FHIR © HL7.org  |  Server Home  |  FHIR Server FHIR Server 3.7.13  |  FHIR Version n/a  User: [n/a]

8793008: Rokitansky sequence (disorder)


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


2 descendants. Search Descendants:

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Rokitansky sequence Pathological process Pathological developmental process true Inferred relationship Some 1
Rokitansky sequence Is a Congenital anomaly of vagina false Inferred relationship Some
Rokitansky sequence Is a Vagina absent false Inferred relationship Some
Rokitansky sequence Finding site Structure of upper third of vagina true Inferred relationship Some 1
Rokitansky sequence Finding site Uterine structure true Inferred relationship Some 2
Rokitansky sequence Pathological process Pathological developmental process true Inferred relationship Some 2
Rokitansky sequence Finding site Structure of middle third of vagina true Inferred relationship Some 3
Rokitansky sequence Pathological process Pathological developmental process true Inferred relationship Some 3
Rokitansky sequence Occurrence Congenital true Inferred relationship Some 3
Rokitansky sequence Is a Congenital absence of uterus true Inferred relationship Some
Rokitansky sequence Associated morphology Absence true Inferred relationship Some 1
Rokitansky sequence Associated morphology Absence true Inferred relationship Some 2
Rokitansky sequence Associated morphology Absence true Inferred relationship Some 3
Rokitansky sequence Associated morphology Congenital anomaly false Inferred relationship Some 1
Rokitansky sequence Is a Agenesis of vagina false Inferred relationship Some
Rokitansky sequence Associated morphology Congenital malformation false Inferred relationship Some 1
Rokitansky sequence Finding site Female genital tract false Inferred relationship Some
Rokitansky sequence Is a Congenital absence of vagina true Inferred relationship Some
Rokitansky sequence Associated morphology Congenital absence false Inferred relationship Some 1
Rokitansky sequence Is a Imperforate vagina false Inferred relationship Some
Rokitansky sequence Is a Malformation sequence true Inferred relationship Some
Rokitansky sequence Associated morphology Congenital absence false Inferred relationship Some 1
Rokitansky sequence Finding site Vaginal structure false Inferred relationship Some 1
Rokitansky sequence Occurrence Congenital true Inferred relationship Some 2
Rokitansky sequence Finding site Vaginal structure false Inferred relationship Some 2
Rokitansky sequence Associated morphology Congenital absence false Inferred relationship Some 2
Rokitansky sequence Associated morphology Congenital absence false Inferred relationship Some 1
Rokitansky sequence Occurrence Congenital true Inferred relationship Some 1
Rokitansky sequence Finding site Vaginal structure false Inferred relationship Some 1
Rokitansky sequence Associated morphology Congenital atresia false Inferred relationship Some 1
Rokitansky sequence Finding site Vaginal structure false Inferred relationship Some 1
Rokitansky sequence Associated morphology Developmental abnormality false Inferred relationship Some 2
Rokitansky sequence Occurrence Congenital false Inferred relationship Some
Rokitansky sequence Finding site Entire genital organ false Inferred relationship Some 2
Rokitansky sequence Course Multiple superficial injuries of lower leg false Inferred relationship Some

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

Back to Start