Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2017. Module: SNOMED CT core
Descriptions:
| Id | Description | Lang | Type | Status | Case? | Module |
| 3332032015 | Double uterus, hemivagina, renal agenesis syndrome (disorder) | en | Fully specified name | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 3332033013 | Double uterus, hemivagina, renal agenesis syndrome | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 3332039012 | Double uterus and obstructed hemivagina syndrome | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 3332040014 | Herlyn Werner syndrome | en | Synonym (core metadata concept) | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
| 3332041013 | Obstructed hemivagina and ipsilateral renal anomaly | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 3332042018 | Wunderlich syndrome | en | Synonym (core metadata concept) | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
| 3332043011 | A rare congenital urogenital anomaly characterized by the presence of double uterus (didelphys, bicornuate or septum-complete or partial), unilateral cervico-vaginal obstruction and ipsilateral renal anomalies (renal agenesis and/or other urinary tract anomalies). Patients are usually diagnosed at puberty after menarche due to recurrent severe dysmenorrhea, chronic pelvic pain, excessive foul smelling mucopurulent discharge, spotting and intermenstrual bleeding (depending on the existence of uterine or vaginal communications). Fever, dyspareunia, and a palpable abdominal, pelvic or vaginal mass (mucocolpos or pyocolpos) may also be present. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
| 3332044017 | A rare congenital urogenital anomaly characterised by the presence of double uterus (didelphys, bicornuate or septum-complete or partial), unilateral cervico-vaginal obstruction and ipsilateral renal anomalies (renal agenesis and/or other urinary tract anomalies). Patients are usually diagnosed at puberty after menarche due to recurrent severe dysmenorrhoea, chronic pelvic pain, excessive foul smelling mucopurulent discharge, spotting and intermenstrual bleeding (depending on the existence of uterine or vaginal communications). Fever, dyspareunia, and a palpable abdominal, pelvic or vaginal mass (mucocolpos or pyocolpos) may also be present. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| Double uterus, hemivagina, renal agenesis syndrome (disorder) | Is a | Congenital uterine anomaly | true | Inferred relationship | Some | ||
| Double uterus, hemivagina, renal agenesis syndrome (disorder) | Is a | Congenital anomaly of the kidney | true | Inferred relationship | Some | ||
| Double uterus, hemivagina, renal agenesis syndrome (disorder) | Is a | Multiple system malformation syndrome | true | Inferred relationship | Some | ||
| Double uterus, hemivagina, renal agenesis syndrome (disorder) | Associated morphology | Developmental anomaly | false | Inferred relationship | Some | 2 | |
| Double uterus, hemivagina, renal agenesis syndrome (disorder) | Occurrence | Congenital | true | Inferred relationship | Some | 2 | |
| Double uterus, hemivagina, renal agenesis syndrome (disorder) | Finding site | Kidney structure | true | Inferred relationship | Some | 2 | |
| Double uterus, hemivagina, renal agenesis syndrome (disorder) | Associated morphology | Developmental anomaly | false | Inferred relationship | Some | 3 | |
| Double uterus, hemivagina, renal agenesis syndrome (disorder) | Occurrence | Congenital | false | Inferred relationship | Some | 3 | |
| Double uterus, hemivagina, renal agenesis syndrome (disorder) | Finding site | Uterine structure | false | Inferred relationship | Some | 3 | |
| Double uterus, hemivagina, renal agenesis syndrome (disorder) | Occurrence | Congenital | true | Inferred relationship | Some | 1 | |
| Double uterus, hemivagina, renal agenesis syndrome (disorder) | Pathological process (attribute) | Pathological developmental process | true | Inferred relationship | Some | 1 | |
| Double uterus, hemivagina, renal agenesis syndrome (disorder) | Associated morphology | Morphologically abnormal structure (morphologic abnormality) | true | Inferred relationship | Some | 2 | |
| Double uterus, hemivagina, renal agenesis syndrome (disorder) | Associated morphology | Morphologically abnormal structure (morphologic abnormality) | true | Inferred relationship | Some | 1 | |
| Double uterus, hemivagina, renal agenesis syndrome (disorder) | Pathological process (attribute) | Pathological developmental process | true | Inferred relationship | Some | 2 | |
| Double uterus, hemivagina, renal agenesis syndrome (disorder) | Finding site | Uterine structure | true | Inferred relationship | Some | 1 |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
This concept is not in any reference sets
FHIR