402452001: Primary systemic (AL fibril type) amyloidosis (disorder)

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

Descriptions:

Id Description Lang Type Status Case? Module

1770376014 Primary systemic (AL fibril type) amyloidosis (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core

1781591014 Primary systemic (AL fibril type) amyloidosis en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core

1770376014 Primary systemic (AL fibril type) amyloidosis (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core

1781591014 Primary systemic (AL fibril type) amyloidosis en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
Primary systemic (AL fibril type) amyloidosis	Is a	Systemic amyloidosis affecting skin (disorder)	false	Inferred relationship	Existential restriction modifier (core metadata concept)
Primary systemic (AL fibril type) amyloidosis	Associated morphology	Amyloid deposition	false	Inferred relationship	Existential restriction modifier (core metadata concept)
Primary systemic (AL fibril type) amyloidosis	Finding site	Skin structure	false	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Primary systemic (AL fibril type) amyloidosis	Associated morphology	Focal amyloid	false	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Primary systemic (AL fibril type) amyloidosis	Finding site	Skin structure	false	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Primary systemic (AL fibril type) amyloidosis	Associated morphology	Focal amyloid	false	Inferred relationship	Existential restriction modifier (core metadata concept)	1

Inbound Relationships	Type	Active	Source	Characteristic	Refinability	Group
Amyloid light chain amyloidosis due to multiple myeloma (disorder)	Is a	False	Primary systemic (AL fibril type) amyloidosis	Inferred relationship	Existential restriction modifier (core metadata concept)
Primary systemic amyloidosis associated with occult plasma cell dyscrasia	Is a	False	Primary systemic (AL fibril type) amyloidosis	Inferred relationship	Existential restriction modifier (core metadata concept)
Macroglossia due to amyloidosis (disorder)	Is a	False	Primary systemic (AL fibril type) amyloidosis	Inferred relationship	Existential restriction modifier (core metadata concept)
Pseudoscleroderma due to amyloid light-chain amyloidosis	Is a	False	Primary systemic (AL fibril type) amyloidosis	Inferred relationship	Existential restriction modifier (core metadata concept)

Reference Sets

Concept inactivation indicator attribute value reference set (foundation metadata concept)

SAME AS association reference set (foundation metadata concept)