AutoICD API

D47.2

Billable

Monoclonal gammopathy

Monoclonal gammopathy

Status

Billable / Specific

Block

D37-D48

Parent Code

D47

ICD-11 Mapping

1 equivalent

Coding Notes

Inclusion Terms

Alternative clinical terms for this condition

  • Monoclonal gammopathy of undetermined significance [MGUS]

Excludes 1

Codes that cannot be used together with this code (mutual exclusion)

Related Codes(6)
ICD-11 Equivalents(1)

ICD-11 Equivalents

View full mapping

Corresponding ICD-11 codes from the WHO crosswalk mapping

Also Known As / Clinical Terms(252)

SNOMED CT

UMLS

Clinical Terms

  • Immunoglobulin G monoclonal gammopathy of uncertain significance
  • Hyperplastic lymph node
  • Monoclonal Gammapathy of Undetermined Significance
  • Benign monoclonal gammopathy
  • Monoclonal Gammopathy, Benign
  • Light chain monoclonal gammopathy of uncertain significance
  • Randall disease
  • Monoclonal Gammapathies
  • Immunoglobulin G deficiency
  • Immunoglobulin D monoclonal gammopathy of uncertain significance
  • Urticarial vasculitis
  • Angiolymphoid hyperplasia
  • Castleman disease with IgM -associated neuropathy
  • Hypogammaglobulinemia due to monoclonal gammopathy of undetermined significance
  • Chronic urticaria
  • Monoclonal gammopathy with three clones
  • Necrotising cutaneous vasculitis
  • Neuropathy in benign monoclonal gammopathy
  • Ectactic nodes
  • Neuropathy associated with dysproteinaemias
  • Triclonal gammopathy
  • Gell and Coombs reaction type III
  • Monoclonal IgG present
  • Monoclonal immunoglobulin G present
  • Monoclonal immunoglobulin G detected
  • Monoclonal Gammopathy of Undetermined Significance
  • Monoclonal Gammapathy
  • Recurrent periodic urticaria
  • TEMPI syndrome
  • MGUS
  • Neuropathy in benign monoclonal gammopathy of undetermined significance
  • Hypersensitivity reaction type III
  • Benign Monoclonal Gammopathies
  • IgG monoclonal gammopathy of uncertain significance
  • Gammapathy, Monoclonal
  • Monoclonal free light chain detected
  • Monoclonal gammopathy of uncertain significance (disorder)
  • Non-amyloid MIDD (monoclonal immunoglobulin deposition disease)
  • Monoclonal immunoglobulin A present
  • Monoclonal gammopathy (clinical)
  • Immunoglobulin M monoclonal gammopathy of uncertain significance
  • Biclonal gammopathy
  • Giant lymph node hyperplasia
  • Monoclonal immunoglobulin A detected
  • Monoclonal gammopathy (disorder)
  • Benign monoclonal gammopathy (disorder)
  • Hypogammaglobulinemia
  • Benign monoclonal hypergammaglobulinaemia
  • Monoclonal paraproteinemia
  • monoclonal gammopathies
  • benign monoclonal gammapathy
  • Immunoglobulin G deficiency due to monoclonal gammopathy of undetermined significance
  • Castleman disease
  • IgM monoclonal gammopathy of uncertain significance
  • Neuropathy associated with dysproteinemias
  • Gammopathy
  • Hypergammaglobulinaemia benign monoclonal
  • Immunosecretory disorder
  • Motor neuron disease due to gammopathy
  • Gammopathy, Monoclonal
  • Hypogammaglobulinaemia due to monoclonal gammopathy of undetermined significance
  • Monoclonal IgA present
  • Benign monoclonal hypergammaglobulinemia
  • Monoclonal Gammapathies, Benign
  • Disorder of increased production of immunoglobulin protein
  • Dysgammaglobulinemia
  • Complex multigenic autoinflammatory syndrome
  • Angiomatous lymphoid hamartoma
  • Non-amyloid monoclonal immunoglobulin deposition disease
  • MGUS - monoclonal gammopathy of uncertain significance
  • gammapathy monoclonal
  • gammopathy monoclonal
  • Hypergammaglobulinemia benign monoclonal
  • Telangiectasia, erythrocytosis, monoclonal gammopathy, perinephric fluid collections and intrapulmonary shunting syndrome
  • Benign Monoclonal Gammapathies
  • Monoclonal Gammopathy of Undetermined Significance (MGUS)
  • Polyneuropathy, organomegaly, endocrinopathy, monoclonal gammopathy, and skin changes (POEMS) syndrome
  • Benign angiofollicular hyperplasia
  • Necrotizing cutaneous vasculitis
  • Neuropathy in benign MGUS (monoclonal gammopathy of undetermined significance)
  • Monoclonal gammopathy of undetermined significance (morphologic abnormality)
  • Polyneuropathy, organomegaly, endocrinopathy, monoclonal gammopathy, and skin changes syndrome
  • Castleman's disease
  • Monoclonal gammopathy of uncertain significance
  • Immunoglobulin A monoclonal gammopathy of uncertain significance
  • Dysgammaglobulinaemia
  • Type III reaction
  • POEMS - Polyneuropathy organomegaly endocrinopathy monoclonal and skin changes
  • Asymptomatic monoclonal gammopathy
  • Urticarial vasculitis with monoclonal immunoglobulin M component, Schnitzler
  • Monoclonal paraproteinaemia
  • POEMS syndrome
  • Castleman's disease with IgM -associated neuropathy
  • Monoclonal free light chain present
  • IgD monoclonal gammopathy of uncertain significance
  • Monoclonal IgD present
  • Urticarial vasculitis with monoclonal IgM component, Schnitzler
  • Monoclonal immunoglobulin D detected
  • Monoclonal gammopathy of undetermined significance [MGUS]
  • Hypogammaglobulinaemia
  • gammopathies monoclonal
  • Hypersensitivity reaction mediated by immune complex
  • MGUS undetermined
  • Monoclonal Gammopathies, Benign
  • Angiofollicular lymph node hyperplasia
  • IgA monoclonal gammopathy of uncertain significance
  • Castleman disease with immunoglobulin M monoclonal gammopathy of uncertain significance
  • Schnitzler syndrome
  • Monoclonal immunoglobulin D present
  • Polyneuropathy organomegaly endocrinopathy monoclonal gammopathy and skin changes
  • MGUS - monoclonal gammopathy of undetermined significance
  • Monoclonal gammopathy with two clones
  • Monoclonal Gammapathy, Benign
  • Monoclonal gammopathy of unknown significance
  • Light chain disease
Frequently Asked Questions
What is the ICD-10 code for monoclonal gammopathy?

The ICD-10-CM code for monoclonal gammopathy is D47.2. The full clinical description is "Monoclonal gammopathy". D47.2 is a billable/specific code that can be used on insurance claims and medical billing.

What does ICD-10 code D47.2 mean?

ICD-10-CM code D47.2 represents “Monoclonal gammopathy”. It is classified under Chapter 2: Neoplasms and is a billable/specific code that can be used on a claim.

Is D47.2 a billable code?

Yes, D47.2 is a billable/specific ICD-10-CM code and can be used to indicate a diagnosis on a medical claim.

What chapter is D47.2 in?

D47.2 is in Chapter 2: Neoplasms (codes C00-D49).

What codes cannot be used with D47.2?

D47.2 has Excludes1 notes indicating codes that cannot be used together with it, including: neoplasms of unspecified behavior (D49.-).

What SNOMED CT codes does D47.2 map to?

D47.2 maps to 38 SNOMED CT concepts: 207036003, 58648008, 52064007, 1259049004, 51611005, and 33 more. SNOMED CT is a clinical terminology used in electronic health records.

What are the UMLS CUIs for D47.2?

D47.2 is linked to 2 UMLS Concept Unique Identifiers: C0026470, C1136085. The UMLS (Unified Medical Language System) integrates multiple biomedical vocabularies maintained by the U.S. National Library of Medicine.

How does D47.2 relate to ICF functioning codes?

ICF (International Classification of Functioning, Disability and Health) codes describe how conditions like monoclonal gammopathy 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 D47.2?

D47.2 maps to the ICD-11 code: 2A83.0 (Monoclonal gammopathy of undetermined significance).

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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.