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46907007: Congenital duplication of gallbladder (disorder)


Status: current, Sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2002. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
78185016 Congenital duplication of gallbladder en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
494677011 Duplication of gallbladder en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
784307013 Congenital duplication of gallbladder (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
78185016 Congenital duplication of gallbladder en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
78185016 Congenital duplication of gallbladder en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
494677011 Duplication of gallbladder en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
494677011 Duplication of gallbladder en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
784307013 Congenital duplication of gallbladder (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
784307013 Congenital duplication of gallbladder (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
4543171000241117 duplication congénitale de la vésicule biliaire fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
4543171000241117 duplication congénitale de la vésicule biliaire fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module


2 descendants. Search Descendants:

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Congenital duplication of gallbladder (disorder) Is a Congenital anomaly of gallbladder false Inferred relationship Existential restriction modifier (core metadata concept)
Congenital duplication of gallbladder (disorder) Associated morphology Double structure true Inferred relationship Existential restriction modifier (core metadata concept) 1
Congenital duplication of gallbladder (disorder) Finding site Gallbladder structure true Inferred relationship Existential restriction modifier (core metadata concept) 1
Congenital duplication of gallbladder (disorder) Finding site Digestive organ structure (body structure) false Inferred relationship Existential restriction modifier (core metadata concept) 2
Congenital duplication of gallbladder (disorder) Associated morphology anomalie du développement false Inferred relationship Existential restriction modifier (core metadata concept) 2
Congenital duplication of gallbladder (disorder) Occurrence Congenital false Inferred relationship Existential restriction modifier (core metadata concept)
Congenital duplication of gallbladder (disorder) Associated morphology anomalie congénitale false Inferred relationship Existential restriction modifier (core metadata concept) 1
Congenital duplication of gallbladder (disorder) Finding site Structure of digestive system (body structure) false Inferred relationship Existential restriction modifier (core metadata concept) 1
Congenital duplication of gallbladder (disorder) Is a Congenital duplication of digestive organs false Inferred relationship Existential restriction modifier (core metadata concept)
Congenital duplication of gallbladder (disorder) Is a Supernumerary gallbladder true Inferred relationship Existential restriction modifier (core metadata concept)
Congenital duplication of gallbladder (disorder) Occurrence Congenital false Inferred relationship Existential restriction modifier (core metadata concept)
Congenital duplication of gallbladder (disorder) Associated morphology Double structure false Inferred relationship Existential restriction modifier (core metadata concept) 1
Congenital duplication of gallbladder (disorder) Finding site Gallbladder structure false Inferred relationship Existential restriction modifier (core metadata concept) 1
Congenital duplication of gallbladder (disorder) Occurrence Congenital false Inferred relationship Existential restriction modifier (core metadata concept) 2
Congenital duplication of gallbladder (disorder) Finding site Gallbladder structure false Inferred relationship Existential restriction modifier (core metadata concept) 2
Congenital duplication of gallbladder (disorder) Is a Liver and/or biliary duplication (disorder) true Inferred relationship Existential restriction modifier (core metadata concept)
Congenital duplication of gallbladder (disorder) Associated morphology Double structure false Inferred relationship Existential restriction modifier (core metadata concept) 2
Congenital duplication of gallbladder (disorder) Occurrence Congenital true Inferred relationship Existential restriction modifier (core metadata concept) 1
Congenital duplication of gallbladder (disorder) Pathological process (attribute) Pathological developmental process (qualifier value) true Inferred relationship Existential restriction modifier (core metadata concept) 1

Inbound Relationships Type Active Source Characteristic Refinability Group
Congenital duplication of gallbladder type 2 (disorder) Is a True Congenital duplication of gallbladder (disorder) Inferred relationship Existential restriction modifier (core metadata concept)
Congenital duplication of gallbladder type 1 (disorder) Is a True Congenital duplication of gallbladder (disorder) Inferred relationship Existential restriction modifier (core metadata concept)

This concept is not in any reference sets

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