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890379002: Congenital duplication of gallbladder type 2 (disorder)


Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Jan 2021. Module: SNOMED CT core module

Descriptions:

Id Description Lang Type Status Case? Module
4012420014 Congenital duplication of gallbladder type 2 (disorder) en Fully specified name Active Entire term case insensitive SNOMED CT core module
4012421013 Congenital duplication of gallbladder type 2 en Synonym Active Entire term case insensitive SNOMED CT core module


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Congenital duplication of gallbladder type 2 Is a Congenital duplication of gallbladder true Inferred relationship Existential restriction modifier
Congenital duplication of gallbladder type 2 Associated morphology Double structure true Inferred relationship Existential restriction modifier 1
Congenital duplication of gallbladder type 2 Occurrence Congenital true Inferred relationship Existential restriction modifier 1
Congenital duplication of gallbladder type 2 Pathological process Pathological developmental process true Inferred relationship Existential restriction modifier 1
Congenital duplication of gallbladder type 2 Finding site Gallbladder structure true Inferred relationship Existential restriction modifier 1

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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