Status: current, Primitive. Date: 31-Jan 2002. Module: SNOMED CT core
Descriptions:
| Id | Description | Lang | Type | Status | Case? | Module |
| 4553711018 | GM2 gangliosidosis (disorder) | en | Fully specified name | Active | Case sensitive | SNOMED CT core |
| 485484018 | GM2 gangliosidosis | en | Synonym | Active | Case sensitive | SNOMED CT core |
| 55591012 | Deficiency of beta-N-acetylhexosaminidase isoenzymes | en | Synonym | Active | Initial character case insensitive | SNOMED CT core |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| GM2 gangliosidosis | Is a | Gangliosidosis | true | Inferred relationship | Some | ||
| GM2 gangliosidosis | Occurrence | Congenital | true | Inferred relationship | Some | 1 | |
| GM2 gangliosidosis | Finding site | Structure of nervous system | true | Inferred relationship | Some | 2 |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
| Retinal dystrophy due to GM2 gangliosidosis | Due to | True | GM2 gangliosidosis | Inferred relationship | Some | 2 |
| Dystonia due to GM2 gangliosidosis | Due to | True | GM2 gangliosidosis | Inferred relationship | Some | 2 |
| Sandhoff disease | Is a | True | GM2 gangliosidosis | Inferred relationship | Some | |
| Adult chronic GM2 gangliosidosis | Is a | True | GM2 gangliosidosis | Inferred relationship | Some | |
| Infantile GM2 gangliosidosis | Is a | True | GM2 gangliosidosis | Inferred relationship | Some | |
| Juvenile GM2 gangliosidosis | Is a | True | GM2 gangliosidosis | Inferred relationship | Some | |
| Tay-Sachs disease | Is a | True | GM2 gangliosidosis | Inferred relationship | Some |
Reference Sets
Australian emergency department reference set
Clinical finding foundation reference set
Australian dialect reference set
Problem/Diagnosis reference set
Description inactivation indicator reference set
FHIR