Inbound Relationships |
Type |
Active |
Source |
Characteristic |
Refinability |
Group |
Monoclonal gammopathy of undetermined significance (MGUS) |
Is a |
False |
Monoclonal gammopathy (disorder) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Secondary monoclonal gammopathy |
Is a |
False |
Monoclonal gammopathy (disorder) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Benign monoclonal gammopathy (disorder) |
Is a |
True |
Monoclonal gammopathy (disorder) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
POEMS syndrome |
Is a |
True |
Monoclonal gammopathy (disorder) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Monoclonal gammopathy of uncertain significance |
Is a |
True |
Monoclonal gammopathy (disorder) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Triclonal gammopathy |
Is a |
True |
Monoclonal gammopathy (disorder) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Waldenström macroglobulinemia (disorder) |
Is a |
True |
Monoclonal gammopathy (disorder) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Light chain disease |
Is a |
True |
Monoclonal gammopathy (disorder) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Biclonal gammopathy |
Is a |
True |
Monoclonal gammopathy (disorder) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Mixed cryoimmunoglobulinemia with monoclonal component |
Is a |
True |
Monoclonal gammopathy (disorder) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Heavy chain disease |
Is a |
True |
Monoclonal gammopathy (disorder) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Other paraproteinemias |
Is a |
False |
Monoclonal gammopathy (disorder) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
paraprotéinémie monoclonale |
Is a |
False |
Monoclonal gammopathy (disorder) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Telangiectasia, erythrocytosis, monoclonal gammopathy, perinephric fluid collections and intrapulmonary shunting syndrome (disorder) |
Is a |
True |
Monoclonal gammopathy (disorder) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Non-amyloid monoclonal immunoglobulin deposition disease (disorder) |
Is a |
True |
Monoclonal gammopathy (disorder) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Paraproteinemia-associated scleredema |
Associated with |
True |
Monoclonal gammopathy (disorder) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
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 (disorder) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|