Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Jan 2017. Module: SNOMED CT core module
Descriptions:
Id | Description | Lang | Type | Status | Case? | Module |
3313728015 | CDG2G - carbohydrate deficient glycoprotein syndrome type 2G | en | Synonym | Active | Entire term case sensitive | SNOMED CT core module |
3313736012 | Carbohydrate deficient glycoprotein syndrome type 2g | en | Synonym | Active | Entire term case insensitive | SNOMED CT core module |
3313737015 | Carbohydrate deficient glycoprotein syndrome type IIg | en | Synonym | Active | Only initial character case insensitive | SNOMED CT core module |
3323076014 | Component of oligomeric golgi complex 1 congenital disorder of glycosylation (disorder) | en | Fully specified name | Active | Entire term case insensitive | SNOMED CT core module |
3323077017 | COG1 congenital disorder of glycosylation | en | Synonym | Active | Entire term case sensitive | SNOMED CT core module |
3324357013 | COG1 (component of oligomeric golgi complex 1) congenital disorder of glycosylation | en | Synonym | Active | Entire term case sensitive | SNOMED CT core module |
3324358015 | Congenital disorder of glycosylation type IIg | en | Synonym | Active | Only initial character case insensitive | SNOMED CT core module |
3327884010 | Component of oligomeric golgi complex 1 congenital disorder of glycosylation | en | Synonym | Active | Entire term case insensitive | SNOMED CT core module |
Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
Component of oligomeric golgi complex 1 congenital disorder of glycosylation | Is a | Autosomal recessive hereditary disorder | true | Inferred relationship | Existential restriction modifier | ||
Component of oligomeric golgi complex 1 congenital disorder of glycosylation | Is a | Carbohydrate-deficient glycoprotein syndrome type II | true | Inferred relationship | Existential restriction modifier | ||
Component of oligomeric golgi complex 1 congenital disorder of glycosylation | Occurrence | Congenital | true | Inferred relationship | Existential restriction modifier | 1 |
Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
This concept is not in any reference sets