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54119007: Congenital pancreatic trypsin 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
89950015 Congenital pancreatic trypsin deficiency en Synonym Active Entire term case insensitive SNOMED CT core module
792315014 Congenital pancreatic trypsin 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
Congenital pancreatic trypsin deficiency Is a Congenital anomaly of pancreas false Inferred relationship Existential restriction modifier
Congenital pancreatic trypsin deficiency Finding site Pancreatic structure false Inferred relationship Existential restriction modifier 1
Congenital pancreatic trypsin deficiency Occurrence Congenital false Inferred relationship Existential restriction modifier
Congenital pancreatic trypsin deficiency Associated morphology Developmental anomaly false Inferred relationship Existential restriction modifier 1
Congenital pancreatic trypsin deficiency Associated morphology Congenital deficiency false Inferred relationship Existential restriction modifier 1
Congenital pancreatic trypsin deficiency Finding site Digestive organ structure false Inferred relationship Existential restriction modifier 1
Congenital pancreatic trypsin deficiency Is a Deficiency of trypsin true Inferred relationship Existential restriction modifier
Congenital pancreatic trypsin deficiency Occurrence Congenital true Inferred relationship Existential restriction modifier 1
Congenital pancreatic trypsin deficiency Associated morphology Congenital anomaly false Inferred relationship Existential restriction modifier 1
Congenital pancreatic trypsin deficiency Finding site Digestive organ structure false Inferred relationship Existential restriction modifier 1
Congenital pancreatic trypsin deficiency Associated morphology Congenital anomaly false Inferred relationship Existential restriction modifier 2
Congenital pancreatic trypsin deficiency Associated morphology Congenital deficiency false Inferred relationship Existential restriction modifier 1
Congenital pancreatic trypsin deficiency Finding site Pancreatic structure false Inferred relationship Existential restriction modifier 1
Congenital pancreatic trypsin deficiency Finding site Digestive organ structure false Inferred relationship Existential restriction modifier 2
Congenital pancreatic trypsin deficiency Finding site Pancreatic structure false Inferred relationship Existential restriction modifier 2
Congenital pancreatic trypsin deficiency Associated morphology Congenital anomaly false Inferred relationship Existential restriction modifier 2
Congenital pancreatic trypsin deficiency Is a Congenital disease true 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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