syndroom van dubbele uterus, hemivagina en renale agenesie (aandoening) | | syndroom van dubbele uterus, hemivagina en renale agenesie | | syndroom van uterus didelphys, bicornis of bilocularis, geobstrueerde hemivagina en ipsilaterale nieragenesie OHVIRA-syndroom 'obstructed hemivagina and ipsilateral renal anomaly'-syndroom syndroom van Herlyn-Werner-Wunderlich HWW-syndroom Herlyn-Werner-Wunderlich-syndroom
| | Double uterus, hemivagina, renal agenesis syndrome | | Double uterus and obstructed hemivagina syndrome Herlyn Werner syndrome Obstructed hemivagina and ipsilateral renal anomaly Wunderlich syndrome
| | 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. |
| Id | 722431007 | Status | Primitive |
DHD Diagnosis thesaurus reference set |
RIVM authorized national diagnosis thesaurus to ICD10 complex mapping reference set | Target | Q51.1 | Term | Verdubbeling van uterus met verdubbeling van cervix en vagina |
Target | Q60.0 | Term | Agenesie van nier, enkelzijdig |
|
SNOMED CT to Orphanet simple map | 3411 |
SNOMED CT to ICD-10 extended map | Target | Q51.1 | Rule | TRUE | Advice | ALWAYS Q51.1 | POSSIBLE REQUIREMENT FOR ADDITIONAL CODE TO FULLY DESCRIBE DISEASE OR CONDITION | Correlation | SNOMED CT source code to target map code correlation not specified |
Target | Q60.0 | Rule | TRUE | Advice | ALWAYS Q60.0 | Correlation | SNOMED CT source code to target map code correlation not specified |
|
|