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190953007: Trypsinogen deficiency (disorder)


Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Jan 2002. Module: SNOMED CT core module

Descriptions:

Id Description Lang Type Status Case? Module
293614016 Trypsinogen deficiency en Synonym Active Entire term case insensitive SNOMED CT core module
574598018 Trypsinogen deficiency (disorder) en Fully specified name Active Entire term case insensitive SNOMED CT core module


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Trypsinogen deficiency Is a Inborn error of metabolism true Inferred relationship Existential restriction modifier
Trypsinogen deficiency Occurrence Congenital true Inferred relationship Existential restriction modifier 1
Trypsinogen deficiency Finding site Body system structure false Inferred relationship Existential restriction modifier

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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