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54119007: Congenital pancreatic trypsin deficiency (disorder)

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
89950015 Congenital pancreatic trypsin deficiency en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
792315014 Congenital pancreatic trypsin deficiency (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
89950015 Congenital pancreatic trypsin deficiency en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
89950015 Congenital pancreatic trypsin deficiency en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
792315014 Congenital pancreatic trypsin deficiency (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
792315014 Congenital pancreatic trypsin deficiency (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
4566971000241115 déficit congénital en trypsine pancréatique fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
4566971000241115 déficit congénital en trypsine pancréatique fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module

0 descendants.

Expanded Value Set

Outbound Relationships Type Target Active Characteristic Refinability Group Values
Congenital pancreatic trypsin deficiency (disorder) Is a Congenital anomaly of pancreas false Inferred relationship Existential restriction modifier (core metadata concept)
Congenital pancreatic trypsin deficiency (disorder) Finding site Pancreatic structure false Inferred relationship Existential restriction modifier (core metadata concept) 1
Congenital pancreatic trypsin deficiency (disorder) Occurrence Congenital false Inferred relationship Existential restriction modifier (core metadata concept)
Congenital pancreatic trypsin deficiency (disorder) Associated morphology anomalie du développement false Inferred relationship Existential restriction modifier (core metadata concept) 1
Congenital pancreatic trypsin deficiency (disorder) Associated morphology Congenital deficiency false Inferred relationship Existential restriction modifier (core metadata concept) 1
Congenital pancreatic trypsin deficiency (disorder) Finding site Digestive organ structure (body structure) false Inferred relationship Existential restriction modifier (core metadata concept) 1
Congenital pancreatic trypsin deficiency (disorder) Is a Deficiency of trypsin (disorder) true Inferred relationship Existential restriction modifier (core metadata concept)
Congenital pancreatic trypsin deficiency (disorder) Occurrence Congenital true Inferred relationship Existential restriction modifier (core metadata concept) 1
Congenital pancreatic trypsin deficiency (disorder) Associated morphology anomalie congénitale false Inferred relationship Existential restriction modifier (core metadata concept) 1
Congenital pancreatic trypsin deficiency (disorder) Finding site Digestive organ structure (body structure) false Inferred relationship Existential restriction modifier (core metadata concept) 1
Congenital pancreatic trypsin deficiency (disorder) Associated morphology anomalie congénitale false Inferred relationship Existential restriction modifier (core metadata concept) 2
Congenital pancreatic trypsin deficiency (disorder) Associated morphology Congenital deficiency false Inferred relationship Existential restriction modifier (core metadata concept) 1
Congenital pancreatic trypsin deficiency (disorder) Finding site Pancreatic structure false Inferred relationship Existential restriction modifier (core metadata concept) 1
Congenital pancreatic trypsin deficiency (disorder) Finding site Digestive organ structure (body structure) false Inferred relationship Existential restriction modifier (core metadata concept) 2
Congenital pancreatic trypsin deficiency (disorder) Finding site Pancreatic structure false Inferred relationship Existential restriction modifier (core metadata concept) 2
Congenital pancreatic trypsin deficiency (disorder) Associated morphology anomalie congénitale false Inferred relationship Existential restriction modifier (core metadata concept) 2
Congenital pancreatic trypsin deficiency (disorder) Is a Congenital disease true Inferred relationship Existential restriction modifier (core metadata concept)
Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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