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722392003: Congenital malabsorptive diarrhea due to paucity of enteroendocrine cells (disorder)

Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Jan 2017. Module: SNOMED CT core module

Descriptions:

Id Description Lang Type Status Case? Module
3326710012 Congenital malabsorptive diarrhea due to paucity of enteroendocrine cells (disorder) en Fully specified name Active Entire term case insensitive SNOMED CT core module
3326711011 Congenital malabsorptive diarrhea due to paucity of enteroendocrine cells en Synonym Active Entire term case insensitive SNOMED CT core module
3331831014 Congenital malabsorptive diarrhoea due to paucity of enteroendocrine cells en Synonym Active Entire term case insensitive SNOMED CT core module
3331832019 Enteric anendocrinosis en Synonym Active Entire term case insensitive SNOMED CT core module

0 descendants.

Expanded Value Set

Outbound Relationships Type Target Active Characteristic Refinability Group Values
Congenital malabsorptive diarrhea due to paucity of enteroendocrine cells Is a Chronic diarrhea of infants AND/OR young children true Inferred relationship Existential restriction modifier
Congenital malabsorptive diarrhea due to paucity of enteroendocrine cells Is a Malabsorption syndrome true Inferred relationship Existential restriction modifier
Congenital malabsorptive diarrhea due to paucity of enteroendocrine cells Is a Congenital disease true Inferred relationship Existential restriction modifier
Congenital malabsorptive diarrhea due to paucity of enteroendocrine cells Is a Autosomal recessive hereditary disorder true Inferred relationship Existential restriction modifier
Congenital malabsorptive diarrhea due to paucity of enteroendocrine cells Is a Digestive system hereditary disorder true Inferred relationship Existential restriction modifier
Congenital malabsorptive diarrhea due to paucity of enteroendocrine cells Clinical course Chronic true Inferred relationship Existential restriction modifier 4
Congenital malabsorptive diarrhea due to paucity of enteroendocrine cells Has definitional manifestation Diarrhea false Inferred relationship Existential restriction modifier
Congenital malabsorptive diarrhea due to paucity of enteroendocrine cells Occurrence Congenital true Inferred relationship Existential restriction modifier 3
Congenital malabsorptive diarrhea due to paucity of enteroendocrine cells Finding site Gastrointestinal tract structure true Inferred relationship Existential restriction modifier 3
Congenital malabsorptive diarrhea due to paucity of enteroendocrine cells Finding site Intestinal structure true Inferred relationship Existential restriction modifier 1
Congenital malabsorptive diarrhea due to paucity of enteroendocrine cells Interprets Bowel action true Inferred relationship Existential restriction modifier 2
Congenital malabsorptive diarrhea due to paucity of enteroendocrine cells Has interpretation Altered true Inferred relationship Existential restriction modifier 2
Congenital malabsorptive diarrhea due to paucity of enteroendocrine cells Interprets Digestive system function false Inferred relationship Existential restriction modifier 5
Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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