Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2002. Module: SNOMED CT core
Descriptions:
| Id | Description | Lang | Type | Status | Case? | Module |
| 175932012 | Hypomyelination | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 627344012 | Hypomyelination (morphologic abnormality) | en | Fully specified name | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 1192091000146115 | hypomyelinisatie | nl | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT Netherlands NRC maintained module (core metadata concept) |
| 1192101000146110 | hypomyelinisatie (afwijkende morfologie) | nl | Fully specified name | Active | Entire term case insensitive (core metadata concept) | SNOMED CT Netherlands NRC maintained module (core metadata concept) |
| 1192111000146112 | dysmyelinisatie | nl | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT Netherlands NRC maintained module (core metadata concept) |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| Hypomyelination | Is a | gebrekkige ontwikkeling (afwijkende morfologie) | false | Inferred relationship | Some | ||
| Hypomyelination | Is a | Morphologically abnormal structure (morphologic abnormality) | true | Inferred relationship | Some |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
| Hypomyelinating leukodystrophy with atrophy of basal ganglia and cerebellum (disorder) | Associated morphology | False | Hypomyelination | Inferred relationship | Some | 4 |
| Epileptic encephalopathy with global cerebral demyelination (disorder) | Associated morphology | False | Hypomyelination | Inferred relationship | Some | 2 |
| Hypomyelination neuropathy arthrogryposis syndrome (disorder) | Associated morphology | True | Hypomyelination | Inferred relationship | Some | 1 |
| Epileptic encephalopathy with global cerebral demyelination (disorder) | Associated morphology | True | Hypomyelination | Inferred relationship | Some | 1 |
| Congenital hypomyelinating neuropathy | Associated morphology | True | Hypomyelination | Inferred relationship | Some | 1 |
| MTHFS-related developmental delay, microcephaly, short stature, epilepsy syndrome | Associated morphology | True | Hypomyelination | Inferred relationship | Some | 5 |
This concept is not in any reference sets
FHIR