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722431007: syndrome d'utérus double-hémivagin-agénésie rénale (trouble)


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
1012041000172110 syndrome d'utérus double-hémivagin-agénésie rénale fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Common French translation module (core metadata concept)
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
758711000241112 syndrome d'utérus double-hémivagin-agénésie rénale (trouble) fr Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT Common French translation module (core metadata concept)
894101000172116 hémivagin obstrué et anomalie rénale ipsilatérale fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Common French translation module (core metadata concept)
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


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
syndrome d'utérus double-hémivagin-agénésie rénale survenue (attribut) congénital true Inferred relationship Some 1
syndrome d'utérus double-hémivagin-agénésie rénale Pathological process (attribute) Pathological developmental process true Inferred relationship Some 1
syndrome d'utérus double-hémivagin-agénésie rénale morphologie associée (attribut) structure anormale sur le plan morphologique true Inferred relationship Some 2
syndrome d'utérus double-hémivagin-agénésie rénale morphologie associée (attribut) structure anormale sur le plan morphologique true Inferred relationship Some 1
syndrome d'utérus double-hémivagin-agénésie rénale Pathological process (attribute) Pathological developmental process true Inferred relationship Some 2
syndrome d'utérus double-hémivagin-agénésie rénale localisation d'une constatation (attribut) utérus (structure corporelle) true Inferred relationship Some 1
syndrome d'utérus double-hémivagin-agénésie rénale est un(e) (attribut) Congenital uterine anomaly true Inferred relationship Some
syndrome d'utérus double-hémivagin-agénésie rénale est un(e) (attribut) anomalie congénitale des reins true Inferred relationship Some
syndrome d'utérus double-hémivagin-agénésie rénale est un(e) (attribut) syndrome de malformations multisystémiques true Inferred relationship Some
syndrome d'utérus double-hémivagin-agénésie rénale morphologie associée (attribut) Developmental abnormality false Inferred relationship Some 2
syndrome d'utérus double-hémivagin-agénésie rénale survenue (attribut) congénital true Inferred relationship Some 2
syndrome d'utérus double-hémivagin-agénésie rénale localisation d'une constatation (attribut) structure d'un rein true Inferred relationship Some 2
syndrome d'utérus double-hémivagin-agénésie rénale morphologie associée (attribut) Developmental abnormality false Inferred relationship Some 3
syndrome d'utérus double-hémivagin-agénésie rénale survenue (attribut) congénital false Inferred relationship Some 3
syndrome d'utérus double-hémivagin-agénésie rénale localisation d'une constatation (attribut) utérus (structure corporelle) false Inferred relationship Some 3

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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