Precursor Condition
Monoclonal Gammopathy of Renal Significance
CI-CAN-00009006MGRSExplore in graph →
HematologicPrecursor2 active trials
- NCIt
- C157343
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Precursor Condition
CI-CAN-00009006MGRSExplore in graph →
Data completeness1 / 7 dimensions
Computed from entity_counters.completeness · refreshed after each connector run
Definition
A condition caused by a B-cell or plasma cell clone resulting in the deposition of the secreted monoclonal immunoglobulin, without evidence for overt lymphoma or myeloma. This category includes a wide spectrum of renal pathology and include such lesions as immunoglobulin-associated amyloidosis, the monoclonal immunoglobulin deposition diseases (MIDDs; light chain deposition disease, heavy chain deposition disease, and light and heavy chain deposition disease), proliferative glomerulonephritis with monoclonal immunoglobulin deposits (PGNMID), C3 glomerulopathy with monoclonal gammopathy, light chain proximal tubulopathy (Fanconi syndrome), and several others.
Data updated 22 days agoSource updated 26.08e
Taxonomy
Several hierarchies coexist; edges are listed per hierarchy type with their source.
Parents
Children (0)
Leaf node — no children.
Anatomy
Data updated 15 hours agoSource updated unknowncounters aggregate over descendants
Names
Only the preferred name is recorded so far.
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Key figures
Each figure carries its unit, period and source; ranks link to "Why this rank?".
Data updated 15 hours agoSource updated unknownregistry figures: cdc-uscs · latest year available per metric · counters aggregate over descendants