Status: current, Primitive. Date: 31-Jan 2017. Module: SNOMED CT core
Descriptions:
Id | Description | Lang | Type | Status | Case? | Module |
3310060017 | Mayer-Rokitansky-Küster-Hauser syndrome type 2 (disorder) | en | Fully specified name | Active | Case sensitive | SNOMED CT core |
3310061018 | Mayer-Rokitansky-Küster-Hauser syndrome type 2 | en | Synonym | Active | Case sensitive | SNOMED CT core |
3993221011 | Atypical MRKH (Mayer Rokitansky Kuster Hauser) syndrome | en | Synonym | Active | Initial character case insensitive | SNOMED CT core |
3993222016 | Mullerian duct aplasia, renal dysplasia, cervical somite anomalies syndrome | en | Synonym | Active | Case insensitive | SNOMED CT core |
Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
Mayer-Rokitansky-Küster-Hauser syndrome type 2 | Pathological process | Pathological developmental process | true | Inferred relationship | Some | 1 | |
Mayer-Rokitansky-Küster-Hauser syndrome type 2 | Is a | Malformation sequence | false | Inferred relationship | Some | ||
Mayer-Rokitansky-Küster-Hauser syndrome type 2 | Finding site | Structure of upper third of vagina | true | Inferred relationship | Some | 1 | |
Mayer-Rokitansky-Küster-Hauser syndrome type 2 | Pathological process | Pathological developmental process | true | Inferred relationship | Some | 2 | |
Mayer-Rokitansky-Küster-Hauser syndrome type 2 | Finding site | Uterine structure | true | Inferred relationship | Some | 2 | |
Mayer-Rokitansky-Küster-Hauser syndrome type 2 | Occurrence | Congenital | true | Inferred relationship | Some | 2 | |
Mayer-Rokitansky-Küster-Hauser syndrome type 2 | Finding site | Structure of middle third of vagina | true | Inferred relationship | Some | 3 | |
Mayer-Rokitansky-Küster-Hauser syndrome type 2 | Occurrence | Congenital | true | Inferred relationship | Some | 3 | |
Mayer-Rokitansky-Küster-Hauser syndrome type 2 | Pathological process | Pathological developmental process | true | Inferred relationship | Some | 3 | |
Mayer-Rokitansky-Küster-Hauser syndrome type 2 | Is a | Congenital absence of vagina | false | Inferred relationship | Some | ||
Mayer-Rokitansky-Küster-Hauser syndrome type 2 | Is a | Congenital absence of uterus | false | Inferred relationship | Some | ||
Mayer-Rokitansky-Küster-Hauser syndrome type 2 | Associated morphology | Absence | true | Inferred relationship | Some | 1 | |
Mayer-Rokitansky-Küster-Hauser syndrome type 2 | Associated morphology | Absence | true | Inferred relationship | Some | 2 | |
Mayer-Rokitansky-Küster-Hauser syndrome type 2 | Associated morphology | Absence | true | Inferred relationship | Some | 3 | |
Mayer-Rokitansky-Küster-Hauser syndrome type 2 | Is a | Rokitansky sequence | true | Inferred relationship | Some | ||
Mayer-Rokitansky-Küster-Hauser syndrome type 2 | Associated morphology | Congenital absence | false | Inferred relationship | Some | 1 | |
Mayer-Rokitansky-Küster-Hauser syndrome type 2 | Occurrence | Congenital | true | Inferred relationship | Some | 1 | |
Mayer-Rokitansky-Küster-Hauser syndrome type 2 | Finding site | Vaginal structure | false | Inferred relationship | Some | 1 |
Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
Reference Sets
Australian emergency department reference set
Clinical finding foundation reference set
Problem/Diagnosis reference set