Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Jul 2016. Module: SNOMED CT core module
Descriptions:
| Id | Description | Lang | Type | Status | Case? | Module |
| 3308700019 | Deficiency of monoamine oxidase A (disorder) | en | Fully specified name | Active | Only initial character case insensitive | SNOMED CT core module |
| 3310405019 | Deficiency of monoamine oxidase A | en | Synonym | Active | Only initial character case insensitive | SNOMED CT core module |
| 3311514018 | Monoamine oxidase A deficiency | en | Synonym | Active | Only initial character case insensitive | SNOMED CT core module |
| 3311515017 | Brunner syndrome | en | Synonym | Active | Entire term case sensitive | SNOMED CT core module |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| Deficiency of monoamine oxidase A | Is a | Inherited metabolic disorder of nervous system | true | Inferred relationship | Existential restriction modifier | ||
| Deficiency of monoamine oxidase A | Is a | X-linked hereditary disease | false | Inferred relationship | Existential restriction modifier | ||
| Deficiency of monoamine oxidase A | Is a | Deficiency of tyraminase | true | Inferred relationship | Existential restriction modifier | ||
| Deficiency of monoamine oxidase A | Occurrence | Congenital | true | Inferred relationship | Existential restriction modifier | 1 | |
| Deficiency of monoamine oxidase A | Finding site | Structure of nervous system | true | Inferred relationship | Existential restriction modifier | 2 | |
| Deficiency of monoamine oxidase A | Is a | X-linked recessive hereditary disease | true | Inferred relationship | Existential restriction modifier |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
This concept is not in any reference sets
FHIR