Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2002. Module: SNOMED CT core
Descriptions:
| Id | Description | Lang | Type | Status | Case? | Module |
| 1009151000172119 | gangliosidose à GM2 | fr | Synonym (core metadata concept) | Active | Entire term case sensitive (core metadata concept) | SNOMED CT Common French translation module (core metadata concept) |
| 418481000241113 | gangliosidose à GM2 (trouble) | fr | Fully specified name | Active | Entire term case sensitive (core metadata concept) | SNOMED CT Common French translation module (core metadata concept) |
| 4553711018 | GM2 gangliosidosis (disorder) | en | Fully specified name | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
| 485484018 | GM2 gangliosidosis | en | Synonym (core metadata concept) | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
| 55591012 | Deficiency of beta-N-acetylhexosaminidase isoenzymes | en | Synonym (core metadata concept) | Active | Only initial character case insensitive (core metadata concept) | SNOMED CT core |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| gangliosidose à GM2 | est un(e) (attribut) | gangliosidose (trouble) | true | Inferred relationship | Some | ||
| gangliosidose à GM2 | survenue (attribut) | congénital | true | Inferred relationship | Some | 1 | |
| gangliosidose à GM2 | localisation d'une constatation (attribut) | système nerveux | true | Inferred relationship | Some | 2 |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
| Retinal dystrophy due to GM2 gangliosidosis | Due to | True | gangliosidose à GM2 | Inferred relationship | Some | 2 |
| Sandhoff disease | est un(e) (attribut) | True | gangliosidose à GM2 | Inferred relationship | Some | |
| Adult chronic GM2 gangliosidosis (disorder) | est un(e) (attribut) | True | gangliosidose à GM2 | Inferred relationship | Some | |
| Infantile GM2 gangliosidosis (disorder) | est un(e) (attribut) | True | gangliosidose à GM2 | Inferred relationship | Some | |
| Juvenile GM2 gangliosidosis (disorder) | est un(e) (attribut) | True | gangliosidose à GM2 | Inferred relationship | Some | |
| Tay-Sachs disease | est un(e) (attribut) | True | gangliosidose à GM2 | Inferred relationship | Some |
Reference Sets
Canada English language reference set (foundation metadata concept)
FHIR