Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Jul 2014. Module: SNOMED CT core module
Descriptions:
| Id | Description | Lang | Type | Status | Case? | Module |
| 2995368018 | HCC - hypomyelination and congenital cataract | en | Synonym | Active | Entire term case sensitive | SNOMED CT core module |
| 2995422017 | Hypomyelination and congenital cataract | en | Synonym | Active | Entire term case insensitive | SNOMED CT core module |
| 2995853012 | Hypomyelination and congenital cataract (disorder) | en | Fully specified name | Active | Entire term case insensitive | SNOMED CT core module |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| Hypomyelination and congenital cataract | Is a | Hereditary disorder of nervous system | true | Inferred relationship | Existential restriction modifier | ||
| Hypomyelination and congenital cataract | Is a | Leukoencephalopathy | true | Inferred relationship | Existential restriction modifier | ||
| Hypomyelination and congenital cataract | Is a | Autosomal recessive hereditary disorder | true | Inferred relationship | Existential restriction modifier | ||
| Hypomyelination and congenital cataract | Finding site | Cerebral white matter structure | true | Inferred relationship | Existential restriction modifier | 1 |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
This concept is not in any reference sets
FHIR