Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Jan 2017. Module: SNOMED CT core module
Descriptions:
Id | Description | Lang | Type | Status | Case? | Module |
3326243010 | Joubert syndrome with congenital hepatic fibrosis (disorder) | en | Fully specified name | Active | Entire term case sensitive | SNOMED CT core module |
3326244016 | Joubert syndrome with hepatic defect | en | Synonym | Active | Entire term case sensitive | SNOMED CT core module |
3326245015 | Joubert syndrome with congenital hepatic fibrosis | en | Synonym | Active | Entire term case sensitive | SNOMED CT core module |
3326246019 | Cerebellar vermis hypoplasia, oligophrenia, congenital ataxia, coloboma, hepatic fibrosis | en | Synonym | Active | Entire term case insensitive | SNOMED CT core module |
3326247011 | COACH syndrome | en | Synonym | Active | Entire term case sensitive | SNOMED CT core module |
3326248018 | Gentile syndrome | en | Synonym | Active | Entire term case sensitive | SNOMED CT core module |
3326250014 | COACH (cerebellar vermis hypoplasia, oligophrenia, congenital ataxia, coloboma, hepatic fibrosis) syndrome | en | Synonym | Active | Entire term case sensitive | SNOMED CT core module |
Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
This concept is not in any reference sets