shortening, shortness›limbed stature, with immunodeficiency → D82.2
- Immunodeficiency›following hereditary defective response to Epstein-Barr virus (EBV) → D82.3
- Syndrome›hyperimmunoglobulin E (IgE) → D82.4
- Immunodeficiency›with›thrombocytopenia and eczema → D82.0
- Hypoplasia, hypoplastic›thymus (gland)›with immunodeficiency → D82.1
- Immunodeficiency›with›short-limbed stature → D82.2
- Disease, diseased›lymphoproliferative›X-linked → D82.3
- Immunodeficiency›with›partial albinism → D82.8
- Immunodeficiency›with›major defect → D82.9
- Deficiency, deficient›immunity›cell-mediated›with thrombocytopenia and eczema → D82.0
- Immunodeficiency›with›major defect›specified type NEC → D82.8
NCHS Alphabetic Index. Index first, then the Tabular List.