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 |
|