Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Jan 2002. Module: SNOMED CT core module
Descriptions:
| Id | Description | Lang | Type | Status | Case? | Module |
| 118325010 | Tay-Sachs disease, variant AB | en | Synonym | Active | Entire term case sensitive | SNOMED CT core module |
| 118326011 | Hexosaminidase activator deficiency | en | Synonym | Active | Entire term case insensitive | SNOMED CT core module |
| 118327019 | GM>2< gangliosidosis, type AB | en | Synonym | Active | Entire term case sensitive | SNOMED CT core module |
| 811399010 | Tay-Sachs disease, variant AB (disorder) | en | Fully specified name | Active | Entire term case sensitive | SNOMED CT core module |
| 1233370019 | GM2 activator deficiency | en | Synonym | Active | Entire term case sensitive | SNOMED CT core module |
| 1233371015 | AB variant | en | Synonym | Active | Entire term case sensitive | SNOMED CT core module |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| Tay-Sachs disease, variant AB | Is a | Tay-Sachs disease | true | Inferred relationship | Existential restriction modifier | ||
| Tay-Sachs disease, variant AB | Occurrence | Congenital | true | Inferred relationship | Existential restriction modifier | 1 | |
| Tay-Sachs disease, variant AB | Finding site | Structure of nervous system | true | Inferred relationship | Existential restriction modifier | 2 |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
This concept is not in any reference sets
FHIR