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237869003: 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
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

9 descendants. Search Descendants:

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
Papular cutaneous 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

GB English

US English

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