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715201005: syndrome du grêle court congénital (trouble)


Status: current, Sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2018. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
3301852017 Congenital short bowel syndrome (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
3301853010 Congenital short bowel syndrome en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
746831000241114 syndrome du grêle court congénital (trouble) fr Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT Common French translation module (core metadata concept)
955241000172112 syndrome du grêle court congénital fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Common French translation module (core metadata concept)
977791000172117 SGC (syndrome du grêle court) congénital fr Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Common French translation module (core metadata concept)
3301854016 A rare intestinal disorder of neonates of unknown etiology. Patients are born with a short small bowel (less than 75 cm in length) that compromises proper intestinal absorption and leads chronic diarrhea, vomiting and failure to thrive. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
3301965010 A rare intestinal disorder of neonates of unknown aetiology. Patients are born with a short small bowel (less than 75 cm in length) that compromises proper intestinal absorption and leads chronic diarrhoea, vomiting and failure to thrive. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core


1 descendants. Search Descendants:

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Congenital short bowel syndrome (disorder) Pathological process (attribute) Pathological developmental process true Inferred relationship Some 1
Congenital short bowel syndrome (disorder) est un(e) (attribut) anomalie morphologique congénitale true Inferred relationship Some
Congenital short bowel syndrome (disorder) est un(e) (attribut) Congenital anomaly of small intestine (disorder) true Inferred relationship Some
Congenital short bowel syndrome (disorder) morphologie associée (attribut) Abnormally short growth true Inferred relationship Some 1
Congenital short bowel syndrome (disorder) survenue (attribut) congénital true Inferred relationship Some 1
Congenital short bowel syndrome (disorder) localisation d'une constatation (attribut) Entire small intestine true Inferred relationship Some 1
Congenital short bowel syndrome (disorder) est un(e) (attribut) Deformity (finding) false Inferred relationship Some
Congenital short bowel syndrome (disorder) est un(e) (attribut) syndrome du grêle court (trouble) true Inferred relationship Some

Inbound Relationships Type Active Source Characteristic Refinability Group
Diaphragmatic hernia, short bowel, asplenia syndrome (disorder) est un(e) (attribut) True Congenital short bowel syndrome (disorder) Inferred relationship Some

This concept is not in any reference sets

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