Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Jul 2018. Module: SNOMED CT core module
Descriptions:
Id | Description | Lang | Type | Status | Case? | Module |
3638504019 | Adrenomyodystrophy (disorder) | en | Fully specified name | Active | Entire term case insensitive | SNOMED CT core module |
3638505018 | Adrenomyodystrophy | en | Synonym | Active | Entire term case insensitive | SNOMED CT core module |
Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
Adrenomyodystrophy | Is a | X-linked hereditary disease | true | Inferred relationship | Existential restriction modifier | ||
Adrenomyodystrophy | Is a | Hereditary disorder of endocrine system | true | Inferred relationship | Existential restriction modifier | ||
Adrenomyodystrophy | Is a | Adrenal cortical hypofunction | true | Inferred relationship | Existential restriction modifier | ||
Adrenomyodystrophy | Occurrence | Congenital | false | Inferred relationship | Existential restriction modifier | 1 | |
Adrenomyodystrophy | Finding site | Adrenal cortex structure | true | Inferred relationship | Existential restriction modifier | 1 |
Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
This concept is not in any reference sets