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 | 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 | |
| Hereditary cerebral hemorrhage with amyloidosis (disorder) | 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
FHIR