Autosomal recessive hyperimmunoglobulin M syndrome due to CTNNBL1 deficiency
Autosomal recessive hyperimmunoglobulin M syndrome due to UNG deficiency
Hyper-IgM syndrome due to uracil N-glycosylase
Hyper IgM syndrome due to INO80
Hyper-IgM syndrome type 1
Autosomal recessive hyper- immunoglobulin M syndrome
Autosomal recessive hyperimmunoglobulin M syndrome due to APRIL deficiency
Autosomal recessive activation-induced cytidine deaminase deficiency
Autosomal recessive hyperimmunoglobulin M syndrome
Autosomal recessive hyperimmunoglobulin M syndrome due to AID deficiency
Hyper-IgM syndrome due to CD40 deficiency
Autosomal dominant hyperimmunoglobulin M syndrome due to activation induced cytidine deaminase deficiency
Immunodeficiency with IgM hypergammaglobulinemia
Hyper-IgM syndrome due to CD40 ligand deficiency
Autosomal recessive combined immunodeficiency due to CD40 mutation
Autosomal dominant activation-induced cytidine deaminase deficiency
Hyperimmunoglobulin M syndrome with susceptibility to opportunistic infection
Hyperimmunoglobulin M syndrome without susceptibility to opportunistic infection
Immunodeficiency with increased immunoglobulin M
Autosomal dominant hyper-IgM syndrome type 2
Hyperimmunoglobulin M syndrome
Autosomal recessive hyperimmunoglobulin M syndrome due to mutator S homolog 6 deficiency
CMMR-D (constitutional mismatch repair deficiency) syndrome
Hyper-IgM syndrome due to UNG
Autosomal recessive hyperimmunoglobulin M syndrome due to uracil DNA glycosylase deficiency
Hyper-IgM syndrome due to CD40L deficiency
Constitutional mismatch repair deficiency syndrome
Autosomal recessive hyperimmunoglobulin M syndrome due to INO80 complex ATPase subunit deficiency
Hyper-IgM syndrome type 5
Hyper IgM syndrome due to MSH6
Autosomal recessive hyperimmunoglobulin M syndrome due to mutS homolog 6 deficiency
Immunodeficiency with IgM hypergammaglobulinaemia
X-linked hyper-immunoglobulin M syndrome
Hyper-IgM syndrome with susceptibility to opportunistic infections
Autosomal dominant hyper IgM syndrome due to AICDA
Autosomal recessive hyper-IgM syndrome type 2
HIGM3 - hyperimmunoglobulin M syndrome type 3
Autosomal recessive hyperimmunoglobulin M syndrome due to activation induced cytidine deaminase deficiency
Hyper IgM syndrome due to TNFSF13
Autosomal dominant hyperimmunoglobulin M syndrome due to AID deficiency
Hyper-IgM syndrome without susceptibility to opportunistic infections
Hyperimmunoglobulin M syndrome type 3
Autosomal recessive hyper-IgM syndrome
Hyper IgM syndrome
Autosomal recessive hyperimmunoglobulin M syndrome due to MSH6 deficiency
X-linked hyper-IgM syndrome
Autosomal recessive hyperimmunoglobulin M syndrome due to catenin beta like 1deficiency
Autosomal recessive hyper IgM syndrome due to AICDA
Autosomal recessive hyperimmunoglobulin M syndrome due to INO80 deficiency
Hyper IgM syndrome due to CTNNBL1
X-linked with hyper-IgM immunodeficiency

Frequently Asked Questions

What is the ICD-10 code for immunodeficiency with increased immunoglobulin m [igm]?

The ICD-10-CM code for immunodeficiency with increased immunoglobulin m [igm] is D80.5. The full clinical description is "Immunodeficiency with increased immunoglobulin M [IgM]". D80.5 is a billable/specific code that can be used on insurance claims and medical billing.

What does ICD-10 code D80.5 mean?

ICD-10-CM code D80.5 represents “Immunodeficiency with increased immunoglobulin M [IgM]”. It is classified under Chapter 3: Diseases of the Blood and Blood-Forming Organs and is a billable/specific code that can be used on a claim.

Is D80.5 a billable code?

Yes, D80.5 is a billable/specific ICD-10-CM code and can be used to indicate a diagnosis on a medical claim.

What chapter is D80.5 in?

D80.5 is in Chapter 3: Diseases of the Blood and Blood-Forming Organs (codes D50-D89).

What codes cannot be used with D80.5?

D80.5 has Excludes1 notes indicating codes that cannot be used together with it, including: autoimmune disease (systemic) NOS (M35.9); functional disorders of polymorphonuclear neutrophils (D71); human immunodeficiency virus [HIV] disease (B20).

What SNOMED CT codes does D80.5 map to?

D80.5 maps to 14 SNOMED CT concepts: 1351570003, 1351572006, 1362020006, 403836001, 1351573001, and 9 more. SNOMED CT is a clinical terminology used in electronic health records.

What are the UMLS CUIs for D80.5?

D80.5 is linked to 1 UMLS Concept Unique Identifier: C0740331. The UMLS (Unified Medical Language System) integrates multiple biomedical vocabularies maintained by the U.S. National Library of Medicine.

How does D80.5 relate to ICF functioning codes?

ICF (International Classification of Functioning, Disability and Health) codes describe how conditions like immunodeficiency with increased immunoglobulin m [igm] affect a person's functioning: body functions, activities, participation, and environmental factors. AutoICD provides ICF Core Sets for 12+ conditions and can map clinical text to ICF categories automatically. Browse the ICF directory to explore functioning codes.

What is the ICD-11 equivalent of D80.5?

D80.5 maps to the ICD-11 code: 4A01.05 (Immunodeficiencies with severe reduction in serum IgG or IgA with normal or elevated IgM and normal numbers of B-cells).

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Includes SNOMED Clinical Terms® (SNOMED CT®) used by permission of SNOMED International. Includes content from the UMLS Metathesaurus, courtesy of the U.S. National Library of Medicine.