FHIR © HL7.org  |  Server Home  |  FHIR Server FHIR Server 3.7.4-SNAPSHOT  |  FHIR Version n/a  User: [n/a]

829971006: Non-amyloid monoclonal immunoglobulin deposition disease (disorder)

Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2020. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
3880130012 Non-amyloid monoclonal immunoglobulin deposition disease (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
3880131011 Non-amyloid monoclonal immunoglobulin deposition disease en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
3880132016 Randall disease en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
3880133014 Non-amyloid MIDD (monoclonal immunoglobulin deposition disease) en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
5408854012 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. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
5408855013 A rare, secondary glomerular disease characterised by proteinuria, dysproteinaemias, 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 organisation and are negative for Congo red staining. Associated signs and symptoms depend on the involvement of other organs, liver, heart, nerve fibres, gastrointestinal tract, or skin. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
3880130012 Non-amyloid monoclonal immunoglobulin deposition disease (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
3880131011 Non-amyloid monoclonal immunoglobulin deposition disease en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
3880132016 Randall disease en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
3880133014 Non-amyloid MIDD (monoclonal immunoglobulin deposition disease) en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
3880134015 A rare secondary glomerular disease characterized by proteinuria, dysproteinemia, 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. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
3880135019 A rare secondary glomerular disease characterised by proteinuria, dysproteinaemia, 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 organisation and are negative for Congo red staining. Associated signs and symptoms depend on the involvement of other organs, liver, heart, nerve fibres, gastrointestinal tract or skin. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
5408854012 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. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
5408855013 A rare, secondary glomerular disease characterised by proteinuria, dysproteinaemias, 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 organisation and are negative for Congo red staining. Associated signs and symptoms depend on the involvement of other organs, liver, heart, nerve fibres, gastrointestinal tract, or skin. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
3424331001000118 Monoklonale Immunglobulin-Ablagerungskrankheit de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
6407511000241116 maladie des dépôts d'immunoglobuline monoclonale non amyloïde fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
6407521000241111 MDIM (maladie des dépôts d'immunoglobuline monoclonale) non amyloïde fr Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
6407531000241113 maladie de Randall fr Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
6407511000241116 maladie des dépôts d'immunoglobuline monoclonale non amyloïde fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
6407521000241111 MDIM (maladie des dépôts d'immunoglobuline monoclonale) non amyloïde fr Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
6407531000241113 maladie de Randall fr Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
3424331001000118 Monoklonale Immunglobulin-Ablagerungskrankheit de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module

1 descendants. Search Descendants:

Expanded Value Set

Outbound Relationships Type Target Active Characteristic Refinability Group Values
Non-amyloid monoclonal immunoglobulin deposition disease (disorder) Is a Glomerular disease true Inferred relationship Existential restriction modifier (core metadata concept)
Non-amyloid monoclonal immunoglobulin deposition disease (disorder) Finding site Glomerulus structure (body structure) true Inferred relationship Existential restriction modifier (core metadata concept) 1
Non-amyloid monoclonal immunoglobulin deposition disease (disorder) Interprets Serum globulin measurement true Inferred relationship Existential restriction modifier (core metadata concept) 2
Non-amyloid monoclonal immunoglobulin deposition disease (disorder) Has interpretation Above reference range true Inferred relationship Existential restriction modifier (core metadata concept) 2
Non-amyloid monoclonal immunoglobulin deposition disease (disorder) Interprets Immunoglobulin measurement true Inferred relationship Existential restriction modifier (core metadata concept) 3
Non-amyloid monoclonal immunoglobulin deposition disease (disorder) Has interpretation Above reference range true Inferred relationship Existential restriction modifier (core metadata concept) 3
Non-amyloid monoclonal immunoglobulin deposition disease (disorder) Has interpretation Present (qualifier value) false Inferred relationship Existential restriction modifier (core metadata concept) 4
Non-amyloid monoclonal immunoglobulin deposition disease (disorder) Interprets Paraprotein measurement true Inferred relationship Existential restriction modifier (core metadata concept) 4
Non-amyloid monoclonal immunoglobulin deposition disease (disorder) Is a Plasma cell neoplasm true Inferred relationship Existential restriction modifier (core metadata concept)
Non-amyloid monoclonal immunoglobulin deposition disease (disorder) Is a Neoplasm of uncertain behavior of kidney (disorder) true Inferred relationship Existential restriction modifier (core metadata concept)
Non-amyloid monoclonal immunoglobulin deposition disease (disorder) Is a Hematologic neoplasm of uncertain behavior true Inferred relationship Existential restriction modifier (core metadata concept)
Non-amyloid monoclonal immunoglobulin deposition disease (disorder) Is a Monoclonal gammopathy (disorder) true Inferred relationship Existential restriction modifier (core metadata concept)
Non-amyloid monoclonal immunoglobulin deposition disease (disorder) Pathological process (attribute) Abnormal immune process (qualifier value) true Inferred relationship Existential restriction modifier (core metadata concept) 1
Non-amyloid monoclonal immunoglobulin deposition disease (disorder) Associated morphology Immunoglobulin deposition disease true Inferred relationship Existential restriction modifier (core metadata concept) 1
Non-amyloid monoclonal immunoglobulin deposition disease (disorder) Is a Neoplasm of parenchyma of kidney (disorder) true Inferred relationship Existential restriction modifier (core metadata concept)
Non-amyloid monoclonal immunoglobulin deposition disease (disorder) Has interpretation Detected (qualifier value) true Inferred relationship Existential restriction modifier (core metadata concept) 4
Inbound Relationships Type Active Source Characteristic Refinability Group
Heavy chain deposition disease Is a True Non-amyloid monoclonal immunoglobulin deposition disease (disorder) Inferred relationship Existential restriction modifier (core metadata concept)

Reference Sets

Component annotation with string value reference set (foundation metadata concept)

Back to Start