190953007: Trypsinogen deficiency (disorder)

SNOMED CT Concept\Clinical finding (finding)\Disease\...

\Genetic disease\Hereditary disease\Hereditary metabolic disease\Inborn error of metabolism\Trypsinogen deficiency

\Disorder of foetus and/or newborn\Congenital disease (disorder)\Inborn error of metabolism\Trypsinogen deficiency

\Metabolic disease\Hereditary metabolic disease\Inborn error of metabolism\Trypsinogen deficiency

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

Descriptions:

Id Description Lang Type Status Case? Module

293614016 Trypsinogen deficiency en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core

574598018 Trypsinogen deficiency (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core

Expanded Value Set

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

Inbound Relationships

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This concept is not in any reference sets