D47.2
BillableMonoclonal gammopathy
Monoclonal gammopathy
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)
D47.0Mast cell neoplasms of uncertain behavior
D47.1Chronic myeloproliferative disease
D47.3Essential (hemorrhagic) thrombocythemia
D47.4Osteomyelofibrosis
D47.9Neoplm of uncrt behav of lymphoid,hematpoetc & rel tiss,unsp
D47.ZOth neoplm of uncrt behav of lymphoid, hematpoetc & rel tiss
ICD-11 Equivalents(1)
ICD-11 Equivalents
View full mappingCorresponding ICD-11 codes from the WHO crosswalk mapping
Also Known As / Clinical Terms(252)
SNOMED CT
- Monoclonal gammopathy with three clones13720003
- Triclonal gammopathy13720003
- Light chain disease51319002
- Chronic urticaria51611005
- Recurrent periodic urticaria51611005
- Biclonal gammopathy52064007
- Monoclonal gammopathy with two clones52064007
- Asymptomatic monoclonal gammopathy58648008
- Benign monoclonal gammopathy58648008
- POEMS - Polyneuropathy organomegaly endocrinopathy monoclonal and skin changes79268002
- POEMS syndrome79268002
- Polyneuropathy organomegaly endocrinopathy monoclonal gammopathy and skin changes79268002
- Polyneuropathy, organomegaly, endocrinopathy, monoclonal gammopathy, and skin changes (POEMS) syndrome79268002
- Polyneuropathy, organomegaly, endocrinopathy, monoclonal gammopathy, and skin changes syndrome79268002
- Gell and Coombs reaction type III83699005
- Hypersensitivity reaction mediated by immune complex83699005
- Hypersensitivity reaction type III83699005
- Type III reaction83699005
- Monoclonal gammopathy109983007
- Monoclonal gammopathy (clinical)109983007
- Monoclonal paraproteinaemia109983007
- Monoclonal paraproteinemia109983007
- Gammopathy111001004
- Hypogammaglobulinaemia119250001
- Hypogammaglobulinemia119250001
- Dysgammaglobulinaemia123782009
- Dysgammaglobulinemia123782009
- Angiofollicular lymph node hyperplasia207036003
- Angiolymphoid hyperplasia207036003
- Angiomatous lymphoid hamartoma207036003
- Benign angiofollicular hyperplasia207036003
- Castleman disease207036003
- Castleman's disease207036003
- Giant lymph node hyperplasia207036003
- Neuropathy associated with dysproteinaemias230585004
- Neuropathy associated with dysproteinemias230585004
- Neuropathy in benign MGUS (monoclonal gammopathy of undetermined significance)230590001
- Neuropathy in benign monoclonal gammopathy230590001
- Neuropathy in benign monoclonal gammopathy of undetermined significance230590001
- Ectactic nodes234088000
- Hyperplastic lymph node234088000
- MGUS - monoclonal gammopathy of uncertain significance277577000
- Monoclonal gammopathy of uncertain significance277577000
- Monoclonal gammopathy of undetermined significance277577000
- IgA monoclonal gammopathy of uncertain significance285423008
- Immunoglobulin A monoclonal gammopathy of uncertain significance285423008
- IgG monoclonal gammopathy of uncertain significance285424002
- Immunoglobulin G monoclonal gammopathy of uncertain significance285424002
- IgM monoclonal gammopathy of uncertain significance285426000
- Immunoglobulin M monoclonal gammopathy of uncertain significance285426000
- IgD monoclonal gammopathy of uncertain significance285428004
- Immunoglobulin D monoclonal gammopathy of uncertain significance285428004
- Light chain monoclonal gammopathy of uncertain significance285430002
- Schnitzler syndrome402415001
- Urticarial vasculitis with monoclonal IgM component, Schnitzler402416000
- Urticarial vasculitis with monoclonal immunoglobulin M component, Schnitzler402416000
- Necrotising cutaneous vasculitis402655006
- Necrotizing cutaneous vasculitis402655006
- Urticarial vasculitis402656007
- Disorder of increased production of immunoglobulin protein414031008
- Immunosecretory disorder414031008
- Monoclonal free light chain detected414766003
- Monoclonal free light chain present414766003
- Monoclonal IgA present414768002
- Monoclonal immunoglobulin A detected414768002
- Monoclonal immunoglobulin A present414768002
- Monoclonal IgD present414769005
- Monoclonal immunoglobulin D detected414769005
- Monoclonal immunoglobulin D present414769005
- Monoclonal IgG present414771005
- Monoclonal immunoglobulin G detected414771005
- Monoclonal immunoglobulin G present414771005
- TEMPI syndrome718614004
- Telangiectasia, erythrocytosis, monoclonal gammopathy, perinephric fluid collections and intrapulmonary shunting syndrome718614004
- Non-amyloid MIDD (monoclonal immunoglobulin deposition disease)829971006
- Non-amyloid monoclonal immunoglobulin deposition disease829971006
- Randall disease829971006
- Castleman disease with IgM -associated neuropathy1259049004
- Castleman disease with immunoglobulin M monoclonal gammopathy of uncertain significance1259049004
- Castleman's disease with IgM -associated neuropathy1259049004
- Motor neuron disease due to gammopathy1263538007
- Complex multigenic autoinflammatory syndrome1295181006
- Hypogammaglobulinaemia due to monoclonal gammopathy of undetermined significance16318061000119108
- Hypogammaglobulinemia due to monoclonal gammopathy of undetermined significance16318061000119108
- Immunoglobulin G deficiency12631000119106
- Immunoglobulin G deficiency due to monoclonal gammopathy of undetermined significance16894671000119102
UMLS
- Asymptomatic monoclonal gammopathyC0026470
- Benign Monoclonal GammapathiesC0026470
- Benign Monoclonal GammapathyC0026470
- Benign Monoclonal GammopathiesC0026470
- Benign Monoclonal GammopathyC0026470
- Benign monoclonal gammopathyC0026470
- Benign monoclonal gammopathy (disorder)C0026470
- Benign monoclonal hypergammaglobulinaemiaC0026470
- Benign monoclonal hypergammaglobulinemiaC0026470
- Hypergammaglobulinaemia benign monoclonalC0026470
- Hypergammaglobulinemia benign monoclonalC0026470
- MGUSC0026470
- MGUS - monoclonal gammopathy of uncertain significanceC0026470
- MGUS - monoclonal gammopathy of undetermined significanceC0026470
- MGUS undeterminedC0026470
- Monoclonal Gammapathies, BenignC0026470
- Monoclonal Gammapathy of Undetermined SignificanceC0026470
- Monoclonal Gammapathy, BenignC0026470
- Monoclonal Gammopathies, BenignC0026470
- Monoclonal Gammopathy of Undetermined SignificanceC0026470
- Monoclonal Gammopathy of Undetermined Significance (MGUS)C0026470
- Monoclonal Gammopathy, BenignC0026470
- Monoclonal gammopathy of uncertain significanceC0026470
- Monoclonal gammopathy of uncertain significance (disorder)C0026470
- Monoclonal gammopathy of undetermined significanceC0026470
- Monoclonal gammopathy of undetermined significance (MGUS)C0026470
- Monoclonal gammopathy of undetermined significance (morphologic abnormality)C0026470
- Monoclonal gammopathy of undetermined significance [MGUS]C0026470
- Monoclonal gammopathy of unknown significanceC0026470
- benign monoclonal gammapathyC0026470
- benign monoclonal gammopathyC0026470
- gammopathy monoclonalC0026470
- mgusC0026470
- monoclonal gammopathyC0026470
- Gammapathy, MonoclonalC1136085
- Gammopathy, MonoclonalC1136085
- Monoclonal GammapathiesC1136085
- Monoclonal GammapathyC1136085
- Monoclonal GammopathiesC1136085
- Monoclonal GammopathyC1136085
- Monoclonal ParaproteinemiaC1136085
- Monoclonal gammopathyC1136085
- Monoclonal gammopathy (clinical)C1136085
- Monoclonal gammopathy (disorder)C1136085
- Monoclonal paraproteinaemiaC1136085
- Monoclonal paraproteinemiaC1136085
- gammapathy monoclonalC1136085
- gammopathies monoclonalC1136085
- monoclonal gammapathiesC1136085
- monoclonal gammapathyC1136085
- monoclonal gammopathiesC1136085
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.