Status: current, Primitive. Date: 31-Jan 2002. Module: SNOMED CT core
Descriptions:
Id | Description | Lang | Type | Status | Case? | Module |
15502012 | Rokitansky sequence | en | Synonym | Active | Case sensitive | SNOMED CT core |
3993218014 | Congenital absence of uterus and vagina | en | Synonym | Active | Case insensitive | SNOMED CT core |
507815011 | Mayer-Rokitansky-Kuster syndrome | en | Synonym | Active | Case sensitive | SNOMED CT core |
830508011 | Rokitansky sequence (disorder) | en | Fully specified name | Active | Case sensitive | SNOMED CT core |
4591688011 | Describes a spectrum of Mullerian duct anomalies with congenital aplasia of the uterus and upper two thirds of the vagina in otherwise phenotypically normal females. It can be classified as either MRKH syndrome type 1 (corresponding to isolated utero-vaginal aplasia) or MRKH syndrome type 2 (utero-vaginal aplasia associated with other malformations). MRKH syndrome was thought to be purely sporadic but familial cases seem to be inherited autosomal dominantly with incomplete penetrance and variable expressivity. | en | Definition | Active | Case sensitive | SNOMED CT core |
Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
Mayer Rokitansky Küster Hauser syndrome type 1 | Is a | True | Rokitansky sequence | Inferred relationship | Some | |
Mayer-Rokitansky-Küster-Hauser syndrome type 2 | Is a | True | Rokitansky sequence | Inferred relationship | Some |
Reference Sets
Australian emergency department reference set
Clinical finding foundation reference set
Problem/Diagnosis reference set