237869003: Localized hereditary amyloidosis (disorder)

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

\Genetic disease\Hereditary disease\Hereditary amyloidosis (disorder)\Localized hereditary amyloidosis (disorder)

\Amyloidosis\Hereditary amyloidosis (disorder)\Localized hereditary amyloidosis (disorder)
\Amyloidosis\Localized amyloidosis\Localized hereditary amyloidosis (disorder)

Status: current, 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

356477010 Organ limited hereditary amyloidosis en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core

356478017 Localised hereditary amyloidosis en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core

356479013 Localized hereditary amyloidosis en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core

626660014 Localized hereditary amyloidosis (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core

356477010 Organ limited hereditary amyloidosis en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core

356477010 Organ limited hereditary amyloidosis en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core

356478017 Localised hereditary amyloidosis en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core

356478017 Localised hereditary amyloidosis en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core

356479013 Localized hereditary amyloidosis en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core

356479013 Localized hereditary amyloidosis en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core

626660014 Localized hereditary amyloidosis (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core

626660014 Localized hereditary amyloidosis (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core

6362321000241114 amylose localisée de forme héréditaire fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module

6362331000241111 amyloïdose localisée de forme héréditaire fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module

6362321000241114 amylose localisée de forme héréditaire fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module

6362331000241111 amyloïdose localisée de forme héréditaire fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
Localized hereditary amyloidosis (disorder)	Is a	Localized amyloidosis	true	Inferred relationship	Existential restriction modifier (core metadata concept)
Localized hereditary amyloidosis (disorder)	Finding site	Body system structure	false	Inferred relationship	Existential restriction modifier (core metadata concept)
Localized hereditary amyloidosis (disorder)	Associated morphology	Amyloid deposition	false	Inferred relationship	Existential restriction modifier (core metadata concept)
Localized hereditary amyloidosis (disorder)	Associated morphology	Focal amyloid	true	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Localized hereditary amyloidosis (disorder)	Is a	Hereditary amyloidosis (disorder)	true	Inferred relationship	Existential restriction modifier (core metadata concept)

Inbound Relationships	Type	Active	Source	Characteristic	Refinability	Group
Familial lichen amyloidosis	Is a	True	Localized hereditary amyloidosis (disorder)	Inferred relationship	Existential restriction modifier (core metadata concept)
Papular cutaneous amyloid	Is a	False	Localized hereditary amyloidosis (disorder)	Inferred relationship	Existential restriction modifier (core metadata concept)
Poikilodermal cutaneous amyloid	Is a	True	Localized hereditary amyloidosis (disorder)	Inferred relationship	Existential restriction modifier (core metadata concept)
Hereditary cerebral amyloid angiopathy, Icelandic type	Is a	False	Localized hereditary amyloidosis (disorder)	Inferred relationship	Existential restriction modifier (core metadata concept)
Hereditary cerebral hemorrhage with amyloidosis (disorder)	Is a	True	Localized hereditary amyloidosis (disorder)	Inferred relationship	Existential restriction modifier (core metadata concept)
Lattice corneal dystrophy	Is a	True	Localized hereditary amyloidosis (disorder)	Inferred relationship	Existential restriction modifier (core metadata concept)
Localized hereditary amyloidosis of heart (disorder)	Is a	True	Localized hereditary amyloidosis (disorder)	Inferred relationship	Existential restriction modifier (core metadata concept)

Reference Sets