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1148888004: Nodular glomerulosclerosis due to heavy chain deposition disease (disorder)

Status: current, Sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2021. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
4552724014 Nodular glomerulosclerosis due to heavy chain deposition disease en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
4552725010 Nodular glomerulosclerosis due to heavy chain deposition disease (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
4552726011 Nodular glomerulosclerosis with heavy chain deposition disease en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
7708961000241117 glomérulosclérose nodulaire due à une maladie des dépôts de chaines lourdes fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module

0 descendants.

Expanded Value Set

Outbound Relationships Type Target Active Characteristic Refinability Group Values
Nodular glomerulosclerosis due to heavy chain deposition disease Due to Heavy chain disease false Inferred relationship Some 2
Nodular glomerulosclerosis due to heavy chain deposition disease Associated morphology Nodular glomerulosclerosis (morphologic abnormality) true Inferred relationship Some 1
Nodular glomerulosclerosis due to heavy chain deposition disease Is a Glomerulosclerosis true Inferred relationship Some
Nodular glomerulosclerosis due to heavy chain deposition disease Finding site Glomerulus structure true Inferred relationship Some 1
Nodular glomerulosclerosis due to heavy chain deposition disease Is a Glomerular disease due to neoplastic disease true Inferred relationship Some
Nodular glomerulosclerosis due to heavy chain deposition disease Due to 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. true Inferred relationship Some 2
Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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