Status: current, Sufficiently defined by necessary conditions definition status (core metadata concept). Date: 01-Aug 2025. Module: SNOMED CT core
Descriptions:
| Id | Description | Lang | Type | Status | Case? | Module |
| 4542657013 | Hypomyelination of central nervous system structure (disorder) | en | Fully specified name | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 4542658015 | Hypomyelination of central nervous system structure | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 4542659011 | CNS (central nervous system) hypomyelination | en | Synonym (core metadata concept) | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| Hypomyelination of central nervous system structure (disorder) | Is a | Disorder of the central nervous system (disorder) | true | Inferred relationship | Some | ||
| Hypomyelination of central nervous system structure (disorder) | Finding site | Structure of central nervous system (body structure) | true | Inferred relationship | Some | 1 | |
| Hypomyelination of central nervous system structure (disorder) | Associated morphology | Hypomyelination | true | Inferred relationship | Some | 1 |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
| Hypomyelination of cerebral white matter | Is a | True | Hypomyelination of central nervous system structure (disorder) | Inferred relationship | Some | |
| Epileptic encephalopathy with global cerebral demyelination (disorder) | Is a | True | Hypomyelination of central nervous system structure (disorder) | Inferred relationship | Some | |
| MTHFS-related developmental delay, microcephaly, short stature, epilepsy syndrome | Is a | True | Hypomyelination of central nervous system structure (disorder) | Inferred relationship | Some |
This concept is not in any reference sets
FHIR