Status: current, Sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2022. Module: SNOMED CT core
Descriptions:
| Id | Description | Lang | Type | Status | Case? | Module |
| 4674116014 | Retinal dystrophy due to GM2 gangliosidosis | en | Synonym (core metadata concept) | Active | Only initial character case insensitive (core metadata concept) | SNOMED CT core |
| 4674524010 | Dystrophy of retina due to GM2 gangliosidosis | en | Synonym (core metadata concept) | Active | Only initial character case insensitive (core metadata concept) | SNOMED CT core |
| 4674525011 | Dystrophy of retina due to GM2 gangliosidosis (disorder) | en | Fully specified name | Active | Only initial character case insensitive (core metadata concept) | SNOMED CT core |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| Retinal dystrophy due to GM2 gangliosidosis | est un(e) (attribut) | Retinal dystrophy | true | Inferred relationship | Some | ||
| Retinal dystrophy due to GM2 gangliosidosis | Due to | gangliosidose à GM2 | true | Inferred relationship | Some | 2 | |
| Retinal dystrophy due to GM2 gangliosidosis | localisation d'une constatation (attribut) | structure de la rétine | true | Inferred relationship | Some | 1 | |
| Retinal dystrophy due to GM2 gangliosidosis | morphologie associée (attribut) | Dystrophy (morphologic abnormality) | true | Inferred relationship | Some | 1 |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
This concept is not in any reference sets
FHIR