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

93268000: Congenital hypoplasia of intestinal tract (disorder)


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

Descriptions:

Id Description Lang Type Status Case? Module
154327010 Congenital hypoplasia of intestinal tract en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
154328017 Rudimentary intestinal tract en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
154329013 Congenital short intestine en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
836965014 Congenital hypoplasia of intestinal tract (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
154327010 Congenital hypoplasia of intestinal tract en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
154327010 Congenital hypoplasia of intestinal tract en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
154328017 Rudimentary intestinal tract en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
154328017 Rudimentary intestinal tract en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
154329013 Congenital short intestine en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
154329013 Congenital short intestine en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
836965014 Congenital hypoplasia of intestinal tract (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
836965014 Congenital hypoplasia of intestinal tract (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
4708971000241119 hypoplasie de l'intestin fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
4708971000241119 hypoplasie de l'intestin fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module


1 descendants. Search Descendants:

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Congenital hypoplasia of intestinal tract Is a Disease of intestine false Inferred relationship Existential restriction modifier (core metadata concept)
Congenital hypoplasia of intestinal tract Is a Congenital anomaly of trunk false Inferred relationship Existential restriction modifier (core metadata concept)
Congenital hypoplasia of intestinal tract Is a Congenital anomaly of gastrointestinal tract false Inferred relationship Existential restriction modifier (core metadata concept)
Congenital hypoplasia of intestinal tract Associated morphology Congenital hypoplasia false Inferred relationship Existential restriction modifier (core metadata concept) 1
Congenital hypoplasia of intestinal tract Occurrence Congenital false Inferred relationship Existential restriction modifier (core metadata concept)
Congenital hypoplasia of intestinal tract Finding site Intestinal structure true Inferred relationship Existential restriction modifier (core metadata concept) 1
Congenital hypoplasia of intestinal tract Is a Congenital anomaly of intestinal tract true Inferred relationship Existential restriction modifier (core metadata concept)
Congenital hypoplasia of intestinal tract Is a Congenital anomaly of digestive tract false Inferred relationship Existential restriction modifier (core metadata concept)
Congenital hypoplasia of intestinal tract Is a Congenital malformation false Inferred relationship Existential restriction modifier (core metadata concept)
Congenital hypoplasia of intestinal tract Occurrence Congenital false Inferred relationship Existential restriction modifier (core metadata concept)
Congenital hypoplasia of intestinal tract Finding site Intestinal structure false Inferred relationship Existential restriction modifier (core metadata concept) 1
Congenital hypoplasia of intestinal tract Associated morphology Congenital hypoplasia false Inferred relationship Existential restriction modifier (core metadata concept) 1
Congenital hypoplasia of intestinal tract Occurrence Congenital false Inferred relationship Existential restriction modifier (core metadata concept) 2
Congenital hypoplasia of intestinal tract Finding site Intestinal structure false Inferred relationship Existential restriction modifier (core metadata concept) 2
Congenital hypoplasia of intestinal tract Associated morphology Hypoplasia false Inferred relationship Existential restriction modifier (core metadata concept) 2
Congenital hypoplasia of intestinal tract Associated morphology Hypoplasia true Inferred relationship Existential restriction modifier (core metadata concept) 1
Congenital hypoplasia of intestinal tract Occurrence Congenital true Inferred relationship Existential restriction modifier (core metadata concept) 1
Congenital hypoplasia of intestinal tract 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 hypoganglionosis of large intestine Is a True Congenital hypoplasia of intestinal tract Inferred relationship Existential restriction modifier (core metadata concept)

Reference Sets

GB English

US English

Back to Start