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890385009: Congenital duplication of gallbladder type 1 (disorder)


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

Descriptions:

Id Description Lang Type Status Case? Module
4012434014 Congenital duplication of gallbladder type 1 (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
4012435010 Congenital duplication of gallbladder type 1 en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
4013202013 Congenital duplication of gallbladder type 1 results from a split primordium, which can be septated, bilobed or Y-shaped. 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
Congenital duplication of gallbladder type 1 (disorder) est un(e) (attribut) Congenital duplication of gallbladder true Inferred relationship Some
Congenital duplication of gallbladder type 1 (disorder) morphologie associée (attribut) Double structure true Inferred relationship Some 1
Congenital duplication of gallbladder type 1 (disorder) survenue (attribut) congénital true Inferred relationship Some 1
Congenital duplication of gallbladder type 1 (disorder) Pathological process (attribute) Pathological developmental process true Inferred relationship Some 1
Congenital duplication of gallbladder type 1 (disorder) localisation d'une constatation (attribut) vésicule biliaire (structure corporelle) true Inferred relationship Some 1

Inbound Relationships Type Active Source Characteristic Refinability Group

Reference Sets

Canada English language reference set (foundation metadata concept)

Canada French language reference set (foundation metadata concept)

GB English

US English

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