237869003: Localized hereditary amyloidosis (disorder)

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

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

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

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

2929561000005113 lokaliseret hereditær amyloidose da Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) Danish module (core metadata concept)

Expanded Value Set

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

Inbound Relationships	Type	Active	Source	Characteristic	Refinability	Group
Familial lichen amyloidosis	Is a	True	Localised hereditary amyloidosis	Inferred relationship	Some
Papuløs kutan amyloid	Is a	False	Localised hereditary amyloidosis	Inferred relationship	Some
Poikilodermal cutaneous amyloid	Is a	True	Localised hereditary amyloidosis	Inferred relationship	Some
Hereditary cerebral amyloid angiopathy, Icelandic type	Is a	False	Localised hereditary amyloidosis	Inferred relationship	Some
A rare genetic cerebral small vessel disease characterized by amyloid deposition in the cerebral blood vessels leading to predominantly hemorrhagic strokes, focal neurological deficits, and progressive cognitive decline eventually leading to dementia.	Is a	True	Localised hereditary amyloidosis	Inferred relationship	Some
Lattice corneal dystrophy (disorder)	Is a	True	Localised hereditary amyloidosis	Inferred relationship	Some
Localised hereditary cardiac amyloidosis	Is a	True	Localised hereditary amyloidosis	Inferred relationship	Some

Reference Sets