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128817004: Immunoglobulin deposition disease (morphologic abnormality)

Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2002. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
207360011 Systemic light chain disease en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
207361010 Primary amyloidosis en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
207362015 Immunoglobulin deposition disease en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
732860017 Immunoglobulin deposition disease (morphologic abnormality) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core

0 descendants.

Expanded Value Set

Outbound Relationships Type Target Active Characteristic Refinability Group Values
Immunoglobulin deposition disease Is a Neoplasm of uncertain behaviour false Inferred relationship Some
Immunoglobulin deposition disease Is a Immunoproliferative morphology false Inferred relationship Some
Immunoglobulin deposition disease Is a Hematopoietic neoplasm of uncertain behavior (morphologic abnormality) true Inferred relationship Some
Immunoglobulin deposition disease Is a Plasma cell neoplasm (morphology) true Inferred relationship Some
Inbound Relationships Type Active Source Characteristic Refinability Group
Primary amyloidosis of light chain type Associated morphology False Immunoglobulin deposition disease Inferred relationship Some 5
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. Associated morphology True Immunoglobulin deposition disease Inferred relationship Some 1
A rare non-amyloid monoclonal immunoglobulin deposition disease characterized by production of monoclonal immunoglobulins with truncated heavy chains and no detectable light chains, which are deposited in tissues and cause organ dysfunction, but do not form amyloid beta-pleated sheets or contain an amyloid P component. The condition frequently occurs in association with multiple myeloma. Patients most commonly present with renal involvement (manifesting as hypertension, progressive renal dysfunction, anemia, and nephrotic syndrome with microhematuria), but other organs (such as the liver or skin) may also be affected. Production of IgG1 or IgG3 isotypes results in hypercomplementemia. Associated morphology True Immunoglobulin deposition disease Inferred relationship Some 5

This concept is not in any reference sets

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