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402454000: Primary systemic amyloidosis due to occult plasma cell dyscrasia (disorder)


Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Jul 2003. Module: SNOMED CT core module

Descriptions:

Id Description Lang Type Status Case? Module
1781593012 Primary systemic amyloidosis associated with occult plasma cell dyscrasia en Synonym Active Entire term case insensitive SNOMED CT core module
3874053014 Primary systemic amyloidosis due to occult plasma cell dyscrasia (disorder) en Fully specified name Active Entire term case insensitive SNOMED CT core module
3874054015 Primary systemic amyloidosis due to occult plasma cell dyscrasia en Synonym Active Entire term case insensitive SNOMED CT core module


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Primary systemic amyloidosis due to occult plasma cell dyscrasia Is a Primary systemic (AL fibril type) amyloidosis false Inferred relationship Existential restriction modifier
Primary systemic amyloidosis due to occult plasma cell dyscrasia Associated morphology Amyloid deposition false Inferred relationship Existential restriction modifier
Primary systemic amyloidosis due to occult plasma cell dyscrasia Finding site Skin structure false Inferred relationship Existential restriction modifier 1
Primary systemic amyloidosis due to occult plasma cell dyscrasia Associated morphology Focal amyloid false Inferred relationship Existential restriction modifier 1
Primary systemic amyloidosis due to occult plasma cell dyscrasia Due to Plasma cell neoplasm true Inferred relationship Existential restriction modifier 2
Primary systemic amyloidosis due to occult plasma cell dyscrasia Associated morphology Focal amyloid false Inferred relationship Existential restriction modifier 2
Primary systemic amyloidosis due to occult plasma cell dyscrasia Finding site Skin structure false Inferred relationship Existential restriction modifier 2
Primary systemic amyloidosis due to occult plasma cell dyscrasia Is a Amyloid light-chain amyloidosis true Inferred relationship Existential restriction modifier
Primary systemic amyloidosis due to occult plasma cell dyscrasia Interprets Immunoglobulin measurement true Inferred relationship Existential restriction modifier 1
Primary systemic amyloidosis due to occult plasma cell dyscrasia Has interpretation Above reference range true Inferred relationship Existential restriction modifier 1
Primary systemic amyloidosis due to occult plasma cell dyscrasia Has interpretation Present true Inferred relationship Existential restriction modifier 3
Primary systemic amyloidosis due to occult plasma cell dyscrasia Interprets Paraprotein measurement true Inferred relationship Existential restriction modifier 3
Primary systemic amyloidosis due to occult plasma cell dyscrasia Associated morphology Amyloid deposition true Inferred relationship Existential restriction modifier 4
Primary systemic amyloidosis due to occult plasma cell dyscrasia Causative agent Immunoglobulin, light chain true Inferred relationship Existential restriction modifier 4
Primary systemic amyloidosis due to occult plasma cell dyscrasia Has interpretation Above reference range true Inferred relationship Existential restriction modifier 5
Primary systemic amyloidosis due to occult plasma cell dyscrasia Interprets Serum globulin measurement true Inferred relationship Existential restriction modifier 5
Primary systemic amyloidosis due to occult plasma cell dyscrasia Pathological process Abnormal immune process true Inferred relationship Existential restriction modifier 6

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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