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 |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| Localised hereditary amyloidosis | est un(e) (attribut) | Hereditary amyloidosis (disorder) | true | Inferred relationship | Some | ||
| Localised hereditary amyloidosis | morphologie associée (attribut) | Focal amyloid (morphologic abnormality) | true | Inferred relationship | Some | 1 | |
| Localised hereditary amyloidosis | localisation d'une constatation (attribut) | structure d'un système corporel | false | Inferred relationship | Some | ||
| Localised hereditary amyloidosis | morphologie associée (attribut) | Amyloid deposition | false | Inferred relationship | Some | ||
| Localised hereditary amyloidosis | est un(e) (attribut) | amyloïdose localisée | true | Inferred relationship | Some |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
| Lattice corneal dystrophy | est un(e) (attribut) | True | Localised hereditary amyloidosis | Inferred relationship | Some | |
| Localised hereditary cardiac amyloidosis | est un(e) (attribut) | True | Localised hereditary amyloidosis | Inferred relationship | Some | |
| Hereditary cerebral amyloid angiopathy, Icelandic type | est un(e) (attribut) | False | Localised hereditary amyloidosis | Inferred relationship | Some | |
| Familial lichen amyloidosis | est un(e) (attribut) | True | Localised hereditary amyloidosis | Inferred relationship | Some | |
| Papular cutaneous amyloid | est un(e) (attribut) | False | Localised hereditary amyloidosis | Inferred relationship | Some | |
| Poikilodermal cutaneous amyloid | est un(e) (attribut) | True | Localised hereditary amyloidosis | Inferred relationship | Some | |
| Hereditary cerebral hemorrhage with amyloidosis (disorder) | est un(e) (attribut) | True | Localised hereditary amyloidosis | Inferred relationship | Some |
Reference Sets
Canada English language reference set (foundation metadata concept)
Description inactivation indicator reference set
FHIR