Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Jul 2019. Module: SNOMED CT core module
Descriptions:
Id | Description | Lang | Type | Status | Case? | Module |
3757887011 | Hereditary gelsolin amyloidosis | en | Synonym | Active | Entire term case insensitive | SNOMED CT core module |
3757888018 | Familial amyloidosis Finnish type | en | Synonym | Active | Only initial character case insensitive | SNOMED CT core module |
3757889014 | AGel amyloidosis | en | Synonym | Active | Entire term case sensitive | SNOMED CT core module |
3757890017 | Hereditary amyloidosis Finnish type | en | Synonym | Active | Only initial character case insensitive | SNOMED CT core module |
3757891018 | Familial amyloid polyneuropathy type IV | en | Synonym | Active | Only initial character case insensitive | SNOMED CT core module |
3757892013 | Hereditary gelsolin amyloidosis (disorder) | en | Fully specified name | Active | Entire term case insensitive | SNOMED CT core module |
3757893015 | Gelsolin amyloidosis | en | Synonym | Active | Entire term case insensitive | SNOMED CT core module |
3788703014 | Lattice corneal dystrophy type II | en | Synonym | Active | Only initial character case insensitive | SNOMED CT core module |
Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
This concept is not in any reference sets