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18735004: Congenital omphalocele (disorder)


Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 01-Jul 2024. Module: IPS terminology module (core metadata concept)

Descriptions:

Id Description Lang Type Status Case? Module
31596019 Congenital omphalocele en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) IPS terminology module (core metadata concept)
31597011 Omphalocele en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) IPS terminology module (core metadata concept)
746271010 Congenital omphalocele (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) IPS terminology module (core metadata concept)
2535837011 Amniocele en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) IPS terminology module (core metadata concept)


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Congenital omphalocele Is a Congenital malformation true Inferred relationship Some
Congenital omphalocele Is a Umbilical hernia (disorder) true Inferred relationship Some
Congenital omphalocele Associated morphology Hernial opening (morphologic abnormality) true Inferred relationship Some 1
Congenital omphalocele Occurrence Congenital true Inferred relationship Some 1
Congenital omphalocele Finding site Umbilical structure true Inferred relationship Some 1
Congenital omphalocele Pathological process (attribute) Pathological developmental process (qualifier value) true Inferred relationship Some 1
Congenital omphalocele Associated morphology Herniated structure (morphologic abnormality) true Inferred relationship Some 2
Congenital omphalocele Occurrence Congenital true Inferred relationship Some 2
Congenital omphalocele Finding site Intra-abdominopelvic structure true Inferred relationship Some 2

Inbound Relationships Type Active Source Characteristic Refinability Group

Reference Sets

International Patient Summary

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