Status: current, Sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2017. Module: SNOMED CT core
Descriptions:
| Id | Description | Lang | Type | Status | Case? | Module |
| 3482130011 | Hereditary amyloidosis (disorder) | en | Fully specified name | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 3482131010 | Hereditary amyloidosis | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 792161000241118 | amylose héréditaire (trouble) | fr | Fully specified name | Active | Entire term case insensitive (core metadata concept) | SNOMED CT Common French translation module (core metadata concept) |
| 951831000172119 | amylose héréditaire | fr | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT Common French translation module (core metadata concept) |
| 976291000172110 | amyloïdose héréditaire | fr | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT Common French translation module (core metadata concept) |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| Hereditary amyloidosis (disorder) | morphologie associée (attribut) | Amyloid deposition | true | Inferred relationship | Some | 1 | |
| Hereditary amyloidosis (disorder) | est un(e) (attribut) | Amyloidosis | true | Inferred relationship | Some | ||
| Hereditary amyloidosis (disorder) | est un(e) (attribut) | maladie héréditaire | true | Inferred relationship | Some |
This concept is not in any reference sets
FHIR