Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Jul 2017. Module: SNOMED CT core module
Descriptions:
| Id | Description | Lang | Type | Status | Case? | Module |
| 3464819018 | Carbohydrate deficient glycoprotein syndrome type 2k (disorder) | en | Fully specified name | Active | Only initial character case insensitive | SNOMED CT core module |
| 3464820012 | Carbohydrate deficient glycoprotein syndrome type 2k | en | Synonym | Active | Only initial character case insensitive | SNOMED CT core module |
| 3464821011 | Carbohydrate deficient glycoprotein syndrome type IIk | en | Synonym | Active | Only initial character case insensitive | SNOMED CT core module |
| 3464822016 | Congenital disorder of glycosylation type 2k | en | Synonym | Active | Only initial character case insensitive | SNOMED CT core module |
| 3464823014 | Congenital disorder of glycosylation type IIk | en | Synonym | Active | Only initial character case insensitive | SNOMED CT core module |
| 3464824015 | TMEM165-CDG - transmembrane protein 165 congenital disorder of glycosylation | en | Synonym | Active | Entire term case sensitive | SNOMED CT core module |
| 3464825019 | Transmembrane protein 165 congenital disorder of glycosylation | en | Synonym | Active | Entire term case insensitive | SNOMED CT core module |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| Carbohydrate deficient glycoprotein syndrome type 2k | Is a | Autosomal recessive hereditary disorder | true | Inferred relationship | Existential restriction modifier | ||
| Carbohydrate deficient glycoprotein syndrome type 2k | Is a | Carbohydrate-deficient glycoprotein syndrome type II | true | Inferred relationship | Existential restriction modifier | ||
| Carbohydrate deficient glycoprotein syndrome type 2k | 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
FHIR