Status: current, Defined. Date: 31-Jul 2020. Module: SNOMED CT core
Descriptions:
Id | Description | Lang | Type | Status | Case? | Module |
356477010 | Organ limited hereditary amyloidosis | en | Synonym | Active | Case insensitive | SNOMED CT core |
356478017 | Localised hereditary amyloidosis | en | Synonym | Active | Case insensitive | SNOMED CT core |
356479013 | Localized hereditary amyloidosis | en | Synonym | Active | Case insensitive | SNOMED CT core |
626660014 | Localized hereditary amyloidosis (disorder) | en | Fully specified name | Active | Case insensitive | SNOMED CT core |
Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
Localised hereditary amyloidosis | Is a | Hereditary amyloidosis | true | Inferred relationship | Some | ||
Localised hereditary amyloidosis | Associated morphology | Focal amyloid | true | Inferred relationship | Some | 1 | |
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 | Is a | Localised amyloidosis | true | Inferred relationship | Some |
Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
Lattice corneal dystrophy | Is a | True | Localised hereditary amyloidosis | Inferred relationship | Some | |
Localised hereditary cardiac amyloidosis | Is a | True | Localised hereditary amyloidosis | Inferred relationship | Some | |
Hereditary cerebral amyloid angiopathy, Icelandic type | Is a | False | Localised hereditary amyloidosis | Inferred relationship | Some | |
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 haemorrhage with amyloidosis | Is a | True | Localised hereditary amyloidosis | Inferred relationship | Some |
Reference Sets
Australian emergency department reference set
Clinical finding foundation reference set
Problem/Diagnosis reference set