Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Jan 2002. Module: SNOMED CT core module
Descriptions:
| Id | Description | Lang | Type | Status | Case? | Module |
| 175932012 | Hypomyelination | en | Synonym | Active | Entire term case insensitive | SNOMED CT core module |
| 627344012 | Hypomyelination (morphologic abnormality) | en | Fully specified name | Active | Entire term case insensitive | SNOMED CT core module |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| Hypomyelination | Is a | Developmental anomaly | false | Inferred relationship | Existential restriction modifier | ||
| Hypomyelination | Is a | Morphologically abnormal structure | true | Inferred relationship | Existential restriction modifier |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
| Hypomyelinating leukodystrophy with atrophy of basal ganglia and cerebellum | Associated morphology | False | Hypomyelination | Inferred relationship | Existential restriction modifier | 4 |
| Epileptic encephalopathy with global cerebral demyelination | Associated morphology | False | Hypomyelination | Inferred relationship | Existential restriction modifier | 2 |
| Hypomyelination neuropathy arthrogryposis syndrome | Associated morphology | True | Hypomyelination | Inferred relationship | Existential restriction modifier | 1 |
| Epileptic encephalopathy with global cerebral demyelination | Associated morphology | True | Hypomyelination | Inferred relationship | Existential restriction modifier | 1 |
| Congenital hypomyelinating neuropathy | Associated morphology | True | Hypomyelination | Inferred relationship | Existential restriction modifier | 1 |
This concept is not in any reference sets
FHIR