Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2018. Module: SNOMED CT core
Descriptions:
| Id | Description | Lang | Type | Status | Case? | Module |
| 3638504019 | Adrenomyodystrophy (disorder) | en | Fully specified name | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 3638505018 | Adrenomyodystrophy | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 3638506017 | An extremely rare genetic endocrine disease with characteristics of primary adrenal insufficiency, dystrophic myopathy, hepatic steatosis, severe psychomotor delay, megalocornea, failure to thrive, chronic constipation, and terminal bladder ectasia which can lead to death. There have been no further descriptions in the literature since 1982. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
| 4175721000052110 | adrenomyodystrofi | sv | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT Sweden NRC maintained module (core metadata concept) |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| Adrenomyodystrophy (disorder) | Is a | X-linked hereditary disease | true | Inferred relationship | Some | ||
| Adrenomyodystrophy (disorder) | Is a | Hereditary disorder of endocrine system (disorder) | true | Inferred relationship | Some | ||
| Adrenomyodystrophy (disorder) | Is a | Adrenal cortical hypofunction (disorder) | true | Inferred relationship | Some | ||
| Adrenomyodystrophy (disorder) | Occurrence | Congenital | false | Inferred relationship | Some | 1 | |
| Adrenomyodystrophy (disorder) | Finding site | Adrenal cortex structure | true | Inferred relationship | Some | 1 |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
This concept is not in any reference sets
FHIR