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 |
| 296986019 | B variant hexosaminidase A deficiency | en | Synonym | Active | Entire term case sensitive | SNOMED CT core module |
| 576606015 | B variant hexosaminidase A deficiency (disorder) | en | Fully specified name | Active | Entire term case sensitive | SNOMED CT core module |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| B variant hexosaminidase A deficiency | Is a | Tay-Sachs disease | true | Inferred relationship | Existential restriction modifier | ||
| B variant hexosaminidase A deficiency | Occurrence | Congenital | true | Inferred relationship | Existential restriction modifier | 1 | |
| B variant hexosaminidase A deficiency | Finding site | Structure of nervous system | true | Inferred relationship | Existential restriction modifier | 2 |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
| B variant hexosaminidase A deficiency - infantile | Is a | True | B variant hexosaminidase A deficiency | Inferred relationship | Existential restriction modifier | |
| B variant hexosaminidase A deficiency - juvenile | Is a | True | B variant hexosaminidase A deficiency | Inferred relationship | Existential restriction modifier | |
| B variant hexosaminidase A deficiency - adult | Is a | True | B variant hexosaminidase A deficiency | Inferred relationship | Existential restriction modifier |
This concept is not in any reference sets
FHIR