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FY2027

ICD-10 Code for Immunodeficiency

The ICD-10-CM code for immunodeficiency is D84.9Immunodeficiency, unspecified. This is the code the Alphabetic Index gives for immunodeficiency with no further qualifier, valid for FY2027 (October 1, 2026September 30, 2027).

BillableUnspecified

D84.9 is billable but unspecified. If the documentation names a type, site or cause, one of the more specific codes below is likely expected.

Which immunodeficiency code should you use?

The Alphabetic Index lists 33 codes under Immunodeficiency. Which one applies depends on the qualifier documented in the record — the type, site, cause, or associated condition. Find the qualifier below, then verify the code in the Tabular List before using it.

By type

autosomal recessive, Swiss typeD80.0Hereditary hypogammaglobulinemia
combinedD81.9Combined immunodeficiency, unspecified
common variableD83.9Common variable immunodeficiency, unspecified
following hereditary defective response to Epstein-Barr virusD82.3Immunodeficiency following hereditary defective response to Epstein-Barr virus
severe combinedD81.9Combined immunodeficiency, unspecified
specified type NECD84.89Other immunodeficiencies
X-linked, with increased IgMD80.5Immunodeficiency with increased immunoglobulin M [IgM]

Immunodeficiency with

adenosine-deaminase deficiencyD81.30Adenosine deaminase deficiency, unspecified
antibody defectsD80.9Immunodeficiency with predominantly antibody defects, unspecified
hyperimmunoglobulinemiaD80.6Antibody deficiency with near-normal immunoglobulins or with hyperimmunoglobulinemia
increased immunoglobulin MD80.5Immunodeficiency with increased immunoglobulin M [IgM]
major defectD82.9Immunodeficiency associated with major defect, unspecified
partial albinismD82.8Immunodeficiency associated with other specified major defects
short-limbed statureD82.2Immunodeficiency with short-limbed stature
thrombocytopenia and eczemaD82.0Wiskott-Aldrich syndrome
antibody defects › specified type NECD80.8Other immunodeficiencies with predominantly antibody defects
major defect › specified type NECD82.8Immunodeficiency associated with other specified major defects

Immunodeficiency antibody with

hyperimmunoglobulinemiaD80.6Antibody deficiency with near-normal immunoglobulins or with hyperimmunoglobulinemia
near-normal immunoglobulinsD80.6Antibody deficiency with near-normal immunoglobulins or with hyperimmunoglobulinemia

Immunodeficiency combined

biotin-dependent carboxylaseD81.819Biotin-dependent carboxylase deficiency, unspecified
severeD81.9Combined immunodeficiency, unspecified
specified type NECD81.89Other combined immunodeficiencies
biotin-dependent carboxylase › biotinidaseD81.810Biotinidase deficiency
biotin-dependent carboxylase › holocarboxylase synthetaseD81.818Other biotin-dependent carboxylase deficiency
biotin-dependent carboxylase › specified type NECD81.818Other biotin-dependent carboxylase deficiency
severe › with › low or normal B-cell numbersD81.2Severe combined immunodeficiency [SCID] with low or normal B-cell numbers
severe › with › low T- and B-cell numbersD81.1Severe combined immunodeficiency [SCID] with low T- and B-cell numbers
severe › with › reticular dysgenesisD81.0Severe combined immunodeficiency [SCID] with reticular dysgenesis

Immunodeficiency common variable

specified type NECD83.8Other common variable immunodeficiencies
with › abnormalities of B-cell numbers and functionD83.0Common variable immunodeficiency with predominant abnormalities of B-cell numbers and function
with › autoantibodies to B- or T-cellsD83.2Common variable immunodeficiency with autoantibodies to B- or T-cells
with › immunoregulatory T-cell disordersD83.1Common variable immunodeficiency with predominant immunoregulatory T-cell disorders

Immunodeficiency due to

conditions classified elsewhereD84.81Immunodeficiency due to conditions classified elsewhere
drugsD84.821Immunodeficiency due to drugs
external causesD84.822Immunodeficiency due to external causes
medicationD84.821Immunodeficiency due to drugs

Immunodeficiency selective, immunoglobulin

AD80.2Selective deficiency of immunoglobulin A [IgA]
GD80.3Selective deficiency of immunoglobulin G [IgG] subclasses
MD80.4Selective deficiency of immunoglobulin M [IgM]

Immunodeficiency severe combined

due to adenosine deaminase deficiencyD81.31Severe combined immunodeficiency due to adenosine deaminase deficiency

Index terms and codes are reproduced from the official ICD-10-CM FY2027 release. The Alphabetic Index is a finding aid — a code must always be verified in the Tabular List before it is reported. Data sources