FHIR © HL7.org  |  Server Home  |  FHIR Server FHIR Server 3.7.4-SNAPSHOT  |  FHIR Version n/a  User: [n/a]

33257003: Congenital duplication of digestive organs (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
55496017 Congenital duplication of digestive organs en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
764637016 Congenital duplication of digestive organs (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
55496017 Congenital duplication of digestive organs en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
55496017 Congenital duplication of digestive organs en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
764637016 Congenital duplication of digestive organs (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
764637016 Congenital duplication of digestive organs (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
3441611001000117 Verdoppelung, gastrointestinale de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
4497881000241115 duplication digestive congénitale fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
4497881000241115 duplication digestive congénitale fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
3441611001000117 Verdoppelung, gastrointestinale de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module


24 descendants. Search Descendants:

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Congenital duplication of digestive organs Is a Congenital anomaly of digestive organ (disorder) true Inferred relationship Existential restriction modifier (core metadata concept)
Congenital duplication of digestive organs Occurrence Congenital false Inferred relationship Existential restriction modifier (core metadata concept)
Congenital duplication of digestive organs Associated morphology anomalie du développement false Inferred relationship Existential restriction modifier (core metadata concept) 1
Congenital duplication of digestive organs Finding site Digestive organ structure (body structure) false Inferred relationship Existential restriction modifier (core metadata concept) 1
Congenital duplication of digestive organs Finding site Digestive organ structure (body structure) false Inferred relationship Existential restriction modifier (core metadata concept) 1
Congenital duplication of digestive organs Associated morphology Double structure false Inferred relationship Existential restriction modifier (core metadata concept) 1
Congenital duplication of digestive organs Finding site Digestive organ structure (body structure) false Inferred relationship Existential restriction modifier (core metadata concept) 4
Congenital duplication of digestive organs Is a Congenital anomaly of digestive tract false Inferred relationship Existential restriction modifier (core metadata concept)
Congenital duplication of digestive organs Finding site Digestive organ structure (body structure) false Inferred relationship Existential restriction modifier (core metadata concept) 4
Congenital duplication of digestive organs Finding site Digestive organ structure (body structure) false Inferred relationship Existential restriction modifier (core metadata concept) 1
Congenital duplication of digestive organs Finding site Digestive organ structure (body structure) false Inferred relationship Existential restriction modifier (core metadata concept) 1
Congenital duplication of digestive organs Is a Congenital malformation false Inferred relationship Existential restriction modifier (core metadata concept)
Congenital duplication of digestive organs Occurrence Congenital false Inferred relationship Existential restriction modifier (core metadata concept)
Congenital duplication of digestive organs Associated morphology Double structure false Inferred relationship Existential restriction modifier (core metadata concept) 1
Congenital duplication of digestive organs Finding site Digestive organ structure (body structure) false Inferred relationship Existential restriction modifier (core metadata concept) 1
Congenital duplication of digestive organs Occurrence Congenital false Inferred relationship Existential restriction modifier (core metadata concept) 2
Congenital duplication of digestive organs Finding site Digestive organ structure (body structure) false Inferred relationship Existential restriction modifier (core metadata concept) 2
Congenital duplication of digestive organs Associated morphology Double structure false Inferred relationship Existential restriction modifier (core metadata concept) 2
Congenital duplication of digestive organs Associated morphology Double structure true Inferred relationship Existential restriction modifier (core metadata concept) 1
Congenital duplication of digestive organs Occurrence Congenital true Inferred relationship Existential restriction modifier (core metadata concept) 1
Congenital duplication of digestive organs Finding site Digestive organ structure (body structure) true Inferred relationship Existential restriction modifier (core metadata concept) 1
Congenital duplication of digestive organs 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 stomach Is a True Congenital duplication of digestive organs Inferred relationship Existential restriction modifier (core metadata concept)
Congenital duplication of biliary duct Is a False Congenital duplication of digestive organs Inferred relationship Existential restriction modifier (core metadata concept)
Congenital duplication of gallbladder (disorder) Is a False Congenital duplication of digestive organs Inferred relationship Existential restriction modifier (core metadata concept)
Congenital duplication of liver (disorder) Is a False Congenital duplication of digestive organs Inferred relationship Existential restriction modifier (core metadata concept)
Congenital duplication of appendix Is a False Congenital duplication of digestive organs Inferred relationship Existential restriction modifier (core metadata concept)
Congenital duplication of intestine Is a True Congenital duplication of digestive organs Inferred relationship Existential restriction modifier (core metadata concept)
Congenital duplication of esophagus (disorder) Is a True Congenital duplication of digestive organs Inferred relationship Existential restriction modifier (core metadata concept)
Liver and/or biliary duplication (disorder) Is a True Congenital duplication of digestive organs Inferred relationship Existential restriction modifier (core metadata concept)
Congenital duplication of anus Is a False Congenital duplication of digestive organs Inferred relationship Existential restriction modifier (core metadata concept)
Duplication of teeth (disorder) Is a False Congenital duplication of digestive organs Inferred relationship Existential restriction modifier (core metadata concept)

This concept is not in any reference sets

Back to Start