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717705004: Mayer-Rokitansky-Küster-Hauser syndrome type 2 (disorder)


Status: current, Primitive. Date: 31-Jan 2017. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
3310060017 Mayer-Rokitansky-Küster-Hauser syndrome type 2 (disorder) en Fully specified name Active Case sensitive SNOMED CT core
3310061018 Mayer-Rokitansky-Küster-Hauser syndrome type 2 en Synonym Active Case sensitive SNOMED CT core
3993221011 Atypical MRKH (Mayer Rokitansky Kuster Hauser) syndrome en Synonym Active Initial character case insensitive SNOMED CT core
3993222016 Mullerian duct aplasia, renal dysplasia, cervical somite anomalies syndrome en Synonym Active Case insensitive SNOMED CT core


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Mayer-Rokitansky-Küster-Hauser syndrome type 2 Pathological process Pathological developmental process true Inferred relationship Some 1
Mayer-Rokitansky-Küster-Hauser syndrome type 2 Is a Malformation sequence false Inferred relationship Some
Mayer-Rokitansky-Küster-Hauser syndrome type 2 Finding site Structure of upper third of vagina true Inferred relationship Some 1
Mayer-Rokitansky-Küster-Hauser syndrome type 2 Pathological process Pathological developmental process true Inferred relationship Some 2
Mayer-Rokitansky-Küster-Hauser syndrome type 2 Finding site Uterine structure true Inferred relationship Some 2
Mayer-Rokitansky-Küster-Hauser syndrome type 2 Occurrence Congenital true Inferred relationship Some 2
Mayer-Rokitansky-Küster-Hauser syndrome type 2 Finding site Structure of middle third of vagina true Inferred relationship Some 3
Mayer-Rokitansky-Küster-Hauser syndrome type 2 Occurrence Congenital true Inferred relationship Some 3
Mayer-Rokitansky-Küster-Hauser syndrome type 2 Pathological process Pathological developmental process true Inferred relationship Some 3
Mayer-Rokitansky-Küster-Hauser syndrome type 2 Is a Congenital absence of vagina false Inferred relationship Some
Mayer-Rokitansky-Küster-Hauser syndrome type 2 Is a Congenital absence of uterus false Inferred relationship Some
Mayer-Rokitansky-Küster-Hauser syndrome type 2 Associated morphology Absence true Inferred relationship Some 1
Mayer-Rokitansky-Küster-Hauser syndrome type 2 Associated morphology Absence true Inferred relationship Some 2
Mayer-Rokitansky-Küster-Hauser syndrome type 2 Associated morphology Absence true Inferred relationship Some 3
Mayer-Rokitansky-Küster-Hauser syndrome type 2 Is a Rokitansky sequence true Inferred relationship Some
Mayer-Rokitansky-Küster-Hauser syndrome type 2 Associated morphology Congenital absence false Inferred relationship Some 1
Mayer-Rokitansky-Küster-Hauser syndrome type 2 Occurrence Congenital true Inferred relationship Some 1
Mayer-Rokitansky-Küster-Hauser syndrome type 2 Finding site Vaginal structure false Inferred relationship Some 1

Inbound Relationships Type Active Source Characteristic Refinability Group

Reference Sets

Australian emergency department reference set

Clinical finding foundation reference set

Problem/Diagnosis reference set

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