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3845008: Congenital duplication of intestine (disorder)


Status: current, Sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2014. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
7479015 Congenital duplication of intestine en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
774034014 Congenital duplication of intestine (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
1229431010 Duplication of intestine en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
7479015 Congenital duplication of intestine en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
7479015 Congenital duplication of intestine en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
774034014 Congenital duplication of intestine (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
774034014 Congenital duplication of intestine (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
1229431010 Duplication of intestine en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
1229431010 Duplication of intestine en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
4400991000241111 duplication congénitale de l'intestin fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
4400991000241111 duplication congénitale de l'intestin fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module


12 descendants. Search Descendants:

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Congenital duplication of intestine Is a Congenital anomaly of lower alimentary tract false Inferred relationship Existential restriction modifier (core metadata concept)
Congenital duplication of intestine Associated morphology Double structure false Inferred relationship Existential restriction modifier (core metadata concept) 1
Congenital duplication of intestine Finding site Intestinal structure false Inferred relationship Existential restriction modifier (core metadata concept) 2
Congenital duplication of intestine Occurrence Congenital false Inferred relationship Existential restriction modifier (core metadata concept)
Congenital duplication of intestine Finding site Jejunum, ileum, colon, rectum, and anal canal false Inferred relationship Existential restriction modifier (core metadata concept) 1
Congenital duplication of intestine Is a Congenital anomaly of digestive tract false Inferred relationship Existential restriction modifier (core metadata concept)
Congenital duplication of intestine Associated morphology anomalie congénitale false Inferred relationship Existential restriction modifier (core metadata concept) 1
Congenital duplication of intestine Finding site Intestinal structure false Inferred relationship Existential restriction modifier (core metadata concept) 2
Congenital duplication of intestine Finding site Intestinal structure false Inferred relationship Existential restriction modifier (core metadata concept) 1
Congenital duplication of intestine Finding site Intestinal structure false Inferred relationship Existential restriction modifier (core metadata concept) 1
Congenital duplication of intestine Is a Congenital duplication of digestive organs true Inferred relationship Existential restriction modifier (core metadata concept)
Congenital duplication of intestine Occurrence Congenital false Inferred relationship Existential restriction modifier (core metadata concept)
Congenital duplication of intestine Is a Congenital anomaly of intestinal tract true Inferred relationship Existential restriction modifier (core metadata concept)
Congenital duplication of intestine Associated morphology Double structure false Inferred relationship Existential restriction modifier (core metadata concept) 1
Congenital duplication of intestine Finding site Intestinal structure false Inferred relationship Existential restriction modifier (core metadata concept) 1
Congenital duplication of intestine Occurrence Congenital false Inferred relationship Existential restriction modifier (core metadata concept) 2
Congenital duplication of intestine Finding site Intestinal structure false Inferred relationship Existential restriction modifier (core metadata concept) 2
Congenital duplication of intestine Associated morphology Double structure false Inferred relationship Existential restriction modifier (core metadata concept) 2
Congenital duplication of intestine Associated morphology Double structure true Inferred relationship Existential restriction modifier (core metadata concept) 1
Congenital duplication of intestine Occurrence Congenital true Inferred relationship Existential restriction modifier (core metadata concept) 1
Congenital duplication of intestine Finding site Intestinal structure true Inferred relationship Existential restriction modifier (core metadata concept) 1
Congenital duplication of intestine 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
Enteric duplication Is a True Congenital duplication of intestine Inferred relationship Existential restriction modifier (core metadata concept)
Congenital duplication of colon Is a True Congenital duplication of intestine Inferred relationship Existential restriction modifier (core metadata concept)
Congenital duplication of anus Is a False Congenital duplication of intestine Inferred relationship Existential restriction modifier (core metadata concept)
Long tubular intestinal duplication Is a True Congenital duplication of intestine Inferred relationship Existential restriction modifier (core metadata concept)
Duplication of intestine, unspecified Is a False Congenital duplication of intestine Inferred relationship Existential restriction modifier (core metadata concept)
Duplication of intestine NOS Is a False Congenital duplication of intestine Inferred relationship Existential restriction modifier (core metadata concept)
Congenital duplication of appendix Is a True Congenital duplication of intestine Inferred relationship Existential restriction modifier (core metadata concept)
Congenital duplication of caecum Is a True Congenital duplication of intestine Inferred relationship Existential restriction modifier (core metadata concept)
Congenital duplication of rectum (disorder) Is a True Congenital duplication of intestine Inferred relationship Existential restriction modifier (core metadata concept)

This concept is not in any reference sets

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