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 |
3773565011 | Merosin-negative congenital muscular dystrophy | en | Synonym | Active | Entire term case insensitive | SNOMED CT core module |
3773566012 | Congenital muscular dystrophy type 1A | en | Synonym | Active | Only initial character case insensitive | SNOMED CT core module |
3773567015 | CMD1A - congenital muscular dystrophy type 1A | en | Synonym | Active | Entire term case sensitive | SNOMED CT core module |
3773568013 | Congenital muscular dystrophy due to laminin alpha2 deficiency | en | Synonym | Active | Entire term case insensitive | SNOMED CT core module |
3773569017 | Congenital muscular dystrophy type 1A (disorder) | en | Fully specified name | Active | Only initial character case insensitive | SNOMED CT core module |
3773570016 | MCD1A - muscular congenital dystrophy type 1A | en | Synonym | Active | Entire term case sensitive | SNOMED CT core module |
Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
This concept is not in any reference sets