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93268000: Congenital hypoplasia of intestinal tract (disorder)


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

Descriptions:

Id Description Lang Type Status Case? Module
154327010 Congenital hypoplasia of intestinal tract en Synonym Active Entire term case insensitive SNOMED CT core module
154328017 Rudimentary intestinal tract en Synonym Active Entire term case insensitive SNOMED CT core module
154329013 Congenital short intestine en Synonym Active Entire term case insensitive SNOMED CT core module
836965014 Congenital hypoplasia of intestinal tract (disorder) en Fully specified name Active Entire term case insensitive SNOMED CT core module


1 descendants. Search Descendants:

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Congenital hypoplasia of intestinal tract Is a Disorder of intestine false Inferred relationship Existential restriction modifier
Congenital hypoplasia of intestinal tract Is a Congenital anomaly of trunk false Inferred relationship Existential restriction modifier
Congenital hypoplasia of intestinal tract Is a Congenital anomaly of gastrointestinal tract false Inferred relationship Existential restriction modifier
Congenital hypoplasia of intestinal tract Associated morphology Congenital hypoplasia false Inferred relationship Existential restriction modifier 1
Congenital hypoplasia of intestinal tract Occurrence Congenital false Inferred relationship Existential restriction modifier
Congenital hypoplasia of intestinal tract Finding site Intestinal structure true Inferred relationship Existential restriction modifier 1
Congenital hypoplasia of intestinal tract Is a Congenital anomaly of intestinal tract true Inferred relationship Existential restriction modifier
Congenital hypoplasia of intestinal tract Is a Congenital anomaly of digestive tract false Inferred relationship Existential restriction modifier
Congenital hypoplasia of intestinal tract Is a Congenital malformation false Inferred relationship Existential restriction modifier
Congenital hypoplasia of intestinal tract Occurrence Congenital false Inferred relationship Existential restriction modifier
Congenital hypoplasia of intestinal tract Finding site Intestinal structure false Inferred relationship Existential restriction modifier 1
Congenital hypoplasia of intestinal tract Associated morphology Congenital hypoplasia false Inferred relationship Existential restriction modifier 1
Congenital hypoplasia of intestinal tract Occurrence Congenital false Inferred relationship Existential restriction modifier 2
Congenital hypoplasia of intestinal tract Finding site Intestinal structure false Inferred relationship Existential restriction modifier 2
Congenital hypoplasia of intestinal tract Associated morphology Hypoplasia false Inferred relationship Existential restriction modifier 2
Congenital hypoplasia of intestinal tract Associated morphology Hypoplasia true Inferred relationship Existential restriction modifier 1
Congenital hypoplasia of intestinal tract Occurrence Congenital true Inferred relationship Existential restriction modifier 1
Congenital hypoplasia of intestinal tract Pathological process Pathological developmental process true Inferred relationship Existential restriction modifier 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

This concept is not in any reference sets

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