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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
747441000052118 medfödd brist på pankreatiskt trypsin sv Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Sweden NRC maintained module (core metadata concept)


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Congenital pancreatic trypsin deficiency (disorder) Is a kongenital anomali i pankreas false Inferred relationship Some
Congenital pancreatic trypsin deficiency (disorder) Finding site Pancreatic structure false Inferred relationship Some 1
Congenital pancreatic trypsin deficiency (disorder) Occurrence Congenital false Inferred relationship Some
Congenital pancreatic trypsin deficiency (disorder) Associated morphology utvecklingsabnormitet false Inferred relationship Some 1
Congenital pancreatic trypsin deficiency (disorder) Associated morphology medfödd brist false Inferred relationship Some 1
Congenital pancreatic trypsin deficiency (disorder) Finding site Digestive organ structure false Inferred relationship Some 1
Congenital pancreatic trypsin deficiency (disorder) Is a Deficiency of trypsin true Inferred relationship Some
Congenital pancreatic trypsin deficiency (disorder) Occurrence Congenital true Inferred relationship Some 1
Congenital pancreatic trypsin deficiency (disorder) Associated morphology kongenital anomali false Inferred relationship Some 1
Congenital pancreatic trypsin deficiency (disorder) Finding site Digestive organ structure false Inferred relationship Some 1
Congenital pancreatic trypsin deficiency (disorder) Associated morphology kongenital anomali false Inferred relationship Some 2
Congenital pancreatic trypsin deficiency (disorder) Associated morphology medfödd brist false Inferred relationship Some 1
Congenital pancreatic trypsin deficiency (disorder) Finding site Pancreatic structure false Inferred relationship Some 1
Congenital pancreatic trypsin deficiency (disorder) Finding site Digestive organ structure false Inferred relationship Some 2
Congenital pancreatic trypsin deficiency (disorder) Finding site Pancreatic structure false Inferred relationship Some 2
Congenital pancreatic trypsin deficiency (disorder) Associated morphology kongenital anomali false Inferred relationship Some 2
Congenital pancreatic trypsin deficiency (disorder) Is a Congenital disease (disorder) true Inferred relationship Some

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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