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

SNOMED CT Concept\Clinical finding (finding)\...

\Procedure related finding\Evaluation finding\Measurement finding\...

\Finding of substance level (finding)\Finding of blood substance level (finding)\Blood substance level above reference range\Gammopathy\Disorder of increased production of immunoglobulin protein (disorder)\Monoclonal gammopathy (disorder)\Light chain disease\AL amyloidosis\Primary systemic amyloidosis associated with occult plasma cell dyscrasia
\Finding of substance level (finding)\Finding of blood substance level (finding)\Finding of protein in serum or plasma\Gammopathy\Disorder of increased production of immunoglobulin protein (disorder)\Monoclonal gammopathy (disorder)\Light chain disease\AL amyloidosis\Primary systemic amyloidosis associated with occult plasma cell dyscrasia
\Finding of substance level (finding)\Finding of protein level (finding)\Finding of paraprotein measurement\Paraprotein detected (finding)\Monoclonal gammopathy (disorder)\Light chain disease\AL amyloidosis\Primary systemic amyloidosis associated with occult plasma cell dyscrasia
\Finding of substance level (finding)\Finding of protein level (finding)\Finding of protein in serum or plasma\Gammopathy\Disorder of increased production of immunoglobulin protein (disorder)\Monoclonal gammopathy (disorder)\Light chain disease\AL amyloidosis\Primary systemic amyloidosis associated with occult plasma cell dyscrasia
\Finding of substance level (finding)\Finding of protein level (finding)\Globulin level - finding\Globulin level outside reference range (finding)\Globulin above reference range\Gammopathy\Disorder of increased production of immunoglobulin protein (disorder)\Monoclonal gammopathy (disorder)\Light chain disease\AL amyloidosis\Primary systemic amyloidosis associated with occult plasma cell dyscrasia
\Finding of substance level (finding)\Finding of protein level (finding)\Finding of immunoglobulin level (finding)\Immunoglobulins outside reference range\Increased immunoglobulin\Disorder of increased production of immunoglobulin protein (disorder)\Monoclonal gammopathy (disorder)\Light chain disease\AL amyloidosis\Primary systemic amyloidosis associated with occult plasma cell dyscrasia

\Measurement finding outside reference range\Measurement finding above reference range (finding)\Blood substance level above reference range\Gammopathy\Disorder of increased production of immunoglobulin protein (disorder)\Monoclonal gammopathy (disorder)\Light chain disease\AL amyloidosis\Primary systemic amyloidosis associated with occult plasma cell dyscrasia
\Measurement finding outside reference range\Measurement finding above reference range (finding)\Increased immunoglobulin\Disorder of increased production of immunoglobulin protein (disorder)\Monoclonal gammopathy (disorder)\Light chain disease\AL amyloidosis\Primary systemic amyloidosis associated with occult plasma cell dyscrasia
\Measurement finding outside reference range\Measurement finding above reference range (finding)\Globulin above reference range\Gammopathy\Disorder of increased production of immunoglobulin protein (disorder)\Monoclonal gammopathy (disorder)\Light chain disease\AL amyloidosis\Primary systemic amyloidosis associated with occult plasma cell dyscrasia
\Measurement finding outside reference range\Immunoglobulins outside reference range\Increased immunoglobulin\Disorder of increased production of immunoglobulin protein (disorder)\Monoclonal gammopathy (disorder)\Light chain disease\AL amyloidosis\Primary systemic amyloidosis associated with occult plasma cell dyscrasia
\Measurement finding outside reference range\Globulin level outside reference range (finding)\Globulin above reference range\Gammopathy\Disorder of increased production of immunoglobulin protein (disorder)\Monoclonal gammopathy (disorder)\Light chain disease\AL amyloidosis\Primary systemic amyloidosis associated with occult plasma cell dyscrasia

\Detected by measurement\Paraprotein detected (finding)\Monoclonal gammopathy (disorder)\Light chain disease\AL amyloidosis\Primary systemic amyloidosis associated with occult plasma cell dyscrasia

\Disease\Disorder of immune function (disorder)\Gammopathy\Disorder of increased production of immunoglobulin protein (disorder)\Monoclonal gammopathy (disorder)\Light chain disease\AL amyloidosis\Primary systemic amyloidosis associated with occult plasma cell dyscrasia
\Disease\Amyloidosis\AL amyloidosis\Primary systemic amyloidosis associated with occult plasma cell dyscrasia

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

Descriptions:

Id Description Lang Type Status Case? Module

1781593012 Primary systemic amyloidosis associated with occult plasma cell dyscrasia en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core

3874053014 Primary systemic amyloidosis due to occult plasma cell dyscrasia (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core

3874054015 Primary systemic amyloidosis due to occult plasma cell dyscrasia en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core

1770378010 Primary systemic amyloidosis associated with occult plasma cell dyscrasia (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core

1770378010 Primary systemic amyloidosis associated with occult plasma cell dyscrasia (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core

1781593012 Primary systemic amyloidosis associated with occult plasma cell dyscrasia en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core

1781593012 Primary systemic amyloidosis associated with occult plasma cell dyscrasia en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core

3874053014 Primary systemic amyloidosis due to occult plasma cell dyscrasia (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core

3874054015 Primary systemic amyloidosis due to occult plasma cell dyscrasia en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core

Expanded Value Set

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

Inbound Relationships

Type

Active

Source

Characteristic

Refinability

Group

Reference Sets

GB English

US English

Back to Start

Id	Description	Lang	Type	Status	Case?	Module
1781593012	Primary systemic amyloidosis associated with occult plasma cell dyscrasia	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
3874053014	Primary systemic amyloidosis due to occult plasma cell dyscrasia (disorder)	en	Fully specified name	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
3874054015	Primary systemic amyloidosis due to occult plasma cell dyscrasia	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
1770378010	Primary systemic amyloidosis associated with occult plasma cell dyscrasia (disorder)	en	Fully specified name	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
1770378010	Primary systemic amyloidosis associated with occult plasma cell dyscrasia (disorder)	en	Fully specified name	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
1781593012	Primary systemic amyloidosis associated with occult plasma cell dyscrasia	en	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
1781593012	Primary systemic amyloidosis associated with occult plasma cell dyscrasia	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
3874053014	Primary systemic amyloidosis due to occult plasma cell dyscrasia (disorder)	en	Fully specified name	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
3874054015	Primary systemic amyloidosis due to occult plasma cell dyscrasia	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core