Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Jan 2019. Module: SNOMED CT core module
Descriptions:
| Id | Description | Lang | Type | Status | Case? | Module |
| 3706585011 | SLC35A2-CDG - solute carrier family 35 member A2 congenital disorder of glycosylation | en | Synonym | Active | Entire term case sensitive | SNOMED CT core module |
| 3706586012 | Congenital disorder of glycosylation type 2m | en | Synonym | Active | Only initial character case insensitive | SNOMED CT core module |
| 3706587015 | Solute carrier family 35 member A2 congenital disorder of glycosylation (disorder) | en | Fully specified name | Active | Only initial character case insensitive | SNOMED CT core module |
| 3706588013 | Congenital disorder of glycosylation type IIm | en | Synonym | Active | Only initial character case insensitive | SNOMED CT core module |
| 3706589017 | Solute carrier family 35 member A2 congenital disorder of glycosylation | en | Synonym | Active | Only initial character case insensitive | SNOMED CT core module |
| 3706590014 | CDG2M - congenital disorder of glycosylation type 2m | en | Synonym | Active | Entire term case sensitive | SNOMED CT core module |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| Solute carrier family 35 member A2 congenital disorder of glycosylation | Is a | X-linked hereditary disease | true | Inferred relationship | Existential restriction modifier | ||
| Solute carrier family 35 member A2 congenital disorder of glycosylation | Finding site | Brain structure | true | Inferred relationship | Existential restriction modifier | 1 | |
| Solute carrier family 35 member A2 congenital disorder of glycosylation | Occurrence | Congenital | true | Inferred relationship | Existential restriction modifier | 1 | |
| Solute carrier family 35 member A2 congenital disorder of glycosylation | Is a | Carbohydrate-deficient glycoprotein syndrome type II | true | Inferred relationship | Existential restriction modifier | ||
| Solute carrier family 35 member A2 congenital disorder of glycosylation | Is a | Hereditary disorder of nervous system | false | Inferred relationship | Existential restriction modifier | ||
| Solute carrier family 35 member A2 congenital disorder of glycosylation | Is a | Metabolic encephalopathy | true | Inferred relationship | Existential restriction modifier | ||
| Solute carrier family 35 member A2 congenital disorder of glycosylation | Is a | Inherited metabolic disorder of nervous system | true | Inferred relationship | Existential restriction modifier |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
This concept is not in any reference sets
FHIR