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ICD-10 and ICD-9 Codes for Immunodeficiencies and Related Disorders, Lecture notes of Immunology

A comprehensive list of ICD-10 and ICD-9 codes for various types of immunodeficiencies and related disorders, including functional disorders of polymorphonuclear neutrophils, immunodeficiency with predominantly antibody defects, combined immunodeficiencies, immunodeficiency associated with other major defects, common variable immunodeficiency, and other specified immunodeficiencies. The document also includes information on diagnostic related groups and applicable conditions.

Typology: Lecture notes

2021/2022

Uploaded on 09/12/2022

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IMMUNODEFICIENCIES DISEASE CODES
ICD-10 CM
ICD-9 CM
D71 FUNCTIONAL DISORDERS OF POLYMORPHONUCLEAR NEUTROPHILS
288.1
Applicable To:
Cell membrane receptor complex [CR3] defect
Chronic (childhood) granulomatous disease
Congenital dysphagocytosis
Progressive septic granulomatosis
D71 is grouped within Diagnostic Related Group(s) (MS-DRG v34.0): 808, 809, 810
D80 IMMUNODEFICIENCY WITH PREDOMINANTLY ANTIBODY DEFECTS
D80.0 Hereditary hypogammaglobulinemia 279.04
Applicable To:
Autosomal recessive agammaglobulinemia (Swiss type)
X-linked agammaglobulinemia [Bruton] (with growth hormone deficiency)
D80.1 Nonfamilial hypogammaglobulinemia 279.01
Applicable To:
Agammaglobulinemia with immunoglobulin-bearing B-lymphocytes
Common variable agammaglobulinemia [CVAgamma]
Hypogammaglobulinemia NOS
D80.2 Selective deficiency of immunoglobulin A [IgA] 279.01
D80.3 Selective deficiency of immunoglobulin G [IgG] subclasses 279.03
D80.4 Selective deficiency of immunoglobulin M [IgM] 279.02
D80.5 Immunodeficiency with increased immunoglobulin M [IgM] 279.05
D80 to D80.5 are grouped within Diagnostic Related Group(s) (MS-DRG v34.0): 814, 815, 816
D80.6 Antibody deficiency with near-normal immunoglobulins or with hyperimmunoglobulinemia 279.09
D80.6 is grouped within Diagnostic Related Group(s) (MS-DRG v34.0): 808, 809 810
D80.7 Transient hypogammaglobulinemia of infancy 279.09
D80.7 is grouped within Diagnostic Related Group(s) (MS-DRG v34.0): 814, 815, 816
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IMMUNODEFICIENCIES DISEASE CODES

ICD-10 CM

ICD-9 CM

D

FUNCTIONAL DISORDERS OF POLYMORPHONUCLEAR NEUTROPHILS

Applicable To: Cell membrane receptor complex [CR3] defect Chronic (childhood) granulomatous disease Congenital dysphagocytosis Progressive septic granulomatosis D71 is grouped within Diagnostic Related Group(s) (MS-DRG v34.0): 808, 809, 810

D

IMMUNODEFICIENCY WITH PREDOMINANTLY ANTIBODY DEFECTS

D80.

Hereditary hypogammaglobulinemia

Applicable To: Autosomal recessive agammaglobulinemia (Swiss type) X-linked agammaglobulinemia [Bruton] (with growth hormone deficiency) D80. Nonfamilial hypogammaglobulinemia

Applicable To: Agammaglobulinemia with immunoglobulin-bearing B-lymphocytes Common variable agammaglobulinemia [CVAgamma] Hypogammaglobulinemia NOS D80. Selective deficiency of immunoglobulin A [IgA]

D80.

Selective deficiency of immunoglobulin G [IgG] subclasses

D80.

Selective deficiency of immunoglobulin M [IgM]

D80.

Immunodeficiency with increased immunoglobulin M [IgM]

D80 to D80.5 are grouped within Diagnostic Related Group(s) (MS-DRG v34.0): 814, 815, 816 D80. Antibody deficiency with near-normal immunoglobulins or with hyperimmunoglobulinemia

D80.6 is grouped within Diagnostic Related Group(s) (MS-DRG v34.0): 808, 809 810 D80. Transient hypogammaglobulinemia of infancy

D80.7 is grouped within Diagnostic Related Group(s) (MS-DRG v34.0): 814, 815, 816

D80.

Other immunodeficiencies with predominantly antibody defects

Applicable To: Kappa light chain deficiency D80. Immunodeficiency with predominantly antibody defects, unspecified

D80.8 and D80.9 are grouped within Diagnostic Related Group(s) (MS-DRG v34.0): 808, 809 810

D

COMBINED IMMUNODEFICIENCIES

D81.

Severe combined immunodeficiency [SCID] with reticular dysgenesis

D81.

Severe combined immunodeficiency [SCID] with low T- and B-cell numbers

D81.

Severe combined immunodeficiency [SCID] with low or normal B-cell numbers

D81.0 to D81.2 are grouped within Diagnostic Related Group(s) (MS-DRG v34.0): 808, 809 810 D81. Adenosine deaminase [ADA] deficiency

D81.3 is grouped within Diagnostic Related Group (MS-DRG v34.0): 642 D81. Nezelof's syndrome

D81.4 is grouped within Diagnostic Related Group(s) (MS-DRG v34.0): 808, 809 810 D81. Purine nucleoside phosphorylase [PNP] deficiency

D81.5 is grouped within Diagnostic Related Group (MS-DRG v34.0): 642 D81. Major histocompatibility complex class I deficiency

Applicable To: Bare lymphocyte syndrome D81. Major histocompatibility complex class II deficiency

D81.6 and D81.7 are grouped within Diagnostic Related Group(s) (MS-DRG v34.0): 808, 809 810 D81.

OTHER COMBINED IMMUNODEFICIENCIES

D81.

Biotin-dependent carboxylase deficiency (not billable, use one of the below codes) D81. Biotinidase deficiency

D81.810 is grouped within Diagnostic Related Group (MS-DRG v34.0): 642 D81. Other biotin-dependent carboxylase deficiency

Applicable To: Holocarboxylase synthetase deficiency Holocarboxylase synthetase deficiency D81. Other biotin-dependent carboxylase deficiency, unspecified

Applicable To: Multiple carboxylase deficiency, unspecified

D

OTHER IMMUNODEFICIENCIES

D84.

Lymphocyte function antigen-1 [LFA-1] defect

D84.0 is grouped within Diagnostic Related Group(s) (MS-DRG v34.0): 814, 815, 816 D84. Defects in the complement system

Applicable To: C1 estrase inhibitor [C1-INH] deficiency (not inherited deficiency in complement components) D84.1 is grouped within Diagnostic Related Group (MS-DRG v34.0): 642 D84. Other specified immunodeficiencies 279.10 or

D84.

Immunodeficiency, unspecified

D84.8 and D84.9 are grouped within Diagnostic Related Group(s) (MS-DRG v34.0): 814, 815, 816

D

OTHER DISORDERS INVOLVING THE IMMUNE MECHANISM, NOT ELSEWHERE CLASSIFIED

D89.

Polyclonal hypergammaglobulinemia

Applicable To: Benign hypergammaglobulinemic purpura Polyclonal gammopathy NOS D89.0 is grouped within Diagnostic Related Group(s) (MS-DRG v34.0): 814, 815, 816 D89. Cryoglobulinemia

Applicable To: Cryoglobulinemic purpura Cryoglobulinemic vasculitis Essential cryoglobulinemia Idiopathic cryoglobulinemia Mixed cryoglobulinemia Primary cryoglobulinemia Secondary cryoglobulinemia D89.1 is grouped within Diagnostic Related Group(s) (MS-DRG v34.0): 820 to 825, 840 to 842 D89. Hypergammaglobulinemia, unspecified 273.1 or

D89.

Immune reconstitution syndrome

Applicable To: Immune reconsitution inflammatory syndrome {IRIS} Use additional code for adverse effect, if applicable to identify drug (T36-T50) with fifth or sixth character 5) D89.2 and D89.3 are grouped within Diagnostic Related Group(s) (MS-DRG v34.0): 814, 815, 816

D89.

Mast cell activation syndrome and related disorders (not billable, use one of the below codes) D89. Mast cell activation, unspecified

Applicable To: Mast cell activation disorder, unspecified Mast cell activation syndrome, NOS D89. Monoclonal mast cell activation syndrome

D89.

Idiopathic mast cell activation syndrome

D89.

Secondary mast cell activation

Applicable To: Secondary mast cell activation syndrome Code also underlying etiology, if known D89. Other mast cell activation disorder Applicable To:

Other mast cell activation syndrome D89.40 to D89.43 and D89.49 are grouped within Diagnostic Related Group(s) (MS-DRG v34.0): 814, 815, 816 D89.

OTHER SPECIFIED DISORDERS INVOLVING THE IMMUNE MECHANISM, NOT ELSEWHERE CLASSIFIED

D89.

Graft-versus-host disease (not billable, use one of the below codes) D89. Acute graft-versus-host disease

D89.

Chronic graft-versus-host disease

D89.

Acute on chronic graft-versus-host disease

D89.

Graft-versus-host disease, unspecified

D89.10 to D89.13 are are grouped within Diagnostic Related Group(s) (MS-DRG v34.0): 808, 809, 810 D89. Autoimmune lymphoproliferative syndrome [ALPS]

D89.82 is grouped within Diagnostic Related Group(s) (MS-DRG v34.0): 545, 546, 547 D89. Other specified disorders involving the immune mechanism, not elsewhere classified

Type 1 Excludes: Human immunodeficiency virus disease (B20) D89.89 is grouped within Diagnostic Related Group(s) (MS-DRG v34.0): D89. Disorder involving the immune mechanism, unspecified

Applicable To: Immune disease NOS D89.9 is grouped within Diagnostic Related Group(s) (MS-DRG v34.0): 814, 815, 816 3/