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109983007: Monoclonal gammopathy (disorder)


Status: current, Sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2005. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
174679017 Monoclonal gammopathy (clinical) en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
617774019 Monoclonal gammopathy (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
2659691014 Monoclonal gammopathy en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
3763340012 Monoclonal paraproteinaemia en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
3763341011 Monoclonal paraproteinemia en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
948501000195114 gammopatia monoclonale it Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
3398134010 gammapathie monoclonale fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
384131000274119 Monoklonale Gammopathie de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
443731000274119 Monoklonale Hypergammaglobulinämie de Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module


33 descendants. Search Descendants:

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Monoclonal gammopathy (clinical) Is a Clonal protein disease false Inferred relationship Some
Monoclonal gammopathy (clinical) Finding site Hematopoietic system structure false Inferred relationship Some
Monoclonal gammopathy (clinical) Finding site Leukocyte false Inferred relationship Some
Monoclonal gammopathy (clinical) Finding site Structure of immune system (body structure) false Inferred relationship Some 1
Monoclonal gammopathy (clinical) Associated morphology Monoclonal gammopathy of undetermined significance false Inferred relationship Some 1
Monoclonal gammopathy (clinical) Is a Neoplastic disease of uncertain behavior false Inferred relationship Some
Monoclonal gammopathy (clinical) Is a Disorder of increased production of immunoglobulin protein (disorder) true Inferred relationship Some
Monoclonal gammopathy (clinical) Has definitional manifestation Serum gamma globulin above reference range false Inferred relationship Some
Monoclonal gammopathy (clinical) Has definitional manifestation Paraprotein detected (finding) false Inferred relationship Some
Monoclonal gammopathy (clinical) Has definitional manifestation Immune system finding false Inferred relationship Some
Monoclonal gammopathy (clinical) Has definitional manifestation Immunoglobulin above reference range (finding) false Inferred relationship Some
Monoclonal gammopathy (clinical) Has interpretation Above reference range true Inferred relationship Some 1
Monoclonal gammopathy (clinical) Interprets Serum globulin measurement true Inferred relationship Some 1
Monoclonal gammopathy (clinical) Interprets Paraprotein measurement true Inferred relationship Some 3
Monoclonal gammopathy (clinical) Is a Paraprotein detected (finding) true Inferred relationship Some
Monoclonal gammopathy (clinical) Has interpretation Above reference range true Inferred relationship Some 2
Monoclonal gammopathy (clinical) Interprets Immunoglobulin measurement (procedure) true Inferred relationship Some 2
Monoclonal gammopathy (clinical) Has interpretation Present (qualifier value) false Inferred relationship Some 3
Monoclonal gammopathy (clinical) Pathological process (attribute) Abnormal immune process (qualifier value) true Inferred relationship Some 4
Monoclonal gammopathy (clinical) Has interpretation Detected true Inferred relationship Some 3

Inbound Relationships Type Active Source Characteristic Refinability Group
Monoclonal gammopathy of undetermined significance (MGUS) Is a False Monoclonal gammopathy (clinical) Inferred relationship Some
Secondary monoclonal gammopathy Is a False Monoclonal gammopathy (clinical) Inferred relationship Some
Benign monoclonal gammopathy Is a True Monoclonal gammopathy (clinical) Inferred relationship Some
POEMS syndrome Is a True Monoclonal gammopathy (clinical) Inferred relationship Some
Monoclonal gammopathy of uncertain significance Is a True Monoclonal gammopathy (clinical) Inferred relationship Some
Triclonal gammopathy Is a True Monoclonal gammopathy (clinical) Inferred relationship Some
Waldenström macroglobulinaemia Is a True Monoclonal gammopathy (clinical) Inferred relationship Some
Light chain disease Is a True Monoclonal gammopathy (clinical) Inferred relationship Some
Biclonal gammopathy Is a True Monoclonal gammopathy (clinical) Inferred relationship Some
Mixed cryoimmunoglobulinemia with monoclonal component Is a True Monoclonal gammopathy (clinical) Inferred relationship Some
Heavy chain disease Is a True Monoclonal gammopathy (clinical) Inferred relationship Some
Other paraproteinemias Is a False Monoclonal gammopathy (clinical) Inferred relationship Some
paraprotéinémie monoclonale Is a False Monoclonal gammopathy (clinical) Inferred relationship Some
TEMPI syndrome is a rare multi-systemic disease characterized by the presence of Telangiectasias, Erythrocytosis with elevated erythropoietin levels, Monoclonal gammopathy, Perinephric-fluid collections, and Intrapulmonary shunting. Is a True Monoclonal gammopathy (clinical) Inferred relationship Some
A rare, secondary glomerular disease characterized by proteinuria, dysproteinemias, nephrotic syndrome, and nodular glomerulopathy leading to renal failure, with or without extra-renal manifestations. The renal biopsy shows typical deposits of monoclonal immunoglobulins that do not show a fibrillar organization and are negative for Congo red staining. Associated signs and symptoms depend on the involvement of other organs, liver, heart, nerve fibers, gastrointestinal tract, or skin. Is a True Monoclonal gammopathy (clinical) Inferred relationship Some
Scleredema associated with paraproteinemia (disorder) Associated with True Monoclonal gammopathy (clinical) Inferred relationship Some 2
A rare hematologic disease characterized by symptoms of mast cell activation in the absence of cutaneous findings, as well as absence of diagnostic criteria of systemic mastocytosis with tryptase levels of less than 20 ng/ml and normal to low burden of mast cells. Bone marrow biopsy reveals the presence of monoclonal mast cells carrying the KIT D816V mutation and/or expressing CD25. Patients present with recurrent episodes of flushing, headache, hypotension, abdominal cramping, nausea, diarrhea, cardiac arrhythmias, bronchoconstriction, and bleeding diathesis, among others. Is a False Monoclonal gammopathy (clinical) Inferred relationship Some

This concept is not in any reference sets

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